It started in the early 1980s best I can remember and I take nothing for it.

I haven't yet need to give him an answer friday pairing

Going from shots to a pill is different.

Dx almost 16 years ago. Have been on Rebif most of the last 12 years. Went off of it briefly to try Tecfedera but noticed that Tecfedera made my MS worse. I had to go back and take the Rebif shots. It works the best for me although I hate the shots.

I was diagnosed on March1, 2011. He sent me to the MS neuro for a second opinion. On March 11, 2011 it was confirmed. He put me on Avonex. My body is getting used to the injections. I control the flu like side effects from Avonex with Aleve. It seems to be doing good for me.

Started having symptoms in 1978.
I was dx'd in 1995.
I took Avonex for 6 months, then stopped them because they made me sicker than a dog.
I have been trying to exercise and I try to stay away from sugar. I eat more fiber, and drink more water.
I can still walk a little, and my tremors have lessened.
I also use medical marijuana. It improved my sleep. It helps to be well rested!

Diagnosed in 2005. Currently on Gilenya and I have no issues with this drug. I have been on almost all the MS treatments at some point over the past nine years and I have to say I much prefer taking a pill instead of a shot.

Diagnosed with Mild MS in Jan 2000. Now Secondray Progressive and been on Gabapentin for couple of years - and it helps.

22 years. Swank diet first 6 years. Then nothing. Copaxone 6 yrs off and on stopped with pregnancies. Rebif 6 months. Now nothing. Still RR.