Emotional Intelligence Report |Multiple Myeloma

Surface Behaviors Show All

  1. Seeking medical advice
  2. Seeking emotional support
  3. Managing side effects
  4. Reflecting on the impact of the disease
  5. Sharing personal experiences and condolences
  6. Engaging in self-care activities
  7. Monitoring progress
  8. Starting treatment
  9. Taking prescribed medication
  10. Emotional distress
  11. Experiencing side effects
  12. Fatigue
  13. Initial symptoms
  14. Sharing personal experiences
  15. Sharing personal experiences and stories
  16. Adhering to treatment plan
  17. Attending medical appointments
  18. Difficulty concentrating
  19. Difficulty sleeping
  20. Expressing gratitude
  21. Offering condolences and sympathy
  22. Offering prayers and well wishes
  23. Prioritizing mental health
  24. Seeking second opinions
  25. Attending follow-up appointments
  26. Diagnosis of cancer
  27. Discussing treatment options with healthcare providers
  28. Emotional ups and downs
  29. Expressing empathy and support
  30. Expressing empathy and understanding

Vulnerable Moments

S. No. Moments Content
1 Receiving diagnosis Link Content
2 Adjusting to lifestyle changes Link Content
3 Receiving a diagnosis Link Content
4 Waiting for test results Link Content
5 Coping with emotional distress Link Content
6 Emotional distress Link Content
7 Experiencing side effects Link Content
8 Feeling exposed and in need of support Link Content
9 Navigating healthcare system Link Content
10 Starting treatment Link Content
11 Coping with physical limitations Link Content
12 Coping with the loss of a loved one Link Content
13 Disease progression Link Content
14 Facing end-of-life decisions Link Content
15 Facing treatment decisions Link Content
16 Facing uncertainty about the future Link Content
17 Feeling burnt out as a caregiver Link Content
18 Hospitalization Link Content
19 Managing financial burden Link Content
20 Receiving the cancer diagnosis Link Content
21 Transitioning between healthcare providers Link Content
22 Uncertainty about the future Link Content
23 Coping with pain or discomfort Link Content
24 End-of-life discussions Link Content
25 Experiencing a relapse Link Content
26 Experiencing disease progression Link Content
27 Experiencing emotional distress Link Content
28 Experiencing grief and sadness Link Content
29 Facing financial challenges Link Content
30 Feeling shaken by grief Link Content
31 Feeling the loss of a loved one Link Content
32 Initial diagnosis Link Content
33 Managing emotional distress Link Content
34 Managing financial burdens Link Content
35 Needing support and understanding Link Content
36 Receiving the diagnosis Link Content
37 Adjusting to new routines Link Content
38 Balancing hope and acceptance Link Content
39 Concerns about treatment effectiveness Link Content
40 Coping with emotional and psychological impact Link Content
41 Coping with the emotional impact of the disease Link Content
42 Coping with uncertainty Link Content
43 Dealing with emotional distress Link Content
44 Dealing with pain and discomfort Link Content
45 Dealing with physical pain Link Content
46 Dealing with side effects Link Content
47 Dealing with side effects of treatment Link Content
48 Dealing with the uncertainty of the future Link Content
49 Dealing with treatment side effects Link Content
50 Dealing with uncertainty Link Content
51 Dealing with uncertainty about the future Link Content
52 Dealing with ups and downs of the disease Link Content
53 Devastation over the loss of a loved one Link Content
54 Diagnosis of the disease Link Content
55 Embarking on the caregiving journey Link Content
56 Emotional impact of diagnosis Link Content
57 Emotional rollercoaster Link Content
58 Experiencing setbacks Link Content
59 Experiencing uncertainty about the future Link Content
60 Facing disease progression Link Content
61 Facing financial challenges related to treatment Link Content
62 Fear of relapse Link Content
63 Feeling exposed Link Content
64 Feeling isolated and alone in the journey Link Content
65 Feeling isolated or misunderstood Link Content
66 Feeling isolated or misunderstood by others Link Content
67 Feeling overwhelmed Link Content
68 Feeling the pain of loss and grief Link Content
69 Feeling uncertain about the future Link Content
70 Financial burden Link Content
71 Financial strain Link Content
72 Going through surgery and treatment Link Content
73 Hearing the diagnosis for the first time Link Content
74 Initial diagnosis and realization of the severity of the disease Link Content
75 Longing for peace and closure Link Content
76 Longing for the presence and guidance of the deceased Link Content
77 Making treatment decisions Link Content
78 Managing emotional and mental well-being Link Content
79 Navigating end-of-life decisions Link Content
80 Near-death experience in the hospital Link Content
81 Need for emotional support Link Content
82 Need for support Link Content
83 Needing comfort and support Link Content
84 Needing emotional support Link Content
85 Needing support Link Content
86 Newly diagnosed patients facing an uncertain future Link Content
87 Preparing for end-of-life decisions Link Content
88 Receiving a diagnosis of myeloma Link Content
89 Receiving the call from the doctor Link Content
90 Receiving the initial diagnosis Link Content
91 Reflecting on the loss of a loved one Link Content
92 Reflecting on the loss of young patients Link Content
93 Seeking advice and experiences from others Link Content
94 Seeking comfort and solace in others' experiences Link Content
95 Seeking emotional support Link Content
96 Seeking guidance and advice Link Content
97 Seeking social support Link Content
98 Seeking support and guidance from healthcare professionals Link Content
99 Seeking support from loved ones Link Content
100 Seeking validation and understanding Link Content
101 Sharing personal experiences of loss Link Content
102 Sharing personal struggles Link Content
103 Starting a new treatment Link Content
104 Transitioning to palliative care Link Content
105 Uncertainty about prognosis Link Content
106 Uncertainty about the duration of remission Link Content
107 Uncertainty about the effectiveness of treatment Link Content
108 Uncertainty about treatment effectiveness Link Content
109 Uncertainty about treatment options Link Content
110 Upon receiving the diagnosis Link Content
111 Witnessing the deterioration of health Link Content
112 Abnormal brain scan patterns Link Content
113 Accepting that there are no more options Link Content
114 Acknowledging the impact on daily life Link Content
115 Acknowledging the limited time remaining Link Content
116 Acknowledging the mother's struggle Link Content
117 Acknowledging the shared fear and dread among others affected by cancer Link Content
118 Acknowledging vulnerability and fear Link Content
119 Adjusting to changes in appearance Link Content
120 Adjusting to changes in appearance or abilities Link Content
121 Adjusting to changes in appetite and dietary restrictions Link Content
122 Adjusting to changes in daily life and routines Link Content
123 Adjusting to changes in relationships Link Content
124 Adjusting to life after treatment Link Content
125 Adjusting to life without the father Link Content
126 Adjusting to new lifestyle Link Content
127 Adjusting to new treatment Link Content
128 Adjusting to physical and emotional changes Link Content
129 Adjusting to self-administering injections Link Content
130 Adjusting to the change in plans and dreams Link Content
131 After a progression of the disease Link Content
132 After ASCT (autologous stem cell transplant) Link Content
133 After being hospitalized due to a fall and receiving the diagnosis Link Content
134 After experiencing a seizure Link Content
135 After SCT failure Link Content
136 After second chemo dose Link Content
137 After taking the 10th dose without Darzalex Link Content
138 After taking the 9th dose without Darzalex Link Content
139 After the first heart attack Link Content
140 After the second heart attack Link Content
141 Allowing oneself to grieve Link Content
142 Alone in the hospital room after diagnosis Link Content
143 Anniversaries or special occasions Link Content
144 Anniversary of Dad's passing Link Content
145 Anticipating the challenges ahead Link Content
146 Anticipating the impact of treatment decisions on the journey Link Content
147 Anticipation of relapse and limited treatment options Link Content
148 Anxiety about long-lasting sequelae Link Content
149 Anxiety about potential differences in treatment options between countries Link Content
150 Anxiety and depression related to cancer diagnosis Link Content
151 Anxiety during bouts of tachycardia Link Content
152 Anxiety during the bone marrow biopsy Link Content
153 Apologies for having to rely on someone Link Content
154 Appointment with neurologist Link Content
155 Appreciating the growth in love Link Content
156 Appreciating the support received Link Content
157 Attending the first immediate family wedding Link Content
158 Awareness of the unpredictability of life Link Content
159 Bacteremia diagnosis Link Content
160 Balancing caregiver responsibilities Link Content
161 Balancing caregiving responsibilities Link Content
162 Balancing caregiving responsibilities with personal life Link Content
163 Balancing caregiving responsibilities with personal needs Link Content
164 Balancing hope and fear during treatment Link Content
165 Balancing hope and realism in the face of remission Link Content
166 Balancing medical treatment with maintaining social connections Link Content
167 Balancing personal and caregiving responsibilities Link Content
168 Balancing personal and family perspectives Link Content
169 Balancing personal and family responsibilities Link Content
170 Balancing personal needs with caregiving responsibilities Link Content
171 Balancing quality of life with safety considerations Link Content
172 Balancing the desire for improvement with the need for caution Link Content
173 Balancing work and health Link Content
174 Balancing work and pain Link Content
175 Battling deep anxieties Link Content
176 Battling multiple illnesses Link Content
177 Battling with multiple serious illnesses Link Content
178 Before and during stem cell transplant Link Content
179 Before starting the treatment Link Content
180 Before stem cell collection and surgery Link Content
181 Being a caregiver for a loved one Link Content
182 Being alone in the hospital room when receiving the diagnosis Link Content
183 Being away from home during the diagnosis Link Content
184 Being back in the caregiver's business Link Content
185 Being diagnosed for a whole month Link Content
186 Being diagnosed with Multiple Myeloma and AL Amyloidosis Link Content
187 Being hospitalized and facing complications Link Content
188 Being in the hospital for an extended period Link Content
189 Being isolated in the hospital Link Content
190 Being officially declared in a coma Link Content
191 Being open to influence Link Content
192 Being open to influence and advice Link Content
193 Being open to influence and guidance Link Content
194 Being open to influence and guidance during the decision-making process Link Content
195 Being open to influence and guidance during the talk Link Content
196 Being open to influence and guidance from others Link Content
197 Being put in an induced coma Link Content
198 Being put on mechanical ventilation Link Content
199 Being recently diagnosed Link Content
200 Being told about remission Link Content
201 Being told about the long-lasting sequelae from the encephalitis Link Content
202 Being under extreme stress Link Content
203 Being with close family Link Content
204 Birthdays or holidays without them Link Content
205 Blood clot occurrence Link Content
206 Boarding the plane Link Content
207 Breaking down emotionally in front of spouse Link Content
208 Caregiver burnout Link Content
209 Caregiver feeling overwhelmed and unsure of how to support the patient Link Content
210 Catching Covid Link Content
211 Celebrating milestones without the person Link Content
212 Challenges in managing physical and emotional well-being Link Content
213 Changing retirement plans due to diagnosis Link Content
214 chudezee: Patient seeking information and support regarding their medical condition Link Content
215 Coma Link Content
216 Coming to terms with limited treatment options and prognosis Link Content
217 Coming to terms with myeloma mutation Link Content
218 Coming to terms with physical limitations Link Content
219 Coming to terms with the impact of the disease on family dynamics Link Content
220 Coming to terms with the reality of the disease Link Content
221 Communicating with healthcare providers Link Content
222 Communication limitations Link Content
223 Comparing their remission journey to others Link Content
224 Concern about hemoglobin levels Link Content
225 Concern about returning to work in January Link Content
226 Concern about the effectiveness of the medications Link Content
