Emotional Intelligence Report |Multiple Myeloma

Surface Behaviors

S. No. Behavior Content
1 Seeking medical advice Link Content
2 Seeking emotional support Link Content
3 Managing side effects Link Content
4 Reflecting on the impact of the disease Link Content
5 Sharing personal experiences and condolences Link Content
6 Engaging in self-care activities Link Content
7 Monitoring progress Link Content
8 Starting treatment Link Content
9 Taking prescribed medication Link Content
10 Emotional distress Link Content
11 Experiencing side effects Link Content
12 Fatigue Link Content
13 Initial symptoms Link Content
14 Sharing personal experiences Link Content
15 Sharing personal experiences and stories Link Content
16 Adhering to treatment plan Link Content
17 Attending medical appointments Link Content
18 Difficulty concentrating Link Content
19 Difficulty sleeping Link Content
20 Expressing gratitude Link Content
21 Offering condolences and sympathy Link Content
22 Offering prayers and well wishes Link Content
23 Prioritizing mental health Link Content
24 Seeking second opinions Link Content
25 Attending follow-up appointments Link Content
26 Diagnosis of cancer Link Content
27 Discussing treatment options with healthcare providers Link Content
28 Emotional ups and downs Link Content
29 Expressing empathy and support Link Content
30 Expressing empathy and understanding Link Content
31 Expressing gratitude for support Link Content
32 Expressing sympathy and empathy Link Content
33 Frequent trips to the emergency room Link Content
34 Loss of appetite Link Content
35 Monitoring disease progression Link Content
36 Offering support and encouragement Link Content
37 Reporting symptoms Link Content
38 Seeking advice and guidance Link Content
39 Seeking alternative therapies Link Content
40 Seeking support from family and friends Link Content
41 Starting maintenance treatment Link Content
42 Thankfulness for each day Link Content
43 Undergoing diagnostic tests Link Content
44 10 months of challenging moments Link Content
45 Adapting daily routines Link Content
46 Adjusting medication Link Content
47 Adjusting to new roles and responsibilities Link Content
48 Adjusting treatment Link Content
49 Apologies for needing help Link Content
50 Appreciation for help Link Content
51 Attending doctor appointments Link Content
52 Avoiding drinking during meals Link Content
53 Caregiver role assumed by family member Link Content
54 Changes in appetite Link Content
55 Changes in daily routines and activities Link Content
56 Changes in physical appearance Link Content
57 Completed chemotherapy in September Link Content
58 Continuous throat and lung infections Link Content
59 Dating throughout high school Link Content
60 Diagnosis of Multiple Myeloma and AL Amyloidosis Link Content
61 Diagnosis of Stage 1 MM Link Content
62 Diagnosis of stage 3 Multiple Myeloma Link Content
63 Dialysis 3 times a week for 4.5 hours Link Content
64 Disease progression Link Content
65 Disintegrated and misaligned T 10 and C 6 Link Content
66 Early recognition of illness Link Content
67 Eating small snack portions Link Content
68 Engaging in self-care Link Content
69 Engaging in treatment options Link Content
70 Experiencing physical symptoms Link Content
71 Experiencing physical symptoms and side effects Link Content
72 Expressing condolences and sympathy Link Content
73 Expressing gratitude and appreciation Link Content
74 Expressing mixed emotions about being in remission Link Content
75 Feeling anticlimactic about achieving remission Link Content
76 Feeling better Link Content
77 Financial strain Link Content
78 Fluctuations in energy levels Link Content
79 Flying back for a bone marrow castration Link Content
80 Getting married in 1968 Link Content
81 Grief Link Content
82 Heart attacks requiring stents Link Content
83 Hospital visits Link Content
84 Hospitalization Link Content
85 Interacting with healthcare professionals Link Content
86 Kidney failure Link Content
87 Lack of motivation Link Content
88 Maintaining a positive attitude Link Content
89 Meeting on Cape Cod Link Content
90 Meeting with lead oncologist Link Content
91 Mention of dexamethasone side effects Link Content
92 Monitoring symptoms Link Content
93 Monitoring symptoms and progress Link Content
94 Multiple air chopper rides Link Content
95 Near-death experience Link Content
96 Need for food/protein and hydration Link Content
97 Numbness and tingling in hands and feet Link Content
98 Offering prayers and support Link Content
99 Offering support and empathy Link Content
100 Participating in clinical trials Link Content
101 Passing away peacefully Link Content
102 Patient considering different treatment options Link Content
103 Patient experiencing extreme pain Link Content
104 Patient receiving information about diagnosis and treatment options Link Content
105 Patients sharing their remission news Link Content
106 Positive response to treatment Link Content
107 Preparing for stem cell transplant Link Content
108 Receiving a call from the doctor Link Content
109 Receiving diagnosis Link Content
110 Receiving news of remission Link Content
111 Receiving X-ray therapy for lesions Link Content
112 Reflecting on the journey Link Content
113 Relapse of MM Link Content
114 Remission after 6 months of treatment Link Content
115 Researching treatment options Link Content
116 Retiring and selling their house Link Content
117 Seeking a second opinion Link Content
118 Seeking advice and support from others Link Content
119 Seeking information about the disease Link Content
120 Seeking information and experiences from others Link Content
121 Seeking information on new treatments Link Content
122 Seeking medical advice and treatment options Link Content
123 Seeking support groups Link Content
124 Seeking validation Link Content
125 Self-administration of bortezomib injections Link Content
126 Sharing memories and stories Link Content
127 Sharing personal experiences and offering condolences Link Content
128 Sharing personal stories and experiences Link Content
129 Sharing personal stories and memories Link Content
130 Sharing personal story Link Content
131 Sharing stories and wisdom Link Content
132 Specialist unit in London for Amyloidosis care Link Content
133 Starting chemotherapy Link Content
134 Starting chemotherapy treatment Link Content
135 Stem cell transplant Link Content
136 Struggle to balance various responsibilities Link Content
137 Suggesting therapy as a coping mechanism Link Content
138 Symptoms come and go Link Content
139 Symptoms worsen under stress Link Content
140 Taking anti-nausea and anti-diarrhea medications Link Content
141 Treatment side effects Link Content
142 Treatment with DVTD (daratumumab, bortezomib, thalidomide, and dexamethasone) Link Content
143 Volunteering at a junior college Link Content
144 Weight loss Link Content
145 1-2% kappa restricted plasma cells Link Content
146 10-month break from work for surgery, cancer treatment, and healing Link Content
147 10th dose without Darzalex Link Content
148 9th dose without Darzalex Link Content
149 Ability to write, speak, and understand Link Content
150 Abnormal brain scan patterns Link Content
151 Abnormal free chains Link Content
152 Abnormal free chains in blood work Link Content
153 Abnormal lab results Link Content
154 Accessing the recorded episode on the Revolution Cancer channel and website Link Content
155 Achieving a marathon milestone Link Content
156 Acknowledging limited time Link Content
157 Acknowledging personal growth Link Content
158 Acknowledging the aggressiveness of the disease Link Content
159 Acknowledging the challenges faced Link Content
160 Acknowledging the challenges of the disease Link Content
161 Acknowledging the difficulty and cruelty of the disease Link Content
162 Acknowledging the difficulty and impact of the disease Link Content
163 Acknowledging the difficulty of living without a loved one Link Content
164 Acknowledging the difficulty of the disease for loved ones Link Content
165 Acknowledging the eloquent writing Link Content
166 Acknowledging the impact of frequent trips to the hospital on quality of life Link Content
167 Acknowledging the importance of remission Link Content
168 Acknowledging the loss and expressing hope for healing Link Content
169 Acknowledging the loss and the difficulty of the journey Link Content
170 Acknowledging the pain and grief Link Content
171 Acknowledging the preciousness of life Link Content
172 Acknowledging the relief of gaining more time Link Content
173 Acknowledging the struggle and adversity Link Content
174 Acknowledging the struggles and emotions experienced Link Content
175 Acknowledging the unexpected nature of the situation Link Content
176 Acknowledgment of progress Link Content
177 Acquiring pneumonia Link Content
178 Acting strong and resilient Link Content
179 Active pneumonia Link Content
180 Acyclovir prescribed to prevent shingles Link Content
181 Adaptation and coping strategies Link Content
182 Adapting daily routines and lifestyle Link Content
183 Adapting daily routines to accommodate the upcoming procedure Link Content
184 Adapting to new normalcy Link Content
185 Adhering to dietary restrictions Link Content
186 Adhering to lifestyle changes Link Content
187 Adhering to medication regimen Link Content
188 Adhering to treatment regimen Link Content
189 Adjusting lifestyle habits Link Content
190 Adjusting medication dosage Link Content
191 Adjusting to reduced income Link Content
192 Adjustments to daily routines Link Content
193 Adrenaline rush Link Content
194 Advising caution and care in daily activities Link Content
195 Advocacy for bladder cancer awareness Link Content
196 Advocating for better access to treatments Link Content
197 Advocating for improved access to CAR-T therapy Link Content
198 Advocating for oneself Link Content
199 Advocating for oneself in healthcare settings Link Content
200 Age as a potential factor Link Content
201 Always in treatment Link Content
202 Anemia Link Content
203 Anemia leading to hospital stay Link Content
204 Annual tests and scan to monitor protein levels Link Content
205 Antibiotic treatment for pneumonia Link Content
206 Anticipating other testing Link Content
207 Anticipating the future without the person Link Content
208 Anticipation of reuniting with Dad in Heaven Link Content
209 Anxiety about seeing test results Link Content
210 Anxiety and worry Link Content
211 Anxiety/depression prone Link Content
212 Apologizing for lack of time Link Content
213 Appearance of a slight band after a few months of ASCT Link Content
214 Appointment with neurologist Link Content
215 Appreciating and relying on a supportive spouse Link Content
216 Appreciating the journey and personal growth Link Content
217 Appreciating the support received Link Content
218 Appreciating the time spent with Dad Link Content
219 Appreciation for advancements in science Link Content
220 Appreciation for supportive spouse Link Content
221 Arm fracture misdiagnosed as rotator cuff pain Link Content
222 ASCT (Autologous Stem Cell Transplant) procedure Link Content
223 Asking about differences in treatment options between countries Link Content
224 Asking about experiences with MRI after induction chemo Link Content
225 Asking about MRI results and the presence of lytic lesions Link Content
226 Asking about the age of the deceased Link Content
227 Asking about the effectiveness of treatments for multiple years Link Content
228 Asking for additional questions Link Content
229 Asking for advice on indoor skydiving with a disease Link Content
230 Asking for personal experiences from others Link Content
231 Asking questions during the session Link Content
232 Assessing overall health status Link Content
233 Assisted suppression Link Content
234 Assisting with daily activities (changing diapers, bathing, feeding, etc.) Link Content
235 Attempt to placate patient's worries Link Content
236 Attempted speech through mouth movements Link Content
237 Attending a family wedding Link Content
238 Attending cancer support groups Link Content
239 Attending doctor's appointments Link Content
