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  1. For both of our sons, the trigger seemed to be mono. When our second son showed symptoms (tics), I remember taking him to our pediatrician and asking for the blood test. He did not show any signs of any illness, but the she tested for strep and mono. Tests came back positive for mono.
  2. Sibling of DS12 started tics during mono (he was a few months from turning 9). We did 30 days of keflex - tics stopped about 2 days after starting treatment with keflex. We saw tics return for a day or two about 4 months later, but we did keflex again for 30 days. It has now been a year and 3 months since the first tics appeared during mono and younger brother remains symptom free. We did 30 days of keflex at initial onset and then 30 days again when tics appears a few months later. He has been totally symptome free with no abx for the last 11 months. So, I would treat sibling for at lea
  3. We've seen increased symptoms after swimming in pools, so we tried the epsom salt baths after swimming and it seemed to help.
  4. I am not sure I can be much help since we feel like we are in a big guessing game ourselves, but I know that hearing the experiences of others can help. I would think that 250 mg once a day of keflex might be too low a dose for prophylaxis. Maybe try 250 mg twice a day and if symptoms improve over time you can try to reduce back down to 250 mg once a day again. Have our son's symptoms gotten worse or are they stable ... interesting question. We have been dealing with PANDAS/PITAND for about 8 years, but did not identify it as that until June 2009. Looking back 8 years ago, it was ver
  5. Our ds is 12 and approx 68 pounds. We did keflex for about 1 1/2 years (started June 2009 - stopping in Jan 2011). Our treatment dose was 1,000 mg (taken as 500 mg twice a day) and the prophylactic dose was 500 mg (taken as 250 mg twice a day). We also had to go back and forth a lot between treatment and prophylactic dosing. In Sept 2010, it seemed keflex was not working anymore and we switched to amox for approx 30 days. Amox seemed to help at first, but then seemed to also stop working. We went back to keflex with some success until Jan 2011, then we felt it was not working again.
  6. We just got the Genova CDSA results and a number of blood test results back today and I want to thank everyone on this forum. I kept reading about mycoplasma p and we continue to struggle with PANDAS/PITAND symptoms so we had ds12 tested. Well, it turned out positive. Out of normal results were as follows: • Mycoplasma p IgG level: While in the indeterminate range, we are going to treat as an ongoing infection • Citrobacter amalonaticus: +4 • Klebsiella oxytoca: +4 We are going to treat for all 3 with doxycycline at 100 mg once a day for about 3 months. Any thoughts on thi
  7. Our ds12 used to get canker sores, too. Never figured out why exactly. We followed the same strategy that monarchcat mentioned and changed his toothpaste to one that does not contain SLS (sodium lauryl sufate) - he is using sensodyne. No canker sores since changing to a different toothpaste.
  8. I remember the day we took our ds (then 10) to the ped and I said he had strep throat. The ped looked in his throat and said there was no sign of any infection. No fever, no stomach ache, no sore throat - no symptoms at all. Somehow, I got the ped to do a rapid anyway and in his own words, "That is the fastest most positive result I have ever seen." These kids make is tricky for us by getting sick and not presenting with symptoms. My own opinion is to wait on the vaccines. Get her healthy, get her tonsils out and let her recover. Then, you can assess the vaccines in a few months.
  9. Yes, I think the doctor does have something in mind like the Myer's cocktail. Luckily, our ds12 does fine with needles - has probably been poked more in his life than I have been in my own life ... Thanks for your feedback - glad to hear there were no negative results.
  10. We were hoping for lots of test results today (myco p, lyme, bartonella, thyroid, celiac, hormones, digestive analysis, etc), but our doc rescheduled to Monday because she wants to consult more with other doctors - wonder what that means ... Anyway, I do know she will be asking us to consider intravenous vitamin therapy because we already know our son has a malabsorption problem. Has anyone else tried this? If so, did you see any bad side affects? Any good results? Any increases in PANDAS/PITAND symptoms following treatment? Any input would be appreciated. Thanks!
  11. When our ds was between 4 and 5 years old, we had to deal with sudden onset of soiling. Our ped tested for parasites, but tests turned out neg. We then turned to lactose intolerance. Removing dairy worked immediately for a few weeks and we thought problem was solved, but then it started again when he was still on no dairy. He would eat something harmless like an apple and have an accident. We ended up treating for systemic candida (yeast overgrowth) and problem cleared up. I never want to put a damper on something when it seems someone has found an answer, but I just wanted to toss this o
  12. I am sorry - I know and understand your frustrations. Our ds had itchy bottom when he had systemic candida (bad yeast infection). Our experience is that it takes months or even years to clear systemic candida, so a week or so on anti fungal may not be enough. Also, being on teh anti fungal is probably causing dye off issues and may be increasing symptoms.
  13. I agree with you - mono is a virus so abx should not make a difference. I have no answers. I look at it from the standpoint that the abx were not to treat mono since it is a virus, but the abx were used to do something to the immune system to stop the PANDAS/PITAND reaction. I just know it worked to stop the tics and we don't have ongoing PANDAS/PITAND symptoms with this child like we have with our older son who was not diagnosed for about 7 to 8 years following first symptoms.
  14. Alternative diets are a lot of work to get started, but once you get in the groove it all becomes a habit that can be maintained. It's all about forming new habits and behaviors. Might be good to see a naturopath to decide what type of alternative diet is best or to do some food sensitivity testing to be sure you don't end up overloading on something that is actually causing more issues (ie eggs). We have always done diets based on the idea of reducing candida(yeast) because of the antibiotics. You can google candida diet and find lots of sites that list foods that are ok, foods
  15. One more thought on the rages. I don't know if the rages we saw in the past with our son were due to PANDAS/PITAND or candida. His rages happened about 7 years ago when he was 5. We were treating him for systemic candida and leaky gut. It was like clockwork. We would give him the supplement to kill the yeast (garlic, other natural supplements that we rotated) and he would be like an angry teenager 30 minutes to an hour later. Each rage would last about the same amount of time (maybe 45 minutes or so). If he didn't have the supplements for the yeast - no rage. When the yeast got better -
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