IMPORTANT NOTICE: The contents of this app are based purely on personal experience with the systemic mast cell activation syndrome and DO NOT claim to be general, they only serve the purpose of trying to help other potentially affected people!
All information in this app are based on the webpage https://systemisches-mastzellaktivierungssyndrom-mcas.de. There you will find more detailed information as well as links to doctors and institutes that you can consult on the subject of MCAS in order to have your personal diagnosis made.
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THIS APP DOES NOT REPLACE THE VISIT TO A DOCTOR!
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In this app you will find important information about symptoms, diagnostics, therapy. Something about salicylate intolerance, histamine intolerance and recipes you will also find.
How do I follow a grace diet to empty my histamine barrel? An overview of food groups that should be avoided can be found in the app. Offers of help: What can I do if I become a care case due to the disease, lonely, where can I ask for support, apply for help?
There is also a contact form for getting in touch and a nutrition diary, which can be used to document the tolerability of food and medication.
From now on, you will always have the most important information about the disease with you and can inform yourself at any time, forward the app to family or friends for better understanding and always be well informed. This app is always being updated and expanded.
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What's New in MCAS & Mastocytosis
1.3.1
June 15, 2024
The nutrition diary can now be shared, e.g. to be printed, saved or sent.
I hope this app helps people get a diagnosis. The app can’t diagnose anything but talk to your doctors.
Now that I know what I have I control it entirely through diet and this app has lots of useful information and tools. I have not used it much but it does seem like the most useful and knowledgeable.
The app states how personal each person’s responses are to every aspect and, that’s not just hedging it’s true. You have to figure it out yourself there’s no universal key.