Viewing 3 posts - 1 through 3 (of 3 total)
  • #75514
    Becker Muscular Dystrophy

    Hi to all,
    My grandson who is 7 and lives with us has recently been diagnosed with Becker.
    Apart from the shock of hearing this has anyone got any advice, tips etc to take on board in the early stages.
    Not even very sure what questions to ask but any advice will be much appreciated.

    Posts: 1
    Joined: 20/02/2015
    Re: Becker Muscular Dystrophy

    Hi, welcome to the forum :welcome:

    You will probably find things a bit daunting at first, there’s so much to take in and get your head around. A good place to start might on the Beckers page on the main site Beckers this page will tell you about the support available which you may find useful in the future.

    Others will be along I’m sure to offer their advice, please feel free to ask anything its what we are here for :)

    Posts: 1,015
    Joined: 05/03/2015
    Re: Becker Muscular Dystrophy

    Welcome to these pages.

    This will be a difficult time for all in your family. You are doing exactly the right thing
    in trying to find out more information. Please follow the links that Vicki has given you
    and read up on it.

    Several of oue members have the Beckers variant of MD so you can ask questions
    on the forum here or go to the search box and search for “Beckers”.

    "Even if you are not paranoid, it does not mean they are not out to get you!".

    Posts: 4,630
    Joined: 27/09/2010
Viewing 3 posts - 1 through 3 (of 3 total)

You must be logged in to reply to this topic.

Keep in touch