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Can people with Mastocytosis and MCAS work? What kind of work can they perform?

See how people with experience in Mastocytosis and MCAS give their opinion about whether people with Mastocytosis and MCAS can work and what kind of jobs are more appropriated for people with Mastocytosis and MCAS

Mastocytosis and MCAS jobs
4 answers
The severity of your disease will determine your mobility, and ability to work. Personally, I work 40+ hours in a leadership role. There are days where I can't get out of bed, brain fog is embarrassing when you are presenting and can't remember the simple word you know, it's hard to be social some days.

I know other Mastos who can't leave their house without a mask. During a repetitive outbreak, some sleep for days, can't eat, who have issues with their blood pressures at dangerous lows. There are many other diseases linked to Mastocytosis that make life limiting.

Again, journaling your symptoms and treatments will help you treat your self during specific outbreaks. Listen to your body. If you think you need help, don't be afraid to call 911 or use your EPI. Most importantly, train your co-workers what to do to help you.

Posted May 20, 2017 by Teepee80 500
Some can. Those of us that trigger to fragrance and common environmental things find it much more difficult to be in public.

Posted Sep 30, 2017 by Meredith 2000
This one is difficult- I have had times where I could and times where I can’t. Currently I do but it is not easy and I only work 3 days.

Posted Jan 19, 2018 by Melissa Ashby 1020
Translated from portuguese Improve translation
Can work provided that the work does not expose the reagents that may release mastocitos or your own employee/patient be able to work around stressful situations.
In short you can work since the patient feels well and is able to work in a controlled environment the level of tactile stimuli.

Posted Mar 3, 2017 by elsa oliveira 1000

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World map of Mastocytosis and MCAS

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Stories of Mastocytosis and MCAS

MASTOCYTOSIS AND MCAS STORIES
Mastocytosis and MCAS stories
I was fist diagnosised with systemic mastocytoisis. A few years later and several medicines added to control my disease I saw a different doctor that was not certain of the first diagnosis. She wanted me to have a bone marrow biopsy to confirm.  Thr...
Mastocytosis and MCAS stories
I have had asthma and eczema since being a baby. .in fact. .I was born with urticaria.. What i perceived as normal I learnt later in life was not. Fast forward ..allot of strange symptoms. .allot of diagnosis. .allot of searching for answers.. Und...
Mastocytosis and MCAS stories
I WAS SITTING IN THE TUB ON JANUARY 2010 EVENING WHEN ALL OF A SUDDEN I COULDN'T BREATHE . I STOOD UP AND I TURNED BLOOD RED FROM HEAD TO TOE .THEY HAD TO CALL AN AMBULANCE I WAS IN FULL-BLOWN ANAPHYLACTIC SHOCK AND THEY DIDN'T KNOW IF I WAS GOING TO...
Mastocytosis and MCAS stories
I will update complete story today after my allergy appointment. Feeling excited and nervous all at once. 
Mastocytosis and MCAS stories
Born a healthy baby girl. Consulted a dermatologist and went for an ECG to rule out suspected Leopard spots. (phew) Mother waited till I was 24months old and went to do a skin biopsy to get a dianogistic... From then, I had been following up with ...

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Mastocytosis and MCAS forum

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Mastocytosis and MCAS forum
Anyone see a good doctor that treats mast cell disorders in or around GEORGIA?? Please share your doctor's name, even if you are in a nearby state! I've seen a hematologist in Gainesville, FL, and am being treated for SM due to having all the symptom...
Mastocytosis and MCAS forum
I would like to know how mastocytosis or MCAS is diagnosed. Are there lab tests or any other test to diagnose it? I'm from Europea and I am diagnosed with chronic fatigue syndrome, postural orthostatic tachycardia syndrome and irritable bowel sy...

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