INDEX: This section gives the descriptions of each section on CPC. You can also view the section's description by hovering the mouse over a section's graphical link.LIVING WITH CP: This section gives my personal experiences on how I love with my own CP. Many of you who are disabled will probably find much of this section's content familiar.TYPES OF CP: This section explains the common types of CP and their classifications based on how they can affect the body.CPC DIRECTORY: This section is a list of links around the web where you might find other useful information on CP and other disability related content.DISABILITY BULLETIN: This section allows people to post disability related questions to other visitors on the site; announce medical studies; any other information not associated with any current section on the CPC site.SHARE A STORY: This section allows people to share their stories (both good and bad) about living with CP. This is a completely anonymous Section (at your discretion) so that you need not fear people finding out who you are if that is your choice.ADA LAWS: This section is a copy of the Americans with Disabilities Act information site.  It contains the guidelines concerning the Americans with disabilities rights, fairness, and public access.AGING AND CP: This section is a report on how the aging process can affect a body with CP. This should be a must read for all visitors to the site. I will continue to add to this report as new information becomes available.DISABILITY WORKPLACE: This section can be used as a tool to help aid a disabled individual looking for a job.  You might be surprised at what some of the experts say about how to approach the job market when you are disabled.
HOW SSI WORKS: This section will aid you in finding out if you qualify for Supplemental Security Income.  These rules and regulations are plentiful. CPC strongly recommends you view this section before perusing the SSI route.MEDICAL NEEDS: This section lists online companies where you can purchase medical supplies and equipment. Ordering what you need online offers privacy, convince, and very often cheaper then purchasing from brick and mortar stores.DISABILITY NEWS: This section allows you to keep up with the latest news and events around the US and the world related to the disability community. The section is updated constantly so please visit often.THERAPIES FOR CP: This section discusses some of the different treatments used to treat CP. Some of these include Physical/Occupational Therapy, HBO, TES, Biofeedback and others.AWARDS & WEBRINGS: This Section contains information about the many web rings CPC has joined and awards we have won. It also includes information on how to sign up for our very own web ring or award.FUN STUFF: Occasionally I like to have a little fun on the web. Here you will find information about my hobbies and my many collections of items. This portion of the site is not directly related to CPC. Its just for fun :o)CONTACT CPC: This section allows you to communicate with CPC is several ways including email, ICQ, and out guest book.RECENT UPDATES: This section can be used to find out what changes have been made since you last visited CPC. This page is always updated when CPC is updated no matter how small the update.CAUSE SUPPORT: This section tries to help disabled individuals by supporting several causes that actively promote the awareness and fair treatment of those with disabilities.
HELP: If you are not sure how to use CPC's menu system, click here to get a graphical description on how to use our menu system. People with CP Parents Support EMAIL DATABASE: This database is the very heart and sole of CPC. It allows people with CP, both young and old, to communicate with each other and share experiences or advice.Page
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Parents of Children with Cerebral Palsy
(Page: 1, 2, 3, 4)

Angela W theark4@aol.com  Hi all. We are the proud parents of two children. They are both are shining stars. We are thankful, and look forward to being apart of this special group.

With  our child we have tried OT, PT, special ed and are waiting to try HBO, and Nacd program

