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Everything posted by monarchcat

  1. I was the OP on this thread so I thought I'd pop back in. I haven't been on the board for a while so I didn't realize this thread had been bumped back up. We never did SSRIs or anti-anxiety meds. In a moment of absolute panic I convinced his dr to prescribe lamictil based on several posts on this board, but I never gave it to him. His therapist at the time didn't think he was a danger to himself so we just held on and tried to get through it. We were seeing a therapist (which he hated) and a adolescent specialist weekly for weight checks. As his nutritional status and weight improved, the body
  2. Really?? We usually use CVS for prescriptions but they did some looking (several months ago) and said they couldn't get dye-free azith tablets. I would think if one CVS could do it, then all could. Ugh. I think I'll bug them again. Do you happen to know the manufacturer of the tablets? Sandoz makes them, but that's the company that Rite Aid is telling me is backordered with no date for fulfillment.
  3. Does anyone have success getting azith pills in dye-free form? It's been such a struggle. My son went back on azith about 4 months ago and he absolutely refuses to take the ones with the red dye (not that I blame him). For a while I was able to get dye-free pills from Rite Aid, but they said they have mostly been filling the script by getting pills from other Rite Aid's that had them. They said the manufacturer (Sandoz) says they are on "backorder" with no date for when/if they will be abel to provide them again. I've called several other pharmacies, and Rite Aid was the only one that said the
  4. I would agree that it bears close watching. My son became vegetarian as part of a year-long progression of food restriction. Started with eating meat, but only grass-fed, organic, etc. That turned into vegetarianism, which progressed to restricting more and more "unhealthy" foods until it became full-blown anorexia, orthoexia, and body dysmorphia. In my son's case, his perfectionist/ scrupulosity ocd was at the root of it for the most part.
  5. I agree with checking titers first. Both my kids have PANDAS and we had a difficult situation recently in that my daughter caught chicken pox from someone in her class (she had one vax as a baby, but not the booster), my son (14) also had one vax as a baby, but not the booster. The state stepped in and said that he could not return to school for 2 weeks unless he had the booster immediately or showed immunity. We tested titers and he had no immunity. We made the decision to vax and he had no negative reaction at all... not even a mild flare. I was very relieved, but I knew I was rolling the di
  6. DS has been on treatment strength abx for approximately 5 years now. I'm not sure they are still doing anything but I'm nervous about just going off completely. He's currently on clarithromycin (biaxin). I'm wondering about moving to a prophylactic dose of something... either the biaxin or something else. Has anyone moved to a prophylactic dose after a long time on treatment strength? What abx do you use and what has your experience been? When he was young, he very clearly and obviously needed the treatment strength. He's now a teenager and we are addressing some other stuff, mainly MTHFR rela
  7. DS has been on it since late fall and I do think it's helping. I know for sure he has methylation issues and based on his SNPs I suspected he would be low in lithium. I just had his blood levels tested and his level came back undetectable, despite having been on the lithium orotate daily since November. I've now upped him to one in the morning and one at night. We've been using this: It's important to understand the dose. One 120mg tablet gives about 4 1/2 mg of lithium, so it is a teeny-tiny dose compared to the scary prescription lithium. I think it's worth a try. Start low and slow. H
  8. So a child in my daughter's 3rd grade class came down with chickenpox a couple weeks ago. My daughter had one varicella vaccine when she was a year old then was diagnosed with PANDAS at 3 1/2 and not vaxx'd further after that point. Can you guess where this is leading? Yep! We have chickenpox! Woot! Back when she was 3 1/2 she was diagnosed quickly and easily with PANDAS due to my 14 year old son already having paved the way, so to speak. She was on antibiotics for several years, and we just pulled her off last June. She has been doing GREAT, no issues at all. Before I knew it was chickenp
  9. It seems as though Yasko advocates for very low dose when possible, though some need higher doses, especially at first. I think ideally aiming for under 5mg of elemental lithium per day (and maybe very low, like 2mg or less for long term?). She has lots of info in the webisode in the link above (I finally watched it and it's really interesting!). The tablets I have are 120mg, which contain 4.8mg elemental lithium. We are doing 1 tablet a day right now, but I think I'll adjust that down in a few months, depending on lab results, though. Yasko definitely says to work with a doctor and check lev
  10. I'm at work so don't have my notes/test results with me, but this link explains it fairly well: http://chronicdiseaserecovery.wordpress.com/2013/04/30/mthfr-and-lithium/ Oh, that link also has a link to Dr. Amy's presentation on lithium! Haven't watched it myself yet, but bound to have great info! Amy Yasko's book "Feel Good Nutrigenomics" has a whole chapter on lithium, though it doesn't get terribly specific about SNPs It's not a "magic pill" for us, but I realize there never will be one. So many factors play into it all. I do feel it's helping, though, as another piece of the pu
  11. I recently started ds13 (120 lbs) on lithium orotate. After investigation, his 23andMe results seem to point in that direction. I haven't had his blood lithium level tested yet, but will do so. As with anything, "low and slow" is the way to take it. I started him on one 120mg (4.6mg elemental lithium) per day. I felt that he probably reacted a bit to that dose so I backed him down to half a pill for a couple weeks, and now give him a whole pill once a day. Lithium assists with transport of B12 into the cells, which I think is a big deal in our case also. My son can't tolerate methyl B12 so I g
  12. Thanks for the reply! Yes, vitamin D levels are low at the moment. Just got test results today actually and his level is 22. Strangely, though, they were up nicely when his depression/anorexia really kicked in last fall (his level was 74 at the time, which really surprised me, but it was after all the summer sun). He is homozygous for VDR-taq, which means we'll probably always struggle with D levels. I haven't been supplementing, but am going to start again. The other thing we CANNOT get rid of is mycoplasma. Tests came back for positive IgG and IgM. This has been a couple years now that w
  13. When we started zinc a year ago we were in the middle of a major depression and eating disorder and ocd. Even with all that already going on, I felt like the first few days or so of zinc (15mg zinc picolinate) caused noticeable herxing. We just recently increased the dose to 15mg twice a day and I didn't notice any increase in symptoms this time. Is this a new supplement or an increased dose for your child? Then again, she could have been exposed to something and is flaring from that?
