Guest guest Posted October 18, 2008 Report Share Posted October 18, 2008 I've been mulling over whether to post for a couple of days and now I'm at the point of Why Not?? Briefly, I have chronic mycoplasma pneumonia and EBV. I haven't tested for Lyme yet. My oldest boy, almost 11, is mostly recovered from autism, but we still have some work to do. My middle boy, 4, has severe anxiety and had some developmental delays, not spectrum. My youngest, 19 mo,was just diagnosed with a speech delay. The two little guys were adopted at birth and are biologically half brothers. Here's my dilemma. I had surgery about 10 months ago, got sick with brochitis 6 weeks later, and have been in a chronic fatige/fibro (??) flare off and on (mostly on) ever since. One of my biggest issues lately is fatigue, followed closely by brain fog. I can't even begin to figure out where to start! I have been scaling back on my outside responsibilities, trying to marshall my energy for taking care of myself and my family, but I'm flummoxed. I've got some basic stuff in place for all of us, but need to step it up, especially for me. If I don't get better, no one's going to get the boys healthy. We do have 2 great DAN doctors on board, but money is tight and I have to delay making some appointmentts. Any suggestions for starting points? Thanks!! Jill Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 19, 2008 Report Share Posted October 19, 2008 Jill: I so can relate. I have to take so many things to stay on my feet. Lithium orotate really helps me. And I just started taking Unda 243 which picked me up even after I ran out of lithium. Usually when I run out, I am out of it, but the Unda 243 is really helping (thank's Limin for that idea). Also, I take the Burbur. Pectasol Chelation Complex really helps, as well as MB12 powder (methylcolbamin). Grapefruit seed extract, turmeric, ginger root and digestive enzymes are also things I take. Would you believe I even take more. If I don't take just one of these, then I notice it. I have only been killing my pathogens about 9 months, so I am hoping, another year, and I will be able to come off of some things. Love and prayers, Heidi N I've been mulling over whether to post for a couple of days and now I'm at the point of Why Not??Briefly, I have chronic mycoplasma pneumonia and EBV. I haven't tested for Lyme yet. My oldest boy, almost 11, is mostly recovered from autism, but we still have some work to do. My middle boy, 4, has severe anxiety and had some developmental delays, not spectrum. My youngest, 19 mo,was just diagnosed with a speech delay. The two little guys were adopted at birth and are biologically half brothers.Here's my dilemma. I had surgery about 10 months ago, got sick with brochitis 6 weeks later, and have been in a chronic fatige/fibro (??) flare off and on (mostly on) ever since. One of my biggest issues lately is fatigue, followed closely by brain fog.I can't even begin to figure out where to start! I have been scaling back on my outside responsibilities, trying to marshall my energy for taking care of myself and my family, but I'm flummoxed. I've got some basic stuff in place for all of us, but need to step it up, especially for me. If I don't get better, no one's going to get the boys healthy.We do have 2 great DAN doctors on board, but money is tight and I have to delay making some appointmentts.Any suggestions for starting points?Thanks!!JillNew MapQuest Local shows what's happening at your destination. Dining, Movies, Events, News more. Try it out! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 19, 2008 Report Share Posted October 19, 2008 Hi Jill, I am so sorry that you are having such a hard time. I know how hard it is to take care of your children when you are ill. I have another suggestion. There are studies that show anesthesia can be really toxic to the system. Many people have experienced the same thing. The visual test on Ritchie Shoemakers site can show damage from the anesthesia. The good news is that you can do something about it. I would get the highest quality phos choline you can get. The best I have ever tried is from xymogen. It is a liquid. It is really expensive though. I got it locally from a friend, but check around. I would take buckets of it to start(a couple of tablespoons a day). It will help your brain and your liver process out the residual toxins. Iherb has phos choline pills (from Now foods I believe)that are not as potent, but I would think you could make that up in volume :-) . I would also take glutathione if you tolerate it. I use the powder from Jomar. For me it has been the more helpful than pills. Gingko will increase the microcirculation to your brain. The dry oxy from opaline solutions would also help because it increases your oxygen capacity. It crosses the blood brain barrier which helps too. I hope this helps. Let us know how you are doing. Love, Peggy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 19, 2008 Report Share Posted October 19, 2008 Wow Peggy, thanks for sharing that great information! Like Jill, I also had a general anesthetic that totally messed me up. Also had amalgam removal just prior, plus gadolinium IV's in diagnostic scans - system overload. I have some phos-choline by Designs for Health. Plus another brand buried somewhere that my son didn't tolerate. Going to add it to my daily pile now. I'll also take some glutathione, but I need to be on PST support supplements for a few days first to be able to tolerate the high sulfur. I'm all out of molybdenum at the moment, so that's going to have to wait. Thanks again! > > Hi Jill, > I am so sorry that you are having such a hard time. I know how hard it > is to take care of your children when you are ill. > I have another suggestion. There are studies that show anesthesia can > be really toxic to the system. Many people have experienced the same thing. > The visual test on Ritchie Shoemakers site can show damage from the > anesthesia. > > The good news is that you can do something about it. I would get the > highest quality phos choline you can get. The best I have ever tried is > from xymogen. It is a liquid. It is really expensive though. I got it > locally from a friend, but check around. I would take buckets of it to > start(a couple of tablespoons a day). It will help your brain and your > liver process out the residual toxins. > > Iherb has phos choline pills (from Now foods I believe)that are not as > potent, but I would think you could make that up in volume :-) . > > I would also take glutathione if you tolerate it. I use the powder from > Jomar. For me it has been the more helpful than pills. > Gingko will increase the microcirculation to your brain. > > The dry oxy from opaline solutions would also help because it increases > your oxygen capacity. It crosses the blood brain barrier which helps too. > > I hope this helps. Let us know how you are doing. > Love, > Peggy > Quote Link to comment Share on other sites More sharing options...
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