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Beker muscular dystrophy
Painterman123
Member Posts: 2 Listener
I am lucky enough to be a bmd sufferer, strange you might think to say lucky, but there are far worse types of md in the world and I aint got them...I don't know any other sufferers and would like to meet someone on line to chat. To compare notes if u like.
Replies
Hi @painterman123
Welcome to the community,
To get you started, take a look through our recent discussions and community guidelines. Feel free to contribute we are a chatty bunch.Let us know if you have questions
The Muscular Dystrophy association may be able to help connect you with other people with Beker Muscular Dystrophy, they say:
So we have set up a number of ways to help you do just that. From our online forum to our local Muscle Groups and our Advocacy Ambassadors, there are hundreds of people who want to help – and who really do understand.
Talk to our peer support volunteers
We have a number of peer support volunteers, people who understand what you are going through, no matter how rare the condition. We can introduce you to one of them so that you can contact them confidentially to talk about how you are feeling. Get in touch to find out more or fill in the form below and we will get in touch.
I was just wondering with your username are you a painter as in an artist or as in a decorator? Would love to hear more!
Senior online community officer
You appear to be the first person to discuss Beker muscular dystrophy here on the community, although there was a related discussion from a parent in the past. Would you like to tell us some more about your experiences?
I'm also tagging in @EmmaP94 who's written some great guest blogs for us and is a content advisor at Muscular Dystrophy UK!
Welcome to the community and thanks Pippa for tagging me.
Yes I’m a member of the Content Advisory Group at Muscular Dystrophy UK. We are a team of volunteers who either have MD, have family or friends with MD or are healthcare professionals working with people who have MD. I know many friends and acquaintances with MD and use my knowledge of MD from them, my overall experience of being disabled (I have CP and registered blind) and my journalism background to help MDUK shape their online, media and marketing content.
Like with Scope, MDUK have a website filled with info on MD, advocacy support, MD groups plus much more: https://www.musculardystrophyuk.org/
We also have a Facebook Group “Muscular Dystrophy UK Trailblazers” where you can share stories and get advice from others with MD - https://m.facebook.com/mduktrailblazers/
hope this helps and do let me know if you need further info?! 😀