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.

via Twitter and Facebook

facebook comments

  • 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.

    Lorraine Brooks posted

  • There are 4 different kinds have they told you what kind?

    Lorraine Brooks posted

  • A friend of mine was just diagnosed. I can connect you with him if you'd like?

    Kelsey Seaberg posted

  • Lorraine At this point, we believe relapsing remitting.

    Derek Brooks posted

  • Kelsey absolutely!

    Derek Brooks posted

  • 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.

    Lorraine Brooks posted

  • 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.

    Lorraine Brooks posted

  • 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.

    Dave Boyd 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

    Lannea Auguste Olson Brooks posted

twitter comments

  • @broox Meet @darthbender. @clint

    ohdeafone posted

  • @broox when did you get your diagnosis? @ohdeafone @clint

    darthbender posted

  • interesting article: t.co/WzqPiBUosh

    gitarrenlabor posted

  • @broox @marihuertas How come? We're in the UK, but curious.

    mssocietyuk posted

  • 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.

    darthbender posted

  • Hi Derek, we gotta lively, highly entertaining community of peops on here affected by #MS, so you come to the right place. *waves*

    mssocietyuk posted

  • @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

  • happy to help! :)

    valyrianarakh posted

  • @Will_Penguin thanks! Can we chat over email? derek@broox.com is me!

    broox posted

  • @AbbieHaslin thanks! Can we chat over email? derek@broox.com is me!

    broox posted

  • @valyrianarakh thanks! Can we chat over email? derek@broox.com is me!

    broox posted

  • @darthbender that's good info. Can we chat over email? derek@broox.com is me!

    broox 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

  • @sarah_29_harris I'd love to. Can we chat over email? derek@broox.com is me!

    broox posted

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

    AbbieHaslin posted

  • of course! I'll drop you an email :)

    valyrianarakh posted

  • @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.

    darthbender posted

  • Dx last year and happy to.help.

    leetherriault posted

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