Hi... I'm Tabitha (23), mom to Cole (2) & Kelsey (8 months). I've been waiting for my activation here for 2 weeks, so I'm glad I can finally join everyone!
I've been dealing with LUQ pain since I delievered my son in 2007. Everyone brushed me off, and I learned to deal with the pain. Since then, I delievered another baby in 2008 and the pain was still there. Some days it's worse than others, some it is barely there... but it's constant. After a bought of horrible abdomen pain/cramps and bloody diarrhea, I finally convinced my PCP that it wasn't just gas being caught in my 'splenic flexure' as he likes to say...
I'm scheduled for my first colonoscopy July 24th -- and I'm very, very READY. I'm just looking for a diagnosis, ready to close the chapter of not knowing.
I was asked by my PCP if I have anyone in my family with Crohns or UC -- my little brother was diagnosed with both at the age of 14. He told me you can't have both (which I find hard to believe, as my brother is proof that you can have both).
Every symptom I've had over the past 2 years, are the exact symptoms my brother experiences during a flare up, and during the time before he was diagnosed. I have no doubt in my mind that it isn't just "gas" and I also do not believe that I have to live feeling as if nothing is wrong with me.
I look forward to talking with you all as I start my journey... any tips, advice would be wonderful. I'm looking into diets, and don't really know where to start.
I've been dealing with LUQ pain since I delievered my son in 2007. Everyone brushed me off, and I learned to deal with the pain. Since then, I delievered another baby in 2008 and the pain was still there. Some days it's worse than others, some it is barely there... but it's constant. After a bought of horrible abdomen pain/cramps and bloody diarrhea, I finally convinced my PCP that it wasn't just gas being caught in my 'splenic flexure' as he likes to say...
I'm scheduled for my first colonoscopy July 24th -- and I'm very, very READY. I'm just looking for a diagnosis, ready to close the chapter of not knowing.
I was asked by my PCP if I have anyone in my family with Crohns or UC -- my little brother was diagnosed with both at the age of 14. He told me you can't have both (which I find hard to believe, as my brother is proof that you can have both).
Every symptom I've had over the past 2 years, are the exact symptoms my brother experiences during a flare up, and during the time before he was diagnosed. I have no doubt in my mind that it isn't just "gas" and I also do not believe that I have to live feeling as if nothing is wrong with me.
I look forward to talking with you all as I start my journey... any tips, advice would be wonderful. I'm looking into diets, and don't really know where to start.
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