240 Attending support groups for CAR-T therapy patients and caregivers Link Content
241 Attending the live premiere of "Everything You Need to Know About Multiple Myeloma - Episode 2" Link Content
242 Attending the talk on myeloma treatments and patient journey Link Content
243 Attention span affected by pain and weariness Link Content
244 Autologous stem cell transplant Link Content
245 Autologous Stem Cell transplant Link Content
246 Avoiding crowds and small enclosed places Link Content
247 Awareness of disease recurrence Link Content
248 Awareness of potential relapse Link Content
249 Awareness of the dangers of the herpes zoster virus Link Content
250 Awareness of things in the pipeline Link Content
251 Balancing personal and family perspectives Link Content
252 Balancing priorities between spending time with the mother and focusing on personal future Link Content
253 Balancing work responsibilities and managing a disease Link Content
254 Battling deep anxieties Link Content
255 Bed sore closure Link Content
256 Being a caregiver for a loved one with myeloma Link Content
257 Being a cheerleader Link Content
258 Being a source of light and positivity Link Content
259 Being able to move her eyes and head a little bit Link Content
260 Being brought home for end-of-life care Link Content
261 Being classified as cancer-free after transplant Link Content
262 Being completely paralyzed Link Content
263 Being deemed cancer-free after one round of chemo Link Content
264 Being diagnosed with central nervous system multiple myeloma Link Content
265 Being hooked up to an IV Link Content
266 Being in remission after 6 months of treatment Link Content
267 Being informed about the rarity of CNS multiple myeloma Link Content
268 Being monitored by a specialist unit in London for Amyloidosis Link Content
269 Being on a second drug regimen Link Content
270 Being on a waitlist for SCT Link Content
271 Being on DVTD treatment regimen Link Content
272 Being stuck in an isolation room Link Content
273 Being stuck in bed Link Content
274 Being thankful for each day despite the uncertainty of the future Link Content
275 Being there for family Link Content
276 Being told that the damage is irreversible Link Content
277 Being underwhelmed when told about remission Link Content
278 Being with close family Link Content
279 Belief in CAR-T's safety profile Link Content
280 Belly swelling Link Content
281 Biopsy results Link Content
282 Blood clots Link Content
283 Blood transfusion Link Content
284 Blood transfusions Link Content
285 Boat neck t-shirts Link Content
286 Bone marrow biopsy shows nothing Link Content
287 Bone or organ damage Link Content
288 Bone pain and difficulty sleeping Link Content
289 Bouts of tachycardia Link Content
290 Brain fog Link Content
291 Brain scan showing white spots Link Content
292 Breathing on her own again with the help of the machine Link Content
293 Bringing activities to stay mentally occupied Link Content
294 Bringing entertainment materials Link Content
295 Bringing entertainment materials (book, iPad, magazines) to pass the time Link Content
296 Broken right humerus Link Content
297 Burning sensation when laying down Link Content
298 Burning sensation when lying down Link Content
299 Busy and stressful lifestyle Link Content
300 Call and text when you can't Link Content
301 CAR-T not working Link Content
302 Cardigans Link Content
303 Carrying bags for emergencies Link Content
304 Carrying the bag of test results and medical information Link Content
305 Catching Covid Link Content
306 Celebrating good news and milestones Link Content
307 Celebrating successful treatment Link Content
308 Celebration of progress Link Content
309 Celebration of remission Link Content
310 Challenging days Link Content
311 Change in IGA score from 3802 to 142 Link Content
312 Change in kappa chain levels from 48.2 to 30.2 Link Content
313 Changes in cognitive function Link Content
314 Changes in daily routine Link Content
315 Changes in daily routines Link Content
316 Changes in emotional well-being Link Content
317 Changes in medication protocol Link Content
318 Changes in mobility Link Content
319 Changes in physical condition Link Content
320 Changes in sleep patterns Link Content
321 Changes in social interactions Link Content
322 Charging into the fray confidently and ferociously Link Content
323 Chemo to normalize kappa/lambda levels Link Content
324 Chemo treatment decision Link Content
325 Chemo treatment for MM destroys the body's natural ability to heal and fight infections Link Content
326 Chemotherapy treatment Link Content
327 Chronic pain Link Content
328 chudezee: Providing dietary advice and reassurance Link Content
329 Clean PET scan Link Content
330 Cleaning hands often Link Content
331 Climbing the mountain inch by inch Link Content
332 Clinical trial participation Link Content
333 Clinical trials and chemo options not viable Link Content
334 Cognitive decline Link Content
335 Cold that took three weeks to get over Link Content
336 Collapsed vertebrae Link Content
337 Collection of stem cells for future transplant Link Content
338 Coma Link Content
339 Coming to terms with the situation Link Content
340 Comment on the appearance of urine and its relation to protein levels Link Content
341 Commenting on the beauty of the post Link Content
342 Commenting on the rarity of finding posts from individuals with MM/AL Amyloidosis Link Content
343 Communication difficulties Link Content
344 Communication through yes/no questions and nods Link Content
345 Comparing CAR-T and SCT treatments and their safety profiles Link Content
346 Comparing experiences Link Content
347 Comparing their expectations to the reality of being in remission Link Content
348 Comparing their remission experience to others Link Content
349 Complete remission Link Content
350 Complete response to CAR-T Link Content
351 Completion of 47th infusion Link Content
352 Completion of chemotherapy Link Content
353 Concealing pain or discomfort Link Content
354 Concern about relapse and disease progression Link Content
355 Concern about the new immune evasive strain of Covid-19 Link Content
356 Concerned about the impact on children Link Content
357 Concerns about being bed bound Link Content
358 Concerns about future health complications Link Content
359 Concerns about preexisting conditions Link Content
360 Condolences and expressions of sympathy Link Content
361 Congratulatory messages from friends and well-wishers Link Content
362 Consideration of disease-specific regulations Link Content
363 Considering a second opinion Link Content
364 Considering a spinal tap for diagnosis Link Content
365 Considering going back to small groups Link Content
366 Considering the seriousness of HZE Link Content
367 Considering therapy for venting and emotional support Link Content
368 Considering turmeric Link Content
369 Constant risk of myeloma relapse Link Content
370 Constant sleep Link Content
371 Consuming protein shakes and electrolyte drinks Link Content
372 Consumption of protein shakes and electrolyte drinks Link Content
373 Contacting Medicare for assistance Link Content
374 Continued medication adherence Link Content
375 Continuing chemotherapy for normalizing light chains Link Content
376 Continuing chemotherapy to normalize light chain levels Link Content
377 Continuing journey with myeloma Link Content
378 Continuing with daily life despite the diagnosis Link Content
379 Contracting a physiotherapist Link Content
380 Contracting various illnesses Link Content
381 Controlling body temperature Link Content
382 Conveying love Link Content
383 Coping with physical limitations Link Content
384 Coping with the loss of a loved one Link Content
385 Coping with uncertainty and fear Link Content
386 Cost of medication Link Content
387 Cough from settled chest Link Content
388 Crashing and being transferred to hospice care Link Content
389 Creating good experiences Link Content
390 Crying Link Content
391 Crying together Link Content
392 CT scan shows growing mass Link Content
393 Currently on a wait list for SCT (stem cell transplant) Link Content
394 Currently on a wait list for SCT (Stem Cell Transplant) Link Content
395 Daily check-ins to monitor vitals Link Content
396 Data on older folks Link Content
397 Dealing with physical complications (disintegrated and misaligned T 10 and disintegrated C 6) Link Content
398 Dealing with physical pain and discomfort Link Content
399 Death at a young age Link Content
400 Death of younger patients Link Content
401 Decline in patience and temperament Link Content
402 Decline in physical abilities Link Content
403 Declining health Link Content
404 Declining health and physical symptoms Link Content
405 Declining mental health Link Content
406 Decorticate posturing Link Content
407 Decrease in K/L ratio from > 1000.00 to 1.82 Link Content
408 Decrease in Kappa light chain from 10706.6 mg/L to 27 mg/L Link Content
409 Decreased appetite Link Content
410 Decreased appetite and potential nausea Link Content
411 Decreased attention span Link Content
412 Decreased mobility Link Content
413 Decreased productivity Link Content
414 Decreased urination Link Content
415 Decreased urine output Link Content
416 Decreasing levels of free lambda light chain Link Content
417 Deepening of love in a relationship Link Content
418 Delayed outpatient dialysis scheduling Link Content
419 Demonstrating resilience and endurance Link Content
420 Demonstrating self-motivation and self-care Link Content
421 Dependence on wife for transportation Link Content
422 Describing personal journey Link Content
423 Describing the bloodwork results as "normal" Link Content
424 Desire for a longer caregiving period Link Content
425 Desire for immune system support during treatment Link Content
426 Desiring a comprehensive understanding of the myeloma journey Link Content
427 Detection of the band on testing where M-spike would be Link Content
428 Deteriorating results with each failed treatment Link Content
429 Devastated and shocked by the diagnosis Link Content
430 Developing rash and blisters Link Content
431 Development of depression Link Content
432 Development of paralytic ileus after 10th dose Link Content
433 Development of paralytic ileus after 9th dose Link Content
434 Diagnosed with AL and MM Link Content
435 Diagnosed with throat cancer Link Content
436 Diagnosis confirmation Link Content
437 Diagnosis of a rare disease Link Content
438 Diagnosis of bladder cancer Link Content
439 Diagnosis of cancer at a young age Link Content
440 Diagnosis of herpes zoster encephalitis Link Content
441 Diagnosis of MGUS (starting of Multiple Myeloma) Link Content
442 Diagnosis of multiple myeloma Link Content
443 Diagnosis of Multiple Myeloma Link Content
444 Diagnosis of stage 3 multiple myeloma Link Content
445 Dialysis Link Content
446 Dialysis treatment Link Content
447 Dialysis treatment for AL Amyloidosis Link Content
448 Dietary restrictions and challenges Link Content
449 Differences in overall health status among older patients Link Content
450 Differentiating between cancer friends, myeloma friends, and friends without illness Link Content
451 Difficulty breathing Link Content
452 Difficulty catching breath while biking Link Content
453 Difficulty eating Link Content
454 Difficulty focusing and decreased work quality Link Content
455 Difficulty in achieving clear results in serum protein analysis Link Content
456 Difficulty in fully celebrating remission Link Content
457 Difficulty in movement due to wearing non-slip slippers Link Content
458 Difficulty sleeping due to anxiety and racing thoughts Link Content
459 Difficulty standing and needing support Link Content
460 Difficulty walking and standing for long periods Link Content
461 Dining out during slow hours Link Content
462 Discovering cheap tiny vacuums on Amazon Link Content
463 Discussing medical treatments and progress Link Content
464 Discussing medication regimens Link Content
465 Discussing personal experiences with chemotherapy and working through it Link Content
466 Discussing response to induction chemotherapy Link Content
