fshd - muscular dystrophy uk...fshd between 10-20 percent of people with the condition eventually...
Embed Size (px)
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