mastocytosis.livejournal.com
Newbie - Mastocytosis support and information
http://mastocytosis.livejournal.com/1641.html
Newbie - Mastocytosis support and information. Mastocytosis support and information. Dec 5th, 2007 09:56 pm. Mastocytosis support and information. I ask because , I have various things that go on with me and I was wondering if thats normal for just the UP or if my symptoms could be something more(systemic). Thank you very much for you time. any information you can give me will be greatly apperciated. 2008-02-28 07:05 am (UTC). Hi, i'm sorry i am replying to this so late. Http:/ www.tmsforacure.org.
dkaaa.org
Health Information - DuKane Allergy Asthma
http://www.dkaaa.org/health-information
American Academy of Allergy, Asthma and Immunology. American College of Allergy, Asthma and Immunology. Food Allergy and Anaphylaxis Network. Allergy and Asthma Relief. Food Allergy Guidelines/Resources - Illinois State Board of Education. Food Allergy Action Plan. Kids With Food Allergies. Food Allergy Anaphylaxis Network. Allergy and Asthma Network - Mothers of Asthmatics. American Latex Allergy Association. US Hereditary Angioedema Association. Is it a Cold or an Allergy?
mastocytosis.livejournal.com
might as well make another update - Mastocytosis support and information
http://mastocytosis.livejournal.com/763.html
Might as well make another update - Mastocytosis support and information. Mastocytosis support and information. Might as well make another update. Jun 6th, 2007 06:07 pm. Mastocytosis support and information. Once i get this stabilized i'll probably end up going into a few studies that my dr is running. i'm not thrilled to have a disease that so little is known about, so i might as well do what i can to change tha. 2007-06-06 11:44 pm (UTC). 2007-06-07 12:52 am (UTC). 2007-06-07 03:31 am (UTC). I feel li...
mastocytosisintexas.blogspot.com
mastocytosisintexas: June 2009
http://mastocytosisintexas.blogspot.com/2009_06_01_archive.html
Saturday, June 27, 2009. This disease is so unpredictable. One minute I can be fine, and the next I'm in the middle of a full blown anaphylactic attack. I know some of my triggers, but many still remain a mystery to me. Sometimes I react to them, sometimes I don't. Here are the triggers that I am aware of:. Heat- I live in South Texas where the temperature is around 105 all summer long. Humidity- a killer for me. Melon- cantaloupe and honey dew. Loud Bass sound- I know, it's weird. Friday, June 26, 2009.
mastocytosisintexas.blogspot.com
mastocytosisintexas: First Post
http://mastocytosisintexas.blogspot.com/2009/06/first-post.html
Wednesday, June 24, 2009. My Family Practitioner stuck with me, and even though he treated me for anxiety disorder, he knew there was more there. It wasn't until February of 2008, when I went to see an allergist, that I had ever even heard of Mastocytosis. Through her persistence and after driving across the country to have a bone marrow biopsy and consultation with a Mastocytosis specialist, I finally had a diagnosis and a treatment plan. Subscribe to: Post Comments (Atom). View my complete profile.
lifewithmastocytosis.blogspot.com
Living with Mastocytosis
http://lifewithmastocytosis.blogspot.com/2012/11/so-as-ive-written-my-hometown-was.html
Life with a chronic illness isn't all about spoons and complaining. Tuesday, November 20, 2012. Utm source=facebook&utm medium=competition&utm campaign=share tool dariusrucker2012 lander. Subscribe to: Post Comments (Atom). View my complete profile. Links of Interest and More. Mast Cell Disorders Forum. Dr Castells - My main Masto Dr. My Mastocytosis Facebook Page. National Organization of Rare Disorders - Mastocytosis. Another Masto Blog - Great Links. A Chronic Dose - A Chronic Ilness Blog.
lifewithmastocytosis.blogspot.com
Living with Mastocytosis: of the utmost importance
http://lifewithmastocytosis.blogspot.com/2012/11/of-utmost-importance.html
Life with a chronic illness isn't all about spoons and complaining. Saturday, November 3, 2012. Of the utmost importance. My town has a website! Usually for my birthday I ask people to donate blood or to the TMS, but this year I'm asking if anyone is so inclined, to please donate to the red cross disaster relief NOW (as opposed to January). For the lazy text RED CROSS to 90999). Here is a list of ways to help if you're in the tri state area. I'll post more ways to help as I learn them. Google Results on ...
lifewithmastocytosis.blogspot.com
Living with Mastocytosis: June 2012
http://lifewithmastocytosis.blogspot.com/2012_06_01_archive.html
Life with a chronic illness isn't all about spoons and complaining. Sunday, June 3, 2012. I may have been going about things wrong. I had a conversation this week about a lot of the drama that had been going on and feelings and stuff. It was super awesome to have a constructive conversation with someone where even though we didn't 100% agree on everything, we respected each others positions and opinions and agreed to disagree while hearing each other out. And i am sorry for it. i think, for me, as i ...
lifewithmastocytosis.blogspot.com
Living with Mastocytosis: August 2009
http://lifewithmastocytosis.blogspot.com/2009_08_01_archive.html
Life with a chronic illness isn't all about spoons and complaining. Monday, August 31, 2009. I didn't let it get me down. today i went hooping with the kids at MIT and went shopping. Not the most adventurous of days, but I easily could've hid with my head under a pillow all day too. Well I guess the positive streak had to come to an end at some point. Tuesday, August 25, 2009. More than a few people with masto have set up google alerts so that they get an email whenever mastocytosis makes the news. 1) Th...
lifewithmastocytosis.blogspot.com
Living with Mastocytosis: January 2012
http://lifewithmastocytosis.blogspot.com/2012_01_01_archive.html
Life with a chronic illness isn't all about spoons and complaining. Monday, January 16, 2012. So my blog made it onto google alerts last night. that was sort of unexpected. hello new people! When i first got diagnosed, i was hugely spoiled by the fact that i lived in boston and had immediate access to a host of doctors who all but specialized in mast cell stuff. out here in LA it's a totally different story. where my last masto doctor had around a hundred or more patients, my current one has 8. I've been...
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