467 Discussing the challenges of treatment and travel Link Content
468 Discussing the disease with others Link Content
469 Discussing the impact of a recent fracture on eligibility for a stem cell transplant Link Content
470 Discussing the impact of frequent hospital visits on quality of life Link Content
471 Discussing the impact of treatment on physical and mental well-being Link Content
472 Discussing the ongoing nature of the disease despite being in remission Link Content
473 Discussing time frame Link Content
474 Discussing treatment options and outcomes Link Content
475 Discussing treatment options and progress Link Content
476 Discussing treatment progress and milestones Link Content
477 Discussion of medical awareness and knowledge Link Content
478 Discussion of MRI/CT scan to check for bone abnormalities Link Content
479 Dismissing symptoms Link Content
480 Displaying optimism Link Content
481 Displaying patience and acceptance Link Content
482 Displaying perseverance and determination Link Content
483 Distance from home (200 miles) Link Content
484 DKRd for four months Link Content
485 Doctors being aware of MM as a possible diagnosis Link Content
486 Downplaying personal achievements Link Content
487 Dr calling with urgent news Link Content
488 Drug combination as standard of care Link Content
489 Eating a lot during the first few days Link Content
490 Eating ice chips or popsicles to prevent mouth and throat sores Link Content
491 Eating ice cream (without nuts) Link Content
492 Eating ice to prevent mouth sores Link Content
493 Elevated creatinine levels Link Content
494 Elevated kappa/lambda light chains Link Content
495 Elevated numbers in diagnostic context Link Content
496 Embracing faith, family, and personal passions as sources of strength Link Content
497 Embracing the present Link Content
498 EMG and nerve conduction study Link Content
499 Emotional and physical exhaustion Link Content
500 Emotional breakdown and sharing diagnosis with spouse Link Content
501 Emotional impact of losing a loved one to multiple myeloma Link Content
502 Emotional pain Link Content
503 Empathizing with the initial stress of the diagnosis Link Content
504 Emphasis on the importance of a supporting spouse Link Content
505 Emphasizing the importance of hope and faith Link Content
506 Emphasizing the importance of staying positive Link Content
507 Encouragement Link Content
508 Encouragement to check in-network care providers, pharmacies, co-pays, deductibles, and prescription coverage Link Content
509 Encouragement to take each day as it comes and not to worry about "what ifs" Link Content
510 Encouraging and motivating the person Link Content
511 Encouraging children to live their best lives Link Content
512 Encouraging friends and others on the cancer journey Link Content
513 Encouraging others to keep fighting Link Content
514 Encouraging self-care Link Content
515 Encouraging self-care and therapy Link Content
516 Enduring the effects of heavy drugs Link Content
517 Engaging in conversations with colleagues Link Content
518 Engaging in medical appointments and tests Link Content
519 Engaging in mountain climbing for fundraising Link Content
520 Engaging in one-on-one conversations Link Content
521 Engaging in online discussions about CAR-T therapy Link Content
522 Engaging in physical activity Link Content
523 Engaging in physical therapy Link Content
524 Engaging in self-care practices Link Content
525 Engaging in self-management Link Content
526 Engaging in support groups and seeking emotional support Link Content
527 Engaging in support groups or seeking emotional support Link Content
528 Engaging with a physical therapist Link Content
529 Enjoying golf and family time at the beach Link Content
530 Enjoying phone calls and visits from children Link Content
531 Enjoying retirement and playing golf Link Content
532 Enjoying the experience Link Content
533 Enjoying the moment Link Content
534 Enjoying time and staying positive Link Content
535 Enrollment in company health insurance plan Link Content
536 Exacerbation of back pains from the hospital bed Link Content
537 Excitement about advances in myeloma treatment Link Content
538 Excitement about teclistamab response Link Content
539 Exhaustion from chemotherapy Link Content
540 Exhaustion from long-term chemotherapy Link Content
541 Expectation of high remission rate with CAR-T Link Content
542 Expecting a few days in the bathroom after transplant Link Content
543 Expecting celebration, but receiving an anticlimactic response Link Content
544 Experience of sleepless nights waiting for test results Link Content
545 Experiencing a reaction to Darzalex Link Content
546 Experiencing a relapse Link Content
547 Experiencing arguments with family members Link Content
548 Experiencing back pain Link Content
549 Experiencing CRS (Cytokine Release Syndrome) Link Content
550 Experiencing decline in health Link Content
551 Experiencing discomfort and frustration Link Content
552 Experiencing elevated light chain levels Link Content
553 Experiencing elevated light chains Link Content
554 Experiencing excruciating back pain Link Content
555 Experiencing fatigue and loss of fight Link Content
556 Experiencing health complications Link Content
557 Experiencing improvement in health Link Content
558 Experiencing improvements in physical abilities Link Content
559 Experiencing leg pain Link Content
560 Experiencing pain and discomfort Link Content
561 Experiencing pain when lifting heavy objects or walking in stores Link Content
562 Experiencing pain when sitting or walking Link Content
563 Experiencing relentless pain Link Content
564 Experiencing symptoms Link Content
565 Experiencing symptoms such as bone pain or fatigue Link Content
566 Experiencing tumor growth in L2 vertebra and sacrum Link Content
567 Experiencing varying levels of fatigue Link Content
568 Experiencing worsening symptoms Link Content
569 Exploring alternative healing methods Link Content
570 Exploring alternative treatment options Link Content
571 Exploring options for inflammation and pain relief Link Content
572 Exploring supplements Link Content
573 Expressing a desire for a better outcome Link Content
574 Expressing a desire for support and guidance Link Content
575 Expressing a lack of motivation or hope for the future Link Content
576 Expressing a need for effective coping mechanisms Link Content
577 Expressing a sense of helplessness or being at a loss for words Link Content
578 Expressing admiration and inspiration Link Content
579 Expressing admiration for adventurous individuals with the disease Link Content
580 Expressing admiration for others' attitudes and handling of their conditions Link Content
581 Expressing anticipation for improvement Link Content
582 Expressing anxiety and anticipation for test results Link Content
583 Expressing comfort and support Link Content
584 Expressing concern about specific medical tests Link Content
585 Expressing concern about spots still lighting up on bones Link Content
586 Expressing concern about the duration of the disease Link Content
587 Expressing condolences Link Content
588 Expressing congratulations Link Content
589 Expressing emotions such as resentment, fear, insecurity, and anxiety Link Content
590 Expressing empathy and support for others affected by myeloma Link Content
591 Expressing feelings of overwhelm and exhaustion Link Content
592 Expressing frustration and anger towards the doctor Link Content
593 Expressing frustration and disbelief about the situation Link Content
594 Expressing gratitude and congratulations Link Content
595 Expressing gratitude and hope Link Content
596 Expressing gratitude and support Link Content
597 Expressing gratitude and well wishes Link Content
598 Expressing gratitude for cherished moments Link Content
599 Expressing gratitude for finding stories from people with both conditions Link Content
600 Expressing gratitude for loved ones Link Content
601 Expressing gratitude for shared experiences and well-wishes Link Content
602 Expressing gratitude for shared moments Link Content
603 Expressing gratitude for the time spent with the loved one Link Content
604 Expressing gratitude for treatment options and research Link Content
605 Expressing gratitude towards the caretaker Link Content
606 Expressing grief Link Content
607 Expressing happiness and congratulations Link Content
608 Expressing happiness and support for the news Link Content
609 Expressing hope Link Content
610 Expressing hope and determination Link Content
611 Expressing hope and frustration about advancements in treatment Link Content
612 Expressing hope for a pain-free and peaceful journey Link Content
613 Expressing hope for peace and comfort Link Content
614 Expressing hope for the future Link Content
615 Expressing joy and celebration Link Content
616 Expressing love Link Content
617 Expressing love and appreciation for the person Link Content
618 Expressing love and care Link Content
619 Expressing love and gratitude towards wife Link Content
620 Expressing numbness or lack of excitement about being in remission Link Content
621 Expressing optimism about treatment progress Link Content
622 Expressing prayers and support Link Content
623 Expressing relief and happiness Link Content
624 Expressing relief and numbness simultaneously Link Content
625 Expressing sadness and empathy Link Content
626 Expressing support and empathy Link Content
627 Expressing sympathy Link Content
628 Expressing the importance of sharing stories and raising awareness Link Content
629 Expression of sympathy Link Content
630 Extended hospital stay far from home Link Content
631 Extended hospital stays Link Content
632 Facing an uncertain future Link Content
633 Facing challenging moments Link Content
634 Fading away and becoming non-responsive Link Content
635 Failure to wake up Link Content
636 Faith in God as a source of comfort and strength Link Content
637 Falling asleep every 30 seconds until called Link Content
638 Family support Link Content
639 Fatigue and exhaustion Link Content
640 Fatigue and lots of napping Link Content
641 Fatigue and napping Link Content
642 Fatigue and pain Link Content
643 Fear of losing mom to cancer Link Content
644 Fear of making mistakes with severe consequences Link Content
645 Fear of remaining bedridden Link Content
646 Fear of setting loved ones back Link Content
647 Feeling a sense of accomplishment Link Content
648 Feeling a sense of loss and grief Link Content
649 Feeling a void without Dad Link Content
650 Feeling alone in the journey Link Content
651 Feeling anxious and unable to sleep Link Content
652 Feeling burnt out from caregiving Link Content
653 Feeling discouraged Link Content
654 Feeling excited and wanting to share Link Content
655 Feeling exhausted Link Content
656 Feeling frustrated Link Content
657 Feeling fuller and experiencing nausea Link Content
658 Feeling gratitude for spouse Link Content
659 Feeling hopeless about the future Link Content
660 Feeling like a shell of former self Link Content
661 Feeling lost Link Content
662 Feeling miserable without mom Link Content
663 Feeling more normal Link Content
664 Feeling numb despite reaching remission Link Content
665 Feeling of being adrift Link Content
666 Feeling of being placated Link Content
667 Feeling of emptiness Link Content
668 Feeling of excitement and anticipation Link Content
669 Feeling of weightlessness Link Content
670 Feeling overwhelmed Link Content
671 Feeling overwhelmed by financial concerns and job security Link Content
672 Feeling overwhelmed by stress, anxiety, and depression Link Content
673 Feeling overwhelmed by the diagnosis and its incurable nature Link Content
674 Feeling poorly and not training enough Link Content
675 Feeling scared and young Link Content
676 Feeling shocked and overwhelmed by unexpected changes in health status Link Content
677 Feeling thankful for each day Link Content
678 Feeling tired all the time Link Content
679 Feeling tired due to lack of sleep Link Content
680 Feeling upset and emotional Link Content
681 Fighting against the disease Link Content
682 Fighting for loved ones and a purpose Link Content
