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
APS and consultants. : Hi I live in the... - Hughes Syndrome A...
APS and consultants.
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DebsT
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MaryFAdministrator
Several of our members do attend clinics in that wider area, so you will get some replies later. MaryF
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
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