Guest guest Posted March 9, 2001 Report Share Posted March 9, 2001 Hi , Yes, I do believe that the molybdenum has helped me alot. My brain fog is gone almost all of the time now, and I don't feel spacey. It's about time! As for the parasite issues, here are some very interesting websites that you all may want to check out. I know it is not a fun issue to think about, but it may be one of the factors that keep up from getting better. http://www.dpd.cdc.gov/dpdx/HTML/Para_Health.htm'>http://www.dpd.cdc.gov/dpdx/HTML/Para_Health.htm http://www.sunsteam.com/search/dir/Nature+and+Science/Science/Biology/Microb iology/Parasites http://www.bodyfixer.com/wormsn.htm http://www.dpd.cdc.gov/dpdx/HTML/Para_Health.htm'>http://www.dpd.cdc.gov/dpdx/HTML/Para_Health.htm Here is a testimony from one of our ladies: " I really did my parasite cleanse last October. I was freaked out big time when they came out of my nose, believe me. Am just doing the maintenance now. But I just had another bout this week. For no reason I got sick as a dog Monday. Felt to rotton to eat or drink anything, had the chills at 80 degrees. Went to bed with my warm fuzzies and my heating pad. Tuesday was a little better, I was able to hold fruit and veggie juices. Did a colema with Aloe Tuesday night because I had a stabbing pain on my favorite right side again and my colon just was painfull. But nothing came out, only water.. Wednesday I struggled on juices and a baked potatoe , no BM for 2 days. Yesterday I had 4. Expelled one super long white something and 2 clusters full of Threadworms. I feel great today :-)) I am only telling you so you know if they are there they don't all want to come out right away.You have to make the environment very uncomfortable for them so they get the message that they are not welcome. And that I have done and still do with the cayenne, lots of garlic and the maintenance herbs. " ----- Original Message ----- From: <summer234562001@...> < > Sent: Wednesday, March 07, 2001 10:47 PM Subject: to Patty > Hi Patty Yes i did see the operative report. It DOES say total > capsulectomy was done........ I just don't trust this PS > Different reasons. He has lied to me on several occasions about > other things, and had no knowledge that is was even necessary, I > wondered if he had even performed a total capsulectomy before, and he > has NO belief the all these symptoms are related to the implants. But > he was the PS that implanted them, and was willing to explant > immediately. I will do some reasearch on this micoplasma, I > appreciate your input. We DO keep running into a lot of brick walls > with the medical field, don't we... This Molybedum.... you said you > took it is it still helping? And what was that I read about > parasites,,,,, WOW could it be that??? that I have??? is there > a test to find out? I'm so new at this. Trying to keep spirits up > and energy, as I work full time. At one point thought I was going > to Die. Still wondering. Hanging on for my kids.Hope i can find > something that will be useful to all you girls too. What a NIGHTMARE! > Thanks for caring. Hugs to you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 23, 2001 Report Share Posted May 23, 2001 Dear Patty: Please remind all that to treat mycoplasma without treating the yeast can lead to severe systemic Candiaiasis. . ----- Original Message ----- From: <summer234562001@...> < > Sent: Tuesday, May 22, 2001 10:58 AM Subject: To Patty > Hi Patty, > I am sorry for taking so long to post but have had no news until > yesterday, when I called the rheumatoid Doctor to find out if tests > came back. His nurse called me at 6 PM to tell me of the mycoplasma, > asked if I wanted to start on Minocycline and I was napping, so was > awoke out of a sleep, ......I said yes, she called in the Rx I > picked it up started taking it last night. I tried to call back to > find out how long the therapy is expected to last, but they had left > for the day, so I called this morning, and asked to have the Doctor > call me with info. I am now waiting for a call back. I asked for the > mycoplasma test as a matter of fact, because of info you had given > me about mycoplasma parasites etc. It stuck in my mind when I went > to the Rheumy, so I have YOU to thank for my even asking for the > test, He was guessing I think on the fibromyalgia before the tests > were taken. I took a test on line of questions refering to > fibromyalgia,( I forget the site now), but the reply I got back was > that I had something more serious, and that I should see a > physician,.....this was AFTER he said he thought I had > fibromyalgia.Anyway, I hope to find out how long I'm to be on > minocycline today. This Rx is for ten days 100mg twice a day, I am to > see him again in three weeks too. Hopefully I will know more then> I > AM SO SORRY TO NOT HAVE POSTED, I CAN BARELY MAKE IT OUT OF BED AT > TIMES. Plus, I had no clues on how to help anyone, even myself. But I > will keep you posted on what I learn. Thanks for the site Patty I > will check it out today. Love to ALL MAry > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2001 Report Share Posted May 30, 2001 Hi , So glad that this info has been able to be helpful. I am very interested in this mycoplasma area, so please keep me informed of your progress with your therapy. Did you find out how long your doctor recommended the therapy? Have you shown him the research info done by Dr. Nicolson on the Immed website? I really hope this helps you out, and that you can start to feel alive again. I know about the feeling of not being able to make it out of bed sometimes, so you don't have to apologize for not writing as often, we truly understand! I'll be continuing to pray for your recovery and good health... Love, Patty ----- Original Message ----- From: <summer234562001@...