Has anybody experienced loss of taste, food tasting bad. If so, did you find anything that helped?

Ive been diagnosed with CLL and i will need financial support. I would like to where/how to start the process. Thx

I got off of Dex in June. I am on Sarclisa and Revlimid. I had a few weeks of upper back pain after getting off Dex which could be from working out or withdrawal from Dex. I'm not missing the Dex now that I have adjusted to being off of it. Interested in others' experience who aren't on Dex anymore.

My husband has stage 4 MCL. He recently completed 6 months on chemo and immunotherapy- with a severe allergic reaction to Rituximab and Gazyva. Never reached remission and cancer is showing an increase on recent PET scan. Currently on Jaypirca and is preparing for Car-t. Hoping this is best next step.

Hello, I am a 71, almost 72 yr old. Was diagnosed with AML 10 mos ago. Was getting regular bloodwork done for my PCP. Had no idea anything was wrong until I got a call from my Dr on a Sat afternoon. She told me that I had "Pancytopenia", she had already contacted an oncologist who saw me promptly the following week. Then, I had a whole panel more of bloodwork and a Bone Marrow Aspiration. I started chemo early Dec. '24. I am on oral chemo, Venetoclax/Inqovi, just finished my 5th cycle. I am in remission, and was informed I was eligible for a BMT. After much discussion with family and friends, decided against the transplant. It's a brutal procedure, even with modifications for my being older and with other health issues. So, I'm staying the course with the oral chemo and when things change or I relapse, we'll go from there.

Good day all: This question is for those on Revlimid; What time of day do you take your Revlimid. I am on 10mg. 3 weeks a month. I also do Darzalex once a month. I have a terrible time waking up in the morning. I take Revlimid at about 8 p.m. I wake up shaking, like I am vibrating. Even my vision is vibrating. I suspect neuropathy. My oxygen is good at around 98, my pulse is around 60. I do have mild sleep apnea, but can not do a C-Pap machine. I only have apnea if I lie on my back. I tried a C-Pap for 18 months I developed some serious problems with air in my stomach and my ears. I am seeing a specialist, who recommended I just sleep on my side. I see her again in 3 weeks. I believe if sleep apnea was causing the shaking my waking pulse would be higher. My waking blood pressure is about 115/65. I wonder if the Revlimid is causing part of the problem. Does anyone take Revlimid in the morning? Thanks, Sharon

I have a question for those taking Darzalex Faspro. My doctor said I could stop my Dex completely. So I’ve been working my way down from 20mg the day of treatment to 4. I get my treatment on Fridays, and on Monday or Tuesday I get a weird feeling that sort of feels like anxiety, and it’s a sign I need to lay down and take a nap. Usually feel better thereafter. When I was on the higher doses, I would feel a tightness around my midsection as well. I Don’t remember experiencing that when I was down to about 12mg. However at 8mg and 4mg, I was feeling an increase in body aches I guess I would call it. So I tried 12 mg again today with my treatment. I do take a daily Claritin for allergies, so that’s not changed. And I still take 2 Benedryl the day of my infusion. I just realized that I also weaned myself off of 50mg of Benedryl I had been taking nightly to help both with sleep and allergies. I took my last dose Jun 16. I had infusions on June 13 (4mg Dex), July 18 (4mg Dex), August 15 (8mg Dex), and September 19 (today 12mg Dex). I’m beginning to wonder if taking the 50mg of Benedryl nightly was holding these body aches at bay, and it’s the lack of that (not the lower dose of Dex) that is causing an increase in body aches. Has anyone been instructed by their doctor to take Benedryl in the days after infusion in addition to the day of? Any insight would be appreciated. I would love to stop the Dex completely, and if that means taking Benedryl for a few extra days a month, I’m okay with that!

Just wondering if anyone else has Igg kappa, high risk, stage2, 17p deletion, aggressive. I was diagnosed July 2024. Received 6 cycles of drvd. Had ASCT February 2025. Had a very good partial response. On maintenance of darzalex monthly and revlimid 10 mg. I’ve been feeling good even though my Dr says I have a poor prognosis.

Hello, I want to hear from people with myeloma who are getting Bite treatments (Bispecific T-Cell Engagers)

hi. I am wondering how I can add my daughter to this app im the one with the cancer and bless her she is right beside me helping coordinate all of the information. it was her idea that I start using this app. my cancer MM IgG Kappa and so far from what we have deciphered from the lab results, most recent was the bone marrow biopsy, looks like stage 2. my younger sister lost her bottle with MM 8 years years ago this past August 17th. I have the Lytic lesions in my skull but so far nowhere else, cannot shake the constant headache.