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335 total results
Comments (309)
Hello @jt67, Sounds like you have a lot going on. Wished I had some magic bullets...
https://connect.mayoclinic.org/comment/770281/
Conference I: Small Fiber Neuropathy, POTS, MCAS ... dysautonomia-international-pots-sfn-mcas-vagus-nerve
I’ve been living with BFS for close to three years. Not terribly debilitating, but within the...
https://connect.mayoclinic.org/comment/914067/
seasonal allergies, but I’ve looked into MCAS ... that testosterone can help those with MCAS
OHHH NOOO! I'm SO sorry you are experiencing this too! You are literally the only other...
https://connect.mayoclinic.org/comment/1001457/
be triggering me, but as far as an MCAS ... that has knowledge of paxlovid/covid/mcas ... prostaglandins work in my body so most MCAS ... And since MCAS does have a lot to do
How did your daughter get diagnosed. My doctor has officially diagnosed me with clinical MCAS but...
https://connect.mayoclinic.org/comment/134377/
officially diagnosed me with clinical MCAS
Cromolyn comes in liquid vials that you take with meals and helps gut symptoms from MCAS--but...
https://connect.mayoclinic.org/comment/773937/
meals and helps gut symptoms from MCAS
This is very interesting because I too suspect MCAS and I'm constantly itchy and it feels...
https://connect.mayoclinic.org/comment/309057/
interesting because I too suspect MCAS
@upnorthmama, you might be interested in reading the EDS blog by Mayo experts here: - Ehlers-Danlos...
https://connect.mayoclinic.org/comment/796639/
discussion:
- Ehlers Danlos Syndrome, MCAS ... /discussion/ehlers-danlos-syndrome-mcas-pots-and-mals
OK, the files that would not load is the Guide for Doctors from Dr Afrin...this attached...
https://connect.mayoclinic.org/comment/709699/
since so many people who are new to MCAS
Regarding Mestinon: I have Post Lyme Disease, small call Neuropathy and MCAS. I suffered from Brain...
https://connect.mayoclinic.org/comment/1254879/
Disease, small call Neuropathy and MCAS
Yes, EDS is a joint disorder and commonly is a comorbidity with MCAS, as it HATs...
https://connect.mayoclinic.org/comment/774447/
and commonly is a comorbidity with MCAS ... practices have decided to not seek MCAS
Hello @pamelars60 -- welcome to Connect. Thank you for posting and sharing here on Mayo Connect....
https://connect.mayoclinic.org/comment/96857/
@jools, who have all talked about MCAs ... Since MCAS is often found in patients
Hello - Unfortunately, GA was given as a diagnosis for my biopsy with an eruption on...
https://connect.mayoclinic.org/comment/717931/
comorbidity with Mast Cell Activation (MCAS ... into and infact POTS could trigger MCAS ... that hers went away by taking the MCAS ... a formal diagnosis with the above MCAS ... the more severe version of that is MCAS
Sorry, yes my left ear developed a whooshing sound that correlates with heartbeat. Do have moderate...
https://connect.mayoclinic.org/comment/766401/
month ago and seem to have developed MCAS
Not too long after my gallbladder removal surgery, my MCAS, which I had not known I’d...
https://connect.mayoclinic.org/comment/1155000/
my gallbladder removal surgery, my MCAS
It may also help to know that it appears to be a mast cell activation problem....
https://connect.mayoclinic.org/comment/1172129/
confirm mast cell activation syndrome- MCAS
Hello @@danmlee, Thank you for sharing your story; I'm truly sorry that you are going through...
https://connect.mayoclinic.org/comment/134285/
@jools, who have all talked about MCAs ... Since MCAS is often found in patients
Hey there, no one actually has checked her for lupus or any other autoimmune. I’m having...
https://connect.mayoclinic.org/comment/767979/
to rule out Lyme, autoimmune & MCAS
That’s great news for you. I’m happy to hear that. Fortunately, research and awareness is growing...
https://connect.mayoclinic.org/comment/885756/
awareness is growing for NETs (and MCAS
Actually when I can get any phlegm out it’s like pellets sized like half-a-pea to twice-a-pea....
https://connect.mayoclinic.org/comment/1039997/
lead me to histamine intolerance or MCAS
Sound like a possible Mast Cell Activation syndrome issue to me…..thats something you need to be...
https://connect.mayoclinic.org/comment/1007817/
I would take a look at MCAS.
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