683 Finding comfort and inspiration in others' stories Link Content
684 Finding comfort and meaning in a symbol Link Content
685 Finding comfort in shared experiences Link Content
686 Finding happiness in seeing children succeed Link Content
687 Finding inspiration in the individual's story Link Content
688 Finding inspiration in the story Link Content
689 Finding new meaning and opportunities in life Link Content
690 Finding solace in coding Link Content
691 Finding support from others with similar experiences Link Content
692 Finding support from spouse and friends Link Content
693 Finding work as a distraction Link Content
694 First 8 doses without complications Link Content
695 Flu shot vaccination Link Content
696 Fluctuating blood levels Link Content
697 Fluctuating symptoms Link Content
698 Fluctuations in delirium Link Content
699 Fluctuations in free light chain test results Link Content
700 Focus on Covid and vaccines Link Content
701 Focus on living a fulfilling life Link Content
702 Focus on nutrition, exercise, and social services Link Content
703 Focus on treatment effectiveness Link Content
704 Focusing on overcoming today's battles Link Content
705 Follow-up appointments Link Content
706 Follow-up with GP Link Content
707 Following a treatment plan Link Content
708 Following aggressive treatment protocols Link Content
709 Following post-transplant guidelines Link Content
710 Following safety instructions Link Content
711 Following treatment plan Link Content
712 Following with eyes Link Content
713 Forgetfulness Link Content
714 Fortifying the mind and cherishing moments with loved ones Link Content
715 Four cycles of VRD treatment Link Content
716 Fractured femur Link Content
717 Fractures Link Content
718 Fractures in multiple areas Link Content
719 Free chain test conducted Link Content
720 Frequent air chopper rides Link Content
721 Frequent blood transfusions Link Content
722 Frequent medical appointments Link Content
723 Friendly_Promise_998: Offering reassurance and suggesting further consultation with a doctor Link Content
724 Frightened and questioning after diagnosis Link Content
725 Frustration and fear Link Content
726 Frustration with healthcare system Link Content
727 Full panel of blood work Link Content
728 Gathering loved ones for support Link Content
729 Generating memories Link Content
730 Genotype of cancer cells impacting individual results Link Content
731 Getting back to activities Link Content
732 Getting bone X-rays Link Content
733 Getting Covid and flu vaccines Link Content
734 Getting Covid and flu vaccines after 90 days Link Content
735 Getting insurance Link Content
736 Getting monthly Zometa for bone strengthening Link Content
737 Getting stronger in palliative care for three days Link Content
738 Getting up and out of bed multiple times a day Link Content
739 Given two treatment options Link Content
740 Going in public places after being released from the hospital Link Content
741 Going on Darzalex treatment Link Content
742 Going on walks Link Content
743 Going through rounds of therapy and treatment Link Content
744 Going to a PC Link Content
745 Going to the ER Link Content
746 Going to the hospital every 4 weeks for daratumumab injection Link Content
747 Going to war with cancer Link Content
748 Good diet Link Content
749 Good energy Link Content
750 Gradual adjustment to new circumstances Link Content
751 Grateful attitude Link Content
752 Gratefulness for each day Link Content
753 Grim prognosis from doctors Link Content
754 Grocery shopping with a mask Link Content
755 Hair loss starting around 12 to 14 days after initial chemo Link Content
756 Having a sleep aid on order Link Content
757 Having a three-medication plan for nausea Link Content
758 Having annual tests and scans to assess protein levels Link Content
759 Having fleeting moments of distraction Link Content
760 Having more seizures Link Content
761 Hearing others' experiences Link Content
762 Heavy drug use Link Content
763 Heavy medieval chemotherapy Link Content
764 Helping with grocery shopping Link Content
765 Helplessness Link Content
766 Hiding true emotions Link Content
767 High dose chemo while working Link Content
768 High levels of creatinine and urea Link Content
769 High risk of infections Link Content
770 Highlighting the continuous advancements in medicine Link Content
771 Highlighting the importance of fall prevention Link Content
772 Highlighting the unfortunate timing of new treatments for some individuals Link Content
773 Hiking for several hours on nice weekends Link Content
774 Hindered mobility Link Content
775 Holding onto hope Link Content
776 Hope for a more permanent solution Link Content
777 Hope for recovery Link Content
778 Hopefulness Link Content
779 Hopefulness and optimism despite challenges Link Content
780 Hopefulness despite setbacks Link Content
781 Hoping for the father to rest peacefully Link Content
782 Hospital visits every 4 weeks for daratumumab injection Link Content
783 Hospitalization and isolation Link Content
784 Hospitalization due to low red counts, pneumonia, and falling Link Content
785 Hospitalization for 3 weeks Link Content
786 Hospitalization for Bronchitis Link Content
787 Hospitalization for C-diff Link Content
788 Hospitalization for Covid-19 Link Content
789 Hospitalization for heart attacks Link Content
790 Hospitalization for pain management Link Content
791 Hospitalization for Pneumonia Link Content
792 Hospitalizations Link Content
793 Hospitalizations and medical treatments Link Content
794 Impact of age on the body's ability to fight infections Link Content
795 Impact of treatment on the body's ability to heal Link Content
796 Impact on daily life Link Content
797 Impact on individuals, families, and communities Link Content
798 Impact on job performance Link Content
799 Impatience and frustration Link Content
800 Impatience and frustration with waiting Link Content
801 Importance of early diagnosis and risk factors Link Content
802 Improved cognitive function Link Content
803 Improvement in numbers with medication Link Content
804 In and out of the hospital for treatment Link Content
805 Inability to sleep Link Content
806 Inability to walk again Link Content
807 Inability to walk through the ward Link Content
808 Inconsistent availability of providers Link Content
809 Incorporating daily walks into routine Link Content
810 Increased forgetfulness Link Content
811 Increased heart rate and blood pressure Link Content
812 Increased knowledge about human biology Link Content
813 Increased need for support Link Content
814 Increased reliance on healthcare professionals Link Content
815 Increased reliance on medical devices Link Content
816 Increased workload due to treatment Link Content
817 Increasing reliance on medical interventions Link Content
818 IndependentMachine62 providing positive news and reassurance Link Content
819 Indifference towards work Link Content
820 Induced coma Link Content
821 Induction chemo for 12 cycles Link Content
822 Infections take a toll on the physical body Link Content
823 Inflammation in the brain Link Content
824 Inquiring about in-patient or out-patient status Link Content
825 Inquiring about lytic lesions and their status Link Content
826 Inquiring about spots still appearing on bones after induction chemo Link Content
827 Instructor guiding the skydive Link Content
828 Insurance approval delays Link Content
829 Intense sciatic nerve pain Link Content
830 Interacting with multiple churches Link Content
831 Interested in knowing what others are using in remission Link Content
832 Irony of cancer remission but vulnerability to pneumonia Link Content
833 Irritability Link Content
834 Keeping the focus on the present moment and decision-making Link Content
835 Kicking ass at job Link Content
836 Kidney condition limiting treatment options Link Content
837 Kidney deterioration Link Content
838 Kidney function not improving Link Content
839 Kissing mom and expressing love Link Content
840 Knowing the next steps and potential pitfalls Link Content
841 Kyphoplasty procedure Link Content
842 Lab work shows high free kappa light chains Link Content
843 Labored breathing Link Content
844 Labs completed on 10/09/2023 show abnormal results Link Content
845 Lack of appetite Link Content
846 Lack of awareness about cancer risk Link Content
847 Lack of awareness about multiple myeloma Link Content
848 Lack of confidence in diagnosis Link Content
849 Lack of exercise Link Content
850 Lack of experience among doctors in making determinations for specific tests Link Content
851 Lack of experience in making determinations for MM Link Content
852 Lack of focus Link Content
853 Lack of intense focus at work after treatment Link Content
854 Lack of sleep Link Content
855 Lack of understanding from others Link Content
856 Landing safely Link Content
857 Layering clothing for temperature regulation Link Content
858 Learning about human biology Link Content
859 Learning about the disease and its effects Link Content
860 Learning about the disease and its impact on the body Link Content
861 Learning curve of dealing with the disease Link Content
862 Learning not to be held hostage by things beyond control Link Content
863 Learning to self-administer injections Link Content
864 Left side paralysis Link Content
865 Lenalidomide Link Content
866 Letting go of previous commitments Link Content
867 Letting go of previous commitments and activities Link Content
868 Lifestyle adjustments Link Content
869 Light chains rising Link Content
870 Limited mobility and confinement indoors Link Content
871 Limited mobility and reliance on bed exercises Link Content
872 Limited movement in feet, head, fingers, and right shoulder Link Content
873 Limited social activities Link Content
874 Limited time remaining Link Content
875 Listening to nurses and staying active Link Content
876 Little remission Link Content
877 Living a fulfilling life despite illness uncertainty Link Content
878 Living a wonderful and fulfilling life Link Content
879 Living for each day and staying positive Link Content
880 Living in a beach community Link Content
881 Long commute for treatment Link Content
882 Long road of treatment ahead Link Content
883 Long-lasting sequelae from encephalitis Link Content
884 Long-term post-SCT and remission Link Content
885 Longing for Dad's advice and support Link Content
886 Longing for the person's smile and presence Link Content
887 Looking dapper Link Content
888 Looking for clinical trials on specific maintenance treatments Link Content
889 Looking for low impact workouts Link Content
890 Looking for personal experiences and insights Link Content
891 Looking for resources to support myeloma patients and their loved ones Link Content
892 Looking for the latest treatments and research Link Content
893 Looking into herpes zoster encephalitis (HZE) Link Content
894 Losing job Link Content
895 Loss of a loved one Link Content
896 Loss of hope Link Content
897 Loss of hope for recovery Link Content
898 Loss of independence and reliance on others Link Content
899 Loved ones desperately wanting to believe it won't reoccur Link Content
900 Low energy levels Link Content
901 Low function kidneys Link Content
902 Maintaining hope and optimism Link Content
903 Maintaining social connections Link Content
904 Maintenance therapy Link Content
905 Making lifestyle changes Link Content
906 Manageable pain Link Content
907 Managing daily routines Link Content
908 Managing emotional and psychological impact Link Content
909 Managing emotions related to the upcoming SCT Link Content
910 Managing fear and uncertainty Link Content
911 Managing financial and logistical challenges Link Content
912 Managing lifestyle changes Link Content
913 Managing medication and treatment schedules Link Content
914 Managing medication and wound care Link Content
915 Managing neuropathy symptoms Link Content
916 Managing others' reactions to results Link Content
917 Managing own health anxiety Link Content
918 Managing side effects of chemotherapy Link Content
919 Managing symptoms Link Content
920 Managing treatment side effects Link Content