227 Concern about the implications of the decrease in kappa chain levels Link Content
228 Concern about the potential consequences of osteopenia (or osteoporosis) Link Content
229 Concern for family over oneself Link Content
230 Concern for the well-being of the family member Link Content
231 Concerns about appetite and weight loss Link Content
232 Concerns about changes in drug coverage and costs Link Content
233 Concerns about getting fired Link Content
234 Concerns about kidney health and potential complications Link Content
235 Concerns about preexisting conditions Link Content
236 Concerns about the impact on relationships, particularly with the spouse Link Content
237 Concerns about the myeloma condition Link Content
238 Concerns about the presence of clonal cells Link Content
239 Concerns about the severity of the fever Link Content
240 Concerns about the side effects of Thalidomide Link Content
241 Concerns about the stem cell transplant Link Content
242 Confronting the reality of the disease progression Link Content
243 Confusion about co-pays, deductibles, and prescription coverage Link Content
244 Confusion at times Link Content
245 Considering alternative healthcare options Link Content
246 Considering medical marijuana for appetite Link Content
247 Considering retiring due to pain and weariness Link Content
248 Considering the impact of RSV and flu season Link Content
249 Considering the impact of the fractured femur on candidacy for a stem cell transplant Link Content
250 Considering treatment options Link Content
251 Contemplating future health complications Link Content
252 Contemplating the impact of age on the virus Link Content
253 Contemplating the impact of the disease on life Link Content
254 Contemplating the impact of the disease on personal and professional life Link Content
255 Contemplating the impact on loved ones Link Content
256 Contemplating the possibility of dying in sleep Link Content
257 Controlling the parachute Link Content
258 Coping with exhaustion Link Content
259 Coping with fear and anxiety Link Content
260 Coping with financial burden Link Content
261 Coping with grief and sadness Link Content
262 Coping with humor Link Content
263 Coping with intense sciatic nerve pain Link Content
264 Coping with isolation and confinement during hospital stays Link Content
265 Coping with major life changes Link Content
266 Coping with ongoing treatment Link Content
267 Coping with pain management issues Link Content
268 Coping with physical and emotional pain Link Content
269 Coping with potential side effects Link Content
270 Coping with PTSD symptoms Link Content
271 Coping with setbacks or relapses Link Content
272 Coping with the burden of caregiving Link Content
273 Coping with the challenges of being a caregiver Link Content
274 Coping with the devastating loss of a loved one Link Content
275 Coping with the diagnosis of stage 3 + high-risk chromosome Link Content
276 Coping with the diagnosis of vasculitis Link Content
277 Coping with the emotional and physical toll of the journey Link Content
278 Coping with the emotional impact of a loved one's diagnosis Link Content
279 Coping with the fear and anxiety of the disease potentially resurfacing Link Content
280 Coping with the fear of disease progression Link Content
281 Coping with the fear of the disease coming back Link Content
282 Coping with the fear of the unknown and the impact of the disease on daily life Link Content
283 Coping with the financial burden of healthcare Link Content
284 Coping with the impact of the disease on personal life Link Content
285 Coping with the impact on daily life Link Content
286 Coping with the impact on relationships Link Content
287 Coping with the impending loss of a loved one Link Content
288 Coping with the loss of a parent Link Content
289 Coping with the loss of independence and physical decline Link Content
290 Coping with the non-curable and terminal nature of multiple myeloma Link Content
291 Coping with the odds of limited success Link Content
292 Coping with the physical and emotional challenges Link Content
293 Coping with the physical and emotional challenges after transplant Link Content
294 Coping with the physical and emotional toll of the disease Link Content
295 Coping with the potential side effects or complications of the procedure Link Content
296 Coping with the pressure to downplay results Link Content
297 Coping with the reality of an incurable disease Link Content
298 Coping with the realization that bones may never fully recover Link Content
299 Coping with the role reversal of caregiver and patient Link Content
300 Coping with the sense of loneliness Link Content
301 Coping with the stigma and lack of awareness surrounding bladder cancer Link Content
302 Coping with the stress and anxiety of supporting mother Link Content
303 Coping with the stress of the journey Link Content
304 Coping with the toll of infections and hospitalizations Link Content
305 Coping with the uncertainty of the disease Link Content
306 Coping with the uncertainty of the future Link Content
307 Coping with treatment side effects Link Content
308 Coping with uncertainty about treatment outcomes Link Content
309 Coping with unexpected challenges Link Content
310 Craving positive news Link Content
311 Craving understanding and empathy Link Content
312 Crying together Link Content
313 Dealing with a struggle that others can't relate to Link Content
314 Dealing with anxiety/depression Link Content
315 Dealing with bone lesions and the need for a walker Link Content
316 Dealing with boredom during the 2-3 week recovery period Link Content
317 Dealing with changes in relationships Link Content
318 Dealing with conflicting emotions and thoughts Link Content
319 Dealing with constant sickness of grandkids from day care centers Link Content
320 Dealing with continuous throat and lung infections Link Content
321 Dealing with criticism or judgment Link Content
322 Dealing with denied insurance claims Link Content
323 Dealing with disease progression Link Content
324 Dealing with emotional impact Link Content
325 Dealing with financial burden Link Content
326 Dealing with financial burden and potential loss of income due to CAR-T therapy Link Content
327 Dealing with financial burdens Link Content
328 Dealing with financial uncertainty Link Content
329 Dealing with grief and loss Link Content
330 Dealing with hair loss and its impact on self-image and confidence Link Content
331 Dealing with hindered mobility and fatigue Link Content
332 Dealing with limited treatment options Link Content
333 Dealing with loss of appetite and nausea Link Content
334 Dealing with low function kidneys and fractures Link Content
335 Dealing with multiple health complications Link Content
336 Dealing with muscle wasting Link Content
337 Dealing with pain and requiring extra pain medications Link Content
338 Dealing with pain or discomfort Link Content
339 Dealing with peripheral nerve damage Link Content
340 Dealing with physical pain and discomfort Link Content
341 Dealing with potential complications Link Content
342 Dealing with potential permanent disabilities Link Content
343 Dealing with potential side effects of treatment Link Content
344 Dealing with self-criticism Link Content
345 Dealing with setbacks Link Content
346 Dealing with severe back pain Link Content
347 Dealing with social stigma and misconceptions Link Content
348 Dealing with stigma Link Content
349 Dealing with stress or pressure Link Content
350 Dealing with symptoms and side effects without proper support Link Content
351 Dealing with the aftermath of a near-death experience Link Content
352 Dealing with the challenges of caregiving Link Content
353 Dealing with the consequences of mini strokes Link Content
354 Dealing with the distance from home and loved ones Link Content
355 Dealing with the emotional and physical challenges of the journey Link Content
356 Dealing with the emotional and physical challenges of treatment Link Content
357 Dealing with the emotional impact of a loved one's diagnosis Link Content
358 Dealing with the emotional impact of caregiving Link Content
359 Dealing with the emotional impact of losing a father Link Content
360 Dealing with the emotional impact of the disease Link Content
361 Dealing with the expectations and reactions of others Link Content
362 Dealing with the fear of cancer returning Link Content
363 Dealing with the fear of relapse Link Content
364 Dealing with the fear of the unknown Link Content
365 Dealing with the illness and impending loss of a parent Link Content
366 Dealing with the impact of the disease Link Content
367 Dealing with the impact on daily life Link Content
368 Dealing with the impending loss and mortality Link Content
369 Dealing with the insidious nature of the disease Link Content
370 Dealing with the long process of treatment Link Content
371 Dealing with the loss of freedom and independence Link Content
372 Dealing with the pain of losing a loved one Link Content
373 Dealing with the physical and emotional challenges of dialysis Link Content
374 Dealing with the physical and emotional challenges of treatment Link Content
375 Dealing with the physical and emotional impact of the disease Link Content
376 Dealing with the physical and emotional toll of cancer Link Content
377 Dealing with the physical and emotional toll of caregiving Link Content
378 Dealing with the reality of having an incurable cancer Link Content
379 Dealing with the uncertainty and fragility of life Link Content
380 Dealing with the uncertainty of the disease Link Content
381 Dealing with the uncertainty of the disease progression Link Content
382 Dealing with treatment-related challenges Link Content
383 Dealing with uncertainty and fear of the future Link Content
384 Dealing with unexpected complications and prolonged hospital stay Link Content
385 Dealing with unexpected health issues Link Content
386 Decision-making about medication options Link Content
387 Declining mental health Link Content
388 Delirium and extreme pain Link Content
389 Dependence on others for daily activities Link Content
390 Dependence on others for daily care Link Content
391 Depending on each other for support and care Link Content
392 Depressing thoughts Link Content
393 Describing the impact of the disease on daily life Link Content
394 Desire for a more permanent solution Link Content
395 Desire for a successful outcome Link Content
396 Desire for accurate explanation of the lab result Link Content
397 Desire for immediate answers Link Content
398 Desire for information on the appearance of urine and its significance Link Content
399 Desire for solid food and normal eating habits Link Content
400 Desire for support and guidance Link Content
401 Desire to take care of her for longer Link Content
402 Desiring comfort and solace Link Content
403 Development of depression Link Content
404 Development of hospital-acquired pneumonia Link Content
405 Development of pneumonia Link Content
406 Diagnosed with AL and MM Link Content
407 Diagnosis Link Content
408 Diagnosis and hospitalization Link Content
409 Diagnosis at 30 years old Link Content
410 Diagnosis disclosure Link Content
411 Diagnosis of herpes zoster encephalitis Link Content
412 Diagnosis of ischemic stroke Link Content
413 Diagnosis of MM Link Content
414 Diagnosis of multiple myeloma Link Content
415 Diagnosis of Multiple Myeloma and AL Amyloidosis Link Content
416 Diagnosis of Plasma Cell Leukemia Link Content
417 Dialysis Link Content
418 Difficulty breathing Link Content
419 Difficulty falling asleep Link Content
420 Difficulty maintaining normal blood levels Link Content
421 Difficulty navigating healthcare system Link Content
422 Difficulty walking and standing Link Content
423 Discovering cytogenetics weren't great Link Content
424 Discovering the arm is broken Link Content
425 Discovering the diagnosis of multiple myeloma after fracturing his femur Link Content
426 Discovering the misdiagnosis and the true disease state Link Content
427 Discovering the presence of white spots on the brain scan Link Content
428 Discovering the seriousness of herpes zoster encephalitis Link Content
429 Discovering the true cause of shoulder pain Link Content
430 Discovering the true cause of the pain Link Content
431 Discussing financial burden Link Content
432 Discussing impact on daily life Link Content
433 Doubt about the individual's capability for the job Link Content
434 Doubt and uncertainty about the future Link Content
435 Doubting one's abilities Link Content
436 Doubting one's strength and ability to prevail Link Content
437 Doubting the effectiveness of the next round of treatment Link Content
438 Doubting the effectiveness of the next treatment Link Content
439 Doubts about the ability to provide for loved ones Link Content
440 During air chopper rides Link Content
441 During DKRd treatment Link Content
442 During hospitalization Link Content
443 During initial treatment Link Content
444 During lifestyle adjustments Link Content
