I'm a newbie!: I was diagnosed in May of... - My MSAA Community

My MSAA Community

9,019 members20,711 posts

I'm a newbie!

bavery207 profile image
3 Replies

I was diagnosed in May of 2015, at age 65, with primary progressive MS. Befor that I was seeing a neurologist for Essential Tremor and considering having deep brain stimulation surgery. I had the surgery in Nov. 2015 and it made an enormous improvement in my tremor, although my right hand and left leg still tremor some. AS for the MS, I have recently started some PT and Speech therapy to help with balance and swallowing/voice issues. I am waiting to see what the FDA (and my insurance co.) have to say about the possible med. for primary progressive that is being looked at. This is not what I imagined retirement being like,but I guess I am lucky that I am retired and have the time and some energy to deal with everything.

Written by
bavery207 profile image
bavery207
To view profiles and participate in discussions please or .
Read more about...
3 Replies
jimeka profile image
jimeka

What is the med you are looking at, hope you get it, I have PPMS so please keep us informed how you get on, hope when you get it, that it works for you, Cheers Jimeka

TonyiaR7 profile image
TonyiaR7 in reply to jimeka

The new drug for PPMS and RRMS is Ocrevus (ocrelizumab). My neurologist wants me to consider the medication. However, B-cell depletion is not insignificant treatment. She wants to watch how others respond and how my MS is progressing. I am on the border of RRMS and SPMS. But for others, she stated they had no choice.

johnMSAA profile image
johnMSAAPartner

Welcome to our My MSAA Community, bavery207 ! Thank you for sharing your MS journey so far, and we certainly want you to keep us posted on here.

- John, MSAA

You may also like...

I'm a fighter.. I'm a Conqueror.. I'm a winner...

currently taking Rebif but I don't see a difference. I am having very bad muscle spasms in my legs...

Hello World from a newbie

referral to a neurologist and lots of tests, got the diagnosis of PPMS. It's possible I may have...

Newbie to community but not to MS

I Have had ms for 12 years now. I am 51 and feel like my life should still lively and to be do lots...

I'm getting AWFULLLLLY tired of this.

if always coming in second. (Am in secondary progressive stage now, and boy is it at a galloping...

Hi, I'm Bonnie and I'm new here

with PPMS. I have been on numerous treatments and nothing has slowed down the progression. My dr...