Hello, I was diagnosed in 2017, had SCT 2018. I am not on any maintenance since 2018 and in remission. This past year, I have been getting neuropathy in both of my feet and hands. (tingling and achy) Is it possible to get neuropathy now after nine years due to treatment? I have diabetes but my A1C 5.3 and on no meds. I do not have blurred vision or headaches that usually coincides with diabetes. I also had my nerves tested in feet and hands and I do not have any damage. Thank you in advance.

Are you concerned about your insurance and possible changes? please let me know. Drop a comment here

Has anyone had the experience that when you get your blood work done, the M Spike result does not show? I was told that meant the M spike was at zero, but I find that a bit hard to believe that they wouldn’t at least say zero or no result.

Where do Ilook for the blood vale's

I am multiple myeloma patient Iga and Lambda light chains in the process of relapse. I have recently started having some skin changes which are not bug bites. These are popping up on different parts of my body and most of them are red and itchy. I also have strange sensations on my skin like something is moving on it but no apparent insects or bugs are present even under magnifying glass. I am wondering if all of these are due to my myeloma being active again, and if anybody else experienced this?

Hi everyone, I’m reaching out to hear from anyone who has gone through or supported a loved one through a stem cell transplant, especially if the patient was a Black man in his60s- 70s. My dad is currently preparing for the process, and we’re trying to gather as much real-life insight as possible. His only major health concerns outside of multiple myeloma are mild kidney disease (sometimes normal), maybe risk for mild malnutrition (thin/skinny body type)Doctors say he’s a good candidate overall, but of course, we know that age, kidney function, and being African American can all play a role in outcomes. If you or someone you know has a similar background, I’d love to hear: • How the transplant went (complications, recovery time, etc.) • How the body handled chemo • When were you able to be around others? (Family) • What helped the most during recovery—mentally, physically • Anything you wish you’d known ahead of time How long have you been in remission after transplant ? Appreciate any insight, encouragement, or lessons you’re open to sharing. Thank you in advance. -Monica

I am signing up for a clinical trial for CAR-T Are there resources to help with travel expenses etc?

Hello I have MM for three years and been ion 5 different medication with the shots in your stomach and nothing is helping me my kappa chain light is going up higher. My doctor wants me to have T Cell done but I'm afraid have anyone had it done yet if so can you share some light on it. My bloodwork is low also have anyone experienced any of this

Evening All 6 months ago got the news of MM with lgg damage and stage 4 kidney failure. Started on Velcae and Dex then they added dara as well. Overall been doing pretty well and the numbers seem to be responding No cancer history in my family and was trying to figure out how this surprise came about Then had a old Coast Guard friend of mine remind me of the high power transmitters(LORAN) I worked on for years and sure enough on the VA site a whole section talking about the ionizing radiation(xrays) that had were emitted that none of us knew about So just wondering if there might be any other Coasties around here going thru the same thing? Thanks and hang in there MikeO

Hi to everyone my first post as I’m new to health tree. I was diagnosed with AML in November 2022. My only symptom was feeling weak and at a regular checkup with my cardiologist bloodwork showed extremely low blood count (5.5). I was admitted to the hospital and 3 days later was diagnosed with AML. I had a great oncologist who started me on vidaza chemo and oral venetoclax (oral) not sure spelling which put me in remission right away and for the exception of getting a case of Mercer while in the hospital I’ve enjoyed great health with little to no side effects unfortunately I’ve lost my oncologist and not in love with my new one. He has reminded me that about 36months is the effectiveness for vidaza but with my mutation he feels good he can get me back into remission and that is when I need to seriously consider a stem cell transplant. I will continue to enjoy my good health and cross that bridge when I have to. Anyone similar journey?? Chris

My husband is 67 with multiple myeloma and his kapper chain light keeps going up is there anything he can take to bring it down

Hi, I need some help, hope someone can tell me! I really hope I am able to send out this email, as I haven't been all day! I went to my oncologist , he took blood, but didn't see me!!! He was 3 hours let!! That was on Friday 11, w2025 and took blood ! Today it comes back and it's only me. Back it says protein is high it 8.5 calling it abnormal, does that mean it's moving? He never called back!!! Thank you guys for your help Geri Fumarola

OK, A lot is happening but not yet written in stone. Most of the proposed changes to Medicare, Social Security, Medicaid, if they garner the needed support, will not be decided until after mid-term elections. There are some proposals that are hidden in the bill, that you want to keep an eye on. It affects Medicare for 2028. The proposal sys that Medicare Advantage plans will be selected by an administrator for beneficiaries who become eligible in 2028. They will be locked into that plan for 3 years unless they opt out. (This will require them keeping up with changes) Also, the Medicare will be based on the lowest premium, not what you need based on your health care needs. This will affect your network , coverage levels, etc. This is a good time to start writing letters to your appointed representatives and advocate!

Hello, I am looking for a good MM specialist in New Orleans LA. I have not been able to find one listed on the Health Tree website. Is there anyone out there that could give me a good reference? Or am I missing something?