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The Magic Brain Kid
Приєднався 12 лют 2020
T. has Agenesis of the Corpus Collosum (ACC). He Created this channel to share with others what its like for a kid to have ACC.
NODCC Conference 2024
This video was taken at the 2024 NODCC Conference in Chicago. Everyone in this video either has a DCC or cares for someone with a DCC.
Переглядів: 139
Відео
Magic Brain Kid interview with Eli
Переглядів 1798 місяців тому
Timmy interviews Eli, a teenager with ACC.
MBK Interview with Lillian
Переглядів 9410 місяців тому
An Interview with Lillian. Lillian shares what ACC is like for her.
Magic Brain Kid Returns
Переглядів 7011 місяців тому
The Magic Brain kid is back to update everyone on what life is like for a child with ACC - Agenesis of the Corpus Callosum.
Five In A Row Minecraft
Переглядів 107Рік тому
Throughout this school year, Timmy has been creating Minecraft builds based on the books we have read together. This video is his final project for the school year. For those familiar with FIAR, I am sure you will spot lots more builds that weren't covered in the video. Comment with your favorites.
A Visit to the Neurologist
Переглядів 9324 роки тому
Did you ever wonder what a visit to a Pediatric Neurologist was like? Join The Magic Brian Kid on his visit to his favorite doctor.
DCC Awareness Day
Переглядів 2,7 тис.4 роки тому
July 2nd is International Disorders of the Corpus Callosum Awareness Day. We are celebrating the wonderful individuals who have a DCC and the joy they bring to the world. For more information about Disorders of the Corpus Callosum, please visit nodcc.org/ , www.ausdocc.org.au/ , or www.corpal.org.uk/
Tae Kwon Do Belt Testing
Переглядів 814 роки тому
TMBK Testing for his Yellow Belt and Baby Dino testing for his Red Stripe
Roller Coaster
Переглядів 474 роки тому
T. created a Roller Coaster from Duplos and toilet paper tubes.
Questions and Answers with The Magic Brain Kid Pt. 2
Переглядів 1094 роки тому
Questions and Answers with The Magic Brain Kid Pt. 2
Egy
Happy DCC Awareness Day. Thanks Magic Brain Kid for sharing your adventures with us!
Awesome video. Keep up the great work, Timmy and crew.
You made we twig. My boy didn’t crawl he rolled. Like his brain realised I can get around like this!
this is all so helpful, I'm 30 weeks and my son has acc.
I am so glad you found this helpful. We have a lot of support groups on Facebook. Please find us there for additional resources and connection.
Don't keep going Tim
You suck at doing that
May know your kid is CACC or PACC? As i feel he is so brilliant and no different like other kids
Great job at your appointment Timmy! You did a wonderful job following directions and answering questions. Ok so proud of you :)
Thank you for uploading this! I’ve just got a diagnosis for my 4months old & I hadn’t got any idea what to expect.
Please find our support groups on Facebook. If you post in the Agenesis of the Corpus Callosum Listserv, I (MBK mom) will find you and get you connected. We have an amazing support system set up.
I am celebrating to because of acc I have it and so does my freind ☺️ And we go to the same college
That's so cool! Thanks for celebrating with us
Awesome video❤️ thanks for letting me be apart of it..
Happy DCC Day!
Beautiful video - thank you for sharing with us! Happy International Disorders of the Corpus Callosum Awareness Day!
Thank you!
What an awesome video!!! Happy ACC Awareness Day!!!
To you to Kara!
OMG. I love this one. H waving in the background and the kids are just adorable! We love you!
R u ok hope u are
We are all doing good. Having a blast with homeschooling and all the fun activities available.
Does Timmy have a neurology doctor because I do
Yes he does. Timmy sees his neurologist every 6 months
I do to I’m just like Timmy I see my neurologist every six months also has he ever had an mri I’m eleven and I struggle with the seizures just like timmy
Timmy does have a neurologist that he sees every six months. Thank you for asking! Timmy used to have seizures but now he takes CBD oil and they have stopped.
I have acc I love ur channel it helps me along the way when I have sadness
This means so much to us. Thank you for sharing
I have ACC as well and this is a great way to spread awareness!
Thanks Kara!
I love these videos. Keep going, Tim! Here is a question for you for your next video: what are some things that are hard for you to do because you have ACC?
Hi from the uk x loving this channel not much out there for us. I'm 34weeks pregnant baby hope has been diagnosed with acc and a cyst and grey matter on her frontal lobes. Just waiting for our 2nd MRI results so we can prepare for her birth and what may be to come. Scariest time ever for us but will love her no matter what! Your son is an inspiration keep up the good work!any help or advice would be much appreciated xx
It is a very scary time. Hopefully, T. can give you some encouragement. And if you haven't yet, please find Agenesis of the Corpus Callosum Listserve on Facebook. I will see your post and can connect you with other parents in the UK and the 2020 birth year group.
Hi my youngest son has acc too he’s struggling with verbal language... he got tested from an iep person and she said he is having some difficulty
This is very common. The IEP is wonderful! Your son will get the services he needs. Please ask any questions. We have learned a lot in over the last 6 years. T. loves to answer questions, and if he doesn't know how to answer we (his parents) will jump on to answer them.