Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 Anita, Not Meenakshi, but I would like to know what immune boosters you may reccommend? Anita Kugelstadt <mysuperteach@...> wrote: Meenakshi, I started my son on a viral protocol without running viral titres (or at least any that were of any use). It is obvious from his reaction that he has viral issues. This, in spite of the fact that he had almost none of the soft signs of viral problems (see viral file for that information and other stuff you might find useful). I also know there are people who have used a viral protocol in spite of the complete viral titres tests showing no high numbers and ahve had success. I personally think that using natural antivirals, like Virastop, in a way where you titrate up cautiously is something many parents of ASD kids should try. The more I read about viruses and our kids compromised immune systems, the more I believe that a good number of our kids have these problems. I would also encourage you, if you are considering a viral protocol, to be sure to use immune boosters, perhaps even in advance to prepare for it. As for Virastop, it will digest the protein sheath of any virus which has one, so it is not formulated for only one particular virus. I hope this helps, Anita > > Hi all, > > We recently did an autism panel testing through > Immunosciences lab. it shows that our son doesn't have > the measeles virus. Apparently, the rubeola titer is > normal. but, I understand from previous posts that > there are other viral panels too which we haven't > done. Would it be o.kay. to try a broad spectrum > antiviral like Virastop, whether or not there are > viral issues. I know that there are several parents in > this list use antivirals for some issues. Is the > antiviral like Virasop tailored to work on a > particular viral issue? Just wanted to get more > information about it. > > Thanks in advance. > > Meenakshi. > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 Anita has put together a wonderful file on viral issues, which includes a discussion on immune boosters, on the Autism_Mercury list. If you are not a member, it is well worth joining, if only for that! Anne > > > > Hi all, > > > > We recently did an autism panel testing through > > Immunosciences lab. it shows that our son doesn't have > > the measeles virus. Apparently, the rubeola titer is > > normal. but, I understand from previous posts that > > there are other viral panels too which we haven't > > done. Would it be o.kay. to try a broad spectrum > > antiviral like Virastop, whether or not there are > > viral issues. I know that there are several parents in > > this list use antivirals for some issues. Is the > > antiviral like Virasop tailored to work on a > > particular viral issue? Just wanted to get more > > information about it. > > > > Thanks in advance. > > > > Meenakshi. > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 We use Colostrum made by Kirkman's. www.kirkmanlabs.com A ton of people I know are useing Transfor Factor which is a huge immune booster supplement. -Crystla > > > > Hi all, > > > > We recently did an autism panel testing through > > Immunosciences lab. it shows that our son doesn't have > > the measeles virus. Apparently, the rubeola titer is > > normal. but, I understand from previous posts that > > there are other viral panels too which we haven't > > done. Would it be o.kay. to try a broad spectrum > > antiviral like Virastop, whether or not there are > > viral issues. I know that there are several parents in > > this list use antivirals for some issues. Is the > > antiviral like Virasop tailored to work on a > > particular viral issue? Just wanted to get more > > information about it. > > > > Thanks in advance. > > > > Meenakshi. > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 Hi , I see you've received some answers already. The file that Anne mentioned is here also at our group, although I recommend autism- mercury to anyone with an autistic child. Well worth joining. When choosing immune boosters you need to consider what each one can do. For example, I use astragalus root and echinacea in rotation to help raise NK cell numbers and IP-6 to help make those NK cells more active. I also use colostrum to boost the immune system generally, and because it is supposed to be good for GI issues related to viruses. Like most parents, I also use zinc, Vit A and C (lots of it sometimes). I would really like to use Thymic Protein but it costs quite a bit, especially here in Canada, so it will have to wait. All of my choices are easy to dose: something that is important when you're giving a three year old 25 different supps a day. I hope this might help, Anita > > Anita, > Not Meenakshi, but I would like to know what immune boosters you may reccommend? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2006 Report Share Posted March 28, 2006 I really thank Anita for undertaking that viral document...done voluntarily under her own initiative. That took some time and effort! Please, if anyone is doing the enzyme program for viruses, do drop me a line or post here about what you experienced. It will be important for refining these guidelines and moing this forward. Oh...and I found a possible explanation for the anti-viral and increased yeast issue which I'll post separately. . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2006 Report Share Posted March 28, 2006 I too would like to thank you Anita, not only for your hard work on the viral file, but also for the supplement file in A-M group. This document has been very helpful for me and I'm certain many others in the group. Your contributions of time and energy are very much appreciated!! Sheresa > > I really thank Anita for undertaking that viral document...done > voluntarily under her own initiative. That took some time and effort! > > Please, if anyone is doing the enzyme program for viruses, do drop me a > line or post here about what you experienced. It will be important for > refining these guidelines and moing this forward. > > Oh...and I found a possible explanation for the anti-viral and > increased yeast issue which I'll post separately. > > . > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2006 Report Share Posted March 28, 2006 You are most welcome :-) Here goes: Vitamins A, B50, C, E MethylB12 Magnesium citrate and magnesium sulfate TD Calcium citrate CLO and High EPA fish oil Evening primrose oil Milk thistle Lecithin Folinic acid zinc picolinate and sulfate in TD Taurine Broad Spectrum Amino Acids Selenium Molybdenum Co-enzyme Q10 TMG Candex GSE (sometimes, as necessary) TD Glutathione Culturelle Super Pro Bio probiotics Sambucol Colostrum Rotating astragalus root and echinacea Virastop Lauricidin DMSA and ALA for chelation Melatonin AFP peptizyde, zyme prime, no fenol Waiting in the wings: biotin (too afraid of the constipation that might result right now), OLE (again, worried about the smooth muscle impact right now), P5P. I think that's it. I didn't write down doses or why I use them. If you have any questions though, I'd be happy to share what I know. As for the VS. I'm not sure if you remember but I did use a viral protocol on my son before. He had a very big reaction which scared me and I stopped the protocol. Now I am increasing things VERY slowly. We've been at this for 14 days and we're up to 4 VS a day and 10 lauricidin, plus the daily sambucol and immune boosters. Each time I increase the VS he gets a small viral rash on his face. I'm glad to see that but I'm just as glad to keep it small. Sometimes just one little red bump. Last night I increased by 1 VS with a night dose of chelator, so very empty stomach, and he woke up this morning with about 8 - 10 little red bumps. He also gets little mini-fevers that last for an hour or so and then leave. I'll stay at this dose for a few days, until all the bumps are gone. I really do want to use OLE because I think it is great, but this time around ONE THING INTRODUCED AT A TIME! And I really mean it. :-) VS is pricey. If you get it over the internet I think the cheapest is usually about $29/ bottle (about 372 Canadian dollars with shipping ;-) just kidding, but it does seem that way some days). I intend to VS the whole family at some point, so cost matters. Best wishes, Anita > > Really good information Anita! > > You are giving 25 supplements everyday? May I ask what they all are? I have been recently going over the different ones I have in stock and get things a little more organized. I feel we are on to something with my son. He has been progressing so well lately. I just want to make sure I am getting him everything he needs. I downloaded and printed the supplement list from this group, SO handy! I just am wondering what all you are doing. I would also be interested in your results from the Virastop trial you are doing. After reading the report we are going to start it very shortly. I need to stock up on a couple bottles and make sure my HFS can keep me in stock! > > Thanks so much! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2006 Report Share Posted March 28, 2006 Anita, Thank you for clarifying that the A_M group is worth joining for more than the antiviral file! I certainly did not do a good job of expressing my thoughts. As I hope you know, I meant that if your viral file were all someone got from the list, it would be well worth signing on. I think that list has incredible people on it and provides incredible resources. So, again, thanks for clearing that up. I will try to be more careful! And thanks for all your work. I am very glad to read that your son is holding up well on your new antiviral protocol. Thanks again, Best, Anne > > > > Anita, > > Not Meenakshi, but I would like to know what immune boosters you > may reccommend? > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2006 Report Share Posted March 28, 2006 , Let me premise all this by saying