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Hello, has anyone who suffers with foot drop found an AFO that helps you to run. I have one of those which clips into the laces of my shoe and it is great for gentle walking. But running is not possible with it. I've looked at some online but they cost a fortune so it's a lot of money to waste if t...

<p>I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.</p>

Hello. Just wondering what people's experience of fatigue following Ocrevus infusion was? We were planning on trying to take a trip away (in the UK) immediately after the second infusion. Trying to understand if that's advisable given energy levels? Thanks

hi

Hello have had MS since 1970, still walking but falling more but I was expecting that. Question I was on Aubagio 4yrs and stopped taking 1 month ago. Now experiencing more balance issues. What are the withdrawal symptoms if any?

Hello Shifters, I will performing some standup comedy "live" over the internet, as per the New Normal. Starts tonight at 8:20 (20:20 - get it? Cause it's the year? see what they did there? ) FB: https://www.facebook.com/events/306540333735425/ YT: https://www.youtube.com/watch?v=7RsMJtmmqOI Tha...

Hello everyone, I've headache which last for a long time. Painkillers can not do anything with it. I really suffer much sometimes like now I do. Does anyone have the same problem and what do you do for coping with it?

Hello I hope everyone is doing well ! I was just wondering if anyone else has experienced hard lumps under the skin !? I spoke to my GP and he told me it could be a cyst or my lymph nodes and I think it is my lymph nodes. Does anyone know how this correlates with Ms ?

I don't qualify for Ocrevus either. What I believe is helping me is Low Level Light Therapy. I found a chiropractor who uses it on primarily MS patients. It take about fifteen minutes a treatment: the doctor uses a wand on my spinal cord on my back. I've been using it weekly until the Stay at Home o...

Hello I've been recently diagnosed, I'm still getting my head round it, fed up with the chronic pain, I'm working mum with two kids. My MS Nurse is coming to see me next week. I feel like people that don't have MS don't really get it. If I say I'm tired they say oh I am too, erm it's not the same!!...