Guest guest Posted September 26, 2007 Report Share Posted September 26, 2007 I am not sure what is going on with my son ethan. He has been on SCD since January and has been medication free since then. For the past 2 and a half weeks he complains of a stinging or burning sensation, with occasional cramping in his stomach and this has been bad enough that he hasn't been able to go to school. GI took blood and his sed rate is 12 which is in the normal range. He put us back on pentasa and flagyl while we await results from Calprotectin test ( a stool test that should see if there is any inflammation in his small or large bowel). He has not had any D or blood this whole time. In the past our flares always involved D. Any suggestions would be appreciated, he is in so much pain and I haven't been able to give him anything that seems to help. Should we go back to intro diet or start a clear liquid diet? I should mention that I inadvertantly gave him a probiotic which contained FOS which i now know is an illegal. I began this about a week and a half after his symptoms started so I know that this isn't the root cause but I am sure it didn't help things any. Again any advice would be appreciated, It is really hard watching him in so much pain. thanks very much, Jill and Ethan 9yo, CD 9/05,SCD 1/07 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2007 Report Share Posted September 26, 2007 Hi Jill and Ethan, <<I am not sure what is going on with my son ethan. He has been on > SCD since January and has been medication free since then. For the > past 2 and a half weeks he complains of a stinging or burning > sensation, with occasional cramping in his stomach and this has been > bad enough that he hasn't been able to go to school. GI took blood> and his sed rate is 12 which is in the normal range. He put us back > on pentasa and flagyl while we await results from Calprotectin test > ( a stool test that should see if there is any inflammation in his > small or large bowel). He has not had any D or blood this whole > time.>> Where is the pain and cramping? Is his stool getting drier (constipated)? In the past our flares always involved D. Any suggestions > would be appreciated, he is in so much pain and I haven't been able to give him anything that seems to help. Should we go back to intro> diet or start a clear liquid diet? I should mention that I > inadvertantly gave him a probiotic which contained FOS which i now > know is an illegal. I began this about a week and a half after his > symptoms started so I know that this isn't the root cause but I am > sure it didn't help things any. Again any advice would be > appreciated, It is really hard watching him in so much pain. > thanks very much, > Jill and Ethan 9yo, CD 9/05,SCD 1/07>> It may help to go back to the intro for a couple of days. Please keep us updated. Sheila, SCD Feb. 2001, UC 23yrs, PCOD 22yrs mom of and Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2007 Report Share Posted September 26, 2007 Sheila, The pain is in the area around his navel. At the start he was constipated but I gave him magnesium citrate and his stools look normal to me. Is it possible to be in a flare without D and with a normal sed rate? Thanks for your help, Jill and Ethan --------------------------------- Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 27, 2007 Report Share Posted September 27, 2007 Hi Jill and Ethan, <<Sheila, The pain is in the area around his navel.>> At the start he was constipated but I gave him magnesium citrate and his stools look normal to me. Is it possible to be in a flare without D and with a normal sed rate? Thanks for your help, Jill and Ethan I don't want to freak you out with these links but thought they may trigger some thought as to what it could be and give you ideas to discuss with his doctor: http://www.nlm.nih.gov/medlineplus/ency/article/003120.htm#top http://www.cnn.com/HEALTH/library/DG/00013.html This link speaks of burning pain around the navel http://www.doctorslounge.com/gastroenterology/forums/backup/topic- 10839.html Please let me know how he is doing. Sheila, SCD Feb. 2001, Uc 23yrs, PCOD 22yrs mom of and Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 28, 2007 Report Share Posted September 28, 2007 --- In pecanbread >Thank you Sheila, those articles were helpful. He still feels lousy with the same stinging pain so we will probably go back to the GI doctor on Monday. We have begun the inro diet. Thanks again, jill and ethan. > Hi Jill and Ethan, > > <<Sheila, The pain is in the area around his navel.>> At the start > he was constipated but I gave him magnesium citrate and his stools > look normal to me. Is it possible to be in a flare without D and > with a normal sed rate? Thanks for your help, Jill and Ethan > > I don't want to freak you out with these links but thought they may > trigger some thought as to what it could be and give you ideas to > discuss with his doctor: > > http://www.nlm.nih.gov/medlineplus/ency/article/003120.htm#top > http://www.cnn.com/HEALTH/library/DG/00013.html > > This link speaks of burning pain around the navel > http://www.doctorslounge.com/gastroenterology/forums/backup/topic- > 10839.html > > Please let me know how he is doing. > > Sheila, SCD Feb. 2001, Uc 23yrs, PCOD 22yrs > mom of and > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2007 Report Share Posted September 29, 2007 I was really surprised that, when my dd had a Crohn's flare, it took several *weeks* for the lab work to correlate with what we were seeing. For us, over a weekend she got very tired and lethargic and had stomach pain. We went back to the intro diet. I took her in on Monday and, although the labs were fine, she started on Pentasa. I think it was two weeks later that her SED rate was finally out of whack. I was stunned. Good luck getting through this. Ellen in Boston 10 year-old (today!) dd SCD since 5/06 for Crohn's Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2007 Report Share Posted September 30, 2007 Just curious - Have they had a 90 Food IGG (delayed reaction) allergy test yet. I know allergy doctors don't like to order it but DAN! docs do. I have a moms group and it is amazing the IGG sensitivites these children have, and I've seen huge things when they were removed. Just a thought. My son is SCD and has been for about a year. His stools improved initially, then started to get worse and didn't come back. We found out he had a Clostridia problem, which, if I'm correct can not be starved out using SCD. It's also possible that since SCD works so well on yeast and bacteria, but not Clostridia, it oopens up pandoras box and Clostridia is allowed to thrive in the absence of the other competing yeast and bacteria. Were taking Flagyl now, Jury is out on if it is helping. I see you are also taking Flagyl. We will be moving on to HBOT ASAP because I have heard some reports about various HBOT pressures killing off Clostridia. (P.S. we are still SCD and will be for years to come) Good Luck, I hate to see hurting bellies, it breaks my heart, my prayers are with you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2007 Report Share Posted October 1, 2007 Hi sarah, Have you looked into S. boulardii? It seems to help some with clostridium overgrowth (one thing it does is it inhibits the bacteria toxins effect on the colon). The S. boulardii also help promote a healthier microflora. http://ndt.oxfordjournals.org/cgi/content/full/15/5/571 http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=96311 http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=174512 Sheila, SCD Feb. 2001, UC 23yrs, PCOD 22yrs mom of and > > Just curious - Have they had a 90 Food IGG (delayed reaction) allergy > test yet. I know allergy doctors don't like to order it but DAN! docs > do. I have a moms group and it is amazing the IGG sensitivites these > children have, and I've seen huge things when they were removed. Just a > thought. > My son is SCD and has been for about a year. His stools improved > initially, then started to get worse and didn't come back. We found out > he had a Clostridia problem, which, if I'm correct can not be starved > out using SCD. It's also possible that since SCD works so well on yeast > and bacteria, but not Clostridia, it oopens up pandoras box and > Clostridia is allowed to thrive in the absence of the other competing > yeast and bacteria. Were taking Flagyl now, Jury is out on if it is > helping. I see you are also taking Flagyl. We will be moving on to HBOT > ASAP because I have heard some reports about various HBOT pressures > killing off Clostridia. (P.S. we are still SCD and will be for years to > come) > Good Luck, I hate to see hurting bellies, it breaks my heart, my > prayers are with you. > Quote Link to comment Share on other sites More sharing options...
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