Vasculitis patients living in London? Do you... - Vasculitis UK
Vasculitis patients living in London? Do you think you could benefit from a support group, meeting people who face similar challenges
That would be helpful and lovely. I have written to the person in charge of London but nothing came through. Please keep me posted if anything comes through. Many thanks!
Possibly! Give it a go!
Hi John..in touch with a couple of people in London area..be good to get some others roped in. We all have egpa
I may be interested , I have ANCA vasculitis mpa
Hi John,I may be interested ; I live in Berkshire and unsure if there is a support group in this area. I was diagnosed with most probable EGPA last year.
I may be interested. I live in Hertfordshire. I’m still wary of travelling into London because of COVID and any risk of infections. I’m terrified of another bout of Vasculitis, for which I was hospitalised suddenly (after my first COVID vaccination) last April (2021) and am still recovering (further complicated by Cirrhosis of the liver).Maybe a zoom forum? It would be helpful to speak with others. I’ve never known anyone else with Vasculitis and it is very lonely.
