Re: Re: Foot Pain--Please HELP!

[Guest guest]

Tom .. thanks I have looked at this site before....what one do you think would

be good for a 12 & 16 year old girls...? Thanks again!! Diane

On Tue Apr 26th, 2011 2:53 PM CDT Tom wrote:

>Immediate but temporary foot pain can be helped by Transcutaneous Electrical

Nerve Stimulation A TENS machine cost about $50 and if used properly work well,

they also stop muscle jerks and twitches by keeping a constant current running

through the nerves, When the right frequency is found there is no pain or

discomfort. I have used this site and had no problems. TOM

>

>http://www.medicalproductsonline.org/?gclid=CI3P9uD6uqgCFcm8KgodQBMHFg

>

>

>>

>> How much did the rife machine cost?  thanks

>>

>>

>>

>>

>> ________________________________

>> From: <msadams@...>

>>

>> Sent: Mon, April 25, 2011 10:24:49 AM

>> Subject: RE: [ ] Foot Pain--Please HELP!

>>

>>  

>> Usually foot pain like that can be indicative of Bartonella. For my wife she

>> was not able to get relief from it until she started using a Meissner DP100

>> rife machine.

>>

>> Perhaps others can suggest different treatments.

>>

>>

>> www.lyme-resource.com

>> You can lead a person to a fact, but you can't make them think! -

>>

>>

>> > [ ] Foot Pain--Please HELP!

>> >

>> > Hi, I've been 'lurking' here for awhile, but have never posted.

>> >

>> > Long story short: RA type joint pain started about three

>> > years ago. I went to a Naturopath, who was able to help the

>> > joint pain and swelling with diet, but then other problems

>> > and symptoms started piling up. The bloodwork did not support

>> > an RA diagnosis, so we pursued the problem with diet and

>> > homeopathic/naturopathic remedies. But the increased number

>> > and intensity of symptoms added up to Lyme, Babesia, Barts

>> > +/or others. Delays in testing were due to my big issue of

>> > lack of money (I am nearly unable to work at all - I am a dog

>> > groomer), and refusal of insurance co to pay for anything

>> > beyond (as in useless) test.

>> >

>> > I've now suffered anything and everything from liver enzyme

>> > issues that refuse to clear up, bleeding retina, continuing

>> > (though decreased with diet) joint pain, eye pain, eye

>> > floaters, recurring fevers, air hunger and dry cough, nearly

>> > constant swollen glands, sinus-like headaches,

>> > stomach/digestion problems and pain, distended 'gut',

>> > sharp-quick-stinging pains all over random parts of body,

>> > random itchiness, facial tics, jaw and ear pain, chronic sore

>> > throat, tooth pain, dry skin, hair loss, calf and foot pain.

>> >

>> > I finally got enough money together (along with help from the

>> > LymeTap program) to get testing done, and blood was drawn and

>> > sent in for testing at SpiroStat this past week.

>> >

>> > Now, the reason I am finally posting - the FOOT PAIN!! OMG,

>> > the pain in the soles of my feet, which I thought was plantar

>> > faciitis this whole past year, has gotten so bad in the last

>> > few months, I am nearly reduced to tears several times a day,

>> > every day.

>> >

>> > Believe me, this means BAD pain, as I have learned to live

>> > with a consistently high level of constant pain, all day, every day.

>> >

>> > I cannot take much of any kind of pain killer, as my liver

>> > function has been compromised for the last few years. A

>> > condition probably associated with whichever co-infection I

>> > have, but also probably exacerbated by the huge amounts of

>> > Tylenol Arthritis I was taking for the year before I found my

>> > dr for the joint pain and swelling. I was just trying to

>> > make it so I could work each day, but it played hell on my poor liver.

>> >

>> > So, has anyone got any good treatments for the foot pain

>> > until I get my test results back and my dr can start

>> > whichever treatments I need? Please! I think I'm going to

>> > lose my mind sometimes, it is so bad.

>> >

>> > My feet feel like they will explode when I step down on them,

>> > and the sharp shooting pains that go right up the calf

>> > muscles, can just about take me down. It is horrible, and

>> > I'm at my wits end.

>> >

>> > Thanks in advance for any ideas you may have.......

>> >

>> > Toni in Oregon

>> >

>> >

>> >

>> > ------------------------------------

>> >

>> > Lyme Disease News continually updated from thousands of

>> > sources around the

>> > net: http://www.topix.net/health/lyme-disease

>> >

>> > MedWorm: The latest items on: Lyme Disease

>> > http://tinyurl.com/23dgy8

>> >