i went to my gp with all my symptoms & that it lined up with mcas but was told it wasn’t diagnosed in the uk - any advice on next steps that aren’t going private?😭
2026-09-04 15:30:12
2
hidden.gems.east.lothian :
Could you do a video about Spondylodysplastic EDS my daughter just been put on the genetic waiting list and need more information than what I’m finding online. Thanks
2026-09-04 15:55:47
3
abbiepicklejohns :
I have mcas but they are only allowed to prescribe H1 and H2 blockers and they don't work. WHERE CAN I BUY PLEASE
2026-09-17 07:47:37
0
Louise Burgwyn :
I was told by a GP yesterday there’s no NICE guideline for MCAS so can’t get a diagnosis on the NHS
2026-09-17 17:34:57
0
Dawn Leete :
mcas here only 10 foods and theyake me ill. been on 3 fexo 180ml a day just started famodine
2026-09-18 23:02:00
0
aleee.bl :
Pls dm me
2026-09-04 15:02:11
1
aleee.bl :
Can you pls Check dm
2026-09-04 15:02:15
1
yh :
my friend and I went full vegan for almost 2 years we decided it wasn't for us . I ended up with diary intolerance and she ended up with Crohn's disease after stopping. 😢
2026-09-06 12:55:07
1
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