Regarding Beckers Muscular Dystrophy. Please help.

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  • #75163
    Regarding Beckers Muscular Dystrophy. Please help.

    Hello,

    My name is Ashleigh and my father was diagnosed with Becker’s Muscular Dystrophy when I was in high school. I am 22 now. After recently looking more into this myself, my current understanding is that since I am the daughter of a man with BMD, I am automatically a carrier, which gives me a 50% chance of having a son with BMD, and a 50% chance of having a daughter who becomes a carrier of BMD.

    As someone who has considered children a future possibility at some point, I am very nervous/saddened and I am just in need of more information and/or advice from anyone who has any input.

    My questions about this include:
    Is there a point for me to have genetic carrier testing done on myself, or is my above understanding correct? (That being that I am indeed a carrier)
    Is there anything at all to do in regards to having kids (in terms of lessening the chances of passing it down)?

    And in general, I would just greatly appreciate anyone with any input whatsoever, or anyone who could offer information. I do plan on going to speak to my doctor about this very soon, but in the meantime thank you very much. This has been bothering me for some time now.

    All the best and thanks,

    Ashleigh

    :new: :ty: :|

    Ashleigh6
    Participant
    Posts: 1
    Joined: 28/12/2013
    #92890
    Re: Regarding Beckers Muscular Dystrophy. Please help.

    Hello Ashleigh – Welcome to the forum .

    I assume you have read the MD’s publication about BMD? You can find it HERE

    There is also one about being a carrier, which can be found HERE

    I have found one to do with pregnancy and screening, don’t know whether it will fully answer your query though – that can be found HERE

    This is just my personal opinion, but if you have the option of being tested, I would go ahead and do so, mainly because it is then officially recorded in your medical documentation, rather than something you have to keep telling medicos about to which they then might not listen falsely thinking ‘Well we don’t know for sure’.

    I'm always the animal, my body's the cage

    I blog about nothingness www.amgroves.com

    AM
    Participant
    Posts: 4,751
    Joined: 05/03/2015
    #92891
    Re: Regarding Beckers Muscular Dystrophy. Please help.

    Hi Ashleigh,

    I’m Rosanne, Information Manager working in the Muscular Dystrophy’s London office. I am sure you have fond the Becker muscular dystrophy factsheet really helpful but I would be happy to talk you through inheritance and carrier information and hopefully be able to help you think decide if you would like to arrange a genetic test.

    My direct phone number is 0207 803 4802

    Hopefully hear from you soon.

    Rosanne

    Info Manager Rosanne
    Participant
    Posts: 16
    Joined: 29/07/2013
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