Tecfidera no more

[JerryD]

I've been on Tecfidera for about 2 years. Although it is easy to take, I have stopped the pills because my neurologist and I have determined that it has had little or no effect on my MS. I will be starting my first week of Lemtrada in 2 weeks. I hope to see some results in a couple of months and I am praying that the results are positive.

[pennstater]

I wanted to wish you good luck on the Lemtrada! I hope this does make a difference for you.

[Marco]

There have been some miracle stories related to the Lemtrada and I hope yours is next.

[REG53]

Good Luck Jerry, I hope this is the med that helps you.

[JerryD]

Thanks for the positive posts, everyone! I've been feeling very well, since I have been using my power wheel chair nearly all day. And, although I feel that I am 'throwing a 'Hail Mary' pass, I am going through with the Lemtrada, full steam ahead, that is if Keystone Blue Cross insurance approves! I plan to post my experiences, here. Maybe my story will be of some help to another MSer!