Has Any One Tried Bee Sting Therapy With Fibromyalgia?

Bee venom is Histamine. We don't need Histamine. We need decongestant; big difference. With the decongestant, we need an expectorant. The most important thing for Fibros is to know which Version of FMS you have. Test Thyroid. If it's ok, test Saliva pH. Then you know what you are dealing with. You can look on the all free site FibroFix and see how to treat FMS based on the version you have. The truth is setting us free.

My mother in law suffers from fibromyalgia and I tell you the poor lady gets stung by bees naturally about 3-4 times every summer and it doesn't help. Maybe she hasn't been stung enough.....but who would want to be stung more?

I've never heard of anyone doing a study on BVT for Fibromyalgia. I wouldn't be part of such a study. Pain tends to snowball for me so no thanks. I've seen a couple of shows on tv about it but I found it to be less than scientific. It could actually be something in the venom that works for MS sufferers or it could just be a massive dose of their own endorphines. But like with many things what works for some is BS to others. If it helps someone, whether it be psychologically or physically, I say more power to them. I hope they raise their own bees cause there's a shortage of them right now! Personally if I want a dose of pain with an endorphine chaser I'll go get a tattoo. Me and stinging insects don't get along too well together.

I have never heard of this for treating Fibromyalgia. What if you are allergic to bee stings which many people are allergic to them? I am not sure that it would be something I would want to try.

I hate bee's but I have suffered from Fibromyalgia for at least 10 years and if it does work, I would be the first one in line for it. I totally freak out at the site of a bee and have been stung numerous times but that was before the fibromyalgia. if you get a true answer to this please let me know because I am so tired of suffering. Do you suffer from fibromyalgia also? I used to get so upset when they first labeled it as ALL IN YOUR HEAD. I would get so angry and then I finally found this site that totally describes it to a T. As I was reading it, I was amazed at all the detailed information and how it seemed like whoever wrote about it had been living in my body and feeling my pain. Doctors used to look at me like I was crazy and it was really upsetting. I would spend hours on hours at the Arthritis Doctors office only for him to feel my muscles for about 2 minutes and say "Yep you still have it". I finally told my primary I wanted to drop that Doctor. It took me an hour to get to his office and an hour home. I would wait sometimes 3-4 hours for him since he always ran late. This Doctor was never on time and it was a true waste of money, my time and milage on my car just to hear the same thing. He never had any new meds that he could offer to help me. He did tell me that I would be living off of pain meds for the rest of my life and I am. Although I am allowed a rather large amount of medication due to all my problems, I take about half of what I am allowed. The reason for that is because when I had to have heart surgery, they couldn't give me anything that was strong enough to take the pain away and I was screaming on the table while I felt all they were doing. I would suggest to anyone out there that even if your allowed the max of pain meds, don't take them all because when it comes time for major surgery, you will find yourself suffering in a lot more pain than the fibromyalgia. Please do get back to me if you find out the truth about this and I will do the same for you.

I heard it before,it is useful to some disease!It is funny,but I wouldn't try it!