LC and Non-food Sensitivities?
Moderators: Rosie, Stanz, Jean, CAMary, moremuscle, JFR, Dee, xet, Peggy, Matthew, Gabes-Apg, grannyh, Gloria, Mars, starfire, Polly, Joefnh
I also am sensitive to scents and have used non-scented products for years. Even as a child the smell of perfume would give me a headache. When I was older, in college, I started wearing expensive Dior Perfume for a while, and that didn't bother me, so I too think it is the artificial odors that are the problem. I use a washer and drier that is shared with other apartments. I always have to check the drier to make sure no one has left a drier sheet inside. Once, when I didn't check, I had to rewash all my clothes because I couldn't tolerate the scent left on my laundry. Fragrances give me a headache.
Jean
Jean
I had an interesting experience today at work- I walked into the common area, which smelled heavily of the 3rd hand smoke of 70 patients then was confronted by the scents of several different colognes. My nose started to run like a faucet and kept running for over an hour. Not fun.
Leni
Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.
Anything is possible one day at a time!
Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.
Anything is possible one day at a time!
All of these problems are due, of course, to inappropriate mast cell degranulation, associated with MC.
Tex
Tex
It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
Hi Leni,
I'm currently trying to consolidate a lot of the data that we've discussed on this site about mast cells, to make it easier to understand. It will take me a few more days to get it done, though. In the meantime, the thread at the following link contains some information to get you started. The post by Mary Beth (the third post in the thread) contains a lot of links to good information sites.
http://www.perskyfarms.com/phpBB2/viewtopic.php?t=17624
Tex
I'm currently trying to consolidate a lot of the data that we've discussed on this site about mast cells, to make it easier to understand. It will take me a few more days to get it done, though. In the meantime, the thread at the following link contains some information to get you started. The post by Mary Beth (the third post in the thread) contains a lot of links to good information sites.
http://www.perskyfarms.com/phpBB2/viewtopic.php?t=17624
Tex
It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
Thanks for the link, tex. I'm slowly trying to digest (pun intended) all of this new information. Some of it is over my head but it's a relief to know that there is a physical cause for these goofy symptoms. I'm not as crazy as I thought I was.
Leni
Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.
Anything is possible one day at a time!
Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.
Anything is possible one day at a time!