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-   -   mental retardation, CP, cortical blindness,seizures (https://www.neurotalk.org/new-member-introductions/46304-mental-retardation-cp-cortical-blindness-seizures.html)

janash 05-22-2008 11:30 AM

mental retardation, CP, cortical blindness,seizures
 
Hi to all!!!

I have an 18 y o son who is severly handicapped. We live everyday with all the above mentioned (title). He has been on a long list of seizure meds and we are now investigating the VNS for seizure control. Would be greatly interested in connecting with any and all who have valid info and or personal knowledge and experience with VNS. Also, I would be interested in comparing notes on any and all the above and below mentioned disorders that, at least for us, fall under the umbrella for the diagnosis of cerebral dysgenesis.

My sons conditions are severe seizures, CP, cortical visual impairment (CVI,CVD). He is non-abulatory, and non-verbal. He also has a Mickey button and thus receives all nutrition and meds via the tube.

AfterMyNap 05-22-2008 11:48 AM

Hi, Janash! :Wave-Hello: Welcome to NeuroTalk!

Your little dude sure has a handful of conditions, it has to be difficult for you. This is a huge community of compassionate and informed people, I hope you'll find some answers.

You might like to look at our CP forum for a start.

CP:
http://neurotalk.psychcentral.com/forum52.html

For questions about specific meds, it might help you to visit our medications forum.

Medications:
http://neurotalk.psychcentral.com/forum72.html

We have an epilepsy forum as well where you might find some specific information on seizures.

Epilepsy & seizure disorders:
http://neurotalk.psychcentral.com/forum11.html

We also have a search engine located in the toolbar near the top of every page where you can locate discussions about specific meds and topics via keywords.

I hope you'll find our community both helpful and supportive. Feel free to join in anywhere and let us know if we can assist you in navigating the forums. :)

DAY1 05-22-2008 11:57 AM

Welcome to the board.

WOW!! I didn't think I would ever come across anyone who's child had the same disorders as my daughter.

My daughter has mental retardation, mild CP and seizures. And now some undx'd auto immune disorder. She is 22 yrs old.
She is a very capable child(adult, I guess) Mentally she is somewhere between 8 and 40. Some days her mentallity is like an 8 yr old. Some days I wonder if she's mentally older than I am.

It sounds like you have many more challenges than I do.
My daughter is able to do most things for herself. Brushing her hair, shaving, cutting nails are some things I do for her.
She is able to do some house hold chores.

I look forward to getting to know you.

DAY

janash 05-22-2008 12:33 PM

Thanks for your prompt attention to my post! I have been browsing the very links that you posted in your reply. I tried to post to a message to one link prior to posting as a new member and received a message saying I had to post at least (x) amount of times before I could respond directly to a message. I am confused to the meaning of that!

BTW I graduated from Pontiac Central and I have family in MI. I love it there!

DAY, I also look forward to getting to know you and sharing with you. As for my son's diagnosis; cerebral dysgenesis means he had abnormal brain cells from birth. The grey matter and white matter in the brain are fused together in some places. Because the brain is abnormal the body does not receive the messages correctly so therefore the CP and seizures as well. Seizures damaged the visual center in the brain causing the cortical visual damage. His eyes can see. His brain does not interpret his vision.

I don't know about more challenges than you! LOL Mine are just different. I have 3 other children. Two older and 1 younger than my special son. At least with my handicapped son I know where he is and what mischief he is not into! My other children only God knows! They are great kids nonetheless and never in any serious trouble.

I do look forward to sharing with you.

Janet

Kitty 05-22-2008 12:56 PM

Hi Janet and welcome to NeuroTalk!


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Curious 05-22-2008 01:02 PM

Quote:

Originally Posted by janash (Post 284765)
Thanks for your prompt attention to my post! I have been browsing the very links that you posted in your reply. I tried to post to a message to one link prior to posting as a new member and received a message saying I had to post at least (x) amount of times before I could respond directly to a message. I am confused to the meaning of that!

BTW I graduated from Pontiac Central and I have family in MI. I love it there!

DAY, I also look forward to getting to know you and sharing with you. As for my son's diagnosis; cerebral dysgenesis means he had abnormal brain cells from birth. The grey matter and white matter in the brain are fused together in some places. Because the brain is abnormal the body does not receive the messages correctly so therefore the CP and seizures as well. Seizures damaged the visual center in the brain causing the cortical visual damage. His eyes can see. His brain does not interpret his vision.

I don't know about more challenges than you! LOL Mine are just different. I have 3 other children. Two older and 1 younger than my special son. At least with my handicapped son I know where he is and what mischief he is not into! My other children only God knows! They are great kids nonetheless and never in any serious trouble.

I do look forward to sharing with you.

Janet

welcome janet.

new members can't post links. it keeps spammers from posting. :)

Koala77 05-22-2008 06:53 PM

Hi Janet and welcome to NeuroTalk from me as well.

I see you have lots of helpful information to wade through, and that you've already met some of our wonderful members.


dorrie 05-22-2008 10:47 PM

Hi Janet!! Welcome to Neurotalk!:)

Darlene 05-23-2008 01:11 AM

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

I have had epilepsy for about 40 years and have never been contol, but my spells are mild. About 5 years ago I had a VNS insected, it help out a good deal by shortening my spells and I am able to block them some. It took at least a year before I really seem to help. I have been able to cut down on meds. Let me know if I can be of any other help to you.

Again welcome, looking forward to seeing you around.

Darlene:hug:

DM 05-23-2008 10:06 AM

Hello Janet and another Welcome to NeuroTalk here. As the others' have posted, this is an amazing, informative and caring place and I hope you will feel at home here.

Sometimes it's great to just come here and let off a lil steam. We are all here for one reason or another, so glad you found us.


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