445 During medical appointments Link Content
446 During the first cycle of treatment Link Content
447 During the hospitalization Link Content
448 During the recovery period Link Content
449 During the slow improvement of her condition Link Content
450 During the stent placement procedures Link Content
451 Edema and swelling Link Content
452 Embracing the uncertainty of the future Link Content
453 Emotional and physical strain of being a caregiver Link Content
454 Emotional and psychological challenges of living with a chronic illness Link Content
455 Emotional and psychological impact of cancer diagnosis Link Content
456 Emotional distress due to the severity of the situation Link Content
457 Emotional distress from grim outlook Link Content
458 Emotional distress upon diagnosis Link Content
459 Emotional exhaustion Link Content
460 Emotional fatigue from constant tiredness Link Content
461 Emotional impact of being rediagnosed Link Content
462 Emotional impact of the diagnosis Link Content
463 Emotional impact on the patient and family Link Content
464 Emotional processing of the situation Link Content
465 Emotional response to positive progress and hope Link Content
466 Emotional vulnerability Link Content
467 Emotional vulnerability due to the anticipation of the procedure Link Content
468 Emotional vulnerability due to the unpredictability of the disease Link Content
469 Emotional vulnerability due to young age and life plans Link Content
470 Emotional vulnerability during the journey Link Content
471 End of second month of chemo Link Content
472 Evaluating the affordability of healthcare services Link Content
473 Evaluating the safety of different environments Link Content
474 Excitement about future plans Link Content
475 Exhaustion from lack of sleep Link Content
476 Experiencing a burning sensation Link Content
477 Experiencing a change in health status Link Content
478 Experiencing a decline in health and breathing difficulties Link Content
479 Experiencing a mix of emotions, including guilt and sadness Link Content
480 Experiencing a range of emotions, including relief, numbness, and uncertainty Link Content
481 Experiencing a reaction to the new treatment Link Content
482 Experiencing a relapse after being cancer-free Link Content
483 Experiencing a sense of helplessness and uncertainty Link Content
484 Experiencing a sense of helplessness or being unable to find the right words Link Content
485 Experiencing anxiety and stress Link Content
486 Experiencing anxiety and uncertainty about the future Link Content
487 Experiencing anxiety during the waiting period Link Content
488 Experiencing back pain and lesions Link Content
489 Experiencing diarrhea or c-diff diarrhea Link Content
490 Experiencing difficulty in concentration Link Content
491 Experiencing difficulty in handling and accepting the situation Link Content
492 Experiencing disease progression or relapse Link Content
493 Experiencing doubt and uncertainty Link Content
494 Experiencing doubts and concerns about physical capabilities and energy levels Link Content
495 Experiencing embarrassment and frustration due to medical procedures and mishaps Link Content
496 Experiencing emotional and mental strain Link Content
497 Experiencing emotional challenges Link Content
498 Experiencing emotional distress related to the disease and treatment Link Content
499 Experiencing emotional exhaustion Link Content
500 Experiencing emotional numbness after achieving remission Link Content
501 Experiencing extreme stress, which may increase vulnerability Link Content
502 Experiencing fear and sadness due to the diagnosis of plasma cell leukemia Link Content
503 Experiencing fear and uncertainty Link Content
504 Experiencing fear and uncertainty about disease progression Link Content
505 Experiencing fear of failure Link Content
506 Experiencing frustration and fear due to infections Link Content
507 Experiencing frustration and impatience with the waiting period Link Content
508 Experiencing grief and loss Link Content
509 Experiencing grief and the need to mourn Link Content
510 Experiencing intense pain and discomfort Link Content
511 Experiencing isolation and loneliness Link Content
512 Experiencing loneliness and isolation Link Content
513 Experiencing loss Link Content
514 Experiencing mental confusion and Car T Cells found in spinal fluid Link Content
515 Experiencing moments of fear and vulnerability Link Content
516 Experiencing mood swings Link Content
517 Experiencing more seizures after opening eyes Link Content
518 Experiencing mouth and throat discomfort during treatment Link Content
519 Experiencing mouth sores Link Content
520 Experiencing nausea and difficulty eating Link Content
521 Experiencing nausea and needing medication Link Content
522 Experiencing numbness and uncertainty despite reaching remission Link Content
523 Experiencing pain or discomfort Link Content
524 Experiencing pain that affects daily activities Link Content
525 Experiencing physical and emotional pain Link Content
526 Experiencing physical and emotional side effects of CAR-T therapy Link Content
527 Experiencing physical limitations that may impact treatment options Link Content
528 Experiencing physical pain Link Content
529 Experiencing relapse and failed treatments Link Content
530 Experiencing relapse and growth of lesions Link Content
531 Experiencing relapse and the growth of new lesions Link Content
532 Experiencing relapse or worsening symptoms Link Content
533 Experiencing setbacks or failures Link Content
534 Experiencing severe fractures Link Content
535 Experiencing side effects and complications during treatment Link Content
536 Experiencing side effects of treatment Link Content
537 Experiencing stress and anxiety during the journey Link Content
538 Experiencing the desire to vent and express emotions Link Content
539 Experiencing the emotional impact of the situation Link Content
540 Experiencing the fear of losing the person Link Content
541 Experiencing the first holiday or special occasion without the loved one Link Content
542 Experiencing the hardships of the disease Link Content
543 Experiencing the loss of hope and uncertainty Link Content
544 Experiencing the loss of hope for recovery Link Content
545 Experiencing the progression of myeloma in bone marrow and kidneys Link Content
546 Experiencing the side effects of dexamethasone Link Content
547 Experiencing the suddenness and speed of the loss Link Content
548 Experiencing the ups and downs of the journey Link Content
549 Experiencing transfusion reactions and needing support Link Content
550 Experiencing treatment setbacks Link Content
551 Experiencing treatment side effects Link Content
552 Experiencing uncertainty about the effectiveness of the treatment Link Content
553 Experiencing uncertainty about the right treatment option Link Content
554 Experiencing uncertainty and anxiety about treatment options and outcomes Link Content
555 Experiencing uncertainty and needing support during treatment Link Content
556 Experiencing worsening symptoms despite improving blood markers Link Content
557 Expressing a deeper connection to the loss experienced Link Content
558 Expressing a need for more effective treatments Link Content
559 Expressing appreciation for hearing about treatment experiences from others Link Content
560 Expressing concern for the well-being of the family Link Content
561 Expressing concerns about the ability to work while undergoing treatment Link Content
562 Expressing deep sorrow and loss Link Content
563 Expressing empathy towards the writer Link Content
564 Expressing fear and anxiety Link Content
565 Expressing fear and worry Link Content
566 Expressing fear or anxiety Link Content
567 Expressing frustration and impatience Link Content
568 Expressing frustration or impatience Link Content
569 Expressing gratitude for finding comfort in others' shared experiences Link Content
570 Expressing gratitude for hearing from others going through similar experiences Link Content
571 Expressing gratitude for hearing from someone going through similar experiences Link Content
572 Expressing love and fear of losing mom Link Content
573 Expressing sadness and empathy Link Content
574 Expressing sadness and grief Link Content
575 Expressing sorrow for the family's pain Link Content
576 Expressing sympathy and support Link Content
577 Expressing the need for comfort and peace Link Content
578 Expressing the need for support and love Link Content
579 Expressing the need for time to fully process and accept the remission status Link Content
580 Expressing the ongoing impact of losing a parent Link Content
581 Expressing the shortness of time spent with the deceased Link Content
582 Expressing uncertainty and the need for pain management Link Content
583 Expressing uncertainty or confusion Link Content
584 Expressing vulnerability and emotional pain Link Content
585 Expressing vulnerability and gratitude towards wife Link Content
586 Expressing vulnerability and sadness Link Content
587 Expressing vulnerability and seeking comfort Link Content
588 Expressing worry and concern Link Content
589 Expressing worry for the future Link Content
590 Extreme hip pain Link Content
591 Facing a new season in life without a mother Link Content
592 Facing an uncertain future Link Content
593 Facing challenges in maintaining weight and body functioning Link Content
594 Facing declining physical and mental health Link Content
595 Facing difficult conversations and decisions with loved ones about the cancer journey Link Content
596 Facing external pressure Link Content
597 Facing fear and dread of cancer Link Content
598 Facing fear and dread related to cancer Link Content
599 Facing financial burdens Link Content
600 Facing high levels of free kappa light chains Link Content
601 Facing immediate neck surgery Link Content
602 Facing limited remission Link Content
603 Facing migraines or similar issues and needing medication Link Content
604 Facing mortality Link Content
605 Facing potential relapse Link Content
606 Facing potential relapses or complications Link Content
607 Facing potential side effects or complications Link Content
608 Facing relapse and uncertainty about future treatment options Link Content
609 Facing setbacks and challenges along the way Link Content
610 Facing social stigma Link Content
611 Facing stigma or discrimination Link Content
612 Facing the challenge of living without the deceased Link Content
613 Facing the challenges of caregiving Link Content
614 Facing the challenges of treatment Link Content
615 Facing the decision between standard treatment and clinical trial Link Content
616 Facing the decision of undergoing stem cell transplant Link Content
617 Facing the decision of whether or not to undergo a spinal tap Link Content
618 Facing the diagnosis of stage 1 MM Link Content
619 Facing the end-of-life stage Link Content
620 Facing the fear of losing a loved one Link Content
621 Facing the fear of losing independence and control Link Content
622 Facing the first holidays and special occasions without the loved one Link Content
623 Facing the ineffectiveness of previous regimen Link Content
624 Facing the limited time remaining Link Content
625 Facing the need for CAR-T treatment Link Content
626 Facing the possibility of a downturn in health Link Content
627 Facing the possibility of cancer recurrence Link Content
628 Facing the possibility of disease relapse or progression after CAR-T therapy Link Content
629 Facing the possibility of losing a loved one Link Content
630 Facing the possibility of permanent consequences from surgery Link Content
631 Facing the possibility of preparing for the worst Link Content
632 Facing the possibility of protein deposits in the kidneys Link Content
633 Facing the possibility of relapse Link Content
634 Facing the progression of the disease Link Content
635 Facing the prospect of intense chemotherapy Link Content
636 Facing the reality of a cancer diagnosis Link Content
637 Facing the reality of a difficult journey Link Content
638 Facing the reality of a life without parental guidance Link Content
639 Facing the reality of a non-curable and terminal disease Link Content
640 Facing the reality of a terminal illness Link Content
641 Facing the reality of a terrible disease Link Content
642 Facing the reality of life without a loved one Link Content
643 Facing the reality of limited time on Earth Link Content
644 Facing the reality of loss Link Content
645 Facing the reality of mortality and the impact on family relationships Link Content
646 Facing the slow process of repairing lesion areas Link Content
647 Facing the uncertainty and anticipation before the transplant Link Content
648 Facing the uncertainty of a high-risk chromosome Link Content
649 Facing the uncertainty of future tests and scans Link Content
650 Facing the uncertainty of recovery Link Content
651 Facing the uncertainty of the future without the loved one Link Content
652 Facing treatment failure Link Content
