Vasculitis Research: Suzy on the VasculitsUK forum... - PMRGCAuk

PMRGCAuk

20,289 members38,005 posts

Vasculitis Research

PMRpro profile image
PMRproAmbassador
6 Replies

Suzy on the VasculitsUK forum has just posted this:

healthunlocked.com/vasculit....

To support a proposed research study into access to timely and coordinated specialist care for vasculitis patients, we urgently need very brief accounts of people's negative experiences of delayed recognition and diagnosis or uncoordinated or inappropriate care.

Maximum 100 words by mid-night Tuesday 29th August!! So no pressure!!

No replies will be accepted here in HealthUnlocked community only replies sent by email to John.mills@vasculitis.org.uk or susan@vasculitis.org.uk

Those of you who have GCA that was not recognised quickly please respond - especially those who have lost vision because of the delay.

They can have all the fast-track options they like - you have to get past the GP first and sometimes even the rheumy! So any research that highlights this is going to benefit us.

Written by
PMRpro profile image
PMRpro
Ambassador
To view profiles and participate in discussions please or .
6 Replies
Rocketronzy profile image
Rocketronzy

Mmm dornting.

Let's see how I go this week

Back to downing after holiday. 😳😬

rosie_jones profile image
rosie_jones

Do they want info on delayed diagnosis of PMR too?

PMRpro profile image
PMRproAmbassador in reply to rosie_jones

Not sure - I sent a message about my 5 year delay in getting a PMR diagnosis but I do have doctors here who agree with me it is probably borderline GCA, just not affecting vision.

If they don't want PMR, they'll ignore it and it only takes a minute to do.

sondya profile image
sondya

Initial diagnosis was TIA but wasn't comfortable with it. Had a second opinion and doctor agreed and checked me into diagnostic assessment unit in North Shore hospital in Auckland (NZ). Tests, scans, positive temporal biopsy pointed to GCA. Prednisone started immediately in Dec 2016. There would have been less of a delay (of three weeks) if I hadn't thought it was the 'flu, but the onset of visual auras scared me. Hospital Rheumatologist (with GP backup) is monitoring assessment and treatment. Now tapering off steroid, everything went to plan. No pain, no headaches, no visual disturbances. Just lessening side-effects to grin and bear. Doctors are confident life will be back to normal in a few months' time.

(Hope I haven't missed your deadline - being in NZ, we are hours ahead, so chanced it!)

HeronNS profile image
HeronNS in reply to sondya

Sondya, did you send those comments to the email in post?

sondya profile image
sondya in reply to HeronNS

Oops. I thought writing it down here was good enough! Ah well - not a major.

You may also like...

Opportunity to participate in research on fatigue in vasculitis

with vasculitis in the UK live with fatigue and adapt to it....

Vasculitis/Tocilizumab

have a PET scan. Today I was informed I have Vasculitis in my major arteries and need to take 40mg...

Neuropathy in vasculitis: A study

https://healthunlocked.com/vasculitis-uk/posts/144815558/your-help-is-needed-neuropathy-study?utm_so

Symptoms of Vasculitis?

it looked like a rash on the Vasculitis website. The doctor, urgent care thought it was an...

Vasculitis poem - here goes

you all I thought I'd share. It's a poem about vasculitis. I've got some poetry out there, but...