Battling My Leaky Gut

QUOTE:”After writing this post, I realized you could replace “Leaky Gut” with “Celiac Disease” or “Food Allergies” or “Multiple Chemical Sensitivities” or “Lupus” or “Lyme Disease” or an other autoimmune illness and the meaning of my words would be the same. Coincidentally, it happens to be “awareness week or month” for just about every autoimmune disease. So if you want to substitute “leaky gut” for the illness you have and share this post (with a link back to me), please feel free to do so.”
WELL MANY MANY MANY OF US WHO SUFFER FROM MCS ALSO SUFFER FROM LEAKY GUT– & MANY MANY OTHER ILLNESS ALSO!!!!

Adventures of an Allergic Foodie

Lately I’ve been feeling like my leaky gut is an alien that’s taken over my body, like in one of those sci-fi movies my boys watched as kids. My leaky gut and all its accompanying symptoms control me physically and emotionally. My gut dictates my family life, my work life, my social life. It tells me where I can eat and what I can eat. It makes me tired and angry. It keeps me from traveling and doing the things I used to do. It makes my brain feel like mush and the wrong words come out of my mouth.

I wish I had an antidote to cure my leaky gut, so that I could return to the person I once was, the one who felt Super Human. Of course, back then,  I didn’t know I felt Super Human. I did not appreciate my health, my energy, my memory, and my…

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About sondasmcschatter

I was encouraged to start a blog as I suffer from MCS /multi chemical sensitivities & other health problems & I have helped several hundred others who suffer from MCS set up "Safe Homes" & given them encouragement & HOPE & share information & lots of laughs along the way also. When you choose to use fragrances, chemicals, or pesticides, You are not simply making a choice for yourself, You are making a choice for everyone around you!!!! What makes me an expert on MCS-- not a darn thing-- BUT have lived with it for years-& years- & have learned lots the HARD WAY-- by experience!! And want to give others help & HOPE & encouragement -- as I know there are not many who understand what it is to live with this illness- & ALL THAT GOES WITH IT!!! Internet has been my way of communication with many who we are confined to their "safe homes" all over the USA & other countries!! I have communicated with many HUNDRED by e-mail-- phone & letters & internet forums-- I hope this blog will help in a better way to share laughter-- hope & information!!! As for many are not any longer able to even leave their homes-- & communication is sooo important & sharing & encouragement & GIVING HOPE!!!
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