653 Facing treatment side effects Link Content
654 Facing treatment uncertainty Link Content
655 Facing treatment-related complications Link Content
656 Facing treatment-related uncertainties Link Content
657 Facing uncertainty Link Content
658 Facing uncertainty about the prognosis Link Content
659 Facing uncertainty and fear Link Content
660 Facing uncertainty and fear about the future Link Content
661 Facing uncertainty and fear after receiving unexpected test results Link Content
662 Facing uncertainty and unpredictability of the disease Link Content
663 Facing unexpected challenges Link Content
664 Facing unexpected leave of absence Link Content
665 Facing unexpected medical expenses Link Content
666 Facing vulnerability to other health issues Link Content
667 Failed chemotherapy treatment Link Content
668 Family gatherings without them Link Content
669 Fatigue and brain fog Link Content
670 Fear and anxiety about the diagnosis and treatment Link Content
671 Fear and anxiety during weekly blood work Link Content
672 Fear of a positive result Link Content
673 Fear of burdening others with the illness Link Content
674 Fear of catching anything Link Content
675 Fear of complications Link Content
676 Fear of developing shingles Link Content
677 Fear of diagnosis Link Content
678 Fear of disease progression or relapse Link Content
679 Fear of having MM Link Content
680 Fear of losing income and insurance Link Content
681 Fear of losing mentor, confidante, and best friend Link Content
682 Fear of needing dialysis Link Content
683 Fear of not being able to handle the physical and mental demands Link Content
684 Fear of not fully recovering Link Content
685 Fear of potential complications or side effects Link Content
686 Fear of recurrence or progression Link Content
687 Fear of recurrence or progression of cancer Link Content
688 Fear of remaining bedridden Link Content
689 Fear of running out of treatment options Link Content
690 Fear of the disease progressing Link Content
691 Fear of the mass not responding to any treatment Link Content
692 Fear of worsening bone or organ damage Link Content
693 Fear of worsening health Link Content
694 Fearing the potential complications and consequences of a delayed diagnosis Link Content
695 Feeling a loss of identity Link Content
696 Feeling a sense of despair and longing for a better outcome Link Content
697 Feeling a sense of disbelief and frustration about the situation Link Content
698 Feeling a sense of urgency to gather information and make informed decisions Link Content
699 Feeling alone and in need of support Link Content
700 Feeling alone and isolated Link Content
701 Feeling alone in dealing with the disease Link Content
702 Feeling alone in the diagnosis and seeking connection with others Link Content
703 Feeling alone in the diagnosis of MM and AL Amyloidosis Link Content
704 Feeling alone in the struggle Link Content
705 Feeling anxious about dexamethasone side effects Link Content
706 Feeling anxious about test results Link Content
707 Feeling anxious about the possibility of spots still appearing on bones Link Content
708 Feeling anxious and concerned about the potential risks during treatment Link Content
709 Feeling anxious and scared about the possibility of having a serious condition Link Content
710 Feeling anxious and unable to sleep Link Content
711 Feeling anxious and uncertain Link Content
712 Feeling anxious and worried about the future Link Content
713 Feeling anxious before undergoing Autologous SCT Link Content
714 Feeling anxious or worried about the procedure Link Content
715 Feeling anxious or worried about the upcoming MRI results Link Content
716 Feeling anxious upon receiving the call about abnormal test result Link Content
717 Feeling at a loss for words Link Content
718 Feeling betrayed and angry towards the doctor for not taking action earlier Link Content
719 Feeling better since treatment started Link Content
720 Feeling bored and isolated during the recovery period Link Content
721 Feeling cleared and free from restrictions Link Content
722 Feeling clueless about insurance plans Link Content
723 Feeling cold or unable to regulate body temperature Link Content
724 Feeling concerned about the severity of HZE Link Content
725 Feeling confused about the diagnosis Link Content
726 Feeling curious and uncertain about the treatment Link Content
727 Feeling dependent on someone else for help Link Content
728 Feeling determined to not be broken Link Content
729 Feeling discomfort and sore throat Link Content
730 Feeling discomfort and soreness in the throat Link Content
731 Feeling discomfort due to body temperature fluctuations Link Content
732 Feeling emotionally drained and exhausted Link Content
733 Feeling emotionally drained and overwhelmed Link Content
734 Feeling emotionally drained from the long journey Link Content
735 Feeling emotionally exposed and fragile Link Content
736 Feeling emotionally exposed and in need of support Link Content
737 Feeling exhausted after a long day Link Content
738 Feeling exhausted and overwhelmed Link Content
739 Feeling exposed after being released from the hospital Link Content
740 Feeling exposed and anxious about potential illness exposure Link Content
741 Feeling exposed and anxious about the disease progression Link Content
742 Feeling exposed and emotional when sharing the diagnosis with spouse Link Content
743 Feeling exposed and in need of support during Bronchitis diagnosis Link Content
744 Feeling exposed and in need of support during C-diff diagnosis Link Content
745 Feeling exposed and in need of support during Covid-19 diagnosis Link Content
746 Feeling exposed and in need of support during Pneumonia diagnosis Link Content
747 Feeling exposed and in need of support during the decision-making process Link Content
748 Feeling exposed and in need of support during the onset of symptoms Link Content
749 Feeling exposed and in need of support during the wait for SCT Link Content
750 Feeling exposed and in need of support while going through treatment Link Content
751 Feeling exposed and in need of support while learning about multiple myeloma treatment Link Content
752 Feeling exposed and in need of support while navigating the myeloma journey Link Content
753 Feeling exposed and needing support after diagnosis Link Content
754 Feeling exposed and needing support after receiving an anticlimactic response Link Content
755 Feeling exposed and needing support while using phone Link Content
756 Feeling exposed and scared during the disease journey Link Content
757 Feeling exposed and uncertain about the effectiveness of vertebra binding Link Content
758 Feeling exposed and uncertain about the future after achieving remission Link Content
759 Feeling exposed and uncertain about the limited time Link Content
760 Feeling exposed and uncertain about the limited time in remission Link Content
761 Feeling exposed and uncertain about the symptoms Link Content
762 Feeling exposed and uncertain about treatment effectiveness Link Content
763 Feeling exposed and vulnerable Link Content
764 Feeling exposed and vulnerable due to the disease Link Content
765 Feeling exposed and vulnerable due to the possibility of spots still appearing on bones Link Content
766 Feeling exposed and vulnerable during medical appointments Link Content
767 Feeling exposed due to a compromised immune system Link Content
768 Feeling exposed due to family's expectations Link Content
769 Feeling exposed due to ongoing treatment Link Content
770 Feeling exposed due to pre-existing myoproliferative disease Link Content
771 Feeling exposed during hospitalization Link Content
772 Feeling exposed during port access Link Content
773 Feeling exposed during rediagnosis Link Content
774 Feeling exposed in standard men's shirts Link Content
775 Feeling exposed to potential risks Link Content
776 Feeling exposed to the possibility of the disease returning Link Content
777 Feeling exposed while sitting next to people in a theater Link Content
778 Feeling exposed while walking past people in a grocery store Link Content
779 Feeling fatigued and vulnerable due to illness Link Content
780 Feeling fatigued and weak Link Content
781 Feeling fragile and unable to lift Link Content
782 Feeling frightened and questioning after diagnosis Link Content
783 Feeling frustrated and overwhelmed Link Content
784 Feeling frustrated and overwhelmed by the long-term nature of the disease Link Content
785 Feeling grief and sadness Link Content
786 Feeling guilty for not doing enough Link Content
787 Feeling held hostage by the situation Link Content
788 Feeling helpless and overwhelmed Link Content
789 Feeling helpless and powerless Link Content
790 Feeling helpless and unsure about how to cope with the situation Link Content
791 Feeling helpless due to pain Link Content
792 Feeling helpless with limited treatment options Link Content
793 Feeling hopeful but uncertain about the effectiveness of teclistamab Link Content
794 Feeling hopeless and in need of encouragement Link Content
795 Feeling hopeless and lacking motivation to continue Link Content
796 Feeling isolated Link Content
797 Feeling isolated and alone Link Content
798 Feeling isolated and disconnected from others Link Content
799 Feeling isolated and in need of support Link Content
800 Feeling isolated and lonely Link Content
801 Feeling isolated and lonely while staying away from others Link Content
802 Feeling isolated and misunderstood by the medical community due to atypical symptoms or age Link Content
803 Feeling isolated and restricted Link Content
804 Feeling isolated or lonely Link Content
805 Feeling jarring mismatch between care team's excitement and personal feelings Link Content
806 Feeling let down by the healthcare system Link Content
807 Feeling like an old man Link Content
808 Feeling like the world is ending Link Content
809 Feeling lonely or isolated Link Content
810 Feeling miserable in the tiny room Link Content
811 Feeling of frustration and helplessness due to limited movement Link Content
812 Feeling of numbness and tingling Link Content
813 Feeling overwhelmed and confused Link Content
814 Feeling overwhelmed and confused after the diagnosis Link Content
815 Feeling overwhelmed and helpless Link Content
816 Feeling overwhelmed and in need of support Link Content
817 Feeling overwhelmed and scared about dealing with a serious illness at a young age Link Content
818 Feeling overwhelmed by emotions Link Content
819 Feeling overwhelmed by medical information Link Content
820 Feeling overwhelmed by medical information and decisions Link Content
821 Feeling overwhelmed by the amount of information to process Link Content
822 Feeling overwhelmed by the challenges of relapsed multiple myeloma Link Content
823 Feeling overwhelmed by the changes Link Content
824 Feeling overwhelmed by the complexity of myeloma treatments and information Link Content
825 Feeling overwhelmed by the complexity of the disease and treatment Link Content
826 Feeling overwhelmed by the diagnosis Link Content
827 Feeling overwhelmed by the diagnosis and treatment options Link Content
828 Feeling overwhelmed by the disease Link Content
829 Feeling overwhelmed by the duration of the journey Link Content
830 Feeling overwhelmed by the impact of the illness Link Content
831 Feeling overwhelmed by the Medicare enrollment process Link Content
832 Feeling overwhelmed by the need to travel long distances for medical appointments Link Content
833 Feeling overwhelmed by the potential need for further tests and procedures Link Content
834 Feeling overwhelmed by the situation Link Content
835 Feeling overwhelmed by the thought of enduring the situation for a long time Link Content
836 Feeling overwhelmed by the uncertainties Link Content
837 Feeling overwhelmed by the uncertainty of the situation Link Content
838 Feeling overwhelmed by treatment Link Content
839 Feeling overwhelmed during the first year after diagnosis Link Content
840 Feeling overwhelmed with dietary choices Link Content
841 Feeling physically and emotionally drained Link Content
842 Feeling physically and emotionally drained during procedures Link Content
843 Feeling physically weak and dependent on others Link Content
844 Feeling poorly and not knowing the cause Link Content
845 Feeling relieved and grateful for the positive outcome Link Content
846 Feeling scared and angry upon hearing the word "cancer" Link Content
847 Feeling shocked and surprised by the diagnosis Link Content
848 Feeling sore and attributing it to physical activity Link Content
849 Feeling stuck in the hospital Link Content
850 Feeling sweaty or sick Link Content
851 Feeling the absence and void left by the loved one Link Content
852 Feeling the absence of a central figure in life Link Content
853 Feeling the absence of Dad during significant life events Link Content
854 Feeling the absence of more time together Link Content
855 Feeling the deep fear and dread associated with cancer Link Content
856 Feeling the emotional impact of the mother's diagnosis at a young age Link Content
