This is about the daily adventures of my family and daughter K who is 6 years old. She has been recently diagnosed with Autism in January 2011.
Wednesday, March 30, 2011
To ipad or not to ipad - that is that question
There is a lot of buzz now about the ipad ... a lot of buzz about this device being helpful to children with Autism and helping them to communicate to the world ... since so many have difficulties being able to do so on their own. (SEE POST: ALL ABOUT AUTISM)
So my question for my family and for K is "To ipad or not to ipad?"
I read and hear about the good that it is doing for non-verbal and limited verbal children (like my K). That for some kids it is limiting or eliminating the tantrums that they would normally have since they are able to communicate their needs and wants.
This is what DH and I both want for K. We want K to communicate with us. If this piece of technology will help her then we are all for it. We just need to factor in the price of this tool and the price of the apps that she will use. It is something that we need to work into our budget.
Now there are some places that are assisting with the cost for ipad for low income families and more research needs to be done on that.
Below are some links relating to the cost of the ipad, news stories and information on apps:
Cost of the Ipad:
Cost of ipad from Amazon.com
News Articles:
Mother sets out to buy iPads for other autistic children
Is the iPad a 'Miracle Device' for Autism?
The Conversation: iPad Gives Voice to the Autistic
Students with autism, Asperger's develop iPad app
Can the iPad Be a Learning Tool for Kids With Autism?
Articles about Apps for the ipad:
iPad for Autism: Selecting the best apps
10 Revolutionary iPad Apps to Help Autistic Children
Tuesday, March 29, 2011
Northern Trip - airplanes & cancer
K & I being picked up from the airport! |
I have not posted for a few days because I have been in the northern portion of the US since the 25th.
K and I left for our destination on 3/25 via airplane. I was sooo nervous about flying with K since it was both our first time flying.
We got to the airport 2 hrs early. I was loaded down with one rolling back, my laptop bag, purse and a backpack loaded to the hilt with K's toys. DH dropped us off and said his goodbyes. We checked in the rolling bag and went through security and no mishaps. K and I stopped at one of the restaurants. We sat by the windows so she could see the airplanes with the people loading and unloading. We shared a thing of fries and she had her grapefruit juice. I pointed out the planes and explained where the people were going and what they were doing with the bags. K' s eyes were glued to the window and she kept saying "airplane" and pointing at them.
Then we had about an hour to wait. We loaded our plane as one of the first families. Once K was on the plane she could not get enough of looking out the window. (We were told to put her "noisy toys" away - I never flown before & did not give thought to the noise of her toys bothering other people - the idea was to keep her happy.) Anyway, she LOVED the flight and looking out the window. K sat for 2 and 1/2 hours with out incident. She got to a point where she would say to me "Ears pop, candy please". During the flight I gave her laughy taffy to chew on to help with the ear popping. Also when she was looking out the window she kept saying "ocean" when she saw the clouds.
When it came time to unload, K was a little restless and started to get cranky. This was because she saw everyone else getting off the plan. Once she was off the plan she was fine. V picked us up and we went to get "real" pizza. K was happy to eat and to play with the ice in her water. From there we went to V's house and stayed the night. K was happy to run up and down the stairs and flop on V's bed. K did this all Friday night and Saturday mourning. V (our cousin) made us breakfast on Saturday. She made scrambled eggs, home fries, toast and sausage. K was only interested in eating the toast with jelly and got jelly all over V's glass topped table and on the chair.
After that we got ready to go to Pop Pop's. We stopped at a florist to get pretty purple roses for Grandmom (she has stage 4 throat and lung cancer - hence the reason for our trip.). We stopped at Grandmom's and then at Pop Pops.
So we have been at Pop Pop's ever since.
Tuesday, March 22, 2011
The Frazzled Woman
This is how I feel and why I have not posted in a few days. I am the frazzle woman ... I did 40 million load of laundry this weekend and put them way. I have cleaned the house and am not done yet. I have to work all this week and finish packing for our trip. SO if I do not find time to post - that would be the reason. Have a great week.
Saturday, March 19, 2011
Leaving on a Jet Plane - tips to flying with a child with autism
Ok so it is one week away or 6 days away that K and I hop on our first 2 hr flight to go visit family. I have being researching and trying to prepare for this adventure by asking people who have flown for tips, calling the US Airways, and looking up things on the computer. So this is what I have gathered:
What to check when ordering the tickets:
- Check details of tickets to make sure your seats are together (K and my seats were not together - I had to call the airlines 2 times to get this resolved with out having to pay extra for "choice seats")
- Call the airlines and state you are traveling with a child with Autism to find out what to do to make the how process smoother for you and your child - especially if you are first time fliers.
- Check to see if there is an Autism Fliers program in your area - this helps kids with autism to learn what to expect when flying - it creates a "mock" flying experience from start to end. (I did not have time to do this.)
What to bring:
- A backpack with toys for K
- My laptop & movies for K & head phones
- A power adapter for that laptop for the plane (consult with airline to see if the plane is equipped with a power source - you will have to provide your own adapter)
- Snacks for K - NO PUDDING CUPS (check with airline for type of drinks they have)
- Business cards that say "My daughter has autism. I am doing the best I can. Sorry for the inconvenience"
- Kiddie leash for K in the airport
- Change of clothes and wipes
- Antibacterial hand cleaner
- Gum or now & laters, taffy or gummi bears to create that chewing motion (I do not give K gum)
- Wear clothes with out metal (zippers, buttons, underwire in bras, etc.) Wear easy slip on clothes.