921 Manufacturing delay Link Content
922 Masking up in crowded places Link Content
923 Masking vulnerability Link Content
924 Mechanical ventilation Link Content
925 Medical appointments Link Content
926 Medical treatment Link Content
927 Medication adherence Link Content
928 Medication options Link Content
929 Meeting with nurse to discuss questions Link Content
930 Melphalan treatment before transplant Link Content
931 Memory problems Link Content
932 Mention of "scanxiety" for blood test results Link Content
933 Mention of abnormal test result Link Content
934 Mention of being rediagnosed every 30 days Link Content
935 Mention of beneficial changes on some drugs and cost assistance Link Content
936 Mention of bone marrow biopsy as a necessary test Link Content
937 Mention of lab error Link Content
938 Mention of lab error possibility Link Content
939 Mention of MRD negative and renewed M spike Link Content
940 Mention of osteopenia (or osteoporosis) and risk of bolts tearing out Link Content
941 Mention of potential skeletal survey Link Content
942 Mention of reduction in kappa light chains and its effect on kidneys Link Content
943 Mention of skeletal survey Link Content
944 Mention of specific treatment options (DVTD) and its effectiveness Link Content
945 Mentioning family involvement Link Content
946 Mentioning specific medications (Lenalidomide, Velcade, Steroids) Link Content
947 Mentioning specific treatments Link Content
948 Mentioning the duration of chemotherapy treatment Link Content
949 Mentioning the impact of caregiving Link Content
950 Mentioning the impact of the disease Link Content
951 Mentioning the normalization of bloodwork and potential achievement of MRD- Link Content
952 Mentioning the possibility of linking the article Link Content
953 Mentioning the possibility of reaching MRD- (minimal residual disease negative) Link Content
954 Mentioning the presence and guidance of a deceased loved one Link Content
955 Mentioning the time of the procedure Link Content
956 Mentioning the unpredictability of time Link Content
957 Mild symptoms Link Content
958 Mind racing about bills and job security Link Content
959 Mini strokes due to lack of oxygen Link Content
960 Minimal pain except for post-surgery and physical therapy Link Content
961 Missing Dad's presence Link Content
962 Mix of pain and advancing age Link Content
963 MM patients may experience complications from infections Link Content
964 Monitoring and managing side effects of CAR-T therapy Link Content
965 Monitoring blood count numbers Link Content
966 Monitoring blood markers and symptoms Link Content
967 Monitoring blood tests Link Content
968 Monitoring blood work and test results Link Content
969 Monitoring body temperature Link Content
970 Monitoring health status Link Content
971 Monitoring of deductible status Link Content
972 Monitoring vital signs Link Content
973 Months of limited fulfillment in life Link Content
974 Motivation Link Content
975 Mourning Link Content
976 Moving a bunch of stuff around the house Link Content
977 Moving into palliative care Link Content
978 MRD found 46 myeloma cells per million Link Content
979 MRD negative Link Content
980 Multiple infections Link Content
981 Multiple medical conditions Link Content
982 Multiple rounds of chemo and targeted radiation therapy Link Content
983 Multiple visits for low-grade fevers Link Content
984 Muscles wasting away Link Content
985 Mutation of myeloma Link Content
986 Neck pain caused by extensive bone lesions Link Content
987 Need for access to treatment and support services Link Content
988 Need for advocacy Link Content
989 Need for follow-up in 6 months Link Content
990 Need for follow-up vaccination Link Content
991 Need for high-calorie intake Link Content
992 Need for information and support from others Link Content
993 Need for interpretation of blood work Link Content
994 Need for long-term medication Link Content
995 Need for medication adjustments Link Content
996 Need for more frequent brief breaks at work Link Content
997 Need for sedation during CT or PET scan Link Content
998 Need to make significant changes in life Link Content
999 Need to make significant life changes Link Content
1000 Need to stop smoking Link Content
1001 Needing assistance and support Link Content
1002 Needing assistance with dressing and showering Link Content
1003 Needing easy access to the arm Link Content
1004 Needing more time with mom Link Content
1005 Needing to undergo stem cell transplant Link Content
1006 Neurosurgeon's warning about limited pain elimination with vertebra binding Link Content
1007 News reminding people about Medicare enrollment deadline Link Content
1008 No evidence of disease in bone marrow or blood Link Content
1009 No metabolism Link Content
1010 No psychiatric issues or personality changes Link Content
1011 Nodding head in acknowledgment Link Content
1012 Non-response to standard treatments Link Content
1013 Nostalgia Link Content
1014 Nostalgia for the best years with Dad Link Content
1015 Not comfortable in theaters or crowded places Link Content
1016 Not currently undergoing multiple myeloma treatments Link Content
1017 Not eating out Link Content
1018 Not letting worry rob blessings of today Link Content
1019 Not requiring registration to attend Link Content
1020 Noticing back pain Link Content
1021 Noting the mother's tiredness Link Content
1022 Noting the presence of many potential solutions in development Link Content
1023 Numerous blood transfusions Link Content
1024 Occasional miracles Link Content
1025 Offering comfort and support Link Content
1026 Offering help and support Link Content
1027 Offering love and healing energy Link Content
1028 Offering prayers Link Content
1029 Offering prayers and support to others Link Content
1030 Offering prayers and thoughts Link Content
1031 Offering prayers or wishes for peace and healing Link Content
1032 Offering specific acts of kindness Link Content
1033 Offering support and assistance Link Content
1034 Offering support and comfort Link Content
1035 Offering support and sympathy Link Content
1036 Offering sympathies to the family Link Content
1037 Offering wishes and support Link Content
1038 Offering words of encouragement and support Link Content
1039 Official relapse classification in December 2018 Link Content
1040 Officially declared in a coma Link Content
1041 Oncologist refusing to guess Link Content
1042 Oncologist sharing the report with a big smile Link Content
1043 One test not ruling out MM definitively Link Content
1044 Opening eyes Link Content
1045 Opening her eyes a bit when called Link Content
1046 Optimism Link Content
1047 Optimism fading as treatments fail Link Content
1048 Ordering medications for migraines or similar issues Link Content
1049 Ordering medications in advance Link Content
1050 Ordering necessary medications in advance Link Content
1051 Ordering regular and extra pain medications Link Content
1052 Oscillation between slight improvement and worsening Link Content
1053 Other forms of infection and inflammation Link Content
1054 Out of options Link Content
1055 Outpatient chemo for three weeks Link Content
1056 Over a dozen fractures Link Content
1057 Overcoming pneumonia Link Content
1058 Pain becoming more unbearable Link Content
1059 Pain in lower back during Thanksgiving holiday Link Content
1060 Pain management issues Link Content
1061 Painful recovery Link Content
1062 Partial paralysis Link Content
1063 Participating in cancer survivor activities Link Content
1064 Participating in clinical trials or research studies Link Content
1065 Participating in support groups Link Content
1066 Participating in support groups or therapy Link Content
1067 Participating in the question and answer session Link Content
1068 Participation in clinical trials Link Content
1069 Passing time until the 1 year mark Link Content
1070 Patient achieving deep response Link Content
1071 Patient acknowledging the role of loved ones in their journey Link Content
1072 Patient being informed about maintenance treatment Link Content
1073 Patient being informed about MRD status Link Content
1074 Patient being informed about the window of time for surgery Link Content
1075 Patient being informed that bones will never be as solid as before but will mend Link Content
1076 Patient being reminded about insurance plan renewals and the opportunity to switch coverage for the coming year Link Content
1077 Patient being told not to worry Link Content
1078 Patient being told surgery is an option if pain persists Link Content
1079 Patient being told that pain will alleviate with treatment Link Content
1080 Patient being told that pain will be alleviated with treatment Link Content
1081 Patient deciding not to have surgery Link Content
1082 Patient deciding to try pain medication and brace instead of surgery Link Content
1083 Patient discussing entertainment options for the recovery period Link Content
1084 Patient discussing medical treatments and procedures Link Content
1085 Patient discussing upcoming SCT procedure Link Content
1086 Patient experiencing chronic back pain and anemia Link Content
1087 Patient experiencing fatigue Link Content
1088 Patient experiencing improvement in overall health Link Content
1089 Patient expressing anxiety and seeking preparation advice for Autologous SCT Link Content
1090 Patient expressing anxiety and worry about potential MM diagnosis Link Content
1091 Patient expressing concern about upcoming blood test results Link Content
1092 Patient expressing gratitude for support received Link Content
1093 Patient expressing hope and determination in fighting the disease Link Content
1094 Patient expressing nervousness and anxiety about the situation Link Content
1095 Patient feeling disappointed Link Content
1096 Patient feeling dismissed by their GP Link Content
1097 Patient finding meaning or purpose in their experience Link Content
1098 Patient inquiring about in-patient or out-patient status for ASCT Link Content
1099 Patient is followed closely by PCP and endocrinologist Link Content
1100 Patient mentioning the involvement of healthcare professionals Link Content
1101 Patient not undergoing surgery Link Content
1102 Patient providing an update on their mother's cancer treatment journey Link Content
1103 Patient reading the paperwork and seeing the phrase "Against all expectations" Link Content
1104 Patient receiving mental advice on how to cope with the treatment process Link Content
1105 Patient receiving positive news about insurance coverage and improved health numbers Link Content
1106 Patient receiving treatment (dara+R) Link Content
1107 Patient reflecting on the impact of their illness on daily life Link Content
1108 Patient relying on pain medication for relief Link Content
1109 Patient seeking advice and sharing experiences with others Link Content
1110 Patient seeking advice and support from online community Link Content
1111 Patient sharing a photo related to their illness journey Link Content
1112 Patient sharing experience with neuropathy and its potential impact Link Content
1113 Patient sharing personal medical history and current diagnostic tests Link Content
1114 Patient sharing their medical journey and experiences Link Content
1115 Patient still needing occasional naps Link Content
1116 Patient's anxiety and fear Link Content
1117 Patient's body slowly repairing but not as solid as before Link Content
1118 Patients celebrating their remission but feeling uncertain about the future Link Content
1119 Patients considering their physical limitations and abilities Link Content
1120 Patients discussing the effects of the disease on different parts of their body Link Content
1121 Patients discussing the results of their medical tests Link Content
1122 Patients discussing their plans with their doctor for guidance Link Content
1123 Patients displaying abnormal blood test results Link Content
1124 Patients exhibiting changes in appetite Link Content
1125 Patients experiencing collapsed vertebra or kidney near failure as a major event leading to diagnosis Link Content
1126 Patients experiencing difficulty breathing Link Content
