Why not leave a short comment below and introduce yourselves. Give as much or as little information as you like. Feel free to ask your own questions here:
Introduce Yourself!: Why not leave a... - The UK Mastocytos...
Introduce Yourself!
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![Jess-UKMasto profile image](https://images.hu-production.be/avatars/5f6da030422577e6ccc9a318abd96aa6_small@2x_100x100.jpg)
Hi all, I'm Jess, one of the moderators here, and have had indolent systemic mastocytosis for more than 30 years. Glad to welcome you here!
![Kay-UKMasto profile image](https://images.hu-production.be/avatars/13c246d8a23b31d107f8d7dac75801dc_small@2x_100x100.jpg)
Hello all. I'm Kay and I have indolent systemic mastocytosis. I probably had urticaria pigmentosa for many years without knowing what it was but was diagnosed when my mastocytosis became systemic and started affecting my digestive tract about 6 years ago.
Hi Kay, I’m new to the group. Just posted a few questions that I’m hoping you may have some insights on
Hello from south london. I don’t have a Mast Cell Disease diagnosis but I have daily hives on my trunk, back, arms and legs. I have had allergy tests which were all negative and have been prescribed anti-histamines. I have found that I don’t get any hives as long as I don’t drink anything. I can go all day without an itch if I like, eating as much as I want (avoiding some known triggers), but one sip of water and I’ll break out.
The only mention that I can find of anyone with remotely similar symptoms mentioned MCAS, so I was interested to try and find out more about it. Thanks.