Guest guest Posted June 21, 2002 Report Share Posted June 21, 2002 Hello Gang, Oldtimers may recall some of my posts about the incredible benefits I've had with Bee Venom Therapy (BVT). I'm the PWC that took the road less traveled, and am in my FOURTH 100% REMISSION from CFS/FM by getting stung with live honeybees! Most PWCs are skeptical because it's so outside the box of known therapies for this DD, but that's exactly why I decided to try it. Early on in my illness (7 1/2 years full blown from sudden onset + previous 4 years with milder symptoms) I realized that we share a lot of symptoms with MS and decided to give it a try because it had helped thousands of MS patients. Now, I know that we have a lot of possible causes and pathogens in common with MS. Bee venom has truly been a Godsend for me! It gives me lots of energy, got rid of my FM pain, cognitive and neurological symptoms, IBS, and all the rest of my CFS/FM symptoms. As a bonus, it gives me a feeling of well being (it's a mood elevator) and it's believed to have cancer protective properties. Bee venom is also used to treat various cancers effectively. Since PWCs are predisposed to a higher incidence of cancer, this is an additional bonus. I've included some Medline references below on studies conducted on melittin, apamin and other components of bee venom that are effective for various cancers. In spite of all the anecdotal and scientific studies showing that bee venom is very effective for many diseases, pharmaceutical companies aren't interested in researching whole bee venom because it's a natural product and can't be patented -- there's no money to be made! Components of bee venom continue to be researched because they can be added to other chemicals and can then be patented. I've been experimenting with BVT for over 5 years and now, I'm convinced it could help other PWCs -- not just from my experience, but because others with CFS/FM are reporting similar results. When I first wrote about my first remission with BVT to this list in 12/99 (copy of this post can be found on Corina's website @ http://www.angelfire.com/stars/cfsrecovery/alternative.html and in list archives) I had just started another round of BVT. Since then, I continued to sting for almost two years averaging 4-6 stings every other day. I did not stop stinging through my second 100% remission that lasted 4 months but relapsed after I came down with a cold. I didn't relapse with the first cold, but the second one got to me! Two months after my third 100% remission, I decided to test the waters and stopped stinging after almost 2 years. I felt 100% " normal " with no stings for 2 more months -- then relapsed! I immediately resumed stinging in January 2002 and am in my fourth remission for over 3 months. What makes this remission even more remarkeable is that I came down with the flu in February 2002, with a fever of 104 that knocked me down for a month (I refuse to get flu shots) and still bounced back to another 100% remisssion! Presently, I'm still using 6 stings every other day. Next time I decide to stop BVT, I will try a maintenance dose -- 2 stings once a week to see if it's effective in keeping things in check. I was advised to use a couple of stings weekly, but never adhered to a maintenance dose since I don't have my own beehive. Having a steady supply of bees year round is not a problem thanks to a couple of companies that ship bees for BVT by mail. Between these four 100% remissions, I fluctuated between 75-95% (function and symptoms) since I began using BVT. I also was able to wean myself off Florinef 2 1/2 years ago when it stopped working for me. It helped with severe NMH episodes that usually left me in a semi-comatose state for several hours. After I stopped using it, I was able to abort them within 15 minutes with just 4 stings on my spine (sounds painful but it's one of the least painful areas to sting). I haven't had any NMH symptoms since then. For me, they were the most debilitating symptoms that left me in a vegetative state. I was unable to stand, sit or think at all! I don't fully understand why BVT worked. Bee venom has a vasodilating effect and is supposed to lower blood pressure -- just the opposite of what I want for NMH! The only possible explanation I can come up with, is that scientific studies indicate that bee venom is an anticoagulant, has a stabilizing effect on blood pressure, the HPA axis (stimulates the pituitary to produce ACTH which stimulates the adrenal glands to produce cortisl) and the autonomic nervous system. In 1972, research conducted at Walter by Vick and on dogs and monkeys documents the rise in their cortisol levels. It probably also had an effect on my " leaky " mitral valve since one of the many substances of bee venom is cardiopep, which has beta adrenergic and anti-arrhythmic properties Dr. Theo Cherbuliez, President of the American Apitherapy Society, www.apitherapy.org, helped me to get started with BVT. He wrote the chapter, Bee Venom in the Treatment of Chronic Diseases, in the book Bee Products: Properties, Applications