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Is anyone as irritated by the sun and heat as me? I can't go 5 mins without feeling hot and sweaty, direct sunlight and heat make me grumpy. I tried escaping this crazy weather in the mall, and now I'm exhausted from all the walking. 😛 Not sure if this is MS-related, but I need a break from the sum...

Hi Everyone I’ve had MS a while now but have recently noticed (probably as I’ve recently been walking slower and with a slight limp and have probably been looking more fatigued than usual) that people, who do know me, talk to me in the same way as they would a child and/or can be very patronising....

I've had depression since I was a teenager. Now, finally diagnosed with MS, last year, I will get to look forward to when I can no longer fend for myself. Hasn't happened yet. Fortunately, I have worked since I was in highschool. I know that after 35+ years of taxes paid, I am now an elder. I deserv...

Hi all. So, I know, a couple of weeks ago, I had an MDT DMT meeting, discussing my medication and recent relapses and new lesions. Still not received a letter from them, but I know that it can take a couple of weeks. However, a nurse from my MS team called me today, telling me that they'll be booki...

I’d love to hear about everyone’s hobbies and interests- whether it’s something you were into pre-diagnosis that you’ve adapted to work around your MS symptoms, or if it’s something completely new to you that you wouldn’t have discovered without your MS. You never know when someone might need an u...

Hi I am 10 years in with RR MS, and had 2 very successful doses of alemtuzumab, in January 2016 and January 2017. I responded very well to the alemtuzumab neurologically (despite being highly prone to any virus, cold or infection going in the 1st year) and in 2018 was in extremely good neurologica...

<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>

I am MS person for 20 years and still suffering from drop leg,spasm

Does anyone else experience bruising easy or not remembering where bruises came from. I find bruises all the time and have no idea where they have came from. Could it be ms or my meds, I recently started tecfidera.

Hi I’m new to this iv had Ms along time iv never got over the lack of understand if you look ok you must be ok very frustrating just wanted to get it out there