truthsearcher

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...

Hi Andrea. Could you please email me Carla's blog link? Thanks

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...

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...

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...

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.

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...

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...

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

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.

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...

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...

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...

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.

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...