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Littllemel

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Celiac.com - Celiac Disease & Gluten-Free Diet Support Since 1995

Everything posted by Littllemel

  1. I'm sorry I guess I could have said it different. I was just trying to help others. I remember how desperate for help I was. Such a hopeless feeling. Anyway, I take such a low dose of MMS that it's harmless. In fact the FDA allows it to be sprayed on fruits and vegetables in much higher doses and the FDA uses it as a drinking water purifier. I remember...
  2. No not my church. I don't belong to any church. I joined your celiac forum early last year when I thought I had celiac disease. You can look through my old posts if you wish. Oh and the FDA puts that notice out because they are in cahoots with big pharma. Anyway I found out later that I actually had Lyme Disease which was mimicking the celiac. Apparently...
  3. Ok, I found some more links. Chlorine Dioxide is also known as MMS. Open Original Shared Link Open Original Shared Link I will keep searching for more... Melissa
  4. You can try these links too. Open Original Shared Link And Open Original Shared Link But the best site seems to be the FB site. Sorry if you can't see it. C/D is Chlorine Dioxide. Melissa
  5. I have no involvement with the site just posted it so everyone can research it more. People are curing all sorts of stuff like autism, malaria and chrons with chlorine dioxide. Melissa
  6. People are curing their gluten issues using C/ D. You might want to look into it, Open Original Shared Link Melissa
  7. I was recently diagnosed with Porphyria. My GI is running more tests to see which type of Porphyria I have but my initial 24 hour urine test came up elevated in porphyrins. I have been poking around the forums and I noticed that heavy metals poisoning can be the problem and not Porphyria. Is there a test my GI DR can do for mercury? She barely believes my...
  8. I have shown my GI the yeast test results but she still will not give me an Anti Fungal medicine. She wants to run more tests first. Gah~ Can this thing drag out any more!!
  9. Ok I saw my Nutritionist today with the DNA stool results. It looks like I have a massive yeast infection in the gut. I asked him why the antibiotics made me feel so much better and he feels the probiotic I was on "theralac" was not the right one I needed and the antibiotics killed it and it made me feel better. I guess it was doing more harm then good. He...
  10. Continuation of other "last ditch rant" post So last week I was in the ER for right flank pain again. I thought it was my liver again since I was having so many problems with it and fats. They took a urine sample and said it looked like I had a UTI but they cultured it to be sure. So Monday the 17th they called and said it was definitely a UTI and called...
  11. So last week I was in the ER for right flank pain again. I thought it was my liver again since I was having so many problems with it and fats. They took a urine sample and said it looked like I had a UTI but they cultured it to be sure. So Monday the 17th they called and said it was definitely a UTI and called in some antibiotics. So I start Keflex Monday...
  12. Well the Garlic was short lived, I was intolerant to it by the end of the day. I started Mastic Gum instead which kills H-pylori and other bacteria. I went and saw another GI for a 2nd opinion and he basically does not believe in Leaky Gut. Says there is no scientific evidence to prove it. He wants me to go on Amatryptaline instead and try the Elemental Nutrition...
  13. It all started with reflux. I had had reflux for the past 2 years and I had been placed on Nexium 1x day to control it. In January of 2012 the Nexium no longer worked. The reflux was so bad it was shooting up into my mouth and burning me constantly. I could not control it. Back then I was part of Tricare Prime and was using the Navy Dr's. I was seen multiple...
  14. I am suffering from food intolerance flare ups presently and I am trying to convince my Dr to let me try Ketotifen or Zaditen. Some of you are already on this drug and I wanted to know if you could send me the name and phone number of your prescribing Dr. My case is my GI Drs first one of a non celiac nature and she would like to discuss it with other Drs...
  15. I am currently on day 5 after my last glutoning. I can't believe I keep being so careless. It was sunflower seeds that must have had CC. Now I am leary of my sunflower oil but I have not had any issues from that. I am down to just olive and sunflower oil as my only sources of good fats now. I am too scared to try others. My IgG shows I am intolerant to dairy...
  16. How can I test for those?
  17. I am not confirmed Celiac but went gluten free due to a Endoscopy that showed lower intestine damage. 2 Biopsies taken came back negative. I have been gluten free since 3/2/12 and then started having all sorts of food intolerance issues. I stopped all corn/soy/yeast/dairy/avacados etc and I keep a diary. I have nothing processed. I am down to veggies, fruits...
  18. My ND instructed me to put a pinch of salt in my water and this is to help maintain electrolytes. I have noticed it works a little better than just regular water but some gatorade would be nice right now but Im too scared to try it. I am seeing a new GI on monday and I will let her know about the GB dyskinesia and ask for a scan. I have researched it a bit...
  19. No I haven't had an HIDA scan. I just had an ultrasound and everything looked fine. According to the ER the tests I took with the DR last week were all negative. I know my kidney pain is from dehydration. That is my number one symptom when I eat a food intolerance. My mouth drys up, my kidneys hurt and water just goes right through me without being absorbed...
  20. Turns out the HMF probiotics I were given were grown in milk. I can't believe my ND gave me those!! I can't believe I trusted her and didn't check on my own!! So i have been sick again, It took me 2 days to figure out what it was. Yesterday was another ER visit for me because I had a panic attack about how this is the way my life will be forever. I will never...
  21. I went to my ND today. She wants me to stop the rotation diet since I seem to be getting worse since I started it. I have to go on an all grain and veg diet since those are the foods that bother me the least. That means quinoa, rice, oatmeal and amaranth for me for awhile. I seem to have trouble digesting proteins. She put me on HCL but only if I eat proteins...
  22. I am drinking bone broth made from chicken bones everyday. Should I be rotating this? Will I become intolerant to it?
  23. I can't take motrin or NSAIDS. I went to a new GP today and she gave me Levsin but I am afraid to take it. Most meds give me dry mouth and sores amoung other side effects. She also said I might have a bladder infection because I have extra white cells in my urine but she is going to wait for the culture to come back before prescribing antibiotics. Now I am...
  24. I am trying not to give up but it is so hard. I was sick again last night!! So it was either the melon, peanuts or my smoothie,i am not sure which one though. Is there anything I can do for these aweful cramps! I can't take it anymore!!
  25. Today is another bad day. I got glutened 3 days in a row by CC and I discovered Old Bay and Pears are new intolerances for me. I have been grappling with C&D for the past week. My husband got mad about how strict my rotation diet is, he wanted to add spices to the chicken. He has been sharing dinners with me from the start but I guess its getting to him...
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