> < > Sent: Tuesday, May 22, 2001 7:58 AM Subject: To Patty > Hi Patty, > I am sorry for taking so long to post but have had no news until > yesterday, when I called the rheumatoid Doctor to find out if tests > came back. His nurse called me at 6 PM to tell me of the mycoplasma, > asked if I wanted to start on Minocycline and I was napping, so was > awoke out of a sleep, ......I said yes, she called in the Rx I > picked it up started taking it last night. I tried to call back to > find out how long the therapy is expected to last, but they had left > for the day, so I called this morning, and asked to have the Doctor > call me with info. I am now waiting for a call back. I asked for the > mycoplasma test as a matter of fact, because of info you had given > me about mycoplasma parasites etc. It stuck in my mind when I went > to the Rheumy, so I have YOU to thank for my even asking for the > test, He was guessing I think on the fibromyalgia before the tests > were taken. I took a test on line of questions refering to > fibromyalgia,( I forget the site now), but the reply I got back was > that I had something more serious, and that I should see a > physician,.....this was AFTER he said he thought I had > fibromyalgia.Anyway, I hope to find out how long I'm to be on > minocycline today. This Rx is for ten days 100mg twice a day, I am to > see him again in three weeks too. Hopefully I will know more then> I > AM SO SORRY TO NOT HAVE POSTED, I CAN BARELY MAKE IT OUT OF BED AT > TIMES. Plus, I had no clues on how to help anyone, even myself. But I > will keep you posted on what I learn. Thanks for the site Patty I > will check it out today. Love to ALL MAry > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2004 Report Share Posted February 24, 2004 Kim, Hey girlie, I'm concerned about you...you're too young to be suffering so. When you say your symptoms have reached a boiling point, what is going on? I know someone who went to Dr., and she lives in Manhattan. If you would like to get in touch with her, I will forward your message to her and hopefully she will respond to you. I think if you are looking for help in terms of someone telling you it's the implants and that you need to get them out, we can do that! If you are looking for someone to treat you for your symptoms, he may be able to help you, but keep in mind, he is a rheumatogist and is going to be giving you things from his little bag of tricks....be careful! In my opinion, you would be better off saving your precious money and putting it toward explant...I know you are struggling with the financial side of this, and the number one thing you need to do right now is get those puppies out of you Kim! There is no question about that. It's the first thing you need to do. That's just my two cents....let me know if you want to be put in touch with my girlfriend in Manhattan who has been to Dr. . Patty ----- Original Message ----- From: kim przybylski Sent: Tuesday, February 24, 2004 2:19 PM Subject: Fwd: RE: TO PATTY Patty, Hi how are you. Long time no talk. Well Ive been doing major reserach becuase my sysmptoms have reached a boiling poit. I have been speakining with Pyn over the phone and also spoke wth in Dr. Fengs office. She recomended DR gary a Rheumy in NY who specilizes in auto-immune breast implants and silicon, the only thing is he does not accept insurance and charges $450 for a visit. do you know anything about him and is it worth the money for hhim to confirm all my sysmptoms with having implants. please e-mail me back.thanks so much.anxious to hear from u. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2004 Report Share Posted February 24, 2004 yes i would like to get in touch with her. can you ask her to e-mail me personally. i read some about him and he beliveves in silicone and disease. dr fengs office reccommened him so i belive he will believe me. its expensive but i think he would be best to treat my dry eye i hope. thats whats killing me the most. still in finicial bound still cant afford it. my ps offered to remove them for free but i dont think he is skilled in explant and removing enbloc. he suggests i dont remove them to avoid severe depression, but i have that now because of symptoms i have no life. i am sure some women on the site can relate to dry eye and life stle changes. it sucks. i want him to confirm the auto immune from them and treat me. i seen his name in a few letters on the net that he studies patentients with these problems and beleieves us. --- In , " ~*Patty*~ " <redeemed7@c...> wrote: > Kim, > Hey girlie, I'm concerned about you...you're too young to be suffering so. When you say your symptoms have reached a boiling point, what is going on? > > I know someone who went to Dr., and she lives in Manhattan. If you would like to get in touch with her, I will forward your message to her and hopefully she will respond to you. I think if you are looking for help in terms of someone telling you it's the implants and that you need to get them out, we can do that! If you are looking for someone to treat you for your symptoms, he may be able to help you, but keep in mind, he is a rheumatogist and is going to be giving you things from his little bag of tricks....be careful! > > In my opinion, you would be better off saving your precious money and putting it toward explant...I know you are struggling with the financial side of this, and the number one thing you need to do right now is get those puppies out of you Kim! There is no question about that. It's the first thing you need to do. > > That's just my two cents....let me know if you want to be put in touch with my girlfriend in Manhattan who has been to Dr. . > Patty > > ----- Original Message ----- > From: kim przybylski > > Sent: Tuesday, February 24, 2004 2:19 PM > Subject: Fwd: RE: TO PATTY > > > Patty, > > Hi how are you. Long time no talk. Well Ive been doing major reserach becuase my sysmptoms have reached a boiling poit. I have been speakining with Pyn over the phone and also spoke wth in Dr. Fengs office. She recomended DR gary a Rheumy in NY who specilizes in auto-immune breast implants and silicon, the only thing is he does not accept insurance and charges $450 for a visit. do you know anything about him and is it worth the money for hhim to confirm all my sysmptoms with having implants. please e-mail me back.thanks so much.anxious to hear from u. Quote Link to comment Share on other sites More sharing options...
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