If you have found your way here and are wondering whether to join in then all I can say is “please do!”. Personally I’ve never used Facebook and never intend to so I’ve missed out on discussions in that arena but I feel this is like a safe place for us to discuss matters relating to masto and to share our experiences and ask for expert help. So even if you’re a bit hesitant why not give this new group a chance and let’s see how we can help each other.
To post or not to post?: If you have... - The UK Mastocytos...
To post or not to post?
![Kay-UKMasto profile image](https://images.hu-production.be/avatars/13c246d8a23b31d107f8d7dac75801dc_small@2x_100x100.jpg)
Kay-UKMastoAmbassador
Written by
![Kay-UKMasto profile image](https://images.hu-production.be/avatars/13c246d8a23b31d107f8d7dac75801dc_small@2x_100x100.jpg)
Kay-UKMasto
Ambassador
To view profiles and participate in discussions please or .
1 Reply
•
Me too! Missed out, that is.
Not what you're looking for?
You may also like...
Help please. MCAS investigation on the NHS?
Hi. Sorry this is quite long but would be grateful if a anyone is able to help. I've been trying...
Cutaneous or Systemic - help please?!
Firstly - I am so happy to have found this place.
Secondly - I am very aware that all my symptoms...
Might I have Mastocytosis rather than MCAS?
Hi, I experienced a very strange phenomenon last night that I've never had before and it's made me...
Survey on your experience with COVID-19 Vaccination
https://www.smartsurvey.co.uk/s/UKMastoVaccines/
I am very pleased to share here the link to our...
MRI with contrast dye
I need some advice / opinions, please.
I have to have a MRI scan of my brain, to help diagnose...