857 Feeling the fragility of life Link Content
858 Feeling the impact of pain on mobility and independence Link Content
859 Feeling the need for a longer charging cord Link Content
860 Feeling the need for more aggressive treatment Link Content
861 Feeling the need for more casual/athletic options Link Content
862 Feeling the need for oversized clothing Link Content
863 Feeling the need for support and understanding from others Link Content
864 Feeling the need for support from close friends and family Link Content
865 Feeling the need for validation or confirmation of the doctor's assessment Link Content
866 Feeling the need to report any unusual symptoms Link Content
867 Feeling the need to surrender a few days for treatment Link Content
868 Feeling the pain and grief of losing a loved one Link Content
869 Feeling the physical and emotional effects of intense chemotherapy Link Content
870 Feeling the presence and guidance of a deceased loved one Link Content
871 Feeling the pressure to be grateful and happy Link Content
872 Feeling the weight of grief and sadness Link Content
873 Feeling the weight of physical limitations Link Content
874 Feeling the weight of the situation affecting mental health Link Content
875 Feeling tired and overwhelmed Link Content
876 Feeling tired due to Revlimid maintenance Link Content
877 Feeling trapped and unable to leave Link Content
878 Feeling unable to sleep Link Content
879 Feeling uncertain about eligibility for a stem cell transplant due to age Link Content
880 Feeling uncertain about how to manage everything Link Content
881 Feeling uncertain about progress Link Content
882 Feeling uncertain about the chosen treatment plan Link Content
883 Feeling uncertain about the disease progression Link Content
884 Feeling uncertain about the effectiveness of maintenance treatments Link Content
885 Feeling uncertain about the effectiveness of treatment Link Content
886 Feeling uncertain about the effectiveness of treatments Link Content
887 Feeling uncertain about the outcome Link Content
888 Feeling uncertain about the progress towards remission Link Content
889 Feeling uncertain about the safety of indoor skydiving with the disease Link Content
890 Feeling uncertain about the significance of normal bloodwork Link Content
891 Feeling uncertain about the time frame Link Content
892 Feeling uncertain about what comes next Link Content
893 Feeling uncomfortable and seeking support Link Content
894 Feeling uncomfortable in crowded spaces Link Content
895 Feeling vulnerable and open to seeking guidance and influence Link Content
896 Feeling worried and concerned about the projected increase in MM cases Link Content
897 Feeling worried and uncertain Link Content
898 Feeling worried and uncertain about the abnormal test results Link Content
899 Finding motivation to continue fighting Link Content
900 Finding peace of mind in a book Link Content
901 Finding solace in others' stories and experiences Link Content
902 Finding solace in reminiscing and sharing stories Link Content
903 First 30 days after treatment Link Content
904 First hospitalization Link Content
905 First time needing help Link Content
906 Freefalling through the air Link Content
907 Friendly_Promise_998: Patient feeling uncertain and seeking reassurance about their blood test results Link Content
908 Frustration and fear of recurring infections Link Content
909 Frustration with healthcare system Link Content
910 Frustration with insurance process Link Content
911 Frustration with seeing a local oncologist with less expertise Link Content
912 Funeral or memorial service Link Content
913 Gathering loved ones together for support Link Content
914 GI bleed episode Link Content
915 Going through a difficult journey Link Content
916 Going through additional testing and procedures Link Content
917 Going through bone marrow castration Link Content
918 Going through chemotherapy and stem cell transplant Link Content
919 Going through previous treatments Link Content
920 Going through surgery and starting chemotherapy Link Content
921 Going through their belongings Link Content
922 Going through treatment again Link Content
923 Going through treatment and steroid withdrawal Link Content
924 Going through treatment procedures Link Content
925 Googling prognosis and facing mortality Link Content
926 Grasping at straws for additional resources Link Content
927 Gratitude and relief upon receiving the all-clear diagnosis Link Content
928 Grief and bereavement Link Content
929 Grieving during special occasions and milestones Link Content
930 Grieving the loss of a loved one to multiple myeloma Link Content
931 Hair not coming off on its own and causing pain Link Content
932 Handling the heavy medieval chemotherapy Link Content
933 Handling ups and downs as a team Link Content
934 Having a hard time eating Link Content
935 Having a lesion that required radiation Link Content
936 Having to rely on medication for relief Link Content
937 Having two collections Link Content
938 Hearing about high free kappa light chains Link Content
939 Hearing about others' experiences with the disease Link Content
940 Hearing about the death of younger patients Link Content
941 Hearing about the difficult journey and loss of a loved one Link Content
942 Hearing about the loss of a loved one Link Content
943 Hearing that the condition is highly unusual for her age Link Content
944 Hearing the diagnosis of cancer Link Content
945 Hearing the diagnosis of MGUS and later smoldering myeloma Link Content
946 Hearing the news of incurable cancer Link Content
947 Hearing the word "cancer" and feeling scared and angry Link Content
948 Hearing their favorite song or seeing their favorite movie Link Content
949 Helplessness in the face of complications Link Content
950 Hoping for a miraculous recovery Link Content
951 Hoping for family's strength Link Content
952 Hoping for improvement in the future Link Content
953 Hoping for positive news and outcomes Link Content
954 Hospital stay Link Content
955 Hospitalization for tumor lysis syndrome Link Content
956 Immediately after transplant surgery Link Content
957 Impact on personal relationships Link Content
958 Impacted mental well-being Link Content
959 Ineligibility for standard forms of treatment Link Content
960 Initial diagnosis and decision to undergo CAR-T treatment Link Content
961 Initial diagnosis of bladder cancer Link Content
962 Initial diagnosis of myeloma Link Content
963 Initial high IGA score Link Content
964 Initial realization of being sick Link Content
965 Investing in each other Link Content
966 Investing in their relationship Link Content
967 Keeping the rest of life together Link Content
968 Kidney deterioration Link Content
969 Kidney failure Link Content
970 Knowing others who are in a similar situation Link Content
971 Lack of financial help Link Content
972 Lack of knowledge about standard procedures in different countries Link Content
973 Lack of support Link Content
974 Laying in bed with racing thoughts Link Content
975 Learning about the cancer diagnosis Link Content
976 Learning about the MRD results Link Content
977 Learning about the potential diagnosis of Multiple Myeloma Link Content
978 Learning about the rarity and potential fatality of CNS multiple myeloma Link Content
979 Learning that the mass is growing Link Content
980 Living alone and single Link Content
981 Long and hard journey of battling multiple myeloma Link Content
982 Long wait time for results Link Content
983 Longing for a definitive answer and resolution to the uncertainty Link Content
984 Longing for a sense of control and empowerment in managing the disease Link Content
985 Longing for Dad's love and support Link Content
986 Longing for emotional support Link Content
987 Longing for immune system support during treatment Link Content
988 Longing for more options Link Content
989 Longing for peace and healing Link Content
990 Longing for the person's smile and presence in Heaven Link Content
991 Longing for the presence and guidance of loved ones Link Content
992 Longing for the presence and support of a father figure Link Content
993 Losing appetite during treatment Link Content
994 Losing hope as treatments fail Link Content
995 Loss of hope for recovery Link Content
996 Loss of independence Link Content
997 Loss of mobility and independence Link Content
998 Making decisions about end-of-life care Link Content
999 Making decisions about treatment options Link Content
1000 Managing caregiver stress Link Content
1001 Managing changes in daily life and routines Link Content
1002 Managing conflicting priorities Link Content
1003 Managing daily activities with limited mobility Link Content
1004 Managing dialysis and its impact on daily life Link Content
1005 Managing emotional well-being during confinement Link Content
1006 Managing emotions related to personal achievements Link Content
1007 Managing expectations and hopes Link Content
1008 Managing expectations and hopes for the outcome of the SCT Link Content
1009 Managing financial and logistical challenges Link Content
1010 Managing financial challenges Link Content
1011 Managing frustration with others' lack of understanding Link Content
1012 Managing pain and discomfort Link Content
1013 Managing the effects of heavy drug use Link Content
1014 Managing the emotional impact of CAR-T therapy on relationships and daily life Link Content
1015 Managing the emotional toll on relationships Link Content
1016 Managing the fear of falls and potential injuries Link Content
1017 Managing the impact on personal relationships Link Content
1018 Managing the impact on relationships and family dynamics Link Content
1019 Managing treatment expectations Link Content
1020 Managing uncertainty Link Content
1021 Managing uncertainty about prognosis Link Content
1022 Mental and physical toll of chemotherapy Link Content
1023 Mental strain during post-op appointment Link Content
1024 Moments of loneliness without Dad Link Content
1025 Moments of questioning faith Link Content
1026 Moments of uncertainty Link Content
1027 Moments of uncertainty and fear during the treatment journey Link Content
1028 Monitoring progress and waiting for updates Link Content
1029 Navigating changes in healthcare providers Link Content
1030 Navigating end-of-life decisions and discussions Link Content
1031 Navigating financial and insurance challenges Link Content
1032 Navigating financial challenges Link Content
1033 Navigating financial implications Link Content
1034 Navigating the challenges and emotions of caregiving Link Content
1035 Navigating the challenges of caregiving and illness Link Content
1036 Navigating the challenges of treatment and travel Link Content
1037 Navigating the complexities of treatment options Link Content
1038 Navigating the emotional journey of grief Link Content
1039 Navigating the emotional toll of the disease Link Content
1040 Navigating the healthcare system Link Content
1041 Navigating the healthcare system and accessing resources Link Content
1042 Navigating the healthcare system and insurance coverage for CAR-T therapy Link Content
1043 Navigating the influence of others' opinions Link Content
1044 Navigating the landing Link Content
1045 Navigating the transition into a new season of life without the loved one Link Content
1046 Near-death experience Link Content
1047 Need for additional support during MM treatment Link Content
1048 Need for clarification and understanding of the CD38 inhibitor's effect on testing Link Content
1049 Need for clear communication Link Content
1050 Need for dialysis and its impact on daily life Link Content
1051 Need for education and understanding of the disease Link Content
1052 Need for further testing Link Content
1053 Need for guidance in interpreting blood work Link Content
1054 Need for guidance on how to protect against Covid-19 Link Content
1055 Need for guidance on maintaining hydration and preventing complications Link Content
1056 Need for medical support Link Content
1057 Need for pain management Link Content
1058 Need for reassurance and encouragement Link Content
1059 Need for reassurance and hope Link Content
1060 Need for reassurance and support Link Content
1061 Need for support during VRD treatment Link Content
1062 Need for support from family and friends Link Content
1063 Need for support in managing symptoms and appointments Link Content
1064 Needing a second opinion for reassurance and confidence Link Content
1065 Needing additional low impact workout options Link Content
1066 Needing assistance with temperature control Link Content
1067 Needing Dad's guidance and wisdom Link Content
1068 Needing easy access to port Link Content
1069 Needing emotional support and understanding Link Content
1070 Needing emotional support during the journey Link Content
1071 Needing emotional support from loved ones Link Content
1072 Needing guidance on how to navigate the situation Link Content
1073 Needing hope for the future Link Content