Caren S. twinstdd@aol.com  My son David (18 months) has a twin brother and it is very hard to watch his brother crawling and walking. The doctors say David will walk and I pray they are right. He is sitting up but cannot get into a sitting position by himself. He is trying to crawl but hasn’t got the hang of it yet. He is very determined to follow his brother. David receives physical therapy 2 times a week
Sue DuPart gaduparts@yahoo.com 
(MSN: (Email addr)
Meredith (4) was premature. She was 31wks. and was recussitated in 2 minutes. She had strabismus, poor sucking and eating and is lagging in her weight gain. She is very friendly and loving. Her epilepsy was diagnosed at age 4. I have epilepsy and am well qualified to be her mother. I want to hear from others who struggle with weight gain and eating habits. We have used Speech, occupational therapy and visual therapy.
Pamela Hoeltke hoeltke@ivillage.com
AOL: hoeltke1
We are very grateful to be the parents of David [2] as we thought that he might not be with us long as an infant. David had a very hard time after birth. We would be grateful for any information that would help us to be better parents for David and maybe we can pass the information along as David gets older.  Currently we are doing the routine of PT and OT with speech therapy. (David is considered hypotonic)
Jennifer F.. JimandJen@stic.net  My son has ataxic CP and I would love to network with other parents of children with CP.
Hillary B. kcmom@i.am  I am looking for other parents with kids with mild cp and I want to know about what their symptoms were and when they were diagnosed. My child is receiving OT 2 hours a week and will be starting PT, speech, adaptive soon.
Adrian V. adrian.voican@excelnet.ro  My child Maria has Spastic Quadriplegia. We are ready to do max to improve condition. of our child. We have used oral Baclofen Amino Acids.  I wish to communicate with other parents.
Julian T. jugs-t@webtribe.net  Josef [9] has severe Spastic Quadriplegic Cerebral Palsy. He does however have the understanding of a nine year old, and is quite intelligent. He cannot however communicate verbally. We are about to try Botox injections on Josef's legs.
Joyce A. abg3@idt.net  Brian is an 8 year old spastic quad. He is bright and mainstreamed in 2nd grade. Uses a power chair and computer with trackball.
Psuleen W. angel52294@aol.com  Our son is 21 months old we got the diagnoses of Stadic Encepholpathy the Dr, was 90% sure it was CP.
Cindy P. cpaine22368@yahoo.com  Cindy has a 16 month old child w/mild CP. Her child is presently in PT/OT co-treat twice a week and speech once a week. Want to try hippotherapy and therapeutic swimming Any stories/experiences from other parents would be appreciated. Would like to talk to parents in similar situation.
Terri M. tlmatt3126@hotmail.com 
AOL: tlkm84
I'm in the Air Force (San Antonio, Texas) and have found it difficult to find good resources for my son. He's a 7 y/o old with Spastic Quadriplegic (or double hemi). Sometimes he's diagnosed as hemiplegic and sometimes as quadriplegic. Once he was diagnosed as double hemiplegic. There just isn't one that describes him. He's in the 1st grade and is a joy to all of his teachers. Cognitively he's right on target which has made it much easier working with the school system. We have done Rhizotomy Tendon Transfers and we're hoping to get approval for TES soon.
Marty N. mjnusbaum@msn.com  Marty's (Chicago, IL) son Eric (11) is in the 5th grade with mild CP. We would like to hear how other parents cope with the challenges associated with keeping up in school, particularly ways to become more effective with using a computer for schoolwork. We have tried P.T., O.T., Speech Therapy, TES, Gait Analysis, leg casts, and orthotics.
Lynn B. Lynn_Brenneman@
hotmail.com
 
I am the mother of three boys. The youngest, Eli, is 3 (Quadriplegia) and has mixed CP. He was born full-term, but complications arose during delivery and he died. He was resuscitated and born a second time 12 minutes later. Currently he cannot talk or move independently. We do daily PT, OT as recommended. I'm interested in finding out more about hyperbaric oxygen therapy. I have become an active lobbyist, both locally and statewide.
Leanne B. l_borrowman@hotmail.com  I'm a single parent of [Samantha (6) Spastic Diplegia]. She is a very bright girl and is ding very well in school. She wants to it all. I'm going to be trying HBO treatments in August.
Gary D. gd@wwa.com  I am a CP parent of a 9 year old with Spastic Diplegic CP. I am also  a member of the Board of Directors of a Conductive Education Center called The Center for Independence through Conductive Education. Conductive Education Physical Therapy Occupational Therapy Botox injections Tendon lengthening surgery
Jennifer B. laurenzmom@aol.com  Brett also has craniosynostosis and had skull surgery (cranial vault remodel) at 9 months. He also has many syndromal features, yet dr.'s cannot fit him with a certain syndrome. He is a very happy, funny, determined and smart little boy!!! We have tried Physical and Occupational Therapy 3 times a week, Speech Therapy Son wears bi-lateral AFO's. Would like to try cranial sacral therapy.
Lillian S. Skimmer82@webtv.net
agridulce@picosito.com 
Kyle (8) is a happy well-adjusted child. He is very comfortable with his "God-given challenge." When people say, "What wrong with you?" Kyle will say, "Nothing is wrong with me, what's wrong with you?" He enjoys horseback riding, basketball, running (as best as he can), working on the car with dad, swimming, and riding his big 3-wheel bike.

Kyle has tried (& still does) horseback riding, physical therapy, occupational therapy, speech, and had surgery. We are interested in trying Neuromuscular/Biofeedback Program.

Carmen L. bulita29@hotmail.com  I went through the process of a lawsuit for malpractice. My daughter [age 4, Mixed CP] disabling condition was caused by that. If anyone wants to know about the procedures or need help or support, feel free to ask. Also, my husband is a military. We are currently on PT, OT, ST, aquatic therapy, NDT. Wants to try horseback riding and neurofeedback and home schooling.
Becky H jbcchaag@aol.com  I have twins born at 24 weeks gestation. We are sure our daughter Claudia has CP, although she has not yet been diagnosed. We expect a diagnosis in October. She has high tone in her lower extremities, mainly right leg. Her twin brother Caleb is doing well.
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