After five years at the MS Society, I’ve decided to move on to pastures new. Over those years, posts in this forum have made me laugh, cry, think and understand the complexities of life with MS.
If ever there was a way to learn about the different way that MS and disabilities affect people and those that care for them- this forum is it.
I’d like to thank you all for your patience, wit, honesty and support. Remember to look after each other and be patient with those you don’t understand or agree with.
Most of all I’d like to thank Val for her brilliant moderation skills and amazing support- I couldn’t have done it without her.
The Digital Team will continue to monitor posts and keep an eye on the tech side of the operation.
Once again- thanks for all you’ve taught me and hope you all continue to be the lively and loving community that you are……
Hi I Have decided to post on here as would like information on disease modifying drugs. I have RRMS and have had a meeting with neurologist who has recommended these. I am in particular looking at taking Tecfidera. I would like to hear from anyone who has been taking these and their experience. I am finding it hard to make a decision bearing in mind the Side effects. Thanks everyone x