1127 Patients experiencing fatigue Link Content
1128 Patients experiencing possible heart damage from amyloid created by myeloma Link Content
1129 Patients experiencing symptoms that can be attributed to other conditions Link Content
1130 Patients experiencing weight loss Link Content
1131 Patients expressing gratitude for reaching remission Link Content
1132 Patients expressing their emotions and concerns about remission Link Content
1133 Patients falling asleep due to toxin buildup Link Content
1134 Patients feeling numb about their remission Link Content
1135 Patients feeling the need to inform local community physicians about their MM diagnosis and treatment Link Content
1136 Patients going through years of not feeling well and multiple doctor visits and tests Link Content
1137 Patients participating in clinical trials Link Content
1138 Patients reaching remission Link Content
1139 Patients relying on Google searches to find answers and seeking support online Link Content
1140 Patients reporting cognitive impairment Link Content
1141 Patients reporting pain Link Content
1142 Patients seeking advice and support from doctors through portals Link Content
1143 Patients seeking advice from others who have similar conditions Link Content
1144 Patients seeking answers through multiple doctor appointments Link Content
1145 Patients seeking medical advice from their GP and other doctors Link Content
1146 Patients sharing their personal experiences with the disease and its impact on their activities Link Content
1147 Patients sharing their success stories and milestones Link Content
1148 Patients showing signs of infection Link Content
1149 Patients showing signs of inflammation Link Content
1150 Patients undergoing more standard of care drugs Link Content
1151 Patients undergoing standard of care drugs Link Content
1152 Patients undergoing stem cell transplant Link Content
1153 Payment of monthly premiums Link Content
1154 Perception of "normal" returning Link Content
1155 Performing household chores Link Content
1156 Peripheral nerve damage and sciatic nerve pain Link Content
1157 Persistent fatigue Link Content
1158 Personal experience with a frightening situation Link Content
1159 PET scan and ultrasound Link Content
1160 PET scan on 10/31 Link Content
1161 PET scans showing solid tumors Link Content
1162 Physical decline Link Content
1163 Physical decline and muscle wasting Link Content
1164 Physical pain Link Content
1165 Physical pain and discomfort Link Content
1166 Physical symptoms Link Content
1167 Physical therapy Link Content
1168 Physical weakness Link Content
1169 Physically and mentally demanding job Link Content
1170 Placement of stents Link Content
1171 Planning aggressive travel Link Content
1172 Planning for future travel and living life to the fullest Link Content
1173 Planning to move to North Carolina Link Content
1174 Planning treatment cycles around a football season Link Content
1175 Planning trips and activities Link Content
1176 Planning trips and making memories Link Content
1177 Playing disc golf Link Content
1178 Playing with child to temporarily escape reality Link Content
1179 Playing with kids Link Content
1180 Political implications Link Content
1181 Poor work quality Link Content
1182 Positive attitude Link Content
1183 Positive attitude towards treatment Link Content
1184 Positive outlook Link Content
1185 Positive outlook on life Link Content
1186 Positive reinforcement Link Content
1187 Positive response to CAR-T treatment Link Content
1188 Post-ASCT bone marrow biopsy on day +60 Link Content
1189 Posting lengthy posts on a Reddit thread Link Content
1190 Posting on Reddit for support Link Content
1191 Posting updates on treatment progress Link Content
1192 Potential future ASCT (Autologous Stem Cell Transplant) Link Content
1193 Potential heart damage Link Content
1194 Potential need for dialysis Link Content
1195 Practicing good hand washing Link Content
1196 Praying for peace Link Content
1197 Preference for CAR-T over SCT Link Content
1198 Preference for ice cream (without nuts) Link Content
1199 Preparing for a stem cell transplant Link Content
1200 Preparing for SCT Link Content
1201 Preparing for the upcoming procedure Link Content
1202 Prescribed 15mg 2x/day morphine Link Content
1203 Prescribed medication Link Content
1204 Presence of blood oxygen and heart monitors Link Content
1205 Presence of CD38 inhibitor (Dara) in maintenance treatment Link Content
1206 Presence of fever Link Content
1207 Presence of pets Link Content
1208 Presence of plasma cells post transplant Link Content
1209 Presence of spinal compression fractures Link Content
1210 Presence of younger patients with the same condition Link Content
1211 Pretending to be fine Link Content
1212 Previous regimen no longer effective Link Content
1213 Primary caretaker role Link Content
1214 Processing emotions in head and heart Link Content
1215 Processing emotions together Link Content
1216 Processing the situation Link Content
1217 Procrastination Link Content
1218 Progress in recovery Link Content
1219 Progression from standard of care drugs to stem cell transplant to more standard of care drugs to clinical trials Link Content
1220 Progression of disease Link Content
1221 Progression of disease despite treatment Link Content
1222 Progression to smoldering myeloma Link Content
1223 Progressive deterioration Link Content
1224 Promoting awareness and education about myeloma Link Content
1225 Promoting awareness and unity Link Content
1226 Providing comfort and encouragement Link Content
1227 Providing encouragement and positive thoughts Link Content
1228 Providing information on the expected timeline for results and recovery Link Content
1229 Providing strength and support Link Content
1230 Providing words of comfort and encouragement Link Content
1231 PTSD from hospital stay Link Content
1232 Pushed to the limit Link Content
1233 Putting into sedation and ventilation Link Content
1234 Putting on a brave face Link Content
1235 Questioning the ability to endure for an extended period Link Content
1236 Questioning the virility of the virus in young patients Link Content
1237 Quick recovery Link Content
1238 Racing thoughts about bills and job security Link Content
1239 Raising awareness about myeloma Link Content
1240 Raising awareness for myeloma Link Content
1241 Reacting to family's expectations Link Content
1242 Reading a 2-case study Link Content
1243 Reading about others' experiences Link Content
1244 Reading an article about projected increase in MM cases Link Content
1245 Realizing the importance of relationships Link Content
1246 Receiving a message from mom expressing guilt and love Link Content
1247 Receiving complete response from treatment Link Content
1248 Receiving Darzalex treatments Link Content
1249 Receiving diagnosis and treatment information Link Content
1250 Receiving old school, heavy chemotherapy drugs Link Content
1251 Receiving platelet infusions, antibiotics, and transfusion Link Content
1252 Receiving positive feedback from healthcare professionals Link Content
1253 Receiving positive news Link Content
1254 Receiving prayers and well wishes Link Content
1255 Receiving support from family and friends Link Content
1256 Receiving the all-clear diagnosis Link Content
1257 Receiving treatment Link Content
1258 Receiving treatment and medication Link Content
1259 Receiving treatment and therapy Link Content
1260 Receiving treatment at Bruno Cancer Center Link Content
1261 Receiving treatment for Multiple Myeloma and AL Amyloidosis Link Content
1262 Receiving treatment in the doctor's office Link Content
1263 Receiving unexpected test results Link Content
1264 Recent cancer survivor Link Content
1265 Reclaiming what cancer has taken Link Content
1266 Recognizing that the story is not over Link Content
1267 Recognizing that the ultimate decision rests with Deb Link Content
1268 Recognizing the challenges of dealing with a loved one's illness Link Content
1269 Recognizing the importance of empathy for others Link Content
1270 Recognizing the presence of new treatments and advancements in the disease Link Content
1271 Recognizing the strength and love of the family Link Content
1272 Recognizing the strength of the mother Link Content
1273 Recognizing the value of unique and unprecedented approaches to myeloma care Link Content
1274 Recommendation against stem cell transplant Link Content
1275 Recommendation for follow-up in 6 months Link Content
1276 Recommendation to continue drinking water for various reasons Link Content
1277 Recommendation to exercise, take calcium & vitamin D supplements, and continue on morphine Link Content
1278 Recovery from muscle loss Link Content
1279 Recovery or remission Link Content
1280 Recovery time after treatment Link Content
1281 Recurrence of symptoms in July Link Content
1282 Rediagnosis every 30 days Link Content
1283 Reduced cognitive abilities Link Content
1284 Reduced mobility Link Content
1285 Reduction of M spike and myeloma in bone marrow and kidneys Link Content
1286 Reference to sleeplessness and hyperactivity Link Content
1287 Referral to a neurologist Link Content
1288 Referral to a Neuromuscular neurologist Link Content
1289 Referred to medical oncology clinic for further evaluation and management Link Content
1290 Referring to specific chemotherapy drugs (Dara+KD) Link Content
1291 Referring to specific medical terms Link Content
1292 Reflecting on gratitude and love Link Content
1293 Reflecting on past experiences and memories Link Content
1294 Reflecting on personal experiences with loss Link Content
1295 Reflecting on personal experiences with similar situations Link Content
1296 Reflecting on personal losses and memories Link Content
1297 Reflecting on personal memories and experiences Link Content
1298 Reflecting on the deceased and their qualities Link Content
1299 Reflecting on the impact of cancer on families Link Content
1300 Reflecting on the impact of caregiving Link Content
1301 Reflecting on the impact of Dad's illness on the family Link Content
1302 Reflecting on the journey of caregiving Link Content
1303 Reflecting on the lasting impact of losing a loved one Link Content
1304 Reflecting on the preciousness of life and relationships Link Content
1305 Reflecting on the preciousness of life and the importance of relationships Link Content
1306 Reflecting on the strength and qualities of the deceased Link Content
1307 Reflecting on the uncertainty of the disease Link Content
1308 Reflecting on the uncertainty of the disease returning Link Content
1309 Reflecting on the unfairness of the disease Link Content
1310 Reflection on past memories with Dad Link Content
1311 Regaining physical ability during initial therapy Link Content
1312 Regular doctor visits Link Content
1313 Regular doses of Kyprolis every two weeks Link Content
1314 Regular exercise Link Content
1315 Regular hospital visits for chemotherapy Link Content
1316 Regular hospital visits for daratumumab injection Link Content
1317 Regular infusions of Darith Tumamal Link Content
1318 Regular phone check-ins Link Content
1319 Regularly swimming in the pool Link Content
1320 Rehired by old company Link Content
1321 Rekindling interest in relationship Link Content
1322 Relapse Link Content
1323 Relapse after failed SCT Link Content
1324 Relapse and emergence of solid tumors Link Content
1325 Relapse with peripheral nerve damage in jaw Link Content
1326 Relying on a caretaker for support Link Content
1327 Relying on a healthy lifestyle for pain management Link Content
1328 Relying on insurance coverage Link Content
1329 Remembering Dad's fun and lively personality Link Content
1330 Remembering good memories of the father Link Content
1331 Reminiscing Link Content
1332 Remission from myeloma Link Content
1333 Renewed M spike Link Content
1334 Renewing health insurance plan annually Link Content
1335 Renewing insurance coverage for 2024 Link Content
1336 Reporting changes in personal information to insurance provider Link Content
1337 Reporting symptoms to healthcare provider Link Content
1338 Reporting symptoms to healthcare providers Link Content
