I was on here a while ago, not sure if anyone remembers, but anyway, I've had a few new updates, and I am soooo LOST! Since the begining of Jly I have had abdominal pain and I've suffered from IBS for the last 12 years. I am only 28 now. I've had 3 kids and during my pregnancies I've had no symptoms. Well, my general doctor is also a natural path and she has tested me like crazy. everything seems to come back fine. I was diagnosed with Hashimoto's but she doesn't want to treat me or send me to a specialist because it will make my diarrhea worse. She did an extensive allergy test (more like a sensativity test) But since then I am gluten free, milk free, and now yeast free. She aslo wants me to stay away from my slight sensativities which involve 34 things, including fruits and vegetables. She thought I have candida because I am allergic to yeast. Well, then she sent me to a GI specialist because crohns runs in my family and I went to see him, he said it sounded just like it. So I recently went and did a colonoscopy and an endoscopy. He said everything looked fine, he didn't see any signs of crohns, he did find a polyp that came back fine (no cancer). He put me on bentyl, but then I had to go to the ER because I had an ellergic reaction to it, so then he told me to take peppermint oil after every meal. I end up burbing that up and tasteing it for hours. Then I did get a yeast infection so I took a diflucan and got yeast coming out with my bowel movements. So I'm now on candex to help kill that, and they want me to stay away from white potatoes and cane sugar. I have been doing all of this and I am still waking up and about an hour after I get this horrible pain and I get diarrhea with it. I am also on a refridgerated probiotic that doesn't cantain soy milk ect, everything I can't eat. I'm soooo at my ending point. I'm almost ready to ask the doc to give me the bag and cut out my colon, just so I can get out of my house. I've tried the aloe vera juice, but haven't been consistant, I need to start that up again. At first when I go to these doctors they seem sooo compassionate and determined to help me, but now that they've run the tests they want or think it could be, I feel like they have dropped off the earth. My husband is getting tired of me looking things up online and trying to diagnose myself, but I don't know whatelse to do. I can't keep living this way. It just feels like there is something they are missing. Is there a simple test for addison's desease? Does this sound like anything that anyone else can think of? How do I know if it's not one of my other organs not working properly? I need help.
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