Posted 6/13/2019 10:50 PM (GMT 0)
Started the Byron White protocol for lyme disease. Have been using for almost a month now off and on. I have had lyme disease now since March of 2012. Used a lot of antibiotics (9months at one time) different protocols etc. Work for a while then start in not feeling well. First had all the symptoms of lyme, bullseye rash,inflammation, horrible leg spasms that knocked me to the floor, headache, fatigue, brain fog, aching, stabbing pain in head. Stabbing pain in leg had to use crutches. Then would later go into other leg and on crutches. So was on crutches off and on for a while. Haven't had that again for a few years so thankful for that. Seems like anywhere that I have had injurys I hurt when I have a flare up. I seem to have fibromyalgia now where I just ache especially on top part of my arm where I can barely raise my arm without pain.I have been bed fast and so sick I couldn't eat (metal taste in mouth). Learned to eat right with no wheat, sugar, milk products. Mess up occaisional and I can really feel it. Have to detox with epson salt baths 4 cups epson salts and 1 cup baking soda to warm water not hot at least 1 x week or more. Hot water makes me sicker and will have major herx. Have had horrible achy pain all over, fatigue, other symptoms and now using the A-L complex, my naturapath dr has had me on. Started out with 2 drops and now up to 16. Get nauseated, major pain in body where I can't sleep just feel achy like flu all over at times.I stop to give it a rest a couple days and start to feel a little better then when I start back up the same herx reactions. I have taken the alka seltzer gold some have used for detox and the burbur penella. Seems to help some. Not sure how long I am suppose to be on this just hoping it will help. I had a bad reaction to my antibiotics so am not using them anymore. I had hives break out and then left horrible bruises all over my arms like someone beat me. They have faded some after almost 2 years but you can still see them. Really weird stuff this disease has. Any others had any improvement with the A-L Byron protocol? Thanks