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I really appreciate your positive personality here. Thanks so much for your thoughts on this. I believe having a deep faith is a main ingredient towards any form of success. I am so sorry to hear that your young daughter is going through all of this horrible stuff. I've been thinking about the fact that she now has RSD in her stomach. Just a thought, have you or her doctors thought of trying digestive enzymes? I was having such horrible stomach pains coming and going on the left side of my body, my rsd side, following my surgery that there was a time where I was concerned that RSD was moving into my intestines too. The doctors were not able to find the source of my pain and I usually shrugged it off as having to do with my chronic constipation. It wasn't until just recently when I added the a full spectrum blend digestive enzyme that the pain stopped. I also take a systemic enzyme for inflammation and now swear by them both. Not only has it helped me with the pain, edema and complete stiffness in my bones, it knocked my chronic sinusitis out of me and I no longer need to take my medication for that. I have way more energy too. I am currently reading an interesting book by Ellen Cutter, DC and Jeremy E Kaslow, MD on the subject of enzymes which is what promted me to give the digestive enzymes a go. I hope this message finds you and your daughter doing well. MsL |
Thanks again,
Hi MsL,
Thanks for the tips. Over the past 4 years, Sarah has seen five different g.i. specialists with none of them providing any help. She is now seeing a new doctor who is addressing some of the things you recommend. He is an MD and naturopath who is willing to go the extra distance to find out what is going on. Recent tests he has ordered have revealed that she has very little, if any, beneficial intestinal bacteria so just last week he started her on probiotics and an "intensive repair complex" which is used to help repair and restore the g.i. lining. It is a combination of plant enzymes, mucilaginous herbs, and amino acids. From time to time others post about stomach difficulties; but it is difficult to find much about it when you research RSD. Recently, I became aware that as many as 70% of Fibromyalgia sufferers have Irritable Bowel, and we have been told that Sarah also has FM as well. One of the tests her doc ran indicated that there was irritation that may be resulting in response to parasympathetic excitability, not really much of a surprise. Please continue to share, as it is most helpful. I will be looking for the book you suggested on my next trip to Borders. Thanks, Jeanne aka Polly |
I also have a suggestion. This is something I found out about MYSELF this summer.
Fructose (and excess sucrose--which is 1/2 fructose) can be an intolerance trigger. I have a GI congenital defect I was born with, twisted malrotation of the whole GI tract. So I tend to get "used" to upheavals there. What I DIDN't realize is that I have a fructose problem. Now with hindsight, I realize it was always there, but it just seemed to become much worse all of a sudden. If your daughter has trouble with fruit, esp. apples and pears, if she cannot tolerate apple juice/cider, that would be a big warning sign of this. I stopped ALL high fructose corn syrup, high fructose fruit, and sucrose and ALL my gas, pain, and diarrhea attacks STOPPED! I looked this up on the net and found one site that claimed a 1 in 3 incidence for this intolerance. I have managed fresh oranges, recently. But I don't drink any juices anymore. I take supplemental Vit C daily instead. I'd suggest an elimination of these sugars for at least two weeks, to see if there is improvement. I discovered my problem during vacation where I became sick and didn't eat ANYTHING for a while besides crackers, water, chicken soup etc. When I had a G2 Gatorade I was sick within 1/2 hour! And that had 1/2 the sugars of a regular Gatorade. Even Jelly on my peanut butter set me off. Now that I am eating sugar/corn syr free, I feel so much better, you can't imagine! Please consider it if IBS symptoms are resistant to other treatment! |
Thanks!!!
