Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.

RiS
Has anyone heard about a stem cell treatment for MS?
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Doctors generally do not try stem cell transplants on MS patients for a few reasons. 1. It is very dangerous. 2. The data to support doing it is not large. 3. Durability is a question.
I am a member of two groups on daily strength, this one and a leukemia group. I was diagnosed with both in early 2015. The MS was considered secondary to my main problem, which was the leukemia. After multiple drug tries it was determined that the only way I could be healed from the leukemia was a stem cell transplant.
It is important to know that there are two types of transplants, autologous and allogeneic. Autologous is when you harvest and use your own stem cells for transplant. Allogeneic is someone else's. Autologous is less dangerous than allogeneic for a variety of reasons.
Without going into too much detail, most MS patient data on stem cell transplant comes from autologous. Mine was allogeneic. Today is Day +265 post transplant for me. In addition to what is hopefully a lasting leukemia remission, my neurologist told me that my lesions are fading, there are no new ones and none are enhancing. All of my MS symptoms have gone. My doc says my MS is also in remission and likely cured.
If interested I can give you more info, but it is important to remember that most docs will not give you an allogeneic stem cell transplant for MS. Your risk of dying in the first year is around 20%. First 3 years is higher than that.
For some, this risk is worth it. Others, no. I am sorry for your situation and hope that God and science will find a way to make something work.
John
it yet. Says its too early & still has many side effects/kinks to work out yet, plus it's not guaranteed to work for everyone. 25% of the people have either stayed the same or got worse.