1339 Researching about SCT Link Content
1340 Researching academic centers and comprehensive cancer centers Link Content
1341 Researching CAR-T therapy Link Content
1342 Researching diet and supplements Link Content
1343 Researching medical condition Link Content
1344 Researching prognosis online Link Content
1345 Researching the impact of chemo and drug treatments Link Content
1346 Researching treatment options for CAR-T therapy Link Content
1347 Resilience and determination Link Content
1348 Responding to Darzalex Link Content
1349 Response to full-strength Kyprolis Link Content
1350 Resuming daily routines Link Content
1351 Retirement Link Content
1352 Returning to SCT clinic for transplant Link Content
1353 Returning to the SCT clinic for transplant Link Content
1354 Reviewing Explanation of Benefits (EOB) Link Content
1355 Reviewing imaging with the doctor Link Content
1356 Reviewing results on the website Link Content
1357 Revlimid as a newer and safer treatment option Link Content
1358 Riding the dialysis train Link Content
1359 Rising lambda count after 14 months Link Content
1360 Risk of infections is high in MM patients Link Content
1361 Routine physical check-up Link Content
1362 Routine physical check-ups Link Content
1363 Running a small art and design business Link Content
1364 Runny nose without taking anti-histamine Link Content
1365 Rushing to the office Link Content
1366 Sadness Link Content
1367 Scheduling activities around good days Link Content
1368 Scheduling and attending appointments Link Content
1369 SCT failure at 2 month mark Link Content
1370 SCT in December Link Content
1371 Searching for diet types Link Content
1372 Searching for information and answers Link Content
1373 Seeing a local oncologist with less expertise for day-to-day management Link Content
1374 Seeing mother's demise in thoughts Link Content
1375 Seeking a time frame from a doctor Link Content
1376 Seeking additional methods for inflammation/pain relief Link Content
1377 Seeking additional support Link Content
1378 Seeking advice and experiences from others with the same condition Link Content
1379 Seeking advice and guidance from others who have experienced similar situations Link Content
1380 Seeking advice and guidance from others who have gone through similar experiences Link Content
1381 Seeking advice and information Link Content
1382 Seeking advice and reassurance from online community Link Content
1383 Seeking advice and resources Link Content
1384 Seeking advice and suggestions for Autologous Stem Cell Transplant preparation Link Content
1385 Seeking advice on managing the situation Link Content
1386 Seeking advice on treatment options Link Content
1387 Seeking alternative options for pain management Link Content
1388 Seeking alternative treatments Link Content
1389 Seeking alternative treatments and clinical trials Link Content
1390 Seeking alternative ways to manage disease Link Content
1391 Seeking answers and support Link Content
1392 Seeking comfort and support Link Content
1393 Seeking comfort and support from others Link Content
1394 Seeking comfort in the presence of loved ones Link Content
1395 Seeking cookbooks Link Content
1396 Seeking distraction through exercise Link Content
1397 Seeking distractions and coping mechanisms Link Content
1398 Seeking emotional support from loved ones Link Content
1399 Seeking FDA approved CAR-T options Link Content
1400 Seeking financial assistance Link Content
1401 Seeking financial assistance for CAR-T therapy Link Content
1402 Seeking further tests and consultations Link Content
1403 Seeking guidance from a social worker Link Content
1404 Seeking guidance on ensuring cutting-edge care for multiple myeloma Link Content
1405 Seeking help from a myeloma specialist Link Content
1406 Seeking hope for a permanent solution Link Content
1407 Seeking information Link Content
1408 Seeking information about CAR-T therapy Link Content
1409 Seeking information about catching the disease early Link Content
1410 Seeking information about coping strategies Link Content
1411 Seeking information about managing a chronic disease Link Content
1412 Seeking information about MRI results after induction chemo Link Content
1413 Seeking information about multiple myeloma Link Content
1414 Seeking information about myeloma Link Content
1415 Seeking information about the disease and treatment Link Content
1416 Seeking information about the procedure Link Content
1417 Seeking information about the timing and development of conditions Link Content
1418 Seeking information about treatment options Link Content
1419 Seeking information and advice on how to make the most of the time with a loved one Link Content
1420 Seeking information and educating oneself about the disease Link Content
1421 Seeking information and resources Link Content
1422 Seeking information on maintenance treatments Link Content
1423 Seeking information on Medicare coverage Link Content
1424 Seeking information on MRD status Link Content
1425 Seeking information on myeloma drugs in clinical trials Link Content
1426 Seeking information online Link Content
1427 Seeking information online about disease prognosis Link Content
1428 Seeking medical advice for persistent pain Link Content
1429 Seeking medical advice for shoulder pain Link Content
1430 Seeking medical care and hospitalizations Link Content
1431 Seeking medical help Link Content
1432 Seeking medical help after recurring symptoms Link Content
1433 Seeking medical help and diagnosis Link Content
1434 Seeking medical help at Barnes Jewish hospital Link Content
1435 Seeking palliative care Link Content
1436 Seeking palliative care to manage symptoms and side effects Link Content
1437 Seeking peace of mind Link Content
1438 Seeking pre-authorization for certain treatments Link Content
1439 Seeking reassurance and advice Link Content
1440 Seeking reassurance and validation Link Content
1441 Seeking reassurance or validation from others Link Content
1442 Seeking recommendations for healthcare providers experienced in CAR-T therapy Link Content
1443 Seeking recommendations for therapists Link Content
1444 Seeking second opinion Link Content
1445 Seeking second opinions or alternative therapies Link Content
1446 Seeking social support Link Content
1447 Seeking social support from friends and family Link Content
1448 Seeking support Link Content
1449 Seeking support and advice Link Content
1450 Seeking support and encouragement Link Content
1451 Seeking support and reassurance Link Content
1452 Seeking support and validation Link Content
1453 Seeking support and validation from others Link Content
1454 Seeking support from a cancer coach Link Content
1455 Seeking support from friends or support groups Link Content
1456 Seeking support from healthcare professionals Link Content
1457 Seeking support from loved ones Link Content
1458 Seeking support from others Link Content
1459 Seeking support from the community Link Content
1460 Seeking support from the Reddit community Link Content
1461 Seeking support from therapist and significant other Link Content
1462 Seeking therapy and applying psychology strategies Link Content
1463 Seeking therapy for emotional support Link Content
1464 Seeking therapy for grief Link Content
1465 Seeking to expand medical awareness and knowledge Link Content
1466 Seeking treatment from MM specialist at a center of excellence Link Content
1467 Seeking vetted resources for diet and supplements Link Content
1468 Seizing the day and trusting in God's guidance Link Content
1469 Seizure occurrence Link Content
1470 Seizures Link Content
1471 Sending virtual hugs and love Link Content
1472 Sending virtual hugs and well wishes Link Content
1473 Sense of loss Link Content
1474 Sensing the wind and speed Link Content
1475 Sequential illnesses (Covid-19, Pneumonia, Bronchitis, C-diff) Link Content
1476 Setting goals and creating a plan for treatment Link Content
1477 Sever pain after sleeping Link Content
1478 Severe back pain Link Content
1479 Sharing a personal story Link Content
1480 Sharing a personal tribute Link Content
1481 Sharing condolences and expressing sympathy Link Content
1482 Sharing condolences and sympathies Link Content
1483 Sharing diagnosis with loved ones Link Content
1484 Sharing experiences Link Content
1485 Sharing experiences and offering support Link Content
1486 Sharing frustrations and challenges related to medical tests and procedures Link Content
1487 Sharing ideas Link Content
1488 Sharing love and affection Link Content
1489 Sharing memories Link Content
1490 Sharing news Link Content
1491 Sharing personal connections and experiences Link Content
1492 Sharing personal experiences and advice Link Content
1493 Sharing personal experiences and emotions related to the disease Link Content
1494 Sharing personal experiences and feelings on online platforms Link Content
1495 Sharing personal experiences and reactions Link Content
1496 Sharing personal experiences and seeking advice Link Content
1497 Sharing personal experiences and sympathies Link Content
1498 Sharing personal experiences and treatment journeys Link Content
1499 Sharing personal experiences as a caregiver for a MM patient Link Content
1500 Sharing personal experiences of loss Link Content
1501 Sharing personal experiences or stories related to loss Link Content
1502 Sharing personal experiences with CAR-T therapy on social media Link Content
1503 Sharing personal experiences with MM and AL Amyloidosis Link Content
1504 Sharing personal experiences with myeloma Link Content
1505 Sharing personal experiences with similar treatments Link Content
1506 Sharing personal experiences with skydiving and disease management Link Content
1507 Sharing personal experiences with treatment and trials Link Content
1508 Sharing personal medical experiences Link Content
1509 Sharing personal medical updates and milestones Link Content
1510 Sharing personal stories Link Content
1511 Sharing personal stories and connections Link Content
1512 Sharing personal stories and tributes Link Content
1513 Sharing personal stories of loss and coping Link Content
1514 Sharing personal struggles and experiences Link Content
1515 Sharing photos and updates Link Content
1516 Sharing positive treatment progress Link Content
1517 Sharing similar experiences and struggles Link Content
1518 Sharing the duration of their remission Link Content
1519 Sharing the news Link Content
1520 Sharing the surprise of being in remission against expectations Link Content
1521 Sharing the victory with others Link Content
1522 Sharing updates on bloodwork results Link Content
1523 Sharing updates on treatment progress and outcomes Link Content
1524 Sharing updates with family and friends Link Content
1525 Sharing updates with loved ones Link Content
1526 Shingles vaccination Link Content
1527 Shirts for port access Link Content
1528 Shopping from clearance racks for affordable clothing options Link Content
1529 Shortness of breath Link Content
1530 Shoulder pain Link Content
1531 Shrinking masses Link Content
1532 Shrinking of masses Link Content
1533 Sickness Link Content
1534 Side effects management Link Content
1535 Signs of brain damage Link Content
1536 Sitting and freaking out Link Content
1537 Sitting next to people in a theater Link Content
1538 Sleeping throughout the day Link Content
1539 Slipping back into darkness Link Content
1540 Slow progress towards remission Link Content
1541 Slower completion of chores Link Content
1542 Smiling despite inner struggles Link Content
1543 Social isolation Link Content
1544 Sore throat from nasal drip Link Content
1545 Specialist unit in London for Amyloidosis Link Content
1546 Specific tests like bone marrow biopsy needed for diagnosis Link Content
1547 Speculating on the impact of dormant chicken pox Link Content
1548 Speech improvements Link Content
1549 Spending time with family and grandchildren Link Content
1550 Spending weekends with mother Link Content
1551 Stable condition Link Content
1552 Standard induction therapy Link Content
1553 Started on antiviral Aciclovir Link Content
1554 Starting a new treatment Link Content
