Can anything prevent peripheral neuropathy after stem cell transplant?
Hi - I am having a stem cell transplant Oct 30 and have some peripheral neuropathy now, so I'm concerned it will get worse after transplant and want to do anything I can to prevent it from getting worse. I'm confused about what causes the PN - is it from the chemo or from GVHD? If it is from the chemo, has anyone tried cool packs on hands/feet during chemo to try to prevent it? Any other ideas or information on how to prevent PN after transplant? Thanks so much.
Interested in more discussions like this? Go to the Bone Marrow Transplant (BMT) & CAR-T Cell Therapy Support Group.
Oops autologous not anthologist.
And yes, sharing a birthday or anniversary would have been my first choice.
I wish you well with your transplant. Don’t hesitate to check in here on Connect. There are many members who have had an autologous BMT for MM or other conditions. It can help being able to talk with someone who has walked the same walk…though your daughter was a brave trailblazer for you already! ☺️ Will she also be your caregiver?
I see this is an older post, but will comment in case it is helpful. I had peripheral neuropathy prior to my cancer diagnosis it worsened someone with Velcade and then at the time of transplant, but at 13 months out, it has improved and really doesn’t cause me any significant problems despite ongoing chemotherapy. Hoping that you have minimal difficulty with this.
Thank you Merrle. That is very helpful because it gives me hope that if my PN does get worse it might get better. It’s all about keeping hope alive 😀 I am about 3 weeks post transplant and so far no increased PN.
I was in pretty rough, shape at three weeks post Transplant but things really did get better and better. Even at month 12 I saw some improvements.Hang in there! Let us know if you have either worried about, maybe we can help.🤗