- Wear socks with your shoes.
- Get to the airport 2 to 1 1/2 hours before flight.
- Bring birth certificate for kids and State Id for yourself (My understating with US Airways is that I cannot check in on the computer systems because I am traveling with a child under 18. So I want to make sure that I have both our IDs just in case.)
- Advise airline when I get there that I am traveling with a child with autism when I check in.
- Bring benadryll or other calming medication - to give before flight - depending on the time it takes to kick in.
- Do not give comfort toy to child until after security to prevent fall outs.
- Provide another comfort item like Lollipop for security process (I am guessing - this works with K as a great motivator - but have not tested it out in airport security.)
- Tell security that my daughter has autism.
- Let the people who work on the plane know that my child has autism.
- Remain calm and positive and hope that the child is the same.
- Hope and pray that it is a smooth flight.
Below are some links to sites I have checked out regarding flying with a child who has autism:
Thursday, March 17, 2011
Happy St. Patty's Day :)
"No man ever wore a cravat as nice, as his own child's arm around his neck."
- Irish Proverb
- Irish Proverb
It is better to be a coward for a minute than dead the rest of your life.
Irish Proverb
Irish Proverb
Dance as if no one's watching, sing as if no one's listening, and live everyday as if it were your last.
Irish Saying
Irish Saying
Three best to have in plenty - sunshine, wisdom and generosity.
Irish Triad
Irish Triad
If you do not sow in the spring, you will not reap in the autumn.
A merry heart lives long.
History of the Shamrock & St. Patrick
- The plant used by St. Patrick to explain the Trinity (the Father, Son and Holy Spirit) when he Christianity to Ireland.
- The sacred plant to the Druids because it formed the Triad and 3 way a mystical number to the Druids.
- "Wearin' o' the green" the shamrock became a symbol of rebellion in the 19th century. If anyone was caught wearing it they risked being hanged. This was because of a government led religious movement against Catholics. It became the sign of the Catholic underground.
- A 4 leaf clover brings good luck.
- St. Patrick banished snakes from Ireland. (Some think that the "snakes" were the Druids.)
- He brought Christianity to Ireland and taught the trinity by using the shamrock.
Tuesday, March 15, 2011
Intro to Irish Fairies Part 2
The Pooka: This fairy is a a shape shifter. He can turn into a scary or pleasing forms. He may appear has a horse, goat, rabbit, dog or goblin. The most common form is that of a horse with dark fur and golden eyes a a flowing mane. The Pooka try to trick a human into taking a ride - and what a wild ride it will be!! As wild as the ride will be this fairy will not do any real harm to the human.
The Dullahan: This fairy is a headless horsemen. He either headless or has his head being carried under one arm. He is normally seen riding on a black horse. The Dullahan is the bringer of death omens.
The Leanhaun Shee: This fairy is a beautiful woman who give inspiration to artists in exchange for their love. The artist thus goes made and dies an early death. If a man refuse, then she must be their slave. If a man accepts, then their is no escape, expect to find another to take their place. The leanhaun shee feeds on the life energy of these men and they waste away.
The Fear Gorta-Man: This fairy walks around during times of famine. He seeks money from people who pass by. He can be a great source of good luck for those who give him a lot of money.
The Banshee: She is a fairy that can either be an ugly, scary hag or a beautiful woman. She is a bringer of death omens. She can heard with her mourning call when someone is about to die.
The Fear Sidhe: These fairies were believed to be "People of the Goddess Danu". They are the survivors who retreated underground/otherworld when they were defeated by the Milesians. These fairies are not named directly, but are know as "The Good Neighbors", "The Fair Folks", and "The Folk". They are often given offerings and care is taken to prevent making the fairies mad. These fairies also are very beautiful, but can be very ugly as well.
Monday, March 14, 2011
Intro to Irish Faries
The Sheoques: These fairies live in thorn bushes that are sacred to them. The fairies play music too lead humans astray. They sometimes switch a child with a fairy child to create a changeling.
The Merrows: Portrayed as small hornless cows. These fairies have fish tails and wear a red cap. The men have green teeth, hair and pig eyes with red noses. The woman merrows are pretty and prefer human mates. (umm, so would I if the men truly look the way they are described ...lol!)
The Leprechaun: A solitary fairy that fixes shoes. He is a thrifty sort. If you catch him you find his pot of gold. But if you take your eyes off of him, the leprechaun will disappear.
The Cluricaun: This fairy is another loner like the leprechaun. He robs wine cellars. Also the cluricaun rides sheep and sheep dogs all through the night.
The Gonconer: This loner is seen smoking a pipe and not doing much accept trying to seduce milkmaids and shepherdesses.
The Fear Darring-Red man: There is not an "exact" photo of this fairy. but I would image him as being a pretty ugly fellow. This fairy is a loner that is describe as being a mean practical joker who likes gruesome pranks and giving bad dreams.
http://mysite.verizon.net/cbladey/irish/faries.html
Sunday, March 13, 2011
Care takers, Date night, and Iguana piss
Woooo Whooo - we FINALLY had date night after a year and five months!!! Normally, our date nights are saved for once a year when we travel up north to see family. Where we live in the south we have no family and we do not have a care taker for K when we choice to go out. We either take her with us - which normally she is pretty good in stores and restaurants, go solo, or don't go at all.
