LongJourney said...
I’d like to thank everyone in this site. I’ve been in treatment for 8 months and I used to visit this site daily when things were bad. I have neuro lyme, and many times I thought I was losing my mind and was very depressed. Reading the posts helped me a lot. Although I never posted anything before, I felt I wasn’t alone in my struggle.
I suffered with migraines for many years until I saw a doctor on youtube saying that lyme can be misdiagnosed as migraines. My symptoms were a perfect match with neuro lyme, and there were a number of testimonies of people getting better in his channel. My GP didn’t want to treat me saying that there is no lyme in Texas. I made some phone calls, and the only doctor in my area that treats lyme doesn’t believe in long term antibiotics.
So, in a leap of faith, and in a bit of an impulse, I flew to Mexico to see the youtube doctor. My family and friends thought I was crazy, but I had to try.
The doctor took me to a lab to see my blood in a dark field examination. I could see the infected red blood cells. It was babesia. I also had giargia and other intestine parasites. Then, my blood was sent to a lab in Mexico City for testing. Three weeks later, it came back positive for borrelia, babesia and ehrlichia.
I’ve been rotating antibiotics and only started feeling better on the seventh month. The 70% is based on a list of symptoms and intensity compared to when I started treatment. I was in really bad shape. The fatigue, cognitive issues, speech problems, shortness of breath and pain were just horrible. People can’t understand how bad it is unless they’ve been through it.
I still get brain fog and fatigue when my hormones are fluctuating. But it’s less intense and I am not in pain anymore. I am back to my normal life, working, buying groceries, going on walks. I can sense a flare up coming hours in advance, so I go home and rest. Napping really helps. The flare ups last three to four days, but I now am able to function.
I’ve tried most of the detox methods (dry brushing, pinella, burbur, alka seltzer, Epson salt, even glutathione which is very expensive). Unfortunately, they made zero difference on my symptoms.
I hope my story helps someone keep hope alive. Treatment is long and it is really hard when you don’t see any improvement day after day, month after month. I don’t know if I will ever get to 100%, but I am grateful I’ve come this far.
Here is a list of the medicine I’ve taken in different times and combinations: clindamycin, chloroquine, doxycycline, metronidazole, nucleo cmp forte, clarithromycin, fluconazol, tinidazole, furazolidone.
Wishing you all a speedy recovery and happy new year.
70% is amazing. Congrats! Could you PM me your doctor's name and email? I am very curious about
getting treatment. How much were the consults and treatments?
I am desparate
Thank you,