Re: Bee sting therapy-Looking for Answers

[Guest guest]

Hi again ArshadIt's so good that you finally found someone to help you in your

beesting therapy quest. :)I'm sorry to say that I cannot recommend w to be stung

as I have no experience in this therapy.

http://www.beevenom.com/beevenomtherapy.htm, From 'How stuff works':'Q: Where

does one get stung? Does it hurt?A: BVT has been done literally from head to toe

(except the eyes and inside the ears). The particular location(s) for getting

stung vary depending on the particular symptoms being treated. Bee stings can be

unpleasant, temporarily leaving swollen, itchy bumps on the skin. But the

" stingy, " hot feeling usually lasts for less than a minute.To reduce these side

effects, many use a light fan or a hot, wet washcloth on the site of the sting.

Others, however, are convinced some reaction to the sting is essential to

successful therapy.' I would REALLY suggest that you invest in some of the many

reputable books on BST because they should give you the correct sites.I know my

answer won't have been much of a help, but I just wanted to let you know that it

is fantastic to hear that you've found a way to get what you were after!

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: a_islam69@...

Date: Sun, 26 Feb 2012 12:37:47 -0800

Subject: Bee sting therapy-Looking for Answers

Dear all,

I am a person with Primary progressive multiple sclerosis, being diagnosed in

2004, am on wheelchair for over two years, and living in Australia. I have been

reading about the bee sting therapy as one of the potential treatments and has

been of great help to people like me. I have been overseas and have started the

bee stings mainly on both sides of my spinal cord on my back, from top to botom

and the affected parts ( both hands and legs) through a local beekeeper @ 30

(average) stings per day and three times a week.

[Guest guest]

Hi Arshad,

Primary Progressive MS was the diagnosis given to the husband of Bradley.

In September of 2002, he began taking Low Dose Naltrexone (LDN), and it quickly

halted the progression of his illness.

Ms. Bradley wrote a book about her husband's successful conquest of PPMS, " Up

The Creek With A Paddle. " For more information about her book, visit

http://tinyurl.com/bk9m8c

There have been two clinical trials of LDN for progressive forms of MS, one in

Germany and one in Italy. For more information, visit

http://tinyurl.com/ldn-trials

For more information about LDN in the treatment of MS, visit

http://tinyurl.com/intro-to-ldn

With best wishes,

Dudley Delany

http://profiles.yahoo.com/dudley_delany