As researchers we spend a great deal of time initially
reading around a topic and examining the published research evidence. In order
to be answerable, research questions are usually very specific, as in this
project where we are focussed on orthotic devices for knee instability in people
who have a neuromuscular disease or central nervous system disorder. So when we
get the opportunity to meet and talk with people our research is aimed at
helping whenever possible we take it!
Such an opportunity was taken when we attended a really
interesting meeting of the Yorkshire
and Humber Muscle Group in York last Friday. When we got in touch with the
group to circulate our advert for patient members to join our Steering Group
they invited us along to the meeting. As well as having an opportunity to tell
the group about our research we heard about the work that the group is doing in
the Yorkshire and Humber region. This included reports from those providing
support to people with neuromuscular conditions in the region, fund raising
successes and possibilities, and advice on new self-managed funding arrangements.
The meeting was hosted by the Muscular
Dystrophy Campaign, who provide details about this group and similar ones
all over the country on their website.
Some of the discussions at the meeting were a very strong
reminder for us that in the context of complex neuromuscular conditions walking
problems can be just one of many challenges people are dealing with. We are
aware that our research is asking very focused and specific questions but the
meeting has made us very mindful of the wider context in which our research
question fits. This will be reflected in the discussion section of our final
report.
Bloggers: Catriona McDaid and Alison Booth
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