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

Optic Neuritis/Steroids

Hello, I don’t know if I will be diagnosed with MS or not yet but I have had optic neuritis for weeks. We have to follow up with further testing...

Undiagnosed/seeking diagnosis

I know all the problems about the summer sweating, but I've been sweating from the neck up all times of the year.. They are so powerful that I have to...

Depression: MS? Genetic?Cope or meds

I've been told I need to at least try Prozac for probably 10 years (MS diagnosed for 30 years). I'm scared to go down the path of mental drugs but...

Social Security Disability Benefits & MS

I wanted to share the latest FUMS Podcast Show episode - all about applying for SSDI when you have MS. It's really interesting and helpful. I hope it help you...

I Have MS, What Should I Eat?

Firstly, I want to say that I am not sharing diet advice, I'm just kind of tired of always wondering what to eat and if it could help my symptoms...

What I've Learned in 20 Years Since My MS Diagnosis

It's been 20 years since my MS diagnosis! When I was first diagnosed I was so afraid for my future and although it's not what I thought it would be...

Practical Tips to Manage Heat Sensitivity and Still Have a Life

The summer weather has knocked me out! Utilizing all the strategies I know to manage heat sensitivity. What do you do to stay cool in the warm weather? https://mswellnessproject.com/practical-tips-to-manage-heat-sensitivity-and-still-have-a-life/...

America living in Australia - worth it to come home?

Hello. I was recently diagnosed with Relapsing-remitting multiple sclerosis (RRMS). Luckily for me it was caught early and I was able to leap onto medication before the lesions had a...

Another Icky Flare up!

Currently going through a flare up being treated with a 5 day solu-medrol treatment. We had to halt my last two dosages due to my sugars going too high now...

Any face to face meeting for the community?

I am living in Melbounre Australia and so much want to know ppl that dealing with MS. I was diagnosed 7 months ago and i think it could be a...

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