On very rare occasions we will have one friend watch K, but he works like 6 days a week and goes to school full time. So the last time he watched K was for a very important meeting with her Doctor in January of this year. It was about her diagnosis of "autism" and it was something that earliest meeting time was at 7 pm or watch until March. So we took what we could.
Now our old neighbors (mother and son) would watch K every so oftern. These neighbors were cool. E the son is about my age. He has a daughter who is 9, but him and his wife are divorced. Anyway, they lived next to us for about 5 to 6 years. They had to move out because J (the mother) got hurt at work and E got hurt at work too. So J moved in with her other son and E moved in with his grandmother.
Anyway, E got fired from his job - he was working at a gas station - the gas station was robbed at gun point while he was working. So they fired him for that. But his grandmother lives where we live and E has always been good with K. So E watched K for 2 hours last night.
Also I should note that I am super picky about who watches K. K is a great kid, but she can be like watching 5 to 10 2 year old kids. When I am looking for a sitter, I do not sugar coat how K can be. I might even scare a few off - rather do that then have them tell me mid way through the job that K is too much to handle or if they knew this how K was then they would charge me more (Yeah have had that happen). I was hired for my current job. I had to attend training for 3 weeks. Which meant I had to find someone to watch K for that time. Hubby took one week off to watch K. For the other two weeks I needed K to be watched I interviewed other people. The other person that I really wanted never called me back. The second woman panned out. I took K to meet her and explained all about K (this was before her diagnosis of Autism), I told her that K can be a hand full and laid out the good, the bad and the ugly. She was fine with it. So the week comes up were K was to go there. After the first day, the woman told me if she knew K was going to this much of a hand full she would have charged me more. Then on Wednesday, this woman told me some BS about having to watch another child the next week because of some emergency that happened and could not watch K that week. OK - thanks for that. So I found a day care that would take her for that 3rd week. Then on Friday, this woman told me she could watch K. Well, I told her that I already placed her in a day care that had no problem with handling my daughter so she was out of luck. K went to this day care for a week and there were no issues and all the kids were fine with her.
Any how, back to date night... Hubby had forgotten that date night was yesterday. I only had planned it out in front of him with E and made sure that DH did not have plans for Saturday. E followed up with us on Friday to make sure that it was still on - and yup Hubby was there in the conversation. Saturday rolls around and I told him I was cleaning for when E comes to watch K for date night. Hubby's reply was "THAT'S TOOO NIGHT?" Oh boy, I was fuming!!! Well everything turned out well, we went out and had a great time. E watched K and had lollipops to bribe her (good motivation tool for her). K had the run of the apartment expect for our bedroom being locked. I warned E that K likes to climb and may play in the bathroom. I let him know that there was apples for her to snack on and some chips and cookies. That she could have as much water as she wanted. I left the you tube play list up on the computer of the wiggles and other random kid songs up on the computer for her. I warned him of all I could before we headed out. Then off we went.
At the pool hall, DH and I had iguana piss (aka beer) and Philly cheese steaks. The only reason I had the beer with dinner is because I could - K was not with us and it was truly and adult night out. Normally I don't drink ever and hate the taste of beer. After that we played 2 games of pool. Now I LOVE playing pool, but I suck. Truly suck at playing pool - I am lucky to get ANY ball in. So Hubby beat my butt 2x. I played a song on the juke box - so I surprised him by playing one of his favorite songs - Megadeath's "Peace Sells". Overall it was fun and a bit weird feeling, because there was a big hole - something missing, that something was that K was not with us.
Well, we get back, K was all smiles. E said she was no problem and he has been around NT kids who are 10x worse then K. He said that he would watch her again - so we have a sitter now - YEAH!!!!
Thursday, March 10, 2011
Tuesday, March 8, 2011
Late today :(
Woke up late today and I was late too work. The only saving grace was Hubby getting us coffee from D&D this morning.
K decided to wake up at 3 am this morning and go into the living room. Hubby is a light sleeper and rounded her up and sent her back to bed. He was already up and could not go back to sleep. She got into bed with me and screamed for a moment because she was not thrilled at having to go back to sleep. Sleep & K are like oil and water - two things that do not go well together. So sleep has been an issue with her forever ...
Finally she went back to sleep and so did I - only to over sleep the alarm clocks. :(
K decided to wake up at 3 am this morning and go into the living room. Hubby is a light sleeper and rounded her up and sent her back to bed. He was already up and could not go back to sleep. She got into bed with me and screamed for a moment because she was not thrilled at having to go back to sleep. Sleep & K are like oil and water - two things that do not go well together. So sleep has been an issue with her forever ...
Finally she went back to sleep and so did I - only to over sleep the alarm clocks. :(
Monday, March 7, 2011
Randomness: Why does all the weird news seem to happen in FL?
Is the heat and the sun from Florida killing the common sense brain cells? See the following news stories:
- Naked drunk woman throws rocks, pulls own teeth, cops say
- Look, there's somebody's credit card — let's get pizza! Millionaire dentist accused of using card dropped in parking lot to buy pies
- Crumby evidence nabs "Cookie Monster"
- Man gets shot 2x in 6 months
- Police: Offier told woman to strip. expose herself to him
- Boy arrested for 5th time ... at 8 years old
- Prostitution sting nets 70-year-old woman
- One-armed suspect surprises deputy when prosthesis pops off after fumbled bank robbery
US Airways problem resolved :)
I got off of work today and called customer service back at US Airways. I got a wonderful rep named Donna who helped me. I told her I was a first time flier going to see my terminally ill Grandmother with my 6 year old daughter who has Autism. I explained the problem of the seats not being together and why K and I need to sit together on the plane. Well, she changed our seats with no problem and no charge. Easy as that ... now Frida from my first call I think needs to be retrained.
US Airways 1st response ..
Auto response from US Airways:
This will acknowledge receipt of your correspondence to the Customer Relations Department. Please be assured your comments and concerns are very important to us, and we are working diligently to provide a personal and professional response to every email we receive. Our current response time is 3-4 business days. A member of our Customer Relations team will respond to your feedback as quickly as possible.
If your question or comment is about an upcoming trip, an unused ticket or your Dividend Miles account, please call our Reservations Department at 1-800-428-4322. If your correspondence is regarding delayed, lost or damaged baggage, please visit our website at www.usairways.com and select the link to our Central Baggage Resolution Office for information on how to contact that department directly.
If you are inquiring about the status of a Refund, please be aware that our current Refunds Department processing time is currently 30 days.
Thank you for your patience. We appreciate your business.
US Airways Customer Relations Team
**This is an automated message. Replies to this message are not viewed or monitored.***
US Airways wants parents to pay extra to sit with kids ....
I printed out my flight information today and noticed that K and my seats are not next to each other. I called into US Airways and was told that I pay $30 extra for choice seats. I have never flown before and when I ordered the tickets I naturally thought that parent and child would be placed together. I was wrong ... I explained K's condition - I was advised of paying $30 for the choice seats or when I get to the airport and letting the agent's desk know of the situation and hope they can put us together.
Anyway, I sent and email to the complaint department and I will see what happens. This is the email that I sent below:
To whom it may concern,
I called into customer service today about an issue regarding my future flight plans. When I ordered the tickets I put in the information that I am flying with one child from the age of 2-17 as per the prompt. When I printed out the flight information I noticed that the seat for myself and my 2-17 year old child were not together. This is a HUGE concern to me and to any parent who has a young child that is not sitting near them. Now in my case my daughter is 6 years old and is disabled - she has Autism. "K" MUST sit next to me because she requires adult supervision because of her condition. I called into customer service and explained my situation. I was told that I can pay $30 dollars extra for choice seating to have our seats changed. There really should be some sort of disclaimer on your site or affiliated sites STATING that seats for children may not be played near the parents and that choice seating would be the better option. Also there should be some sort of prompt on the websites that asks if the child's age falls into a bracket of 2-4,5-8,8-11, etc and if the child (regardless of age) is disabled. Depending on the answers then there should be something that brings of the choice seating option up. The customer service agent also said that I can go to the agent desk at the airport and tell them about my daughter's condition and then they may be able to do something about the seating, but that is not guaranteed. I just wanted to bring this to your attention that there need to be some changes made to the websites to bring this to the attention of any parent. Thank you in advance for your time and attention on this matter. Sincerely, "CM"
Anyway, I sent and email to the complaint department and I will see what happens. This is the email that I sent below:
To whom it may concern,
I called into customer service today about an issue regarding my future flight plans. When I ordered the tickets I put in the information that I am flying with one child from the age of 2-17 as per the prompt. When I printed out the flight information I noticed that the seat for myself and my 2-17 year old child were not together. This is a HUGE concern to me and to any parent who has a young child that is not sitting near them. Now in my case my daughter is 6 years old and is disabled - she has Autism. "K" MUST sit next to me because she requires adult supervision because of her condition. I called into customer service and explained my situation. I was told that I can pay $30 dollars extra for choice seating to have our seats changed. There really should be some sort of disclaimer on your site or affiliated sites STATING that seats for children may not be played near the parents and that choice seating would be the better option. Also there should be some sort of prompt on the websites that asks if the child's age falls into a bracket of 2-4,5-8,8-11, etc and if the child (regardless of age) is disabled. Depending on the answers then there should be something that brings of the choice seating option up. The customer service agent also said that I can go to the agent desk at the airport and tell them about my daughter's condition and then they may be able to do something about the seating, but that is not guaranteed. I just wanted to bring this to your attention that there need to be some changes made to the websites to bring this to the attention of any parent. Thank you in advance for your time and attention on this matter. Sincerely, "CM"
Sunday, March 6, 2011
To harness or not?!?!? That is my question
To harness or not ...
K and I are taking a trip in 19 days up north via airplane. Now I have never flown and neither has she.
Also I have never placed a harness on my child. I thought that I would never have to do that ... but since I will be in two busy airports I figure I better do the whole leash/harness thing with K. I have settled on a low cost front facing backpack style that seems to snap in the back or under the arms. So this way she can undo the whole leash and get away.
The winner was - Munchkin Bear with Me Safety Harness and Handstrap :
See harness at Amazon.com.
So once I get it I will update on what I think of it.
K and I are taking a trip in 19 days up north via airplane. Now I have never flown and neither has she.
Also I have never placed a harness on my child. I thought that I would never have to do that ... but since I will be in two busy airports I figure I better do the whole leash/harness thing with K. I have settled on a low cost front facing backpack style that seems to snap in the back or under the arms. So this way she can undo the whole leash and get away.
The winner was - Munchkin Bear with Me Safety Harness and Handstrap :
See harness at Amazon.com.
So once I get it I will update on what I think of it.
Saturday, March 5, 2011
ALL ABOUT AUTISM
Information taken from the National Institute Of Neurological Disorders and Stroke
What is autism?
Autism spectrum disorder (ASD) is a range of complex neurodevelopment disorders, characterized by social impairments, communication difficulties, and restricted, repetitive, and stereotyped patterns of behavior. Autistic disorder, sometimes called autism or classical ASD, is the most severe form of ASD, while other conditions along the spectrum include a milder form known as Asperger syndrome, the rare condition called Rett syndrome, and childhood disintegrative disorder and pervasive developmental disorder not otherwise specified (usually referred to as PDD-NOS). Although ASD varies significantly in character and severity, it occurs in all ethnic and socioeconomic groups and affects every age group. Experts estimate that three to six children out of every 1,000 will have ASD. Males are four times more likely to have ASD than females.
What are some common signs of autism?
The hallmark feature of ASD is impaired social interaction. A child’s primary caregivers are usually the first to notice signs of ASD. As early as infancy, a baby with ASD may be unresponsive to people or focus intently on one item to the exclusion of others for long periods of time. A child with ASD may appear to develop normally and then withdraw and become indifferent to social engagement.
Children with ASD may fail to respond to their names and often avoid eye contact with other people. They have difficulty interpreting what others are thinking or feeling because they can’t understand social cues, such as tone of voice or facial expressions, and don’t watch other people’s faces for clues about appropriate behavior. They lack empathy.
Many children with ASD engage in repetitive movements such as rocking and twirling, or in self-abusive behavior such as biting or head-banging. They also tend to start speaking later than other children and may refer to themselves by name instead of “I” or “me.” Children with ASD don’t know how to play interactively with other children. Some speak in a sing-song voice about a narrow range of favorite topics, with little regard for the interests of the person to whom they are speaking.
Children with ASD appear to have a higher than normal risk for certain co-occurring conditions, including Fragile X syndrome (which causes mental retardation), tuberous sclerosis (in which tumors grow on the brain), epileptic seizures, Tourette syndrome, learning disabilities, and attention deficit disorder. About 20 to 30 percent of children with ASD develop epilepsy by the time they reach adulthood. While people with schizophrenia may show some autistic-like behavior, their symptoms usually do not appear until the late teens or early adulthood. Most people with schizophrenia also have hallucinations and delusions, which are not found in autism.
Children with ASD may fail to respond to their names and often avoid eye contact with other people. They have difficulty interpreting what others are thinking or feeling because they can’t understand social cues, such as tone of voice or facial expressions, and don’t watch other people’s faces for clues about appropriate behavior. They lack empathy.
Many children with ASD engage in repetitive movements such as rocking and twirling, or in self-abusive behavior such as biting or head-banging. They also tend to start speaking later than other children and may refer to themselves by name instead of “I” or “me.” Children with ASD don’t know how to play interactively with other children. Some speak in a sing-song voice about a narrow range of favorite topics, with little regard for the interests of the person to whom they are speaking.
Children with ASD appear to have a higher than normal risk for certain co-occurring conditions, including Fragile X syndrome (which causes mental retardation), tuberous sclerosis (in which tumors grow on the brain), epileptic seizures, Tourette syndrome, learning disabilities, and attention deficit disorder. About 20 to 30 percent of children with ASD develop epilepsy by the time they reach adulthood. While people with schizophrenia may show some autistic-like behavior, their symptoms usually do not appear until the late teens or early adulthood. Most people with schizophrenia also have hallucinations and delusions, which are not found in autism.
How is autism diagnosed?
ASD varies widely in severity and symptoms and may go unrecognized, especially in mildly affected children or when it is masked by more debilitating handicaps. Very early indicators that require evaluation by an expert include:
A comprehensive evaluation requires a multidisciplinary team, including a psychologist, neurologist, psychiatrist, speech therapist, and other professionals who diagnose children with ASD. The team members will conduct a thorough neurological assessment and in-depth cognitive and language testing. Because hearing problems can cause behaviors that could be mistaken for ASD, children with delayed speech development should also have their hearing tested.
Children with some symptoms of ASD but not enough to be diagnosed with classical autism are often diagnosed with PDD-NOS. Children with autistic behaviors but well-developed language skills are often diagnosed with Asperger syndrome. Much rarer are children who may be diagnosed with childhood disintegrative disorder, in which they develop normally and then suddenly deteriorate between the ages of 3 to 10 years and show marked autistic behaviors. Girls with autistic symptoms may have Rett syndrome, a sex-linked genetic disorder characterized by social withdrawal, regressed language skills, and hand wringing.
- no babbling or pointing by age 1
- no single words by 16 months or two-word phrases by age 2
- no response to name
- loss of language or social skills
- poor eye contact
- excessive lining up of toys or objects
- no smiling or social responsiveness.
- impaired ability to make friends with peers
- impaired ability to initiate or sustain a conversation with others
- absence or impairment of imaginative and social play
- stereotyped, repetitive, or unusual use of language
- restricted patterns of interest that are abnormal in intensity or focus
- preoccupation with certain objects or subjects
- inflexible adherence to specific routines or rituals.
A comprehensive evaluation requires a multidisciplinary team, including a psychologist, neurologist, psychiatrist, speech therapist, and other professionals who diagnose children with ASD. The team members will conduct a thorough neurological assessment and in-depth cognitive and language testing. Because hearing problems can cause behaviors that could be mistaken for ASD, children with delayed speech development should also have their hearing tested.
Children with some symptoms of ASD but not enough to be diagnosed with classical autism are often diagnosed with PDD-NOS. Children with autistic behaviors but well-developed language skills are often diagnosed with Asperger syndrome. Much rarer are children who may be diagnosed with childhood disintegrative disorder, in which they develop normally and then suddenly deteriorate between the ages of 3 to 10 years and show marked autistic behaviors. Girls with autistic symptoms may have Rett syndrome, a sex-linked genetic disorder characterized by social withdrawal, regressed language skills, and hand wringing.
What causes autism?
Scientists aren’t certain about what causes ASD, but it’s likely that both genetics and environment play a role. Researchers have identified a number of genes associated with the disorder. Studies of people with ASD have found irregularities in several regions of the brain. Other studies suggest that people with ASD have abnormal levels of serotonin or other neurotransmitters in the brain. These abnormalities suggest that ASD could result from the disruption of normal brain development early in fetal development caused by defects in genes that control brain growth and that regulate how brain cells communicate with each other, possibly due to the influence of environmental factors on gene function. While these findings are intriguing, they are preliminary and require further study. The theory that parental practices are responsible for ASD has long been disproved.
What role does inheritance play?
Twin and family studies strongly suggest that some people have a genetic predisposition to autism. Identical twin studies show that if one twin is affected, there is a 90 percent chance the other twin will be affected. There are a number of studies in progress to determine the specific genetic factors associated with the development of ASD. In families with one child with ASD, the risk of having a second child with the disorder is approximately 5 percent, or one in 20. This is greater than the risk for the general population. Researchers are looking for clues about which genes contribute to this increased susceptibility. In some cases, parents and other relatives of a child with ASD show mild impairments in social and communicative skills or engage in repetitive behaviors. Evidence also suggests that some emotional disorders, such as manic depression, occur more frequently than average in the families of people with ASD.
Do symptoms of autism change over time?
For many children, symptoms improve with treatment and with age. Children whose language skills regress early in life—before the age of 3—appear to have a higher than normal risk of developing epilepsy or seizure-like brain activity. During adolescence, some children with ASD may become depressed or experience behavioral problems, and their treatment may need some modification as they transition to adulthood. People with ASD usually continue to need services and supports as they get older, but many are able to work successfully and live independently or within a supportive environment.
How is autism treated?
There is no cure for ASD. Therapies and behavioral interventions are designed to remedy specific symptoms and can bring about substantial improvement. The ideal treatment plan coordinates therapies and interventions that meet the specific needs of individual children. Most health care professionals agree that the earlier the intervention, the better.
Educational/behavioral interventions: Therapists use highly structured and intensive skill-oriented training sessions to help children develop social and language skills, such as Applied Behavioral Analysis. Family counseling for the parents and siblings of children with ASD often helps families cope with the particular challenges of living with a child with ASD.
Medications: Doctors may prescribe medications for treatment of specific ASD-related symptoms, such as anxiety, depression, or obsessive-compulsive disorder. Antipsychotic medications are used to treat severe behavioral problems. Seizures can be treated with one or more anticonvulsant drugs. Medication used to treat people with attention deficit disorder can be used effectively to help decrease impulsivity and hyperactivity.
Other therapies: There are a number of controversial therapies or interventions available for people with ASD, but few, if any, are supported by scientific studies. Parents should use caution before adopting any unproven treatments. Although dietary interventions have been helpful in some children, parents should be careful that their child’s nutritional status is carefully followed.
What research is being done?
In 1997, at the request of Congress, the National Institutes of Health (NIH) formed its Autism Coordinating Committee (NIH/ACC) to enhance the quality, pace and coordination of efforts at the NIH to find a cure for autism (http://www.nimh.nih.gov/health/topics/autism-spectrum-disorders-pervasive-developmental-disorders/nih-initiatives/nih-autism-coordinating-committee.shtml). The NIH/ACC involves the participation of seven NIH Institutes and Centers: the National Institute of Neurological Disorders and Stroke (NINDS), the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the National Institute of Mental Health, the National Institute on Deafness and Other Communication Disorders, the National Institute of Environmental Health Sciences, the National Institute of Nursing Research, and the National Center on Complementary and Alternative Medicine. The NIH/ACC has been instrumental in the understanding of and advances in ASD research. The NIH/ACC also participates in the broader Federal Interagency Autism Coordinating Committee (IACC) that is composed of representatives from various component agencies of the U.S. Department of Health and Human Services, as well as the U.S. Department of Education and other government organizations.
In fiscal years 2007 and 2008, NIH began funding the 11 Autism Centers of Excellence (ACE), coordinated by the NIH/ACC. The ACEs are investigating early brain development and functioning, social interactions in infants, rare genetic variants and mutations, associations between autism-related genes and physical traits, possible environmental risk factors and biomarkers, and a potential new medication treatment.
In fiscal years 2007 and 2008, NIH began funding the 11 Autism Centers of Excellence (ACE), coordinated by the NIH/ACC. The ACEs are investigating early brain development and functioning, social interactions in infants, rare genetic variants and mutations, associations between autism-related genes and physical traits, possible environmental risk factors and biomarkers, and a potential new medication treatment.
Where can I get more information?For more information on neurological disorders or research programs funded by the National Institute of Neurological Disorders and Stroke, contact the Institute's Brain Resources and Information Network (BRAIN) at:
BRAIN
P.O. Box 5801
Bethesda, MD 20824
(800) 352-9424
http://www.ninds.nih.gov
Information also is available from the following organizations:
Association for Science in Autism Treatment P.O. Box 188 Crosswicks, NJ 08515-0188 info@asatonline.org http://www.asatonline.org | Autism National Committee (AUTCOM) P.O. Box 429 Forest Knolls, CA 94933 http://www.autcom.org |
Autism Network International (ANI) P.O. Box 35448 Syracuse, NY 13235-5448 jisincla@syr.edu http://www.ani.ac | Autism Research Institute (ARI) 4182 Adams Avenue San Diego, CA 92116 director@autism.com http://www.autismresearchinstitute.com Tel: 866-366-3361 Fax: 619-563-6840 |
Autism Society of America 7910 Woodmont Ave. Suite 300 Bethesda, MD 20814-3067 http://www.autism-society.org Tel: 301-657-0881 800-3AUTISM (328-8476) Fax: 301-657-0869 | Autism Speaks, Inc. 2 Park Avenue 11th Floor New York, NY 10016 contactus@autismspeaks.org http://www.autismspeaks.org Tel: 212-252-8584 California: 310-230-3568 Fax: 212-252-8676 |
Birth Defect Research for Children, Inc. 800 Celebration Avenue Suite 225 Celebration, FL 34747 betty@birthdefects.org http://www.birthdefects.org Tel: 407-566-8304 Fax: 407-566-8341 | MAAP Services for Autism, Asperger Syndrome, and PDD P.O. Box 524 Crown Point, IN 46308 info@aspergersyndrome.org http://www.aspergersyndrome.org/ Tel: 219-662-1311 Fax: 219-662-1315 |
National Dissemination Center for Children with Disabilities U.S. Dept. of Education, Office of Special Education Programs 1825 Connecticut Avenue NW, Suite 700 Washington, DC 20009 nichcy@aed.org http://www.nichcy.org Tel: 800-695-0285 202-884-8200 Fax: 202-884-8441 | National Institute of Child Health and Human Development (NICHD) National Institutes of Health, DHHS 31 Center Drive, Rm. 2A32 MSC 2425 Bethesda, MD 20892-2425 http://www.nichd.nih.gov Tel: 301-496-5133 Fax: 301-496-7101 |
National Institute on Deafness and Other Communication Disorders Information Clearinghouse 1 Communication Avenue Bethesda, MD 20892-3456 nidcdinfo@nidcd.nih.gov http://www.nidcd.nih.gov Tel: 800-241-1044 800-241-1055 (TTD/TTY) | National Institute of Environmental Health Sciences (NIEHS) National Institutes of Health, DHHS 111 T.W. Alexander Drive Research Triangle Park, NC 27709 webcenter@niehs.nih.gov http://www.niehs.nih.gov Tel: 919-541-3345 |
National Institute of Mental Health (NIMH) National Institutes of Health, DHHS 6001 Executive Blvd. Rm. 8184, MSC 9663 Bethesda, MD 20892-9663 nimhinfo@nih.gov http://www.nimh.nih.gov Tel: 301-443-4513/866-415-8051 301-443-8431 (TTY) Fax: 301-443-4279 |
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NINDS health-related material is provided for information purposes only and does not necessarily represent endorsement by or an official position of the National Institute of Neurological Disorders and Stroke or any other Federal agency. Advice on the treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient's medical history.
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Last updated February 24, 2011
Intro: K is a girl with Autism
"K" is a sweet & silly & affectionate 6 year old girl. She loves school and riding the bus. K enjoys The Wiggles and Dora the Explorer. Also she loves most any type of music and dancing too it. K loves when she listens to music with Daddy and Daddy sings to her. She loves toys that light up and play music or make random sounds. She also likes toys that have to have to do with ABC's. K enjoys playing outside and going to the park. She likes to ride her bike and go swimming. She also likes to play with play dough and puzzles and painting and drawing. K loves to be tickled!!! She will ASK to be tickled!!! K also like riding on horses. K is afraid of cows (only when trying to feed them). K like to go to McDonald's for the Happy Meal toy and likes the occasional soda and fries. She loves Birthday Cake Ice from Baskin Robbins. K likes pizza but LOVES, LOVES to eat salad and yogurt. K also loves clothes - especially clothes that are glittery, metallic, light up or has some sort of graphic on it.
K may sound like any other 6 year old girl, but January 2011 she was diagnosed with Autism - Infantile Autism to be exact. This diagnosis did not come as a surprise to us - we have know all along for the past 2 years that she had Autism. We just had to go threw the motions of Early Steps, Child Find, and "The Official Diagnosis" from her Pediatric Neuro Developmental Doctor. Child Find had done the evaluation on K when she was 3 or 4 years of age. In January 2010 they placed her in a pre-K program for kids with Autism after everything was said and done based on the ADOS.
Based upon my experience of working with kids inside a day care setting and working with kids in a summer camp for the disabled, I had knew that K had Autism. I did do my research and I knew with 110% certainty. K is more of a 2 year old inside a 6 year old's body. K has the speech and social skills and understanding of a 2 year old. Her speech is like really bad broken English - ie: "Potty minute" (Meaning "I will go potty in a minute"), "Please Ahhh" (meaning: "Please open your month"), "tickle", "Piggies" for "This little piggy..." she will say "Piggy Market" or "Piggy Home" or "Piggy Nine" or "Piggy Roast Beast" etc, and various other short and slitted phrases. She knows enough to get her point across most of the time. She knows all her shapes and colors and her ABC's and can identify her letters and some numbers. She has a very had time with her handwriting - she can make a circle, but is having the toughest time trying to write a square or letters. She can cut with scissors but not like a Neurotypical child. Her social skills are very much like a 2 year old - she will play with things but does not want to share, she is better with older kids or adults. Her understanding is the same - she will climb and you can tell her no a thousand times and she will keep doing it. She can be placed in time out or redirected and she will still do it. Her gross motor skills (walking, running, riding) a bike are right where they should be.
Now when K get upset or frustrated she will do what I call her "hell cat"/"feral cat" mood (may seem like harsh phrasing but it is used ONLY to sum up a series of actions). This mood is when she will yell or scream or growl, she will hit/kick walls and doors, she will hit her head, she will throw things, she will squeeze someone's arm (with me she will try to dig her nails into my skin when doing this - but only to me - and this is where the "hell/feral cat" comes in).
Currently K goes to school full time at the local public school that has an Autism Program and she is in extended care because both I and my husband work until about 5 pm. K goes to therapy 2 times a week. Once for OT and once for speech. I sit in the sessions so I can do the same out home with her. Occasionally I will take her to C.A.R.D. She is goes to Girl Scouts and I do have her go to church - but I am in the process of finding the "right" church for her. We do work related to speech and OT during the week.
I started a few days ago to start a Twitter Account to detail brief daily adventures of K. Then I found with only so much space to type in that I may need a Blog if I want to elaborate on a subject. So here we are today with a better explanation of the Makings of K.
K may sound like any other 6 year old girl, but January 2011 she was diagnosed with Autism - Infantile Autism to be exact. This diagnosis did not come as a surprise to us - we have know all along for the past 2 years that she had Autism. We just had to go threw the motions of Early Steps, Child Find, and "The Official Diagnosis" from her Pediatric Neuro Developmental Doctor. Child Find had done the evaluation on K when she was 3 or 4 years of age. In January 2010 they placed her in a pre-K program for kids with Autism after everything was said and done based on the ADOS.
Based upon my experience of working with kids inside a day care setting and working with kids in a summer camp for the disabled, I had knew that K had Autism. I did do my research and I knew with 110% certainty. K is more of a 2 year old inside a 6 year old's body. K has the speech and social skills and understanding of a 2 year old. Her speech is like really bad broken English - ie: "Potty minute" (Meaning "I will go potty in a minute"), "Please Ahhh" (meaning: "Please open your month"), "tickle", "Piggies" for "This little piggy..." she will say "Piggy Market" or "Piggy Home" or "Piggy Nine" or "Piggy Roast Beast" etc, and various other short and slitted phrases. She knows enough to get her point across most of the time. She knows all her shapes and colors and her ABC's and can identify her letters and some numbers. She has a very had time with her handwriting - she can make a circle, but is having the toughest time trying to write a square or letters. She can cut with scissors but not like a Neurotypical child. Her social skills are very much like a 2 year old - she will play with things but does not want to share, she is better with older kids or adults. Her understanding is the same - she will climb and you can tell her no a thousand times and she will keep doing it. She can be placed in time out or redirected and she will still do it. Her gross motor skills (walking, running, riding) a bike are right where they should be.
Now when K get upset or frustrated she will do what I call her "hell cat"/"feral cat" mood (may seem like harsh phrasing but it is used ONLY to sum up a series of actions). This mood is when she will yell or scream or growl, she will hit/kick walls and doors, she will hit her head, she will throw things, she will squeeze someone's arm (with me she will try to dig her nails into my skin when doing this - but only to me - and this is where the "hell/feral cat" comes in).
Currently K goes to school full time at the local public school that has an Autism Program and she is in extended care because both I and my husband work until about 5 pm. K goes to therapy 2 times a week. Once for OT and once for speech. I sit in the sessions so I can do the same out home with her. Occasionally I will take her to C.A.R.D. She is goes to Girl Scouts and I do have her go to church - but I am in the process of finding the "right" church for her. We do work related to speech and OT during the week.
I started a few days ago to start a Twitter Account to detail brief daily adventures of K. Then I found with only so much space to type in that I may need a Blog if I want to elaborate on a subject. So here we are today with a better explanation of the Makings of K.
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