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

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...

Overwhelmed and scared

Hello all, I'm new to the forum. My wife was diagnosed back in 2006 and has slowly been progressing down the path of losing her ability to walk. I've been...

Cooling Vests

Any suggestions or recommendations for cooling vests? Pros and cons of different styles?...

Frustrated &anxious

Really need advice on how to care for my daughter . She is 25 and living at home. She has RRMS and has now isolated herself. I can cope with...

Any information on Cladribine

Have been reading about Cladribine which appears to be an off label drug. It seems as though it is quite effective for MS without as many dangerous side effects as...

moving

I'm new to the MS online world , but not to MS...I've had it for 29 years and now, after a quite nasty fall down our stairs my,husband thinks we...

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?...

The advantages of MS

Let me first introduce myself before you read this so you can better appreciate my stance. My name is John, I am a primary/elementary school teacher from the UK with...

Waiting to see dr

About 6 months ago I developed a tremble in my right shoulder. At first I thought it was just nerves. I've been through a very trying past 2 years and...

A caregiver's mistake and a lesson learned

My fiancee Tracey is in the advanced stages of SPMS, and is also fighting a five year battle with stage 4 bedsores. Despite this, we still manage to travel from...

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