Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Mastocytosis--anyone Have This Or Heard About It?


Judyin Philly

Recommended Posts

Judyin Philly Enthusiast

HI

This can effect the digestive system tho it's not the main issue with this.

Has something to do with Mast cells??? :blink::(

Good grief, more things to concider..and still no answers...


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Mastocytosis, I had never heard of this either. The links are interesting reading especially for folks who may not have had complete resolution of problems gluten-free. I wonder which genes this is associated with they mention finding them but not the ones they are. Curiosity will most likely make me look further. I am wondering if that reaction could cause a thickening of the intestinal wall and swelling. That was found on my last CT and is something that has been with me since my diverticullitis attack. Thanks for posting this, if nothing else it is interesting reading.

Open Original Shared Link

Open Original Shared Link

Judyin Philly Enthusiast

OMG DID YOU STEAL MY CAT :lol:

WHAT A RIOT. THEY LOOK SO MUCH ALIKE

OK THE FIRST LINK IS THE ONE ROBBIN (GLUELESS) SENT ME.

TOOK TO GI YESTERDAY.

HERE ARE THE THINGS IN THE ARTICLE THAT FIT ME

Possible symptoms of mastocytosis

Red, itchy rash

Rash that looks like freckles

Hives

One large lump on the skin

Diarrhea

Stomach pain Fainting

Difficulty breathing

SHE HAD JUST BEEN TO A CONFERENCE ON THIS CONDITION.

SHE JUST SMILED AND SAID' ...LOOK AT THIS SENTENCE' WHEN I ASKED HER TO TO THE BLOOD WORK FOR IT.

IT SAID...'ELLIMINATE ALL FOODS, TRIGGERS, SO BACK TO SQUARE ONE.

WHAT ARE THEY???????????????????????????

GOTTA LOVE IT

OFF TO READ THE SECOND ONE.

ALSO SINCE I HAVE FIBROUS DYSPLAISA OF THE BONE AND MULTIPLE TUMORS ALL OVER MY BODY LINKED TO PUB MED AND FOUND SOME LINKS TO BONE DISORDERS..

INTERESTING.

THANKS FOR CARING

JUDY

gluless Newbie
Mastocytosis, I had never heard of this either. The links are interesting reading especially for folks who may not have had complete resolution of problems gluten-free. I wonder which genes this is associated with they mention finding them but not the ones they are. Curiosity will most likely make me look further. I am wondering if that reaction could cause a thickening of the intestinal wall and swelling. That was found on my last CT and is something that has been with me since my diverticullitis attack. Thanks for posting this, if nothing else it is interesting reading.

Open Original Shared Link

Open Original Shared Link

I read that first link when I stumbled on this by accident, BUT the second one with the reference to "orphan diseases" made me take notice. There is a doctor at Cleveland Clinic who specializes in "orphan diseases" ---I forget his name--starts with a W, I think. I am wondering if maybe your next course of action would be to try to get to see him. Ask your primary doc if he can refer you and find out who this doctor is. I read an article about him a few years ago and he is a life saver for a lot of people, from what I read.

I hope to God this helps you and others who are still suffering. Hugssss.

Judyin Philly Enthusiast

THANKS TO BOTH OF YOU

YOU KNOW ROBBIN, THIS MAZABRAUD SYNDROME I HAVE IS A ORPHAN DISEASE..

WILL SEE IF IT'S ON THE LIST..I KNOW MC CLUNE ALBRIGHT JUST GOT ON THE LIST BUT THIS NEW ONE NOT SURE OF.

THERE WERE ONLY 80 DOCUMENTATED MEDICAL JOURANAL PUBLICATIONS WHEN I WAS SEARCHING FOR MY DOC WHEN I WAS WORKING IN 1999.

TAKING A BREAK FROM RESEARCH TODAY.

BUT HOPE MAYBE SOME OTHERS WILL SEE THIS AND KNOW ABOUT IT.

HUGS

JUDY

PS.. WE WANTED A LADIES 'GET-A-WAY' BUT DIDN'T HAVE THE CLEVELAND CLINIC IN MIND :lol:

WANTA COME WITH ME :lol:

Judyin Philly Enthusiast
Open Original Shared Link

found this in this article.

Mast cells seem to have other roles as well. Found to gather around wounds, they may play a part in wound healing. For example, the typical itching you feel around a healing scab may be caused by histamine released by mast cells. Researchers also think mast cells may have a role in the growth of blood vessels

Maybe this can be why this area where the heating pad burned me and hasn't really had the lymph system heal...could be the reason listed here.

wow amazing to me.

Judy

blueeyedmanda Community Regular

I have never heard of this either but I am going to look up on it. Sounds different.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,960
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.