1074 Needing medications but not having them ordered in advance Link Content
1075 Needing pain management Link Content
1076 Needing quality time and support without focusing solely on the diagnosis Link Content
1077 Needing reassurance Link Content
1078 Needing reassurance about the test results Link Content
1079 Needing reassurance and comfort Link Content
1080 Needing reassurance and hope for a more permanent solution Link Content
1081 Needing reassurance and support from loved ones Link Content
1082 Needing soothing and comforting sensations Link Content
1083 Needing support and encouragement Link Content
1084 Needing support and guidance for managing nutrition Link Content
1085 Needing support and guidance from a specialist Link Content
1086 Needing support and guidance from healthcare professionals Link Content
1087 Needing support and hope Link Content
1088 Needing support and information from doctors and fellow survivors Link Content
1089 Needing support during emergency room visits Link Content
1090 Needing support during grocery shopping Link Content
1091 Needing support during the journey Link Content
1092 Needing support during the waitlist period Link Content
1093 Needing support from spouse Link Content
1094 Needing support from spouse during cancer journey Link Content
1095 Needing support in ordering medications in advance Link Content
1096 Needing support in preparing children for the situation Link Content
1097 Needing time spaced away Link Content
1098 Needing to find a solution for hair removal Link Content
1099 Needing to grieve and process emotions Link Content
1100 Needing to maintain a positive attitude and sense of humor Link Content
1101 Needing to rely on insurance for support Link Content
1102 Needing validation and validation Link Content
1103 Nervousness about test results and consultations Link Content
1104 New diagnosis of light chain MM Link Content
1105 Not fully comprehending the news of remission Link Content
1106 Not knowing where to turn or what to do Link Content
1107 Not knowing who to talk to Link Content
1108 Not seeking medical help initially due to dismissal of symptoms Link Content
1109 Not thinking much of the initial pain Link Content
1110 November, the month Dad passed away Link Content
1111 Offering prayers for comfort Link Content
1112 Offering support and understanding to the grieving individual and their family Link Content
1113 Onset of cellulitis Link Content
1114 Open to considering alternative treatment options Link Content
1115 Open to influence and guidance during the treatment journey Link Content
1116 Open to influence and seeking answers for the cause of symptoms Link Content
1117 Opening the parachute Link Content
1118 Opening up about fears and uncertainties Link Content
1119 Openness to considering alternative treatment options and lifestyle changes Link Content
1120 Openness to influence and advice Link Content
1121 Openness to influence and advice from others Link Content
1122 Openness to influence and guidance from others who have gone through similar experiences Link Content
1123 Openness to learning about cancer and treatment options Link Content
1124 Overcoming fear of heights Link Content
1125 Overwhelm and fear upon hearing statistics and potential outcomes Link Content
1126 Pain and healing during recovery Link Content
1127 Pain becoming unbearable and affecting sleep Link Content
1128 Pain management Link Content
1129 Panicking during the CT or PET scan Link Content
1130 Patient dealing with the emotional and psychological challenges of their illness Link Content
1131 Patient desiring to hear positive news Link Content
1132 Patient experiencing fear and uncertainty about potential permanent neuropathy Link Content
1133 Patient experiencing fear and uncertainty about the future Link Content
1134 Patient experiencing heightened anxiety due to constant back pain Link Content
1135 Patient experiencing physical pain and discomfort Link Content
1136 Patient experiencing sleeplessness Link Content
1137 Patient expresses concern about the small percentage of clonal plasma cells found after stem cell transplant Link Content
1138 Patient expressing concern for their mother's health and treatment process Link Content
1139 Patient facing potential complications and risks associated with surgery Link Content
1140 Patient facing the possibility of relapse or worsening of their condition Link Content
1141 Patient feeling anxious about undergoing Autologous SCT Link Content
1142 Patient feeling anxious and worried about potential MM diagnosis Link Content
1143 Patient feeling clueless about insurance plan renewals and unsure about how to improve coverage Link Content
1144 Patient feeling disappointed about MRD status Link Content
1145 Patient feeling dismissed and unheard by their GP Link Content
1146 Patient feeling dismissed by doctors and seeking validation Link Content
1147 Patient feeling exposed and in need of support due to extreme pain Link Content
1148 Patient feeling exposed and in need of support while awaiting SCT procedure Link Content
1149 Patient feeling exposed and overwhelmed with information Link Content
1150 Patient feeling exposed and uncertain about their diagnosis Link Content
1151 Patient feeling hyperactive Link Content
1152 Patient feeling isolated and in need of support during recovery Link Content
1153 Patient feeling nervous and anxious about the diagnostic tests and upcoming appointments Link Content
1154 Patient feeling overwhelmed by information and risks of surgery Link Content
1155 Patient feeling uncertain about the future Link Content
1156 Patient feeling vulnerable due to the possibility of ongoing pain Link Content
1157 Patient finding solace and inspiration in symbolic representations Link Content
1158 Patient going through chemotherapy and stem cell transplant Link Content
1159 Patient needing emotional support during the journey Link Content
1160 Patient questioning the effectiveness of treatment Link Content
1161 Patient questioning the impact of low cell count Link Content
1162 Patient relying on heavy pain medication Link Content
1163 Patient relying on the support of loved ones and friends Link Content
1164 Patient seeking guidance based on their in-patient or out-patient status Link Content
1165 Patient seeking guidance from a social worker for assistance with insurance plan decisions Link Content
1166 Patient seeking information about hibernating cells Link Content
1167 Patient seeking reassurance about MRD- status Link Content
1168 Patient seeking reassurance and validation of progress Link Content
1169 Patient seeking recommendations for media to distract and pass the time Link Content
1170 Patient seeking support and validation from others Link Content
1171 Patient seeking support or information about side effects Link Content
1172 Patient seeking validation and connection through sharing their story Link Content
1173 Patient seeking validation and reassurance from online community Link Content
1174 Patient seeks advice from Signal-Engineer-7325 on going to a university hospital Link Content
1175 Patient seeks reassurance about husband's current condition and the effectiveness of the transplant Link Content
1176 Patient struggling to make a decision due to pain and emotional distress Link Content
1177 Patient struggling to make a decision due to pain and information overload Link Content
1178 Patient uncertain about the long-term effects of treatment Link Content
1179 Patient undergoing surgery and medical procedures Link Content
1180 Patient wanting to understand the significance of MRD- status Link Content
1181 Patient worrying about the effectiveness of maintenance treatment Link Content
1182 Patients being open to influence from healthcare professionals Link Content
1183 Patients constantly living with the risk of relapse Link Content
1184 Patients expecting a grand celebration but feeling let down Link Content
1185 Patients experiencing fear and uncertainty after a major event like collapsed vertebra or kidney near failure Link Content
1186 Patients experiencing mixed emotions after reaching remission Link Content
1187 Patients experiencing myeloma relapse Link Content
1188 Patients experiencing the impact of cancer cell genotype on treatment outcomes Link Content
1189 Patients experiencing tingling sensations and seeking reassurance or information Link Content
1190 Patients experiencing years of uncertainty and searching for a diagnosis Link Content
1191 Patients expressing concerns about the impact of the disease on their daily life Link Content
1192 Patients facing deteriorating results with each failed treatment Link Content
1193 Patients facing the possibility of a stem cell transplant and its potential challenges Link Content
1194 Patients feeling anxious and desperate as they search for answers online and seek support Link Content
1195 Patients feeling concerned about possible heart damage and seeking support from their oncologist Link Content
1196 Patients feeling exposed and in need of reassurance Link Content
1197 Patients feeling exposed and in need of support Link Content
1198 Patients feeling exposed and numb after reaching remission Link Content
1199 Patients feeling frustrated and exhausted after years of not feeling well and undergoing numerous tests Link Content
1200 Patients feeling frustrated and marginalized due to not fitting the typical patient demographic Link Content
1201 Patients feeling uncertain about the future and the possibility of the disease returning Link Content
1202 Patients feeling uncertain about their ability to engage in certain activities Link Content
1203 Patients feeling uncertain about their diagnosis Link Content
1204 Patients feeling uncertain about their diagnosis and seeking support from online communities Link Content
1205 Patients finding solace in daily walks Link Content
1206 Patients grappling with the unpredictability of the disease Link Content
1207 Patients mourning the loss of a loved one to the disease Link Content
1208 Patients reaching the stage of clinical trials with limited options Link Content
1209 Patients realizing the potential impact of a late MM diagnosis on their health Link Content
1210 Patients seeking specialized care from MM specialists Link Content
1211 Patients seeking support and guidance from healthcare professionals Link Content
1212 Patients struggling to achieve clear results in serum protein analysis Link Content
1213 Patients struggling to forget they have cancer even after remission Link Content
1214 Patients struggling to fully celebrate their success due to the fear of recurrence Link Content
1215 Patients undergoing aggressive treatment protocols Link Content
1216 Patients undergoing dialysis treatment and managing the impact on their daily lives Link Content
1217 Patients with cancer cells that mutate in response to treatment Link Content
1218 Patients with positive m-protein spike in serum protein analysis Link Content
1219 Personal experience with a loved one's health scare Link Content
1220 Personal understanding of the disease that others may not have Link Content
1221 PET scans showing solid tumors Link Content
1222 Physical and emotional challenges of paralysis Link Content
1223 Post-surgery and physical therapy period Link Content
1224 Potential for accidents or falls due to slippery surface Link Content
1225 Preparing for a medical procedure Link Content
1226 Preparing for a stem cell transplant and its potential impact Link Content
1227 Preparing for and undergoing the Autologous Stem Cell transplant Link Content
1228 Preparing for end-of-life decisions and transitions Link Content
1229 Preparing for stem cell transplant Link Content
1230 Preparing for the arrival of an unborn child amidst the turmoil Link Content
1231 Preparing for the stem cell transplant Link Content
1232 Presence of a large bed sore Link Content
1233 Processing emotions Link Content
1234 Processing emotions related to the disease Link Content
1235 Processing the heavy burden of the disease Link Content
1236 Processing the impact of prayers and well wishes Link Content
1237 Processing the news of remission Link Content
1238 Putting on the skydiving gear Link Content
1239 Quarantine period after cancer treatment Link Content
1240 Questioning one's own purpose and existence Link Content
1241 Questioning the accuracy and reliability of the test results Link Content
1242 Questioning the effectiveness of current treatment Link Content
1243 Questioning the effectiveness of efforts Link Content
1244 Questioning the effectiveness of traditional medical treatments Link Content
1245 Questioning the fairness of the situation Link Content
1246 Questioning the fairness of the timing of treatments Link Content
1247 Questioning the future and contemplating the impact of the disease Link Content
1248 Questioning the motivation behind questioning someone's fitness for a job Link Content
1249 Questioning the purpose and meaning of life Link Content
1250 Questioning the purpose and meaning of the journey Link Content