1555 Starting anti-convulsants Link Content
1556 Starting CAR-T therapy Link Content
1557 Starting Dara-Revlimid-kyprolis-dex treatment at Stanford Link Content
1558 Starting medication Link Content
1559 Starting to get around crowds Link Content
1560 Starting treatment with Darzalex Link Content
1561 Starting treatment with revlimid and other drugs Link Content
1562 Starting treatment within the next 10 days Link Content
1563 Staying away from others to avoid illness exposure Link Content
1564 Staying positive despite the challenges Link Content
1565 Stem cell collection Link Content
1566 Stem cell collection for future transplant Link Content
1567 Stem cell transplant after initial treatment Link Content
1568 Stem cell transplant mentioned as a future treatment Link Content
1569 Steroid side effects Link Content
1570 Steroids (Dexamethasone) Link Content
1571 Stopped sedation but no awakening Link Content
1572 Stopping sedation Link Content
1573 StrangeJournalist7: Discussing Steve Scalise's political aspirations without expressing personal opinions Link Content
1574 Stretchy t-shirts Link Content
1575 Stretchy tank tops for easy access during procedures Link Content
1576 Struggle to get up and get through the day Link Content
1577 Struggling to process and cope with the situation Link Content
1578 Struggling with PTSD Link Content
1579 Struggling with the impact of anti-infection measures on family dynamics Link Content
1580 Subtle movement improvements Link Content
1581 Successful immunotherapy treatment Link Content
1582 Sudden decrease in running ability Link Content
1583 Sudden diagnosis of multiple myeloma Link Content
1584 Suffering in pain Link Content
1585 Suggesting consulting a doctor for personalized advice Link Content
1586 Support from spouse Link Content
1587 Support group participation Link Content
1588 Supporting others affected by myeloma Link Content
1589 Supportive language Link Content
1590 Supportive phone calls and check-ins Link Content
1591 Surgery to fix a bone Link Content
1592 Surgery to insert rod in the bone Link Content
1593 Surgery to place a rod in arm Link Content
1594 Suspected encephalitis caused by Herpes virus Link Content
1595 Suspected myeloma condition Link Content
1596 Switching doctors Link Content
1597 Symmetrical functioning of left and right side Link Content
1598 Symptoms mainly at night and when sitting at the desk Link Content
1599 Symptoms starting before official diagnosis Link Content
1600 Symptoms worsen Link Content
1601 Systematic process of adjustment Link Content
1602 Systematic process of coming to terms with changes Link Content
1603 Taking a break from treatments Link Content
1604 Taking a leave of absence from work Link Content
1605 Taking Bortezomib and Dexamethasone Link Content
1606 Taking care of a 95-year-old father Link Content
1607 Taking care of diet and nutrition Link Content
1608 Taking care of her Link Content
1609 Taking care of legal and will matters Link Content
1610 Taking Darzalex Link Content
1611 Taking it day by day and step by step Link Content
1612 Taking leftover Norco for relief Link Content
1613 Taking methylphenidate Link Content
1614 Taking Naproxen Link Content
1615 Taking pain killers Link Content
1616 Taking pride in work Link Content
1617 Taking time for oneself Link Content
1618 Talking and recovered Link Content
1619 Talking to spouse for support Link Content
1620 Tank top undershirts Link Content
1621 Tank tops with low necklines Link Content
1622 Team effort to obtain available CAR-T treatment Link Content
1623 Team offering Teclistomab as a last resort Link Content
1624 Team spirit Link Content
1625 Team-based approach to care Link Content
1626 Temporary elevation of light chains Link Content
1627 Temporary relief after the test Link Content
1628 Test results came back Link Content
1629 Thalidomide treatment for MM Link Content
1630 Throat and lung infections continuously occur during MM treatment Link Content
1631 Time taken to reach complete remission (2 years) Link Content
1632 Tingling sensation in lips/around mouth Link Content
1633 Tingling/numbness as the only symptoms Link Content
1634 Tired of being isolated Link Content
1635 Tiredness Link Content
1636 Tiredness and decreased stamina Link Content
1637 Tracking of healthcare expenses Link Content
1638 Transition from ICU to home care Link Content
1639 Traumatic experience Link Content
1640 Traveling long distances for medical appointments Link Content
1641 Treatment at Fred Hutch, University of Washington Link Content
1642 Treatment for Covid Link Content
1643 Treatment for depression and anxiety Link Content
1644 Treatment for sciatic nerve pain Link Content
1645 Treatment initiation Link Content
1646 Treatment interventions Link Content
1647 Treatment no longer working Link Content
1648 Treatment options presented by doctor Link Content
1649 Treatment progress discussion Link Content
1650 Treatment with Dara-Revlimid-kyprolis-dex Link Content
1651 Treatment with Darith Tumamal Link Content
1652 Treatment with darzalex, revlimid, velcade, and decadron Link Content
1653 Treatment with heavy chemotherapy options Link Content
1654 Treatment with various chemotherapy regimens Link Content
1655 Treatment-related side effects Link Content
1656 Trend of increasing free light chain levels Link Content
1657 Trouble eating Link Content
1658 Trouble eating for the first 60 days post-transplant Link Content
1659 Trouble with decision-making Link Content
1660 Trusting the instructor Link Content
1661 Trying a new treatment option (Darzalex) Link Content
1662 Trying different drugs Link Content
1663 Trying different treatments and medications Link Content
1664 Uncertain future after diagnosis Link Content
1665 Uncertainty about future expectations Link Content
1666 Uncertainty about holiday plans Link Content
1667 Uncertainty about the future Link Content
1668 Uncertainty and lack of confidence in diagnosis Link Content
1669 undefined: Providing no specific response or contribution Link Content
1670 Undergoing chemotherapy and autologous stem cell transplant surgery Link Content
1671 Undergoing dialysis 3 times a week for 4.5 hours Link Content
1672 Undergoing heavy chemo treatment Link Content
1673 Undergoing immediate neck surgery Link Content
1674 Undergoing immunotherapy treatment Link Content
1675 Undergoing light radiation on the arm Link Content
1676 Undergoing medical tests and procedures Link Content
1677 Undergoing periodic rounds of intense chemotherapy Link Content
1678 Undergoing stem-cell transplant Link Content
1679 Undergoing surgery for bone fracture Link Content
1680 Undergoing surgery for broken arm Link Content
1681 Undergoing treatment with Revlimid Link Content
1682 Underwent chemotherapy and autologous stem cell transplant surgery Link Content
1683 Underwhelmed by the news of being in remission Link Content
1684 Underwhelmed reaction to being told about remission Link Content
1685 Underwhelmed reaction to being told in remission Link Content
1686 Underwhelmed response to being told in remission Link Content
1687 Unexpected risk factor Link Content
1688 Unpredictable and worsening symptoms Link Content
1689 Use of CAR-T therapy Link Content
1690 Use of urine specimen collectors (hats) Link Content
1691 Use of walker and wheelchair Link Content
1692 Using a 10ft long charging cord for phone Link Content
1693 Using a lint roller Link Content
1694 Using a selfie stick as a cheap tripod Link Content
1695 Using a waterpik for oral hygiene Link Content
1696 Using a waterpik to clean teeth due to sensitive gums Link Content
1697 Using a waterproof allergy barrier cover for the bed Link Content
1698 Using an n95 mask Link Content
1699 Using family rallying as a coping mechanism Link Content
1700 Using journaling as a coping mechanism Link Content
1701 Utilization of healthcare services Link Content
1702 Utilizing advanced technology for diagnosis and treatment Link Content
1703 Valuing understanding and support from manager Link Content
1704 Varying levels of physical activity in older patients Link Content
1705 Varying treatment plans Link Content
1706 Vasculitis diagnosis Link Content
1707 Velcade (Bortezomib) Link Content
1708 Visible signs of illness Link Content
1709 Visit to the Cancer Center Link Content
1710 Visit when you can Link Content
1711 Visiting healthcare facilities Link Content
1712 Visiting healthcare professionals Link Content
1713 Visiting with friends in small groups outside Link Content
1714 Vulnerability to other health issues Link Content
1715 Waiting and praying during infusion Link Content
1716 Waiting for blood test results Link Content
1717 Waiting for bone marrow biopsy results Link Content
1718 Waiting for CAR-T treatment to be approved Link Content
1719 Waiting for test results and monitoring progress Link Content
1720 Waiting for the next BM/MRD report Link Content
1721 Waiting period before transplant Link Content
1722 Walking for at least half an hour daily Link Content
1723 Walking past people in a grocery store Link Content
1724 Wanting to prepare for potential changes in quality of life Link Content
1725 Wanting to stay updated on the latest advancements in myeloma treatment Link Content
1726 Wanting to understand the first stages of treatment Link Content
1727 Watching things on phone using the selfie stick on tray Link Content
1728 Watching things on phone while lying on the couch Link Content
1729 Weakened immune system during treatment Link Content
1730 Wear out faster Link Content
1731 Wearing a heavier coat for outdoor activities Link Content
1732 Wearing a tank and light zip-up hoodie Link Content
1733 Wearing a thoracic brace Link Content
1734 Wearing a well-fitted N95 mask Link Content
1735 Wearing a zip-up hoodie Link Content
1736 Wearing button-up shirts for easy access to the triple lumen Link Content
1737 Wearing buttoned flannel shirts Link Content
1738 Wearing comfortable clothing Link Content
1739 Wearing hospital gowns Link Content
1740 Wearing loose and comfortable clothing Link Content
1741 Wearing loose comfortable clothing Link Content
1742 Wearing short sleeve button-ups with different designs Link Content
1743 Wearing soft and comfy clothing Link Content
1744 Wearing standard men's shirts Link Content
1745 Wearing V-neck shirts Link Content
1746 Wishing for a speedy recovery Link Content
1747 Wishing for love, peace, and comfort Link Content
1748 Wishing for pain-free and peaceful moments Link Content
1749 Wishing for peace for the mother Link Content
1750 Wishing love, peace, and comfort Link Content
1751 Withdrawing cells for engineering Link Content
1752 Working full time despite pain Link Content
1753 Working remotely during treatment Link Content
1754 Working remotely from the hospital Link Content
1755 Worsening shoulder pain Link Content
1756 Worsening tremors Link Content
1757 Wrap jackets Link Content
1758 X-ray therapy for lesions Link Content
1759 Yearly tests and scans to monitor protein levels Link Content
1760 Younger patients being diagnosed with the disease, which is unexpected among the general medical community Link Content
1761 Zero traces of myeloma in latest tests and bone marrow biopsy Link Content
1762 Zip-up hoodies Link Content

Vulnerable Moments Show All

  1. Receiving diagnosis
  2. Adjusting to lifestyle changes
  3. Receiving a diagnosis
  4. Waiting for test results
  5. Coping with emotional distress
  6. Emotional distress
  7. Experiencing side effects
  8. Feeling exposed and in need of support
  9. Navigating healthcare system
  10. Starting treatment
  11. Coping with physical limitations
  12. Coping with the loss of a loved one
  13. Disease progression
  14. Facing end-of-life decisions
  15. Facing treatment decisions
  16. Facing uncertainty about the future
  17. Feeling burnt out as a caregiver
  18. Hospitalization
  19. Managing financial burden
  20. Receiving the cancer diagnosis
  21. Transitioning between healthcare providers
  22. Uncertainty about the future
  23. Coping with pain or discomfort
  24. End-of-life discussions
  25. Experiencing a relapse

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