Chronic Neurological Lyme Treatment

Chyanne is 10 years old and has been battling late stage neurological Lyme disease hard core for the last two years.

She has had it undiagnosed for 6 years before being diagnosed at age 8.

Chyanne has been treated 4 times by 4 different doctors all non-Lyme literate doctors.

We have since had to seek a very special dr. out of New York City thanks to a corrupt and conspiracy over treatment protocol for neurological late-stage Lyme disease.

We have to pay 100% out of pocket.

The problem is there is no time to save for the cost of her treatment or even the start of getting her treated.

She is not doing well since the last IV antibiotic treatment and needs to be treated ASAP due to her declining health issues.

They can cause long-term damage to her as she gets older; Lyme disease has already robbed her of her childhood.

The cost to get started with Dr. Elena Frid is $3,000 ($1500 for consult; the rest for extensive testing which she needs and never got thanks to the "protocol").

Dr. Frid truly is our last hope to get Chy better from this chronic disease.

Follow-up visits and medications are also very expensive.

Living here in NY most of us are living pay check to paycheck as it is.

Without the help of Dr. Frid, Chyanne could end up with no quality of life taking medications just to cover her symptoms like so many other victims of Lyme disease (and that's what the PROTOCAL wants).

I'm not one to ever ask for help; I am always doing the helping, but I have no choice.

There is no time to save my weekly left-over pennies as she needs treatment now.

Chyanne does not go to school and hasn't for well over a year. This is no way of life for my little girl.

Half or our problem has been solved and that was finding a Lyme literate doctor.

Thank you all in advance weather you donate or not al;l the support from the Lyme community has helped us so much.

Please SHARE our story.   Thank you for your thoughts and prayers to get Chy into remission.