and Apitherapy (Mizrahi, A. and Lensky, Y. Editors) Plenum, London, UK 1997, pp. 213-220. To explain why bee venom is effective for many chronic diseases, he wrote, " Bee Venom includes some forty components, of which a dozen have been extensively examined. They include 11 peptides, 5 Enzymes, 3 physiologically active Amines, Carbohydrates, Lipids and amino-acids. Of the peptides, the most represented are Melittin, Apamin, Mast Cell Degranulating Peptide and Adolapin. All together, they have systemic actions: anti-inflammatory, anti-fungal, anti-bacterial, anti- pyretic, stimulating ACTH, stimulating vascular permeability. The Enzymes, act on the cardiovascular system and locally at the point of administration of the venom. In the most summarized way one can say that Bee Venom acts on the immune system, redirecting some of its faulty mechanism. Bee venom acts on all afflictions influenced by cortisone, however without any of the side effects of the drug. " " As for the constituents, adolapin has an analgesic effect.* Phospholipase A2 decreases arterial pressure and heart rate, and increases capillary permeability.* Melittin lends anti-bacterial and antifungal properties, and increases resistance to radiation.* Cardiopep possesses anti-arrhythmic properties. Bee venom is a vasodilator, which increases local circulation, and works against spread of bacteria, countering arthritis.* Note that little research has been done in this country regarding bee venom, however, considerable studies have been conducted in Europe which indicate it's efficacy. " With CFS or any chronic disease, the immune system is stuck in the " chronic mode " . Bee venom challenges the immune system, giving it an opportunity to rebalance itself so the body can heal itself. Every time I start a new round of BVT, I experience a " healing crisis " (herxing with fever and flu-like symptoms) and swelling and itching on sting sites. In the early stages of therapy, they're excellent indications that the immune system is responding and that BVT will be effective. Herxing doesn't last long (for me about 2 days 3-4 times) and swelling and itching lasts about a month until the body becomes used to the venom. Hamerman, the father of homeopathy, said, " You can never cure a chronic illness, the best you can hope for is to make it acute, and then you can cure it. " Since a small percentage of the population (.5-2%) is allergic to bee venom resulting in anaphylactic shock, there are safety measures that are always followed -- no one has ever died from BVT! I don't take any medications for CFS/FM. Besides BVT, I use fresh pollen, royal jelly, honey, propolis, a multivitamin, vitamin C, folic acid and probiotics daily. I still take monthly cyanocobalamin B12 shots -- it's all my doctor is willing to give me. I have been taking thyroid medication for 11 years, after my thyroid was destroyed with radioactive iodine when I was treated for another autoimmune illness, Graves' disease. This month, I went for my annual thyroid checkup and tests showed that I could lower the dose of thyroid medication I've been using all these years! I urge those that find this information too good to be true, to research bee venom on their own, and hope that some of you will finally take the BVT plunge! For all still searching that elusive magic bullet, I offer you hope. I am living proof that, in spite of everything our bodies have been subjected to, most of the damage is reversible. I'm 53 and in the early stages of menopause (no symptoms -- BVT of course) and haven't felt this good in over 11 years! Thanks to the humble honeybee, I know what " normal " feels like once again. For the scientific minded, references are below. Bzzz... " All truth passes through three stages: First, it is ridiculed; Second, it is violently opposed; and Third, it is accepted as self- evident. " -- Schopenhauer REFERENCES 1. Marsh NA, Whaler BC. The effects of honey bee (Apis mellifera L.) venom and two of its constituents, melittin and phospholipase A2, on the cardiovascular system of the rat. Toxicon. 1980;18(4):427-35. No abstract available. PMID: 7210027 [PubMed - indexed for MEDLINE] 2. Lin SC, Huang TF, Ouyang CH. Characterization of the purified anticoagulant principles from Apis mellifera (honey bee) venom. Taiwan Yi Xue Hui Za Zhi. 1983 May;82(5):629-39. No abstract available. PMID: 6579218 [PubMed - indexed for MEDLINE] 3. Ouyang C, Lin SC, Teng CM. Anticoagulant properties of Apis mellifera (honey bee) venom. Toxicon. 1979;17(2):197-201. No abstract available. PMID: 442111 [PubMed - indexed for MEDLINE] 4. Vick, J.A., G.B. Warren and R.B. . (1975) The Effect of Treatment with Whole Bee Venom on Daily Cage Activity and Plasma Cortisol Levels in the Arthritic Dog. Am. Bee J. 115, 52-53,58. 5. Couch TL, Benton AW. The effect of the venom of the honey bee, Apis mellifera L., on the adrenocortical response of the adult male rat. Toxicon. 