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
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
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