that the reason I wrote the viral file was because I knew NOTHING. I'm just barely one step up from that now, so please don't think I'm any sort of expert. Now, most of what I know about the rash is what I've learned from 's write-up that she posted earlier: http://www.enzymestuff.com/rtVirusStudyReport.htm#6 I need to read her work again--it is extremely helpful. What she theorizes is that perhaps when the virus is being attacked, it travels up through the nerves until it reaches the skin. Because the rash seems to localize, this theory makes sense (unless, of course you have viruses all over your body, which might be the case for some people). My son seems to get the rash on his face. Once he had a bit on one spot on his arm. Nowhere else on his body. I have read on another list the theory that the rash is in fact a sign of metals being excreted. I don't believe this. Although viruses and metals may very well be related in our ASD kids, I don't think that attacking viruses will actually cause our kids to start excreting metals. Further to that, kids who are chelating do not get this rash. My son, for example, has gotten the rash within less than 60 minutes of taking the antivirals. There is no way that he could start excreting metals in that short period of time. Even during periods where urine and fecal test prove he is excreting a lot of metals he has no rash. So, the significance of a rash appearing is that something in your viral protocol is helping your child's body to attack the virus. This is good. What is bad is if the attack is so strong that it overwhelms your child (and you). This is what happened during the first viral protocol I tried. I did too much too quickly while chelating and had to stop. I talk about this a lot not because I enjoy admitting to lots of people that I screwed up in a very big way, but because I hope that other people can learn from my mistake. When you read 's work, you'll see how things like rashes (not everyone gets them) and other responses will help you adjust your viral protocol up or down as the case may be. I hope this helps. :-) Anita > > Anita, > I have seen rashes mentioned before when folks use antivirals. I believe I have a kid that does not have gut, yeast or bacteria issues. Please tell me the significance of seeing a rash appear...it seems to be good news! I hate to sound ignorant, but on this, I AM a duh! > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2006 Report Share Posted March 29, 2006 FWIW, my son had some rashes and fever on and off before chelating. He had even more rashes and fever going on and off after we started chelation. The rash he had seemed to match the " mercury rash " some people described. I do not know. We've chelated for two years. He does not get anymore rash or fever, but still has lots of viral issues causing seizures (that's what I believe nobody knows for sure!). > > > > Anita, > > I have seen rashes mentioned before when folks use antivirals. I > believe I have a kid that does not have gut, yeast or bacteria > issues. Please tell me the significance of seeing a rash appear...it > seems to be good news! I hate to sound ignorant, but on this, I AM a > duh! > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2006 Report Share Posted March 30, 2006 > > Anita, > I have seen rashes mentioned before when folks use antivirals. I believe I have a kid that does not have gut, yeast or bacteria issues. Please tell me the significance of seeing a rash appear...it seems to be good news! I hate to sound ignorant, but on this, I AM a duh! For my son, I give anti-virals and he develops a rash [which comes and goes in waves]. For him, it means the viruses are coming out of his body. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2006 Report Share Posted March 31, 2006 how would you describe a " mercury rash " ? We just started chelation last weekend so this would be something I could be on the lookout for. Thanks Sheresa > > > > > > Anita, > > > I have seen rashes mentioned before when folks use antivirals. > I > > believe I have a kid that does not have gut, yeast or bacteria > > issues. Please tell me the significance of seeing a rash > appear...it > > seems to be good news! I hate to sound ignorant, but on this, I AM > a > > duh! > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2006 Report Share Posted March 31, 2006 , Have you done a viral protocol? I know of one person whose daughter stopped seizing within a few hours of starting VS. Now, this protocol wasn't followed through with for a variety of reasons, and the mom has been dealing with a number of other more pressing problems with her child, so this mighth have been only temporary and there definitely isn't an end to this story yet, but I thought I'd mention it. Anita > > FWIW, my son had some rashes and fever on and off before chelating. > He had even more rashes and fever going on and off after we started > chelation. The rash he had seemed to match