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I started intermittent fasting a few months after my diagnosis,my diet switched to heavy on the veggies,and i run away from any stressfull people and situations ,i work out and keep a positive outlook,at this point no one even beleives i have m.s,i do not know if everyones outlook is the same ,a bit...

I've been swimming down that river called denial. I was diagnosed in March. And not coping very well. Only my boss and a work bestie knows of my diagnosis. My family don't check in on me since they were told, my two friends i do have don't even ask about it anymore. My partner doesn't seem to a...

Would anyone describe the ms hug as feeling like a panic attack. I've had what I think is one a few times, mainly when under stress. The pain was so unbearable and just scary but because of the situation I was in I thought it was a panic attack. These all happened before my diagnosis, my last one be...

Hi I just wondered what I should expect on my first neurology appointment, will it be to discus/ start treatment? They diagnosed me only by MRI and said I had multiple many lesions on brain and neck. Any advice please thankyou. X

Since my SPMS diagnosis less than two years ago, I’ve been seriously struggling with getting social interactions. I’ve always been an extremely social person but since MS I’ve become the complete opposite. And struggle with anxiety, chronic fatigue, depression, and mobility issues that make socia...

I have my first MRI next week. How long until you got your diagnosis after your scan?

Hey there! Newly diagnosed this summer and have been putting off starting a treatment out of anxiety and fear. I’m trying to determine which is better, Tysabri or Zeposia. Anyone have any input on either medications? Curious of side effects, efficacy, etc. Thank you!

What is THIS 😭 I need tips asap my symptoms are so much worse & I’m freezing and the next minute hot.. also bad restless legs 😳

What all tests were run to confirm your diagnosis of MS?

Anyone else get diagnosed with POTS after their MS diagnosis? I’m wondering what your experience was like, because I’m experiencing many symptoms in addition to my MS symptoms. Thanks!