Hello everyone I'm new to this!

[Ladybriars]

Hello I am Ladybriars, I was diagnosis 6/2009 RRMS. I'm started out with Rebif for 6 months. Too much flu like symptoms. Now I take Avonex and so far doing alot better.

[falalalala]

Welcome!

[CraigS]

Well, Ladybriars

You have landed in a good place. This forum group is full of wonderful supportive people with much to share. I look forward to hearing more about your journey through the magical land of MS.

Craig

[greaterexp]

Welcome!

[RoyceNewton]

G'day

[Jackjosh]

Hello and welcome

[rjoneslaw]

welcome

[Jazzihorsecat]

A very warm welcome Ladybriars. Blessings🙏💐💗

[twooldcrows]

WELCOME ...HAVE A GREAT DAY AND ENJOY THIS WONDERFUL SITE AND A GREAT GROUP OF PEOPLE...

[leking1]

Welcome to the family! We are glad that you have joined us. We all have one thing in common...MS. We live it every day, in all it's various forms and

messes, each day, and each person, differently, but with the same MS. We get it! Welcome!

[carolek572 CommunityAmbassador]

Welcome to this forum, Ladybriars and I am looking forward to hearing more from you!

[Pia7]

Welcome!!!

[MarkUpnorth]

Welcome! Names of my favorite DMT's? A & R. I ran the gauntlet of the DMT's in my day. I've had M.S. for over 20 years, Oh boy! I started on Avonex, the 1-1/4" beast, ended with Rebif, with a couple in between. I spent the last 2.5 years of my DMT's with non-stop flue like symptoms. Got about 1/2 a day 3x per week, right before the next shot, where I didn't ache, shake, and live with the fever. After almost 2 decades, my neuro pulled me off all DMT's, as my history showed as he said, little benefit. I have a history of lots and lots of relapses, often more than one at a time. I can tell you stories, (or look them up on my past postings), such as the broken old TV relapse, where my vision went crazy in a unique way for about a month and a half... BUT, I'm also the success story in my part of the country according to my neuro, but not the only one. "Apparently old farts? Sometimes get a break?" We seem to have gotten over any new relapses, for me it's been over 5 years now, and I've been off of all DMT's and any other drugs (okay, except for the green leafy stuff to fight the nightly burning feet pains). Step 1, keep a positive attitude. Never give up! Even if you're the frog in the beak of the big bird, with your hands around the bird's neck so as not to be able to swallow you. Step 2, eliminate all processed food.... Okay, I went too far, unless you want to research my history via this site. Or just stick around.... I preach what I believe to be my best defense against M.S.

But, your post...DeJaVu.... The Drugs I Used To Take, to the sound of my grade school daughter, now neuroscientist gone teacher, used to play the dum, dum, dum, da dum on the piano every shot night. She hates shots to this day. Passes out at most flue shots.... A neuroscientist who studied rats, gave drugs therapy, then sliced their brains wafer thin to see how they were affected by the drugs. I can't blame here for the math geek turning teacher?

We're a fun group with history of M.S. and life. And then some more. Welcome

I'm Mark Upnorth, I hope to go west again some day. But it's fall, and it's cool, and the colors...yeah I talk too much!

[stepsforNeeC]

Hello Ladybriars! Welcome and you'll find comfort and support from a group of wonderful caring folks in our community. I also have RRMS was dx around 2008(ish) and currently on Copaxone 40 mg 3x per week. I haven't heard, but thank you for sharing new treatment options, I always like to stay well informed.

Peace and Blessings

NeeC

[Horse714]

Welcome you asked me about Avonex vs Ocrevus. I did the split dose of Ocrevus but I’m back on the Avonex.

[Horse714]

I personally like Avonex.