Hya all! First let me apologize for not being a very "talkative"
host! Those that know me will tell you that I never shut up! :)
I have been so very busy and I have so many projects going at one
time that it is sooo very hard to find time to get on here and talk.

Welcome to our newest members! And to those waiting for a reply from
me...it is coming in the next week! :)

One of my projects is very promising! I have been talking with a Dr.
who is very respected in the Autism community about getting new
research done. Here is my gut feeling about the rise of Autism...

Every single childhood vaccine has aborted fetal cell lines in them!
EVERY ONE OF THEM!!! Of course they have not been there since the
beginning of vaccines as abortion was illegal. So why are they in
there now? Anywho, there is a lot in the news about stem cell lines
and Parkinsons disease. The claim is that Parkinsons can be reversed
or improved by injecting cell lines into those affected. Sooooo, if
that is the case....what are we doing to our own children's DNA with
EACH childhood vaccine??? Is it a possibilty that we are in fact
altering our children's DNA/molecular structure??? It IS a
possiblity!! So when the CDC claims...it is genetic...they could be
right! I am in no way saying that enviroment, vaccines, and possibly
herditary genes are not a role some times or in some children. But we
NEED to see if we are actually altering our children's DNA. This Dr.
is speaking with a few different scientists to see if we can get this
ball rolling!!! WOOHOO! (can you tell I am pumped?) ;)

Okay, I found a new group today and am posting it here for you to
check into. They are wwanting to get organized and push insurance
companies to pay for the treatment of our children! And the larger we
stand together...the better chance we will have! South Carolina got a
bill passed in their state. And my state, WV, has a bill being
presented (which means it will be years if and when it gets passed).
So let's all B.A.N. with this group!!! There are many who are losing
their material items to treat their children with biomedical
treatment (I had my only vehicle repoed due to this very issue). And
their are others who want to try it but simply can not afford to. It
is NOT right!!! ARRRGH!

Oops, I almost forgot, I found a company that makes...are you
ready....Organic GF/CF hotdogs and other lunch meat!!! I was
shocked!!! Matthew Cody does not eat meat but I am trying to have
meals where we are all eating the "same" food. (only difference is
that ours has gluten and casein in it). I would love for my whole
family to eat GF/CF but can not afford that. So for now, Matthew Cody
will be the only one...and hopefully we can all "look" like we are
eating the same thing! :)

Okay, here is the info on the new group....

Q. What is NAPC and How do I join?

A. The NAPC is the "National Association of Parents and
Caretakers" of children and adults with special needs. Whether you
are a caretaker or you have special needs yourself, this association
is for you and your rights to provide alternative therapies like
Hyperbaric Oxygen Therapy, Chelation Therapy, or any other therapy
which works better than what mainstream Medicine and drugs have to
offer. Insurance and Medicaid should pay for anything that works
better than what is offered. It is your right.

Q. What do I have to do, I have no time for anything else?

A. All you have to do is simply join. No membership fees,
nothing to fill out, no work or time-consuming expectations. We
simply need you as a member to show politicians and those who make
decisions that we have strength and voters who can make changes. We
need enough members to have an influence on decisions in Washington
when it come to providing healthcare solutions for our members.

The NAPC will be a non-profit membership organization. As a Parent,
Grandparent, or Caretaker or anyone who is supportative of someone
with special needs who may benefit from an alternative therapy which
is not recognized, you will be represented and you will be a part of
the process by just joining and being a member.

The NAPC will only be possible if you join. The NAPC can only help if
you are a part of it because you are the NAPC. If there is not
enough interest to turn this into a large membership organization with
some power, then the plans for the NAPC will be dropped. It will fail
because you were not willing to support it by simply becoming a
member. The power is in numbers. Children and adults with special
needs are not being represented by anyone who does not have a
self-promoting agenda. This will be your association, run by you and
the people you select as your leaders. But first we need you to
become a member. After the membership reaches 1000, we will begin to
select your leadership (by your vote online).

This may be the only chance you will ever have to have your own
organization so you will have a voice in the care of that special
needs child or adult you are responsible for. You are there voice and
they depend and rely on you to make their decisions.

To join the NAPC, simply go to the Yahoo group at
http://health.groups.yahoo.com/group/TheNAPC/

or you can simply send a blank email from the email address you want
to use to
TheNAPC-subscribe@yahoogroups.com

The success or failure of the NAPC is entirely dependant on you. Your
part is to simply join. If that is too much……………. Oh, well……..




HUGS!!!!!!!!!!!!!!!!
Tammy Lynne