ATTN TENNESSEANS-vaccine /mercury litigation

[Guest guest]

Hi everyone,

I am sending this message to hopefully reach out to fellow Tennesseans out

there with kids with autism. This is not a commercial of any kind. I am

just a mom motivated about the possibilities and wanted to share my

enthusiasm.

Think back to when your child was born. Before autism. Did he/she receive

all of the recommended vaccines back then during the first two years of his

life? Most included the Hep B, Hib, Dpt, polio, etc. Most of the time it

seemed like it was at least two shots per well visit that first year or two.

Did you notice any regression during the first year or second year? Can you

attribute the autism to any other thing?

My husband,, and I, and several other families, met with an attorney

from Miami last week (invited by our ASA chapter) to find out more about

litigation against the vaccine manufacturers who put thimerosal into the

vaccines and then, these were injected into our children...... This is a

very serious legal battle that is just now being to brew hot and heavy.

Even so, it is still just the beginning of it all. His name is o

Villasante and he is part of the firm, Robles Law Center, one of the three

main firms litigating against the vaccine manufacturers for this. The

website is robleslawcenter.com

The firm he is with is one of the big ones that litigated against the

tobacco companies and asbestos companies. So, he is not one of the

ambulance chasers that runs commercials on TV. He is respectful and very

professional.

To retain his services costs NOTHING. You do not pay a dime unless you win,

and his fees come from the winnings. The whole entire process could take a

while, maybe 1-3 years. and I are definitely pursuing this for our

oldest son with autism and also our baby boy, as he has a speech delay and

other " autistic like " behaviors. In our opinion, what on earth do we have

to lose?

These are not class actions suits like some of the other vaccine cases.

Each individual child's case is separate. What he needs us to do as

parents is to fill out some information, which includes a very detailed

history on each child, obtain copies of ALL MEDICAL RECORDS FROM ALL DOCTORS

THAT HAVE TREATED YOUR CHILD, obtain the vaccine records showing the

vaccinations and the lot numbers (which most offices do not include in

copies of the records, but by law must have on record, and you are entitled

to that), etc. We just need to do a little leg work on the front end and

give them the information. And, again, it costs us nothing to retain him.

Fellow Tennesseans, please look into this if you are interested. Since the

attorney is from out of state, he must have a Tennessee attorney to contact

to facilitate the relationship. My husband (who is an attorney), and

another local attorney with many years of experience with these type law

suits are going to help him in assisting the Tennessee families. Go to the

website if you want to pursue this litigation or email me and I can put you

in contact with my husband or the other attorney that is assisting Mr.

Villasante.

We are feeling good about this. In talking to Mr. Villasante, he felt very

confident that if a family has all of the medical records, the child showed

signs of neurological damage, etc., that there is a good chance for his firm

to take the case and move forward and hopefully win. He'll review all of

the information on each child and let you know if he thinks it is a good

case. He said this is going to be much bigger than the whole tobacco

litigation ever thought about being. Wow.

Give it some thought. This could be the answer for us families to help

financially provide for our disabled kids for the rest of their lives. No

more having to fight for crappy services from the schools, etc. We could

finally afford good services. And, as we all worry about, it could secure

safe and effective therapies for them as adults. I know I worry about " what

if something happens to me- who will take care of my sons or watch out for

them to make sure their needs are being met... " Just maybe this can give us

some assurance that we can afford to pay good care workers or provide

appropriate services and therapies for them for throughout their adulthood,

without burdening the other family members financially or completely going

bankrupt ourselves. There is no guarantee, but what do we have to lose?

Trina, mom to four boys: Landon(8yr, autism), Chandler (7yr), Holden (3yr),

Keller (1yr, expressive language delay)

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