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Read conversations, start a discussion, and connect with others about multiple sclerosis.

Steroids

Hello all from Canada. I am so surprised when reading postings about PWMS in the US about how early on and how frequently you are put on steroids. Here it...

Stem Cell Institute

has anybody been treated by the stem cell institute in Panama?...

Anyone have experience with LDN (low-dose Naltrexone)?

My GP suggested I research LDN, as she has one patient with MS who takes it. Anyone have experience with this medication? Thanks! Echo...

Zinbryta anyone?

I have been on a handful of meds since 1994. Avonex,copaxone, Rebif and Tecfidera. I was taken off my last meds due to low white count (Tecfidera) and my doctor...

Fatigue

Long before I was diagnosed with MS I had problems with fatigue, which have only gotten worse, and I know this is a problem that is widely shared. I'm wondering...

HSCT treatment in Sweden

A close relative is looking into treating her RRMS with HSCT. As Europe is the most viable option I'm interested to hear about any experience from Karolinska University hospital in...

Feeling worse since meds stopped

Hey all, So I was diagnosed 12 years ago, I am been through some different treatments, most recent was tecfidera. Well my lymphocytes and wbcs took a nose dive and...

Switching drug therapy after 10+ yrs

I have been on Copaxone for 10 1/2 years. my skin cannot take much more. Im concerned about switching to an oral medication. Thoughts?...

Terrified of Tysabri...

Tomorrow's my first Tysabri infusion and I am scared to death. I tested positive for JC Virus but apparently the cutoff is 1.0 and I'm at 0.77. I really, really...

Treating exacerbations

Share your experience with treating relapse / exacerbations. Get the conversation started....

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