The Truth

I am writing because I am reading some disturbing posts on here and people are not getting the correct information from Doctors. Even most LLMD do not have the correct information.

 

Chiari Malformation I is a co infection of Lyme disease. Plain and simple.

 

I know. I was shocked too. I didn't find out until recently.

 

I am 51 years old, had my first child 16 years ago. This is when I found out I had Chiari Malformation. 

 

My whole life I've been sick, but for the 20 it's been worse.

 

I broke out with EBV (Ebstein Barr Virus) last year which led me to Lyme. I had just been diagnosed with Lyme and co infections.

 

If you want to learn more and get to a REAL doctor in any state, please join FB "Lyme disease and co infections".  There are administrators there to help you with anything you need help with.

 

This is a covered up disease by the government. Look up "Plum Island" and you will read the truth in all this. It is a cover up and that is why it is not covered by insurance. They would have to recognize it then.

 

People are dying of this and committing suicide and it makes me sick. I just hope no one reading this decides to choose that.

 

There are so many ways to help you get better along with antibiotics (abx).

 

Please join the site and let the high qualified people help you. I have belonged to it for over a year and cannot believe all that I have learned.  God be with you all.

Yes, it is caused a co infection but I am not sure of which one. The administrator on that FB has the information on that. When I found out, from his site, I was too upset to even care to ask frankly. I have just been diagnosed with Lyme and I also have co infections. I won't go to see my LLMD (Lyme Literate Medical Doctor) for a couple of months. It won't be until then that I will get the correct testing. If you've had a western blot for testing the accuracy rate is not good. There are so many false negatives. Treating with a LLMD, they will go over your history, do testing and do treatment based on clinical diagnosis. A regular MD will not do this. Even if you are positive on a blood test, a regular MD will only give a couple weeks to a month of meds which is not enough.

There is a lab called Igenex in California that does much better testing and this is what people are forced to use because a western blot by a regular lab is not enough.

Please, if you can join the FB site you will learn so much information. I have had this for so long and have researched it for a year because I suspected.

The site again is: Lyme disease and it's co infections.

There are so many people there that can help you.

Good luck and hope to see you on there!  (my name is Wendy)

I didn't come here just to get people to join another group. I came here for information to help myself and it doesn't matter how long people have been here. They still aren't clear on their facts.

Don't worry. I won't post on this site anymore.