Iron infusion and histamine
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
What symptoms did you have?
A subreddit dedicated to sufferers of Anemia. Anything anemic related can be discussed here, whether it’s questions, support or advice. For more info on Iron Deficiency with or without Anemia, check out The Iron Protocol FB Group Guides and www.theironprotocol.com
What did 23andMe help you with?
This community is made for those interested in clinical genetics and its implications for human health and well-being. It is aimed at genetic counselors, medical geneticists, laboratory geneticists, and those affected by, or with experience of, genetic conditions/diseases. Please feel free to share knowledge and ideas, network, provide resources to other professionals and laypersons, and discuss subjects that may arise in everyday practice.
Does anyone actually get better?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Are home kit genetic tests worth it?
A place to share your heritage, genetic ancestry, and explore the amazing family stories people have to share!
What were your low ferritin symptoms?
A subreddit dedicated to sufferers of Anemia. Anything anemic related can be discussed here, whether it’s questions, support or advice. For more info on Iron Deficiency with or without Anemia, check out The Iron Protocol FB Group Guides and www.theironprotocol.com
Did anyone develop dysautonomia BEFORE MCAS?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Has anyone in the UK found their root cause?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Is it possible to heal from this?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Chances of my children developing MS?
Focusing on issues facing people with MS and their family and friends. Conversations about support, research, drug therapies, nutrition, exercise, and more.
Is histamine intolerance real?
For questions and information about Histamine Intolerance and other Mast Cell disorders. This subreddit is for research purposes only. Please do not take medical advice from this subreddit. If you have any medical issues please visit a licensed doctor.
Does neuropathy cause MCAS?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Are we more at risk of autoimmune diseases with MCAS?
Discussion of immunology related topics. Peer review, pop science or news articles allowed. Please do not post questions asking for medical advice or espousing pseudo-science.
If I heal my gut, will I cure my MCAS/HI?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Did anyone's dysautonomia get triggered by pregnancy?
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
Did this happen to anyone else?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Has anyone in the UK been able to access genetic testing to determine the cause of MCAS?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Best tests for MCAS cause
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
If MCAS is triggered by pregnancy, can it ever go away?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Has anyone managed to sustain a normal life after getting MCAS from Covid?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Why is MCAS getting worse?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
How to solve MCAS/Histamine Intolerance
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
What is going on with my body?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.