HBOT

[Guest guest]

Hi,

I have been fighting for HBOT coverage for my own daughter for 10

years. It is appauling that it is not covered, I agree. Owning a

center for four years now, I just cant seem to find the right Doctor

to join in and fight, once I do look out.... Yet I must say thanks

to the man above for looking over us and being able to some what

afford the therapy for because I would still be sitting here 10

years later and be wondering if it would help. SOOO my only other

contribution I am able to do for the children is charge $50.00 a

session for the hard multi chamber, 100% oxygen. Some ideas that I

personally have done to fundraise were " Pennies for " Three

schools in the area gave each classroom a jar for the kids to drop in

spare change. The " winning " class recieved a pizza party in each

school. Since was in one of the schools and the children all

knew each other, the amount of change and CHECKS from the parents

kept coming in. It was truly unbelievable how much people cared and

dumpped the change. The high school then offered to wrap and count

the change!! It got in the news paper with out my doing. We asked our

families instead of gifts to buy a session (they " bought " more than

one). I am so thankful every time I go back and read the articles

about and all of her strides. If you truly want HBOT you can do

it now. Waiting for insurance is wasting precious time for the kids.

It takes work to fund raise, I have done many other fundraisers over

the years if any one needs some help just contact me. Instead of all

the arguing I choose to be of help to get HBOT at least at a

reasonable cost. Any Drs on the list, give me a call if your

interested in a partnership to help the children.

Regards,

Elaine CHT EMT CMA (Mom of Rose)

www.thejennyrosecenter.com

570-421-3415 or email me