fshd - muscular dystrophy uk...fshd between 10-20 percent of people with the condition eventually...

1
94,276 visited our online forum to support each other and talk about the things that matter to them 9,059 understand more about their condition after downloading info factsheets 985 cases were supported by our advocacy team Facioscapulohumeral (FSHD) muscular dystrophy is a genetic muscle-wasting condition that causes muscles to weaken and waste over time leading to increasing disability. We believe everyone living with a muscle-wasting condition should have what they need to live full and independent lives. Here are some of the ways we supported people during 2019/20: FSHD Between 10-20 percent of people with the condition eventually require a wheelchair FSHD mostly causes weakness in muscles of the face, shoulders and upper arms. However, weakness in muscles of the trunk, hips and legs can also develop over time HERE FOR YOU Several generations of a family are often affected by the condition 3,225 requests were made for support through our helpline and clinics 81,764 new users joined our TalkMD forum www.musculardystrophyuk.org Muscular Dystrophy UK, 61A Great Suffolk Street, London SE1 0BU Registered Charity No. 205395 and Registered Scottish Charity No. SC039445 FSHD muscle weakness is often asymmetrical (one side of body affected more than other) Physiotherapists, occupational therapists and podiatrists can help people to live well with the condition There is currently no treatment available targeting the underlying genetic causes of FSHD although there is much research taking place Severity and age of onset are variable for people with FSHD AWARENESS DAY 20 JUNE 2020 THERE ARE ABOUT 2,500 PEOPLE IN THE UK LIVING WITH FSHD

Upload: others

Post on 27-Jan-2021

2 views

Category:

Documents


0 download

TRANSCRIPT

  • 94,276 visited our online

    forum to support each other and talk about

    the things that matter to them

    9,059 understand

    more about their condition after

    downloading info factsheets

    985 cases were supported by our advocacy team

    Facioscapulohumeral (FSHD) muscular dystrophy is a genetic muscle-wasting condition that causes muscles to weaken and waste over

    time leading to increasing disability.

    We believe everyone living with a muscle-wasting condition should have what they need to livefull and independent lives. Here are some of the ways we supported people during 2019/20:

    FSHD

    Between 10-20 percent of people with the condition eventually require a wheelchair

    FSHD mostly causes weakness in muscles of the face, shoulders and upper arms. However, weakness

    in muscles of the trunk, hips and legs can also

    develop over time

    HERE FOR YOU

    Several generations of a family are often affected by the condition

    3,225requests were made for support through

    our helpline and clinics

    81,764 new users joined

    our TalkMD forum

    www.musculardystrophyuk.org

    Muscular Dystrophy UK, 61A Great Suffolk Street, London SE1 0BU

    Registered Charity No. 205395 and Registered Scottish Charity No. SC039445

    FSHD muscle weakness is often asymmetrical (one side of body affected more than other)

    Physiotherapists, occupational therapists and podiatrists can help people to live well with the condition

    There is currently no treatment available targeting the

    underlying genetic causes of FSHD although there is

    much research taking place

    Severity and age of onset are variable for people with FSHD

    AWARENESS DAY 20 JUNE 2020

    THERE ARE ABOUT 2,500 PEOPLE IN THE UK LIVING WITH FSHD