Cerebral Palsy
Family Support Network TM
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Cerebral Palsy Family Support TM |
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Contact us page. Here you can find our emails to
talk with us and share your own stories. We learn from our
mistakes but we can help others avoid making the same as us.
Send your stories and help others find help and/or avoid the
pitfalls. We could also use any links you might have to
disability sites in
you locality or state that we may post on this site for the benefit of
all disabled.
Alphabetical listing of
most pages on this site: Exceptions
will be state and county pages. Some are not linked from
this sidebar but from within a page
The CP Links Page is where you will find most Federal, State and local County pages. My attempt to clarify CP you may find the information provided by NINDS is more specific and detailed There are many different treatments and I only name those I am familiar withHow it is essential to maintain range of motion How it is essential to maintain quality of life What I know through my experience By far not even close to what you should know and Orthotics Again what I know through experience Much more can be had searching the net or talking with doctors and therapists CP LINKS Cerebral Palsy Glossary More Information of CP provided by NINDS Specific Neurological
Disorders My take on the IEP,
IDEA 2004 (Public Law 94-142 & Public Law 101-476), and the 504 plan. IEP overview 504 plan & IDEA Q&A
Parent & Educator Guide of 504 Plan concepts and real life accommodations. Drafted by the OSPI and 5 Puget Sound area School Districts but would be a valuable asset to any fighting for their child's 504 accommodations anywhere U.S.A. IDEA 2004 summary& Washington State Chapter 392-172 WAC
SPED special education and the IEP FORUMS (BBS)
MEMBER PAGES
Pierce County Events
AMBER'S STORY In the share your story section people like you will post their unique experiences and through what is said you may find you are not alone. You may also find a friend and someone you can relate to. And possibly a way to realize your own goals. Websites created by people who have CP or someone in their family has CP. Net-etiquette applies. All sites are subject to approval. Banners and text allowed on these links. NON CP RELATED All sites are subject to approval. All Non-CP links are text only with a line or two of information of the link posted. Please notify me of any broken links so I can remove or fix them. Join with me in trying to educate the public of CP and other disabilities What motivated me to build this site Direct your comments to Robert. Robert wrote a Science Fiction trilogy while being laid up. It took 4 years to complete and he has for sale Book 1 of the trilogy HERE He is awaiting editing and copyrights on books 2 & 3 before sending them to the publisher. Book 1 can stand alone and is a complete novel of 237 pages and 135,000+ words in PDF format. Making Money Online (or not) Other sites I have or to be more precise the wife has and I take care of.
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CONTACT US INFO
We have posted this site as a means for you to navigate through the links to self-help. We are not Doctors or Lawyers and cannot in anyway provide you with medical or legal assistance. We can only point you in a direction through the links. So please do not contact us for this type of advise. That said if you need to contact us here is the information. Please when sending an email place something in the subject line that will let us know it is not spam. Just placing our name will not do it. If you are at a loss place CP or Cerebral Palsy in the subject. If you expect a reply and do not receive one in a week or so resend the email with another subject. Amber's Parents: Robert Taormina ~ Amber's father and host of this site Any thoughts or questions about the site should be directed to me as webmaster.
Snail mail: P.O. BOX 4463 Spanaway, WA. 98387
Snail mail: P.O. BOX 4463 Spanaway, WA. 98387 Ph. (253) 846-5787 (No collect calls accepted)
Make a secure donation/gift through Paypal by clicking on the link below:
Donations/Gifts are graciously accepted, Just log on to www.Paypal.com , Click "Send Money" tab and follow the instructions to send money from an existing Paypal account or by any major Credit Card. Use the email address below to make a Donations/Gifts on Paypal.
If you do not see an email address it is because you need to enable javascripts. The email is in javascript to foil the spambots. You can also mail a Donation/Gift to Tami Taormina P.O. Box 4463 Spanaway, WA. 98387
If you have a website that conforms to simple net-etiquette and would like to place a link here is our preferred link. You may use a text only link if you'd prefer.
And here is the code for this link. Just copy it to a simple text editor to take out any garbage FrontPage put in and paste it in your html. <a href="http://www.cpfsn.org"><img border="0" src="http://www.cpfsn.org/images/buttonsbglogosetc/cpfslogo.gif" width="159" height="151" alt="The Cerebral Palsy Family Support Network dedicated to helping support families with a Disabled Child and or disabilities. Helping the disabled find resources and providing a place for the disabled or their parents to congregate and have their questions answered."></a><BR><b><font face="Arial,Helvetica" color="#000000" size="4"><a href="http://www.cpfsn.org">Cerebral Palsy Family Support Network</a></font></b><BR><b><font face="Arial,Helvetica" color="#FF0000" size="2"> Dedicated to helping families find the support, resources and services they need.</font></b>
I cannot force any to use the forums but I would
encourage you to do so if you have questions you would like answers to or
have a statement you would like to make. I know that having to register
and using the anti-spambot code makes you have to do one more step than
most, but it also insures that the forums are not bombarded by spambots
posting crap on the site. I try to check the forums at least weekly (often
daily) and I have to say that so far I am disappointed that none have
chosen to take advantage of this free opportunity to get and give
information. I built this site to help the disabled get information and
the use of the forums and sharing your stories is a huge part of that
endeavor. Please help one another and I will try to answer what I can as
well. We are a community of the disabled or parents of disabled children
and we should do whatever we can to help each other gain the upper hand or
help each other cope with difficult situations. Just go to the forums page
and write down the anti-spambot question and enter it on the registration
page. You only need do this once to have full access to the forums. If you have a site that deals with any disabilities
then consider either joining CPFSN.org (it
is totally free) and having a link to your site on the appropriate page
(e.g. State, County) as well as the ‘Members’ page or doing a simple
link exchange and having your site appear on the ‘CP Family’ links
page, if you or your child has CP or any disability. If you do not have CP or a child with CP or have a
site devoted to any disability you can still have a reciprocating link
placed on the Non-CP related links page. A link exchange would not only
show your support of this site but would increase your ranking with search
through having another outside link (SEO).
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