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| Waiting for Carlie, Still Slightly Flushed In the ER at St Joe's |
I have been having a hard time writing this blog entry in part, because I was still deciding how I could best utilize this blog for awareness raising. Not everyone wants to hear the nitty gritty day to day of living with chronic illness. And how Mast Cell Activation Disorder (MCAD) affects me is not the same as how it affects everyone else. But I have decided to go ahead and blog here on the main page, and the various other pages of this blog will be for general information, interviews with other people dealing with mast cell disorders, and the like. Please
check out some other great and very informative blogs on Mastocytosis, MCAD and Idopathic Anaphylaxis in the links section to the right.
If you would like to see something on this blog which is not yet here, has not been discussed, etc. please feel free to ask. As I get the time and energy I will be adding blog entries, links, information, etc. Done with the housekeeping/site upkeep, on to the meat of the entry: How starting Singulair went for me:
check out some other great and very informative blogs on Mastocytosis, MCAD and Idopathic Anaphylaxis in the links section to the right.
If you would like to see something on this blog which is not yet here, has not been discussed, etc. please feel free to ask. As I get the time and energy I will be adding blog entries, links, information, etc. Done with the housekeeping/site upkeep, on to the meat of the entry: How starting Singulair went for me:
