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Sensory Processing Disorder

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Uploaded by on Mar 14, 2009

Talking about some of the major sensory issues I have. Some doctors believe that it is another form of Autism Spectrum Disorder. It's still in question of whether or not I have Aspergers. I deal with it the best I can and ways to cope.

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Uploader Comments (DarkWaterfall)

  • Great video. Did you tippy toe as a toddler or clumbsy or poor body awareness?

  • @toptalkradio Yes, to all three! Sometimes even now, I'll find myself walking on my tiptoes!! Always very clumsy and poor proprioception (awareness of own body in space). I've learned that its not uncommon in people with Ehlers-Danlos Syndrome, and I suppose having Sensory Processing Disorder makes it all that more difficult.

  • You're welcome! I was only diagnosed as an adult, and turns out my mom has it too! I'm glad your little girl was diagnosed young and can work on learning tools to help her throughout life! Take care!

  • Thank you for posting this. My 7 year old son has a ton of what you are explained. I hope he grows up to be like you. It was very encouraging to hear you articulate your thoughts and emotions. He struggles in school (2nd grade) and he is very challenging to deal with the behavior issues (lot's of oppotional things).

    I liked your statement, "You do what you gotta do, it's a trial and error process." This really resinated with me. People don't seem to get it and pass judgment on us.

  • @derwin22 I'm sorry to hear that you struggle, but glad that my video helped. Have you read the "Out of Sync Child"? If not, I HIGHLY encourage that you do. It's geared towards parents with children who suffer from SPD. It helped me understand so much! I'm sure you know this, but a lot of his behavior is probably from him being in pain or uncomfortable from some sort of unpleasant stimuli. If you have more questions or just want to talk, feel free to send me a message!

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  • God you are sooo cute....I just OD on your cuteness :-/

  • @toptalkradio thanks for the info. You seem to have a pretty good fight in you and are determined to beat this thing and I have a feeling you will. You are a champion my friend, I will keep on watching!

  • Thank you for posting this video. My oldest daughter will be 7 soon, and has been diagnosed with SPD for over 3 years. It is great, as a parent to see an adult who is well spoken about her own SPD. I hope my daughter will grow up with confidence and eloquence too. Thank you!

  • Hi :) My name is Diane and I wrote a children's book about my daughter, "Meghan's World: The Story of One Girl's Triumph over SPD." Meghan only had SPD and nothing else. At 5 years old Meghan was diagnosed with severe SPD and has since lost her diagnoses...years ago...she is now 14 years old. There are many traditional and alternative therapies that help. Berard AIT helps a lot. Detoxing toxins from vax and envirn., foods and digestive enzymes, epson salt baths. most are intuitive too

  • Hi :) My name is Diane and I wrote a children's book about my daughter, "Meghan's World: The Story of One Girl's Triumph over SPD." Meghan only had SPD and nothing else. At 5 years old Meghan was diagnosed with severe SPD and has since lost her diagnoses...years ago...she is now 14 years old. There are many traditional and alternative therapies that help. Berard AIT helps a lot. Detoxing toxins from vax and envirn., foods and digestive enzymes, epson salt baths

  • @dreamspell22 *frustrating to not be able to get a diagnosis*

  • Thanks for the book recommendation. Ive been struggling to get a diagnosis for my son. he's had meltdowns since he was 15 months old and is now at 3 1/2 starting to tell me that things hurt him.. Like his feet.. the seams in his socks hurt or if he gets any food on his feet/hands that bother's him, or being wet; he has to change his outfit,etc.. Ive just requested he be reevaluated but thankfully his headstart teachers have noticed also.. It's been frustrating for me and im sure upsetting to him

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