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

No Help

I was diagnosed with MS in 2009. Since then I've been to 3 other neurologists. I have lifelong epilepsy but no help...

Possible income sources of MS Patients

Employers are not inclined to hire me because of my disability. I am unable to earn my living. They consider my being...

Frustration with job and disability

I am newly diagnosed in June @ 57yrs and have been out of work since then I used up my sick leave...

Caregiver - Good Payback

I share a house with a friend who is often my MS caregiver, especially when it comes to doing things in the...

Am I being unfair?

Me and my then pregnant wife moved back from Scotland last year, staying with her in-laws. My wife then gave birth to...

http://www.amazon-lady.com/amazon-lady-celebrates-50th-post

Believe it or not we have reached 50 posts, I have come a long way and have written a lot about all...

How my life has changed since being diagnosed.

I find it hard to believe that it was July 2013 that I was given the diagnosis that I have Secondary Progressive...

Anyone have good experience with these types?

Anyone have any good experiences with alternative therapies i.e., massage, reflexology, feldenkrais, reiki, rolfing? Oils for spasticity?...

Just tired

So this is maybe just a pity party, and if you are already feeling down, don't read! I'm fortunate, I know, but...

How MS affects my day.

To day I thought I would write a post about how MS affects my day… It might make an interesting read to...

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