broox

I'd love some intros to other people with Multiple Sclerosis so I could buy them coffee/dinner/drinks and chat about their experiences.

My mom has had it for years. My family has experienced alot with Ms and we know alot about it. My mom is doing pretty well. They have come along way in medicine helping it.
There are 4 different kinds have they told you what kind?
A friend of mine was just diagnosed. I can connect you with him if you'd like?
Lorraine At this point, we believe relapsing remitting.
Relapsing remitting is what mom has she will have flare ups but she will recover from them. There is alot they can do for relasping remitting. Mom found out at 62 wished she would have found out earlier due to she could have been helped way sooner. But she is really pretty normal for a 82 year old. So I think they will figure out what works for Kari and it will be few and far between in flare ups. I know she is probably so frustrated.
Vicki's friend Linda McGhee has it she had it since she was like 27 or so . You could maybe have Vicki connect you with her.
I think Gary Parson's wife Kay here in Newton has had some for form of it for several years as has Julie Broderson who is Linda Boyd's cousin by marriage - also here in Newton. I'd be glad to make a contact if you want.
@broox Meet @darthbender. @clint

ohdeafone posted

@broox when did you get your diagnosis? @ohdeafone @clint
@broox @marihuertas How come? We're in the UK, but curious.
it was actually my wife who was diagnosed. but 3 weeks ago.

broox posted

my wife was recently diagnosed and we would love to chat with others to learn from their experiences.

broox posted

2 months for me. Immediately started Copaxone.
Hi Derek, we gotta lively, highly entertaining community of peops on here affected by #MS, so you come to the right place. *waves*
@broox @mssocietyuk My wife was diagnosed in 2004 with relapsing remitting. Ask away.

Will_Penguin posted

@broox @mssocietyuk RR for the last 15 years (42 now) and still working and active. Happy to give info.

AbbieHaslin posted

diagnosed on 18th may this year been a rollercoaster and eye opener at the same time i have RR went on tysabri instantly happy 2 tlk

sarah_29_harris posted

@broox my email@is being temperamental at the moment but hopefully I will send you a message with my address.

AbbieHaslin posted

Derek, there are fantastic online forums with amazing communities of people with MS and supporters. It sounds cliche, but google for them. Big Hugs
of course! I'll drop you an email :)
@broox hey. I was diagnosed last year. I know it can be as hard for the boyfriends too, if you ever want to chat @mickycurling is on here x

beccyhuxtable posted

certainly, I'll send you an email.
Dx last year and happy to.help.

leetherriault posted

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