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

long wait to see neurologist

I have a new, tentative diagnosis of MS. My neuro-opthalmologist said that I meet criteria and they've found a few active demyelinating lesions on my MRIs that I am currently...

Possible covid positive - but what about my MS treatment

Hello again, when it rains it pours , as the saying goes. My house mates have tested positive to covid, im sure I'll get covid, being in close contact. Which...

Meds

I was diagnosed in 2019 and since then I have had no meds prescribed for my MS. My neurologist doesn't even seem to listen to me when I see her...

Covid vax dose 3 timing?

I just received the 'invite' to book my 3rd Pfizer vaccine dose. After a recent call with my neurologist (before she knew I'd gotten the booking email), I was left...

Neurologist frustrations: what to do?

I am unsure of my neurologist as he is frustrating me. Leg pain, no sleep, nothing works....

How Do Veterans Affairs Benefits Work With MS?

I have a lumbar puncture this week to verify the presumed MS diagnosis. Was wondering if anyone had any experience with how the VA handles these things, my neurologist seems...

Early Symptoms.

Symptoms of MS can take on so many forms. I was hospitalized multiple Times prior to being diagnosed....

Chronic Constipation

Hello all! I've seen some posts in here regarding constipation. But none answered my question. I am dealing with chronic constipation, have been for years. I feel like I may...

How do you suggest I find a new doctor and answers to my questions?

I'm lost every time I turn around something new is going on and I don't know what is due to this illness and what may be due to some other...

Comminicating Symptoms to your Doctors (and the resulting frustrations)

I had a very disturbing visit with my (old) Neurologist yesterday. I was recently referred to a different Neuro doc because my first was SO hard to see for follow-ups...

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