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Lyme Disease gives you DEPRESSION-Anxiety and Anger.. SUICIDE..GET CHECKED
Ms Sans Serif
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[quote:Anonymous Coward 26741443:MV8yMDY2MDc4XzM0NzY0Mzg0X0Y1MjY1OTE0] [quote:Anonymous Coward 27243618:MV8yMDY2MDc4XzM0NzY0MTg3XzZGQUJEQ0Mw] [quote:Anonymous Coward 26741443:MV8yMDY2MDc4XzM0NzY0MDc0XzcwRjhGQjgy] [quote:Anonymous Coward 27243618:MV8yMDY2MDc4XzM0NzYzNzM0XzhDMEMxMEJB] I agree 110% with OP. I've had lyme and still have it. I caught it somewhere in Northeastern Ohio where I live. About 8 years ago a new symptom would appear every two weeks. I have no clue when I was bitten, I never even saw a stupid rash. I honestly suspected a nasty horsefly bite but I'll never know and that isn't the point. I kept going back to the family dr with new symptoms. He was puzzled. We tested for everything possible. Syphilis, HIV etc. The generic family dr lyme test came back negative. I honestly thought I was losing my mind. My Dr wanted me to go to a neurologist and claimed that everything pointed towards MS. Great, MS is almost identical in symptoms but MS treatment doesn't do crap. I was 27 years old at the time. So I convinced my Dr to draw my blood one last time and send it to a lab that specializes in Lyme. I finally found an answer to all the retarded 70 symptoms I had. So i went and visited a Lyme dr across the border into Pennsylvania. He started me on high dose, long term antibiotic treatment because my family dr would only give me 30 days of doxycycline according to the CDC(what a joke that was). So about 4 years of antibiotics got me to a point of symptom free. But when I stop antibiotic treatment, the symptoms start to slowly creep back after about a month. So what I do is just one doxycycline pill per day to keep the symptoms away. It's much better to take just one a day then have those nasty symptoms return. I have also had to take acidphilus the entire time to keep the good bacteria living in my intestine. I also take an antifungal every 3 months to keep the yeast at bay. I had tried many different alternative treatments for lyme but found that doxycycline was the cheapest and worked the best. My lyme Dr noticed that different antibiotics worked for different people or strains of the lyme bacteria. I also tried just about every antibiotic possible while experimenting with my Lyme Dr. The other challenge is treating the stupid co-infections that come along with the insect bite. Below are some of the treatments I tried. Cats claw(samento),garlic, oregano, olive leaf extract, hh capsules, black walnut, clove, nano silver, grapefruit seed extract etc etc Doxycycline, Roxithromycin, Clarithromycin, Bactrim, Amoxicillin, Levaquin(that stuff was hell), Cipro, Pennecillin, Tetracycline, Minocycline, Flagyl, Rifampin, Keflex etc etc Below are my symptoms at the peak of the illness. Depression Anxiety Increase eye floaters Night sweats on my head and chest area only(drenching) tingling on one side of face stange images in peripheral vision double vision flashes of light in my vision during the day flashes of light at night when i close my eyes feelings of impending doom or death in the middle of the night(severe panic attack) insomnia uregency for a nap in the middle of the day anger at about 3 pm every day light headed brain fog forget common words weak muscles joint paint(especially in lower back) and old injuries tingling sensations on hands constant muscle twitches irregular heart beat, heart palpitations worse hangovers from very little alcohol lack of interest in hobbies increase in face tingling when laying down excessive saliva constant thirst light sensitivity(wore sunglasses, even on rainy days) Pain on bottom of feet in the AM swollen gland in neck, near ear and jaw swollen glands in armpits pain in gall bladder area etc etc etc [/quote] OMG. You poor thing. Please try the teasel. You will never regret it. [/quote] Thanks. I don't feel bad for myself. I don't even talk about lyme much anymore. But I just had to post my story out there because I really feel bad for those that might have it and not know what the heck is wrong with them. I've heard of Teasel. Is there a more exact name for it? Some kind of root? [/quote] I had almost all of your symptoms. I couldn't move. I felt like I was dying. Teasel really helped. And everyone I know who has used it has found immense relief. I truly believe I'm cured. Yes, it is a tincture. Read Matthew Wood. He has a book. http://www.lyme-disease-research-database.com/lyme_disease_blog_files/mathew-wood.html Also, check out http://www.ladybarbara.net/html/using_teasel.html This woman really inspired me. There is a picture of her with the weed. I'm sure you've seen it at some point on the side of the road...or growing wild in fields. http://www.amazon.com/Teasel-Root-Tincture-LYME-Organic/dp/B0067C5LWM I bought on Amazon. This is what I used. Good luck. I've been there. It's horrible. You can turn it around. :hf: [/quote]
They go hand in hand. Many new reports. Get checked if you haven't. iGenix blood test in California..It could save your life! Do you have any weird symptoms that can't seem to be cured your entire life? Approx. 1 BILLION people have LYME disease on earth according to many researches. Since this is a biological WEAPON, nobody is excluded, even Ex President BUSH!
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