  14. Thanks, for the info Dedee. I'm looking forward to trying it. I'm waayy past the point of thinking that anything will be a magic cure-all, but I'll settle for building a healthier, happier child day by day, week by week, month by month, year by year....
  15. Thanks for the input. I emailed his pediatrician and asked him if we can do a blood test to get a baseline level before starting and he said yes, so I think we'll do that first. I suspect it might be a good supplement for him.
  16. Over the past year we've been dealing with major depression with ds13. Last winter was awful - depression, eating disorder, anger, etc. He's on biaxin for PANDAS and I started him on zinc, CoQ10, Iron (his levels were low) and hydroxy B12. We've done 23andMe and he has a bunch of mutations. He can't tolerate ANY methyl donors (yet symptomatically he's an undermethylator). I feel like there are big pieces of the puzzle to figure out with the MTHFR and genetic stuff and I'm working through that. He seemed to come out of the depression last Spring. He had gained weight and was eating really w
  17. It looks like he has crazy strep. If his doctor won't treat - find one who will. That's ridiculous that a doctor won't treat an ACTIVE strep infection just because he's asymptomatic. Never mind if he doesn't believe in PANDAS, what about rheumatic fever, sydenham's chorea or glomerulonephritis? Surely he's heard of those? It sounds like your doctor is not going to be helpful. I would seek a doctor knowledgeable about PANDAS as quickly as possible. Good luck!
  18. Definitely more than just puberty, though I'm sure puberty is wreaking havoc as well. This is severe depression, body dysmorphia, eating disorder (orthorexia heading toward anorexia). He won't play video games or watch tv or movies ever because he feels they are not good for him. He is obsessed with how "unhealthy, fat and lazy" he was in the past (he wasn't) and terrified that he will be that way in the future.
  19. Thank you so much for your advice. It sounds like a good plan. Interesting on the Sacc B. He's been on it for years (through the good and the bad) but I'm definitely willing to stop it and see what happens. I know inherently it's a bad idea to try to rush things. Really can't wait for the 23andMe results!
  20. I have another post right now about how we are in crisis - DS 12.5 has severe depression, body dysmorphia, and an eating disorder which has all developed over the past few months. We are in MA and I'm wondering if anyone has been to MGH or has investigated the new "PANDAS Clinic" (are they accepting new patients?). I was at the conference back in November and had mixed feelings when it was spoken about, but that was before DS nose-dived completely. I feel like MGH would definitley be the road to psych meds, and I've been avoiding that, but maybe it's necessary at this point. Just curio
  21. I'm actually waiting for his 23andme results, but will probably be another month or so. I'm convinced he's undermethylated, but haven't wanted to push too many supplments without really knowing the big picture. I see interesting things about anoxeria and zinc deficiency. I have started zinc and magnesium over the past couple weeks, but no change (things are worse actually). I just ordered P-5-P: http://www.amazon.com/gp/product/B0019GXQK0/ref=oh_details_o00_s00_i01?ie=UTF8&psc=1 and 5-methylfolate http://www.amazon.com/gp/product/B001LQY9ZO/ref=oh_details_o00_s00_i00?ie=UTF8&psc=1 and
  22. Thanks for all the input, guys! Ugh.. this just sucks so much. He's miserable and I'm a stress-ball. He has had high myco-p numbers for a year and a half, but no real symptoms. He had a fantastic year last year. These past few months feel very different from past PANDAS episodes. It's textbook depression and eating disorder, which we've never really dealt with before. I'm wondering if puberty is changing the way PANDAS expresses itself (he's most definitely in puberty). We switched from Biaxin to Minocycline for several months to try to bring the myco numbers down, but I could see that he was
  23. We are in probably the worst flare we've ever experienced. DS 12 1/2 has had PANDAS since he was at least 5, treated starting at age 8 1/2. We did 3 IVIG treatments with Dr. B 3 years ago with great succeess. Never back to 100% but really, really good. The past few months he's been sliding into major depression and an eating disorder. He has perfectionist OCD. In the past he's had minor OCD, mostly in his thinking so it was never really noticable or overt. These days he is completely obsessed with healthy eating, calories, reading labels, exercise, etc. He feels hopeless and worthless and is a
  24. This just in - http://blog.23andme.com/news/23andme-provides-an-update-regarding-fdas-review/ So.. it seems as though they will still sell the kits and then provide the ancestry results and raw data, but not the health-related report. Seems to me, the "good stuff" is all in the raw data anyway and can be interpreted genetic genie or livewello. So... not a great result, but better than a total shut-down, I think. Hopefully they can iron out the issues with the FDA. I think it's obscene that apparantly the FDA assumes consumers can't be trusted with their own health information, but that's n
  25. We are on year five of constant abx for my son (12 1/2) with no issues. He's been on augmentin, then azithromycin, then biaxin and now minocycline. My daughter (7) has been on azith and then biaxin for 3 years with a few breaks. She also has tolerated them remarkably well. Some of the PANDAS doctors have remarked that PANDAS kids in general tend to do very well on long-term abx without the issues that others may have. Not to say that's true across the board, but in our case, fortunately, it has been. Having said that, I HATE the fact that my kids need constant abx... I wish it wasn't so an
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