Looking for
something specific?

Ok this is probably a bad idea to post as people will judge but it is called fun drugs so it must be on others people's minds too so here it goes anyway. I used to be the biggest party animal ever from my teens trough my twenties. I'm Dutch and all thing that are party feeling enhancing are readily ...

So since I had COVID almost a year to the day and had the fun delta variant I've noticed my legs retaining water. I tried more potassium, lower my salt intake, drink more water, water pills both over the counter and prescribed, compression socks but all to no avail. So my neurologist after trying al...

I didn’t think MS could still humiliate me. I feel bad about how I’m effecting those around me and how I am going to be a greater burden on my family. I lost it and tore into my wife. I was in such a haze that I can’t remember what I said. I acutely remember the feeling of being mortified. Of c...

Does anyone smoke cannabis or use cannabis to relieve their symptoms

Can you use cannabis oil when taking fingolimod?

Evening folks, Sorry its been a while since I last posted... Has anyone given Cranio-sacral Therapy a shot? I decided to give it a go. Its a very gentle massage - and no meds/drugs so I figured at worst case it was an hour of relaxation.... The after effects were suprising, in that my walking w...

I havnt myself, although I’ve never been asked. I’m not sure what my response would be. That brings me to my next question. Are there any “game changer” close to if not a cure drugs in trials at the moment ?

Hi everyone, it's been a while I have been working so much my free time is almost non existent. I hope everyone is doing ok. Alright the meat of my post. I have decided I'm not hiding anymore, I am telling every single person I know I have MS. I am doing this because I felt like I was hiding mys...

We look forward to your post on the topic For all of you interested: watch out for news of TOLEBRUTINIB and FENEBRUTINIB, for us progressive MSers, in the upcoming Euopean Congress of MS in Copenhagen, Denmark (ECTRIMS). Currently in phase III (the last before filing to EMA or FDA), the drugs coul...

I'm having an active flare up and have been placed on 500mg of methylprednisolone daily for 5 days, and am using paramol and tiger balm to try keep the pain at bay. I've been looking into CBD oil as I used to be a heavy cannabis user around 4 years ago, before my diagnosis was confirmed, and did fi...