the " mercury rash " some > people described. I do not know. We've chelated for two years. He > does not get anymore rash or fever, but still has lots of viral > issues causing seizures (that's what I believe nobody knows for > sure!). > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 2, 2006 Report Share Posted April 2, 2006 Thanks Anita. Yes, I am trying to do some viral stuff right now but it is not easy. He is reacting very strongly in term of behaviors, even with very low doses and sometimes it causes lots of seizures. Thanks, > > > > FWIW, my son had some rashes and fever on and off before > chelating. > > He had even more rashes and fever going on and off after we > started > > chelation. The rash he had seemed to match the " mercury rash " some > > people described. I do not know. We've chelated for two years. He > > does not get anymore rash or fever, but still has lots of viral > > issues causing seizures (that's what I believe nobody knows for > > sure!). > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2006 Report Share Posted April 4, 2006 I remember back when everybody got measles, it was always considered a good sign when the measles rash actually " came out. " (As opposed to just the fever, etc.) Now I am not sure why people thought this, just kind of interesting. I had another friend whose husband worked at the virology lab at Cornell and she told me that when measles rashes appeared on the skin, similar lesions were also appearing on all the internal organs--did not sound very appealing to me. Peace, Kathy E. On Mar 29, 2006, at 1:02 AM, Anita Kugelstadt wrote: > > What she theorizes is that perhaps when the virus is being attacked, > it travels up through the nerves until it reaches the skin. Because > the rash seems to localize, this theory makes sense (unless, of > course you have viruses all over your body, which might be the case > for some people). My son seems to get the rash on his face. Once > he had a bit on one spot on his arm. Nowhere else on his body. > > I have read on another list the theory that the rash is in fact a > sign of metals being excreted. I don't believe this. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2006 Report Share Posted April 4, 2006 LOL, Anita, does your child have any room left for FOOD? (just kidding) Kathy E. On Mar 28, 2006, at 4:26 PM, Anita Kugelstadt wrote: > You are most welcome :-) > > Here goes: > > Vitamins A, B50, C, E > MethylB12 > Magnesium citrate and magnesium sulfate TD > Calcium citrate > CLO and High EPA fish oil > Evening primrose oil > Milk thistle > Lecithin > Folinic acid > zinc picolinate and sulfate in TD > Taurine > Broad Spectrum Amino Acids > Selenium > Molybdenum > Co-enzyme Q10 > TMG > Candex > GSE (sometimes, as necessary) > TD Glutathione > Culturelle > Super Pro Bio probiotics > Sambucol > Colostrum > Rotating astragalus root and echinacea > Virastop > Lauricidin > DMSA and ALA for chelation > Melatonin > AFP peptizyde, zyme prime, no fenol > > Waiting in the wings: biotin (too afraid of the constipation that > might result right now), OLE (again, worried about the smooth muscle > impact right now), P5P. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2006 Report Share Posted April 4, 2006 It would certainly make sense to me given my daughter's history of grand mal seizures after her mumps vaccine at 12, and also the number of VAERs reports of seizures. Peace, Kathy E. On Mar 30, 2006, at 12:24 AM, ferdeson wrote: > . We've chelated for two years. He > does not get anymore rash or fever, but still has lots of viral > issues causing seizures (that's what I believe nobody knows for > sure!). > > > > > > > > , > > > > Let me premise all this by saying that the reason I wrote the viral > > file was because I knew NOTHING. I'm just barely one step up from > > that now, so please don't think I'm any sort of expert. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 5, 2006 Report Share Posted April 5, 2006 > > I remember back when everybody got measles, it was always considered > a good sign when the measles rash actually " came out. " (As opposed > to just the fever, etc.) Now I am not sure why people thought this, > just kind of interesting. Possibly because this meant the virus was coming out of the body, instead of just staying inside the body where it could emerge later and cause additional problems. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 5, 2006 Report Share Posted April 5, 2006 > > Well, my two cents into this converstaion is that strangely, my son's bad rash on his one leg misteriously disappeared with the vomitting he had a couple days ago!! I could not believe it! Probably viruses leaving his body... The rash has been there off an on for the past 2 years... Both my #2 and #3 will vomit when a virus " breaks " . For them, it is a good sign. Dana Quote Link to comment Share on other sites More sharing options...
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