1251 Questioning the reasons behind the disease Link Content
1252 Questioning the significance of achieving remission Link Content
1253 Questioning the significance of being in remission due to the likelihood of the disease returning Link Content
1254 Questioning the significance of the victory Link Content
1255 Questioning the value of hope in the face of a terminal disease Link Content
1256 Reaching the deductible limit Link Content
1257 Realization of being sick Link Content
1258 Realization of disease progression Link Content
1259 Realization of kidney failure Link Content
1260 Realizing kidney function is not improving Link Content
1261 Realizing missed opportunities for learning Link Content
1262 Realizing that dialysis can no longer be done Link Content
1263 Realizing the disease may come back Link Content
1264 Realizing the high stakes involved in the disease Link Content
1265 Realizing the impact of treatment on the body's healing ability Link Content
1266 Realizing the importance of dental care for his specific cancer Link Content
1267 Realizing the limited time left with loved ones Link Content
1268 Realizing the limited time left with the person Link Content
1269 Realizing the size and extent of the mass Link Content
1270 Rebuilding oneself Link Content
1271 Recalling the traumatic experience of being shot Link Content
1272 Receiving a diagnosis of MGUS Link Content
1273 Receiving a diagnosis of multiple myeloma Link Content
1274 Receiving a diagnosis requiring CAR-T therapy Link Content
1275 Receiving a message from a loved one expressing feelings of guilt and love Link Content
1276 Receiving a myeloma diagnosis Link Content
1277 Receiving cancer diagnosis at a young age Link Content
1278 Receiving Darzalex treatments and experiencing side effects Link Content
1279 Receiving medical bills Link Content
1280 Receiving message from mom Link Content
1281 Receiving short notice call from nurse coordinator Link Content
1282 Receiving test results Link Content
1283 Receiving the devastating news of PCL diagnosis Link Content
1284 Receiving the diagnosis of 1-2% kappa restricted plasma cells Link Content
1285 Receiving the diagnosis of multiple myeloma Link Content
1286 Receiving the diagnosis of Multiple Myeloma and AL Amyloidosis Link Content
1287 Receiving the diagnosis of Stage 1 MM Link Content
1288 Receiving the initial cancer diagnosis Link Content
1289 Receiving the myeloma diagnosis Link Content
1290 Receiving the news of relapse Link Content
1291 Receiving the news of starting chemo again Link Content
1292 Receiving the news of the loss Link Content
1293 Receiving the news that it was her last shot and needing to react Link Content
1294 Receiving the recommendation against stem cell transplant Link Content
1295 Receiving the same medications as others Link Content
1296 Receiving the worst possible news Link Content
1297 Receiving treatment and hoping for positive results Link Content
1298 Receiving unexpected test results Link Content
1299 Recognizing the challenges of frequent hospital visits and their impact on quality of life Link Content
1300 Recognizing the current limitations of available options Link Content
1301 Recognizing the emotional impact on the family Link Content
1302 Recognizing the impact of age on susceptibility to infections Link Content
1303 Recognizing the importance of cherished memories Link Content
1304 Recognizing the mismatch between personal feelings and others' excitement Link Content
1305 Recovery from muscle loss Link Content
1306 Recurrence of symptoms Link Content
1307 Recurrence or relapse Link Content
1308 Reflecting on a dark time Link Content
1309 Reflecting on fears and dread Link Content
1310 Reflecting on financial concerns and job security Link Content
1311 Reflecting on mortality Link Content
1312 Reflecting on mortality and life priorities Link Content
1313 Reflecting on mortality and the brevity of life Link Content
1314 Reflecting on mortality and the impact of the disease Link Content
1315 Reflecting on past experiences and hoping for better outcomes Link Content
1316 Reflecting on the adventure Link Content
1317 Reflecting on the emotional impact of the remission diagnosis Link Content
1318 Reflecting on the end of the journey Link Content
1319 Reflecting on the fragility of life Link Content
1320 Reflecting on the fragility of life and relationships Link Content
1321 Reflecting on the fragility of life and the uncertainty of losing loved ones Link Content
1322 Reflecting on the future and mortality Link Content
1323 Reflecting on the impact of myeloma on life Link Content
1324 Reflecting on the impact of new treatments arriving too late Link Content
1325 Reflecting on the impact of the disease on life and purpose Link Content
1326 Reflecting on the impact of the disease on relationships Link Content
1327 Reflecting on the impact of the loss Link Content
1328 Reflecting on the impact of the person's absence Link Content
1329 Reflecting on the impact of the situation Link Content
1330 Reflecting on the initial treatment process and the possibility of relapse Link Content
1331 Reflecting on the journey and finding meaning Link Content
1332 Reflecting on the limitations of being in remission Link Content
1333 Reflecting on the limitations of treatment Link Content
1334 Reflecting on the limited time together Link Content
1335 Reflecting on the memories and qualities of the deceased Link Content
1336 Reflecting on the memories and the impact of the relationship Link Content
1337 Reflecting on the mother's journey Link Content
1338 Reflecting on the possibility of losing a loved one to cancer Link Content
1339 Reflecting on the potential impact of the journey on oneself and others Link Content
1340 Reflecting on the purpose of the journey Link Content
1341 Reflecting on the shock of relapse Link Content
1342 Reflecting on the shortness of the time spent with the loved one Link Content
1343 Reflecting on the shortness of time Link Content
1344 Reflecting on the shortness of time spent with a loved one Link Content
1345 Reflecting on the significance of remission Link Content
1346 Reflecting on the slow progress of treatment Link Content
1347 Reflecting on the suddenness and unfairness of the disease Link Content
1348 Reflecting on the support of a spouse Link Content
1349 Reflecting on the uncertainty of the future Link Content
1350 Reflecting on the uncertainty of time on Earth Link Content
1351 Reflecting on the unexpectedness of the disease Link Content
1352 Relapse Link Content
1353 Relapse or recurrence Link Content
1354 Reliance on regular hospital visits for treatment Link Content
1355 Reliance on wife for support and care Link Content
1356 Relying on support from loved ones Link Content
1357 Relying on support from loved ones and friends Link Content
1358 Remembering and holding onto memories of a deceased loved one Link Content
1359 Remembering mother's battle with cancer Link Content
1360 Remembering the pain of losing a parent Link Content
1361 Requiring assistance with IV management and clothing changes Link Content
1362 Returning to work after treatment with reduced focus Link Content
1363 Running out of treatment options Link Content
1364 Rushing to the nearest hospital Link Content
1365 Sapped strength from being confined Link Content
1366 Searching for comfort Link Content
1367 Searching for information and answers Link Content
1368 Second hospitalization Link Content
1369 Seeing photos of Dad Link Content
1370 Seeing reminders of the person Link Content
1371 Seeing the stress on family Link Content
1372 Seeking a safe space to express emotions Link Content
1373 Seeking advice and information from online community Link Content
1374 Seeking advice on how to create meaningful experiences for a loved one with a limited time Link Content
1375 Seeking advice or recommendations Link Content
1376 Seeking clarification or additional information during the question and answer session Link Content
1377 Seeking comfort and convenience in clothing choices Link Content
1378 Seeking comfort and peace Link Content
1379 Seeking comfort and reassurance Link Content
1380 Seeking comfort and soothing sensations Link Content
1381 Seeking comfort and support from family and friends Link Content
1382 Seeking emotional support to cope with the chronic disease Link Content
1383 Seeking guidance and advice from others who have been through similar experiences Link Content
1384 Seeking guidance and support in navigating the challenges of a loved one's illness Link Content
1385 Seeking guidance on incorporating turmeric into the diet Link Content
1386 Seeking help for dad's diagnosis Link Content
1387 Seeking hope for a permanent solution Link Content
1388 Seeking opinions and input from others Link Content
1389 Seeking peace and comfort Link Content
1390 Seeking peace of mind and support Link Content
1391 Seeking positive energy Link Content
1392 Seeking post-cancer information and guidance for the new life ahead Link Content
1393 Seeking reassurance Link Content
1394 Seeking reassurance about the effectiveness of induction chemo Link Content
1395 Seeking reassurance about the significance of bloodwork results Link Content
1396 Seeking reassurance and encouragement Link Content
1397 Seeking reassurance and hope Link Content
1398 Seeking reassurance and information about the success rate of CAR-T treatment Link Content
1399 Seeking reassurance and support from others Link Content
1400 Seeking reassurance and support from others who have faced similar challenges Link Content
1401 Seeking reassurance and validation for positive outlook Link Content
1402 Seeking reassurance and validation from healthcare professionals and peers Link Content
1403 Seeking reassurance and validation in the face of a cancer diagnosis Link Content
1404 Seeking reassurance from others Link Content
1405 Seeking reassurance from others who have gone through similar experiences Link Content
1406 Seeking reassurance from others who have had similar results Link Content
1407 Seeking relief and understanding for the symptoms Link Content
1408 Seeking relief from pain through medication Link Content
1409 Seeking resources Link Content
1410 Seeking solace and comfort in spirituality and faith Link Content
1411 Seeking solace and strength in difficult times Link Content
1412 Seeking solace and understanding Link Content
1413 Seeking someone to talk to Link Content
1414 Seeking support and advice from the online community Link Content
1415 Seeking support and comfort from others Link Content
1416 Seeking support and connection with others who share the same condition Link Content
1417 Seeking support and guidance in making decisions about maintenance treatments Link Content
1418 Seeking support and information from others Link Content
1419 Seeking support and reassurance from healthcare provider Link Content
1420 Seeking support and reassurance from others Link Content
1421 Seeking support and understanding from others who have experienced remission Link Content
1422 Seeking support and validation from others Link Content
1423 Seeking support from a cancer coach Link Content
1424 Seeking validation and reassurance for pursuing bucket list activities Link Content
1425 Seeking validation and understanding from loved ones Link Content
1426 Seeking validation for concerns and experiences Link Content
1427 Seizures and brain involvement Link Content
1428 Sharing concerns about side effects Link Content
1429 Sharing emotional pain Link Content
1430 Sharing personal connections and experiences Link Content
1431 Sharing personal emotions and tears Link Content
1432 Sharing personal experiences and memories Link Content
1433 Sharing personal experiences and struggles related to being in remission Link Content
1434 Sharing personal experiences of family members Link Content
1435 Sharing personal experiences with a supportive online community Link Content
1436 Sharing personal fears and emotions Link Content
1437 Sharing personal medical updates and concerns Link Content
1438 Sharing personal stories and memories Link Content
1439 Sharing personal struggles and challenges Link Content
1440 Sharing personal struggles and hardships Link Content
1441 Sharing physical and emotional pain Link Content
1442 Sharing the impact of the disease on daily life Link Content
1443 Shock and disbelief upon receiving the diagnosis Link Content
1444 Showing signs of improvement on day 9-11 Link Content
1445 Showing support during a difficult time Link Content
1446 Side effects of medication Link Content
1447 Signs of brain damage Link Content
1448 Sitting in the oncology office with a loved one Link Content
1449 Sitting in the SCT clinic before transplant Link Content
1450 Sleepless nights waiting for test results Link Content
1451 Slip in and out of consciousness Link Content
1452 Spending time with loved ones before passing away Link Content
1453 Standing at the edge of the plane before jumping Link Content
1454 Starting a new treatment trial Link Content
1455 Starting first cycle of treatment Link Content