Hi mrs. D.,
Thanks so much for the advice. It is great that you realized that this was causing such difficulty for you. It is interesting because I would have never made the Fructose association with Gatorade. Several years ago my daughter had hydrogen breath tests done for fructose & lactose intolerance. If I remember correctly, they came back o.k. with the only insight provided was that she was a "rare non hydrogen producer" ... something I really didn't have an explanation for until Sarah started seeing her new doctor. She had been taking Protonex, and thus the lack of stomach acid was likely the explanation. She took this med for 10 months, something I am now reading can do lot more harm than good to the gut. Now that I think about it, I wonder if those tests would provide an accurate result for this reason?? Over the past four years, Sarah has unintentionally been on an "elimination diet" as she has discovered that many things do not agree with her. She has a very difficult time getting enough calories with solids, so the majority of her calories come from GNC Weight Gainer Shakes. We even add flax oil to those as they do not provide enough fat. I am suspecting that there is lots of Fructose in those? I very much appreciate your input. There is so much to be learned from others ... and with an illness with so few answers ... that is invaluable. Thanks again, Jeanne |
Appreciate Your Knowledge!
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I pray that you are still hanging around as I very much appreciate your insight and generosity in taking the time to share. My mind is full of questions, and I am attempting to remain calm and not overreact to the new questions that are surfacing. I will talk with Sarah's doctor about blood tests. Do you know if the bacteria associated with Th1 infections are anaerobic? The reason I ask is that we address Sarah’s pain with hyperbaric oxygen treatments. If they are anaerobic, hyperbarics kill those bacteria and could affect tests results … but I suppose that if results come back normal, we might be able to assume that there was never a problem or that we are addressing it through hyperbarics??? The fact that Sarah’s pain resurfaces when treatments are stopped is concerning when considering an infection connection, as that would indicate that it is not being completely killed off. Please, please continue to share. At this time we are attempting to rule out the possibility of Lyme. Is that too a Th1 infection? I hope you will excuse me if I ask some dumb questions. This is a whole new “world” for me. Is it possible to provide a basic, easy to understand summary of the Marshall Protocol for Th1 infections or do you know where I might find such an explanation. When things get too in depth, especially initially, I must admit that much of it goes right over my head. Thanks, Jeanne |
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I can't find a label...to see what kind of sugar has in it. Sucrose is easier on people than fructose. There are two types of fructose intolerance.. one is GI mostly, the other is a liver reaction (genetic). Also you need to look at magnesium content. Some shakes have high magnesium added and this can cause diarrhea in some people. You might try simple Whey protein...with no added sugar. Adding the flax oil is great. I have never been able to drink apple juice like others...so I think I have had this forever, and it just became acute when I was ill. I seem to be able to eat some cereals, but not others. Plain oatmeal is okay for me, but not the flavored instant type (lots of sugars in them). At one point last year my doctor had me have abdominal ultrasound thinking I had gall bladder problems...it was horrible gas/pain every day...but all was negative. I was so surprised when I cut out all fructose...it was amazing the CHANGE! Long term use of drugs like Protonix (proton pump inhibitors) can mess up absorption of some nutrients: B12 folic acid calcium magnesium zinc iron. Those drugs also prevent protein digestion, which leads to bacterial fermentation in the bowel by bacteria, and the subsequent gas and diarrhea. Short term use is okay, but the way that doctors hand them out "for life" with no supervision, is just terrible IMO. You can PM me anytime, if you have other questions. I don't often get to this forum commonly ;) |
Hi ,
I have been drinking Vitamin Shakes called Alive. I really don't know much about it though. Here is a link about it. http://www.vitasprings.com/alive-ric...ure-s-way.html Hugs, Roz |
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I hope these lines find you truly blessed. My own mum died from R-fever from strep. I have had to have tests that have just been unbelievable lately. I want to thank you for sharing. Much Love, Roz |
Vitamin D deficiency could help explain infection correlation
I think there may be connection -- or rather a correlation -- between RSD and infectious disease. Recent research with Vitamin D has shown many if not most of us are deficient and that Vitamin D is necessary for many physiological functions. So, when inflammation is triggered by an injury, isn't it possible that Vitamin D plays a role in turning it off? When we don't have enough Vitamin D to activate the anti-inflammatory compounds in our bodies (like Interleukin-10), then the inflammation continues and spreads throughout the sympathetic nervous system and beyond. In case you are not aware, Vitamin D has been shown to reduce cancer risk as well as bacterial and viral infections and may play a whole host of other roles in the body -- Check out the Vitamin D council website.
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Thanks so much for your wisdom and intergrity. May you be blessed abundantly. Much Love, Roz |
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