1972 Jan;10(1):55-62. No abstract available. PMID: 5015541 [PubMed - indexed for MEDLINE] 6. Marsh NA, Whaler BC. The effects of honey bee (Apis mellifera L.) venom and two of its constituents, melittin and phospholipase A2, on the cardiovascular system of the rat. Toxicon. 1980;18(4):427-35. No abstract available. PMID: 7210027 [PubMed - indexed for MEDLINE] 7. Bee venom enhances guanylate cyclase activity. Science. 1981 Jul 17;213(4505):359-60. PMID: 6113689 [PubMed - indexed for MEDLINE] http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve & db=PubMed & list_uids=6113689 & dopt=Abstract 8. Vick JA, Shipman WH, R Jr. Beta adrenergic and anti-arrhythmic effects of cardiopep, a newly isolated substance from whole bee venom. Toxicon. 1974 Mar;12(2):139-44. No abstract available. PMID: 4152790 [PubMed - indexed for MEDLINE] 9. Vick JA, Mehlman B, R, Philips SJ, Shipman W. Effect of the bee venom and melittin on plasma cortisol in the unanesthetized monkey. Toxicon. 1972 Oct;10(6):581-6. No abstract available. PMID: 4198739 [PubMed - indexed for MEDLINE] 10. Vick JA, Shipman WH. Effects of whole bee venom and its fractions (apamin and melittin) on plasma cortisol levels in the dog. Toxicon. 1972 Jun;10(4):377-80. No abstract available. PMID: 5070576 [PubMed - indexed for MEDLINE] 11. McHugh SM, Deighton J, AG, Lachmann PJ, Ewan PW. Bee venom immunotherapy induces a shift in cytokine responses from a TH-2 to a TH-1 dominant pattern: comparison of rush and conventional immunotherapy. Clin Exp Allergy 1995; 25:828–838. [MEDLINE] http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve & db=PubMed & list_uids=8564721 & dopt=Abstract 12. Kosnik M, Wraber B. Shift from TH2 to TH1 response in immunotherapy with venoms. Pflugers Arch 2000;440(5 Suppl):R70-1. [MEDLINE] http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve & db=PubMed & list_uids=11005617 & dopt=Abstract 13. Shipman WH, Cole LJ. Increased resistance of mice to x-irradiation after the injection of bee venom. Nature. 1967 Jul 15;215(98):311-2. No abstract available. PMID: 6059526 [PubMed - indexed for MEDLINE] 14. Vick, J.A. and , R.B. 1972. Pharmacological studies of the major fractions of bee venom. Amer. Bee J., 112 (8): 288-289 15. Saini SS, Chopra AK, JW. Melittin activates endogenous phospholipase D during cytolysis of human monocytic leukemia cells. Toxicon. 1999 Nov;37(11):1605-19. PMID: 10482394 [PubMed - indexed for MEDLINE] 16. Wu YL, Jiang XR, Newland AC, Kelsey, SM. Failure to activate cytosolic phospholipase A2 causes TNF resistance in human leukemic cells. J Immunol. 1998 Jun 15;160(12):5929-35. PMID: 9637506 [PubMed - indexed for MEDLINE] 17. Winder D, Gunzburg WH, Erfle V, Salmons B. Expression of antimicrobial peptides has an antitumour effect in human cells. Biochem Biophys Res Commun. 1998 Jan 26;242(3):608-12. PMID: 9464264 [PubMed - indexed for MEDLINE] 18. Shin SY, Lee MK, Kim KL, Hahm KS. Structure-antitumor and hemolytic activity relationships of synthetic peptides derived from cecropin A-magainin 2 and cecropin A-melittin hybrid peptides. J Pept Res. 1997 Oct;50(4):279-85. PMID: 9352466 [PubMed - indexed for MEDLINE] 19. Wachinger M, Saerman T, Erfle V. Influence of amphipathic peptides on the HIV-1 production in persistently infected T lymphoma cells. FEBS Lett. 1992 Sep 14;309(3):235-41. PMID: 1516693 [PubMed - indexed for MEDLINE] 20. Gerst JE, Salomon Y. Inhibition by melittin and fluphenazine of melanotropin receptor function and adenylate cyclase in M2R melanoma cell membranes. Endocrinology. 1987 Nov;121(5):1766-72. PMID: 3665846 [PubMed - indexed for MEDLINE] 21. Bernard PJ, Bazan M, Seagar, M. [Effect of apamin on the action potential and cell current of neuroblastoma N1E 115] Rev Med Chir Soc Med Nat Iasi. 1986 Jan-Mar;90(1):93-100. French. No abstract available. PMID: 3764186 [PubMed - indexed for MEDLINE] 22. Hait WN, Grais L, Benz C, Cadman EC. Inhibition of growth of leukemic cells by inhibitors of calmodulin: phenothiazines and melittin. Cancer Chemother Pharmacol. 1985;14(3):202-5. PMID: 3995682 [PubMed - indexed for MEDLINE] 23. Spoerri PE. Changes induced by apamin from bee venom on differentiated mouse neuroblastoma cells in culture. Acta Anat (Basel). 1983;117(4):346-54. PMID: 6666537 [PubMed - indexed for MEDLINE] 24. Hugues M, Romey G, Duval D, JP, Lazdunsky M. Apamin as a selective blocker of the calcium-dependent potassium channel in neuroblastoma cells: voltage-clamp and biochemical characterization of the toxin receptor. Proc Natl Acad Sci U S A. 1982 Feb;79(4):1308-12. PMID: 6122211 [PubMed - indexed for MEDLINE] 25. Jentsch J. [On the biological activity of the bee venom melittin] Z Naturforsch B. 1969 Feb;24(2):263. German. No abstract available. PMID: 4388835 [PubMed - indexed for MEDLINE] 26. Cerrato PL. A therapeutic bee sting? RN. 1998 Aug;61(8):57-8. Review. No abstract available. PMID: 9739302 [PubMed - indexed for MEDLINE] 27. Fisher RB. Bee venom and chronic inflammatory disease. N Z Med J. 1986 Aug 27;99(808):639. No abstract available. PMID: 3462567 [PubMed - indexed for MEDLINE] Quote Link to comment Share on other sites More sharing options...
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