1456 Starting the clinical trial and facing uncertainty Link Content
1457 Starting to panic upon hearing the mention of MM (multiple myeloma) Link Content
1458 Starting treatment again with revlimid and other drugs Link Content
1459 Stranded in a distant hospital Link Content
1460 StrangeJournalist7: No vulnerable moment identified Link Content
1461 Struggling to balance work responsibilities and managing a disease Link Content
1462 Struggling to find hope and motivation Link Content
1463 Struggling to find light at the end of the tunnel Link Content
1464 Struggling to find suitable recipes Link Content
1465 Struggling to focus on work Link Content
1466 Struggling to keep food down Link Content
1467 Struggling to maintain a sense of normalcy Link Content
1468 Struggling to reconcile hope with the terminal nature of the disease Link Content
1469 Struggling to stay motivated Link Content
1470 Struggling to support the patient Link Content
1471 Struggling with appetite issues Link Content
1472 Struggling with declining mental health Link Content
1473 Struggling with eating post-transplant Link Content
1474 Struggling with emotional and psychological challenges associated with myeloma Link Content
1475 Struggling with imposter syndrome Link Content
1476 Struggling with life challenges and illness Link Content
1477 Struggling with mental health Link Content
1478 Struggling with PTSD from hospital stay Link Content
1479 Struggling with self-confidence Link Content
1480 Struggling with self-doubt Link Content
1481 Struggling with sleep and relying on sleep aids Link Content
1482 Struggling with the absence of a loved one Link Content
1483 Struggling with the impact of cancer on daily life Link Content
1484 Struggling with the physical and emotional toll of chemotherapy Link Content
1485 Struggling with the physical and emotional toll of treatment Link Content
1486 Struggling with the uncertainty of the future Link Content
1487 Struggling with the weight of grief and sadness Link Content
1488 Struggling with understanding from others Link Content
1489 Struggling with various emotions related to the situation Link Content
1490 Suffering in pain for a long time Link Content
1491 Support needed during the fight Link Content
1492 Supporting a loved one through the journey Link Content
1493 Supporting each other emotionally Link Content
1494 Suspected encephalitis diagnosis Link Content
1495 Talking about them with others Link Content
1496 Telling his daughter about the diagnosis Link Content
1497 Throughout months of limited fulfillment in life Link Content
1498 Throughout the treatment process Link Content
1499 Transition from hospital to home Link Content
1500 Transition to a new hospital Link Content
1501 Transition to palliative care Link Content
1502 Transitioning between insurance plans Link Content
1503 Transitioning to maintenance therapy Link Content
1504 Treatment decision-making Link Content
1505 Treatment for Covid Link Content
1506 Treatment for depression and anxiety Link Content
1507 Treatment initiation Link Content
1508 Trusting the equipment Link Content
1509 Trying to go to the bathroom Link Content
1510 Trying to prevent negative emotions from impacting daily life Link Content
1511 Trying to understand what's happening Link Content
1512 Uncertainty about available treatment options Link Content
1513 Uncertainty about diagnosis Link Content
1514 Uncertainty about holiday plans Link Content
1515 Uncertainty about how long the remission will last Link Content
1516 Uncertainty about in-network care providers and pharmacies Link Content
1517 Uncertainty about life expectancy Link Content
1518 Uncertainty about maintaining focus and concentration Link Content
1519 Uncertainty about managing a chronic disease Link Content
1520 Uncertainty about symptoms Link Content
1521 Uncertainty about the cause of the change in kappa chain levels Link Content
1522 Uncertainty about the cause of the slight band Link Content
1523 Uncertainty about the definition of "doing ok" Link Content
1524 Uncertainty about the disease progression Link Content
1525 Uncertainty about the effectiveness of blood transfusions Link Content
1526 Uncertainty about the effectiveness of supplements Link Content
1527 Uncertainty about the effectiveness of Teclistomab Link Content
1528 Uncertainty about the effectiveness of the current chemotherapy regimen Link Content
1529 Uncertainty about the effectiveness of the drug regimen Link Content
1530 Uncertainty about the effectiveness of treatments Link Content
1531 Uncertainty about the effectiveness of vaccinations Link Content
1532 Uncertainty about the future and prognosis Link Content
1533 Uncertainty about the masses Link Content
1534 Uncertainty about the outcome of the SCT Link Content
1535 Uncertainty about the success of maintenance therapy Link Content
1536 Uncertainty about treatment outcomes Link Content
1537 Uncertainty about what comes next Link Content
1538 Uncertainty about what to expect Link Content
1539 Uncertainty about what's next Link Content
1540 Uncertainty and anxiety about future treatments Link Content
1541 Uncertainty and confusion while looking at the test results Link Content
1542 Uncertainty and doubt about the next round of treatment Link Content
1543 Uncertainty of being an in-patient or out-patient Link Content
1544 undefined: No vulnerable moment identified Link Content
1545 Undergoing a 24-hour urine test Link Content
1546 Undergoing chemotherapy Link Content
1547 Undergoing radiation and chemotherapy Link Content
1548 Undergoing stem cell transplant and CAR-T therapy Link Content
1549 Undergoing treatment and experiencing potential side effects Link Content
1550 Undergoing treatment and facing uncertainty Link Content
1551 Undergoing X-ray therapy for pain relief Link Content
1552 Understanding the impact of brain inflammation Link Content
1553 Understanding the irony of cancer remission but vulnerability to pneumonia Link Content
1554 Understanding the possibility of disease recurrence Link Content
1555 Understanding the possibility of relapse Link Content
1556 Upon arrival at the hospital Link Content
1557 Waiting for bed sore closure Link Content
1558 Waiting for biopsy results Link Content
1559 Waiting for blood test results Link Content
1560 Waiting for blood work results and fearing negative outcomes Link Content
1561 Waiting for bone marrow biopsy results Link Content
1562 Waiting for CAR-T therapy treatment to begin Link Content
1563 Waiting for CAR-T treatment to become available Link Content
1564 Waiting for improvement in medical conditions Link Content
1565 Waiting for more information Link Content
1566 Waiting for MRI results Link Content
1567 Waiting for PET scan results Link Content
1568 Waiting for results of bone marrow and blood tests Link Content
1569 Waiting for SCT Link Content
1570 Waiting for SCT and feeling exposed Link Content
1571 Waiting for test results and biopsy Link Content
1572 Waiting for test results and experiencing anxiety about the outcome Link Content
1573 Waiting for test results and fearing disease progression Link Content
1574 Waiting for test results and feeling anxious Link Content
1575 Waiting for test results and medical updates Link Content
1576 Waiting for test results and scan outcomes Link Content
1577 Waiting for test results and treatment outcomes Link Content
1578 Waiting for the availability of CAR-T options Link Content
1579 Waiting for the doctor's call regarding abnormal blood work Link Content
1580 Waiting for the outcome of CAR-T therapy Link Content
1581 Waiting for the results of the bone marrow biopsy Link Content
1582 Waiting for the results of the M-spike number Link Content
1583 Waiting for the results of the stem-cell transplant Link Content
1584 Waiting for transplant and uncertain outcomes Link Content
1585 Waiting for transplant and undergoing more chemo Link Content
1586 Waiting for treatment outcomes and potential methods like stem cell transplants Link Content
1587 Waiting for treatment to normalize kappa/lambda levels Link Content
1588 Waiting to see if Darzalex would work Link Content
1589 Waiting to see the effects of stopping sedation Link Content
1590 Waking up completely paralyzed on day 12 Link Content
1591 Wanting a convenient way to watch things on phone Link Content
1592 Wanting to gather information and opinions from others Link Content
1593 Wanting to retreat and hide during chemo and radiation Link Content
1594 Wanting to see tangible results Link Content
1595 Weekend before he died Link Content
1596 When acquiring pneumonia Link Content
1597 When adjusting to lifestyle changes Link Content
1598 When analyzing and understanding information from healthcare professionals Link Content
1599 When considering alternative options and seeking advice Link Content
1600 When contemplating the impact of the disease on daily life Link Content
1601 When current methods of relief are not effective Link Content
1602 When dealing with the physical and emotional toll of treatment Link Content
1603 When developing a sore throat Link Content
1604 When discussing prognosis Link Content
1605 When discussing treatment options with healthcare professionals Link Content
1606 When encountering potential infection risks Link Content
1607 When encountering triggers or temptations Link Content
1608 When experiencing a cough Link Content
1609 When experiencing constant runny nose Link Content
1610 When experiencing excruciating back pain and limited mobility Link Content
1611 When experiencing frustration and distress due to the pain Link Content
1612 When experiencing intense inflammation or pain Link Content
1613 When experiencing side effects or complications Link Content
1614 When facing emotional challenges Link Content
1615 When facing test results and medical appointments Link Content
1616 When facing treatment side effects Link Content
1617 When facing uncertainty about future mobility and quality of life Link Content
1618 When facing uncertainty about the future Link Content
1619 When feeling dependent on others for support and care Link Content
1620 When feeling lonely Link Content
1621 When feeling overwhelmed or helpless Link Content
1622 When in need of emotional support Link Content
1623 When making decisions about treatment protocols Link Content
1624 When patients experience infections continuously Link Content
1625 When patients face the fundamental cruelty of the disease Link Content
1626 When patients feel frustrated and scared due to complications from infections Link Content
1627 When patients realize the impact of infections on their weakened state Link Content
1628 When patients struggle to come to terms with the disease and its effects Link Content
1629 When receiving a diagnosis Link Content
1630 When receiving test results Link Content
1631 When reviewing imaging with the doctor Link Content
1632 When seeking emotional support Link Content
1633 When starting off walking with a walker Link Content
1634 When transitioning back to work or school Link Content
1635 When vertebrae collapse Link Content
1636 Wishing for a faster recovery Link Content
1637 Wishing for more time together Link Content
1638 Witnessing multiple complications in a loved one Link Content
1639 Witnessing physical changes in the patient Link Content
1640 Witnessing the decline in health Link Content
1641 Witnessing the decline in health and non-responsiveness Link Content
1642 Witnessing the deterioration of a loved one Link Content
1643 Witnessing the deterioration of physical and mental health Link Content
1644 Witnessing the final moments Link Content
1645 Witnessing the impact on family and loved ones Link Content
1646 Wondering about in-patient or out-patient status Link Content
1647 Wondering about the dormancy of chicken pox Link Content
1648 Worries about ability to perform at a high level Link Content
1649 Worries about the impact of the recent fracture on treatment eligibility Link Content
1650 Worrying about the battles of tomorrow Link Content
1651 Worrying about the impact on relationships Link Content
1652 Worsening condition Link Content
1653 Worst days of the caregiver's life Link Content
1654 Yearning for Dad's comforting presence Link Content
1655 Yearning for improvement Link Content
1656 Yearning for reassurance Link Content
1657 Younger patients feeling isolated and misunderstood due to the unexpected age for the disease Link Content

Choice Points Show All

  1. Choosing between different treatment options
  2. Deciding on treatment options
  3. Selecting healthcare providers
  4. Choosing a treatment plan
  5. Considering alternative therapies
  6. Considering alternative treatment options
  7. Deciding on end-of-life care
  8. Deciding on end-of-life care preferences
  9. Decision to undergo stem cell transplant
  10. Selecting a healthcare provider
  11. Choosing to participate in clinical trials
  12. Deciding on medication options
  13. Deciding on palliative care
  14. Making end-of-life decisions
  15. Opting for alternative therapies