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Hughes Syndrome APS Forum

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APS and consultants.

DebsT profile image
5 Replies

Hi I live in the Manchester area. Has anyone seen a Consultant for APS in Manchester that they would reccommend? My symptoms are mainly numbness and migraines. I have got the list from the Hughes Syndrome Foundation.

Thanks

Deb

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DebsT profile image
DebsT
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MaryF profile image
MaryFAdministrator

Several of our members do attend clinics in that wider area, so you will get some replies later. MaryF

amy1808 profile image
amy1808

Hi , I see professor hay at Manchester royal but if I'm honest I don't rate him . Seriously thinking of making a trip to see the main man himself . .i suffer dreadful migraines and numbness with weakness x

DebsT profile image
DebsT in reply to amy1808

Thanks. They have referred me to Professor Ian Bruce.

DebsT profile image
DebsT in reply to amy1808

Yes I was thinking that!!

DebsT profile image
DebsT

Just out of interest does anyone know any private consultants in the Manchester area?

Thanks

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