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truthsearcher

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Everything posted by truthsearcher

  1. Castor, I had Darkfield Microscopy done on my blood as well by an ND. Those little white dots floating around were probably yeast/candida and I too saw with my very own eyes parisites swimming around. My ND called them 'blood parasites" but I know now they were lyme by all the pictures I compared. My red blood cells were very clumped and sticking...
  2. Hi Andrea. Could you please email me Carla's blog link? Thanks
  3. Yes stress flares my Lyme. Also stress causes you adrenals to work harder and many people with Lyme have adrenal fatigue or exhaustion which makes dealing with the smallest of stress almost impossible. When I;m stressed I often get the chills w/o fever, fatigue, severe brain fog, aches and pains throughout my whole body and a very hot flushed feeling...
  4. I sure have had those electrical feelings. I've had them sence childhood. It would be a huge jolt of pain in my neck then go away. This grew into constant pain in my cervicals as I got older. The pain is constant around the C5 area and shoots up into my occipital (back of head). I get tingly. prickly feelings all over and get the buzzing, electrical...
  5. Susie, Sorry to hear your getting the run around. When you see your LLMD you can list what Dr.s receive info concerning your treatment. I opted not to have info sent to my PCP for lots of reasons. I don't see him anyway and would only see him if I broke my leg. He's the one who diagnosed me with CFS and Fibro after a 3 minute visit and offered...
  6. I ordered my second round HW. Ordered on 5/10. Shipped on 5/13 and arrived 5/15. I was amazed at how fast they did my custom order. This time I got extra strength without cascara sagrada and psyllium. We'll see how it goes second time round Did the last one in January with good results. I think I'll start next week.
  7. Sarah, Sorry about Ezra. Definetly get treatment right away to erradicate it quickly. It can be done if treated very promptly. Susie, Yeah! You got the lab slip signed! Wow good news! Keep us posted! If you don't hear in two weeks give your Dr. a call because if they thing it's negative they may never call you. And make sure you get copies, both...
  8. LMA, What helps my horrid constipation is stuff called 3MA. It's Magnesium Oxide. I take 6 of those babies almost every night except when I'm taking my DMSA for my heavy metals. This has helped more than anything so far. It's made by Lane Medical. I get it through my health practioner. Also a cup of Rhubarb tea. Don't know if you can tolerate this...
  9. Yes I recall there are some Canadians on Lymenet who have Lyme. I think Peacesoul is one of them. You could browse around over there and check it out and pm some fellow Canadians and you'll gets lots of good advise. hth
  10. Hi Fedora. Thank you so much for thinking of my dd. My dd is exactly the same way you use to be. The only thing she can eat if she doesn't eat that very minute and gets sick is a banana. Weird huh? It surely sounds like a sugar low doesn't it? Thanks again, and I agree with what Carla said above.
  11. Hi again LMA, I talked to my LLMD about my kids IgeneX results, and he said "they were not remarkable", to not treat unless something really changed. My 6yo d has frequent tummy aches, odd aches and pains, has to eat in a seconds notice when she is hungry or gets ill that she can't eat. (I can't figure that one out?) So... this could be anything...
  12. Hi LMA, I can totally relate. I have 3 little ones to care for with Lyme, it's not fun. I have had many of the symptoms you have including a enlarged spleenic artery. I hope you are able to get the best of care with a LLMD. I went far too long without one. I am now on the road to recovery. On abx 2 months and feeling tons better but a ways to go...
  13. Hi Susie It really is worth it tho it is expensive. I don't know how much you already have invested in your health, but I have spent 10 years of my life searching, spending tons of money for treatments that never lasted. Seeing Chiros, Accupuncture, GI Drs, Orthopedic Drs. Holistic Drs. Naturalpaths, cranial, and osteopathic treatments, tmj specialists...
  14. Yeah right?????? and if you lived in NJ, the Dr. would say there no lyme in NJ, it's more likely if you lived in NY. Duh????? Clueless I say.
  15. Susie, Don't be discouraged. I expected that this would happen. It's happened to me multiple times and sometimes it wasn't so pretty. I had one Dr. tell me that my fibro was not curable and I needed drugs for the rest of my life, and that diet would have no bearing on my recovery. He wouldn't even offer the standard lyme test. Lyme is in NY. All...
  16. Lizard, I'm so happy to hear you making progress with your Dr. Great Work! Keep us posted. Patty, I agree with Carla, get your son to a LLMD. I hear Dr. J in Conn is the best. My son also has speech issues. Stuttering that comes and goes , now gets stuck and can't think of a word. It totally frustrates him because it could be a very simple...
  17. Just wanted to say hi susieg. I'm from Upstate western NY. Lyme is big here. Vets are dx'ing more and more cases of Lyme in this area than ever before in cats and dogs. My LLMD believes I've had Lyme sence I was 5yo. I'm 36 now, and misdiagnosed with Fibro/CFS for nine years. If you are anywhere close to me we have a awesome support group that...
  18. Lizard, I believe that there are others in N.C that treat Lyme. I checked there once because my in laws live there. There is one in Asheville. Don't know if thats close to you. The llmd there has a PA that works with him who charges much less and I've heard is very good. You could post in" seeking Dr's " at Lymenet as well for more info. I can also...
  19. Lonewolf and Tom I was nauseous in the beginning then it went away in about a week. I remember feeling raveously hungry after that. Imo I don't think eating within that 30 min would be bad if you are gonna get sick, but the idea is the paresites get a good dose of killer herbs before you eat so the worms arn't eating your good food. hth
  20. Our whole family did a 30 day round of HM. The cats absolutly hated the stuff. They would hide so I couldn't get to them with the pet syringe full of HM. I ended up not finishing d/t the traumatic experience for the cat's sake. Dogs may be totally different, they eat anything. My cat's are very particular. My two eldest dc age 6 and 8 finished...
  21. Hi. I've been diagnosed Fibromyalgia 9 years ago. All your symptoms and then some. Today have a positive Lyme diagnosis via Igenex western blot. My doctor tells me I never had fibro, it was lyme all along. I'm GFCFSF.
  22. Mftnchn, Hi do you mind sharing what Vit C and Mg you found helpful. I've tried all kinds of both to no avail. Very high doses do nothing. The only Mg I found that helped somewhat was 3A Magnesia by Lane Medical. I have to take the full dose of 6 at bedtime to get any affect and this is the complete colon cleanse. thanks BTW I'm GFCFSF as...
  23. Thanks for that post. I too chronic C for years and lost my gallbladder. All fiber acts like a plug in me. I had all the GI colonoscopys and barium studies as well. I have a very redundant, sluggish colon. Food goes through me like jagged glass and a bowling ball and still no bm. Feels like I'm having baby contractions. Avoiding casein and gluten...
  24. Count me in on the NO epinephrine (vasoconstrictors) I get all those symptoms that the dentists say is "perfectly normal" When I had my amalgams removed last year I had the septocane sp? without the epi and had no problems whatsover, I just had to get more frequent shots because the numbness wore off more quickly. Also worthy of note is those...
  25. Yep just about every poop remover known to man. Mega doses of Vit C do nothing. Milk of Mag doesn't touch me anymore. I drink Turkey Rhubarb tea in combo with something called 3mA magnesia and this gives me at least something once a day. Thank God without it, nothing. I really think the lyme messed with my digestion big time. I have to address...
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