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    Hi

    Greetings, I'm a limbo lander. I have a lil sister with PPMS so I actually know way more about the disease than I ever wanted to.

    Now, it's a disease on the short list for myself. I qm at the very beginning of this process but am very stressed, knowing what is to come and knowing it can take years.

    I just wish I could feel my hands at this point.

    #2
    Greeting Kaitar and welcome! Being in limbo is especially stressful and I feel for you. I, too, had to wait many years but it was a very long time ago. The diagnostic tools have improved since then as have the medications. I hope they find answers for you soon.

    Hope you have checked out our LimboLanders forum here? We also have a live chat session called Patiently Waiting for those in limbo. It's every Wednesday from 8 PM until 9 PM EST in case you're interested! Hope you can make it sometime.

    Again, welcome!
    1st sx '89 Dx '99 w/RRMS - SP since 2010
    Administrator Message Boards/Moderator

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      #3
      Hi and welcome.

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