This Is MS Multiple Sclerosis Knowledge & Support Community

Hi, I'm posting this for my husband. He's had these issues for years now. Was diagnosed RRMS in 2007, now the MS is continually having a go at him. We've found that with him this raw/burning sensation generally is nerve pain. Not sure if you want to know this, but he has eventually gone numb, total ...

I am very sorry to hear about your son. May he rest in peace.
Thankyou for your advice. My husband won't see a counselor, nor my son, but if I start, maybe they will also.
If you feel like talking, I'm willing to listen.

I started LDN 10 days ago. I'm currently on 1.5mg, not having any side-affects yet. Since my diagnoses, I've been put on betaferon, then copaxone. All they did was heighten my symptoms, especially the fatigue. Had enough of the conventional meds. Now am on David Wheldons ABX protocol, going very slo...

when I was a toddler, my older brother ran me into a stoby pole and bashed my head. when I was about 10 fell off a chair onto a concrete floor on my head. when 16 I rolled my first car and got severe injuries to my neck. broke the benchseat clean in half with my back and landed on my head on the roo...

Over time Jases emotions have become erratic. It's affecting our son and his relationship with his father. I'm unsure as what to do. I'm trying to hold it together for the sake of them both. Jase seems to think I'm always taking our sons side when things don't go well, but I don't think I am? We don...

Hi, Not sure if you want to hear this, but it may be MS. As you may know MS isn't always the same with everyone. Especially the symptoms you have when diagnosed. When diagnosed I had same symptoms as you, plus a heap more. It's just gone 6 years since I was diagnosed RRMS. Think I'm now in the next ...

Hi all, i'm new on this site. I was on Betaferon at first, then Copaxone. Found both drugs made my hair thin-out and made me feel like shit. Decided neither of them were doing anything for me so now I don't take anything and I've gone on Wheldons Anti-biotic CAP. You've got to be extremely lucky for...

Hi, thought I'd introduce myself. My name's Renee 35 yrs age and I'm the wife and carer for Jase. We share the same email, hence the user name. We have a 16 year old son, who finds Jases MS difficult. Jase was diagnosed RRMS in 2007,32 yrs age. He's got all symptoms plus some. Lately we've thought h...

Hi All,
I'm new on here and found this topic interesting. I've used this for years and it has helped me with nerve pain and coping in general with this prick of a disease. Be nice if they legalized it here in Australia, the natural, not the synthetic shit!

cheers
Jason and Renee

Hi Everyone, Thought I'd introduce myself. My name is Jason and I'm from Australia. I'm 38 yrs old. I am married to Renee, who is my carer and who writes on this forum for me. We have a 16 yr old son. I was diagnosed RRMS in 2007. Have been on 2 conventional MS drugs, betaferon, then copaxone. Now i...