SOA E2

Spirit of Autism Web TV Episode 2 – Improv for Autism

What’s a fun way for people on the Autism spectrum to learn vital life skills and mind flexibility in a safe and unique environment? Find out on the second episode of Spirit of Autism Web TV , where I interview my good friend Sandy Bruce, founder of Shenanigans!

Thanks for tuning in! Look for the next episode on Wednesday, September 10 at 9:45 pm on AmericanHeartsRadio.com. If you have a topic you’d like to see covered or are struggling with a certain issue related to Autism, drop me a line and I’ll see if I can answer your question on the show!

best buddies

Best Buddies Program

best buddiesI recently heard about a great program that has my son’s name written all over it! (Naturally, when I told him this, he literally looked for his name written all over the program page. It wasn’t there :))

Contrary to popular belief, my son can be very social. By social, I mean friendly and open-hearted when meeting new people. However, if after an introduction the conversation doesn’t revolve around computer code or video games, there is an awkward disconnect.

He has friends all over the world that he Skypes with. Yes, I’ve seen the video chats and know 100% that his friends are real kids his age and not some creepy 50 year-old man pretending to like Minecraft! J has been hacked before and that was super scary!

Anyway, our problem is that my kids homeschool and I work outside of the home part of the time. We miss a lot of homeschool gatherings due to my hours, leaving my kids little opportunities to meet peers. Additionally, being a single parent, I tried to apply for Big Brothers Big Sisters for my son so he has a positive male role model in his life. I was told there was a 4+ year-long waiting list. Whoa! Seriously?

That’s why I was absolutely THRILLED to see this come across my inbox. Although this post refers to the Atlanta chapter, you can go to their website to see if there are programs in your area, as it is an international organization.

The Best Buddies program connects individuals that have intellectual or development disabilities with students from Emory. Each participant will be matched with either one or two Emory students to form a “buddy pair/trio.” The program encourages buddies to contact each other several times a month in addition to hanging out at chapter events. You can also request that your son or daughter to be matched in a same-gender pair.

Once paired with a Buddy, they meet as a chapter once a month during the school year for activities such as movie screenings, arts and crafts, field days and more. Events are typically held on Sunday afternoons on or near Emory’s campus, located in Druid Hills. These usually last for two hours. The first event will likely be in mid-September.

As a result of their involvement with Best Buddies, people with IDD secure rewarding jobs, live on their own, become inspirational leaders, and make lifelong friendships.

Online registration for the 2014-2015 school year is now open. If you are interested, you may register your son or daughter to participate by clicking this here (select Emory University as the chapter).

If you are interested in volunteering, click here.

I will be reporting back on J’s progress once the program is in full swing! Perhaps I will see you there.

Spirit of Autism Puberty

Puberty, Autism and Emotional Shutdowns

Spirit of Autism Puberty“The universe hates me!”

My son came stomping out of his room and collapsed onto the floor, heaving a huge sigh of frustration.

Unfortunately, this is not a new scene in my house, as I also have a 16-year old daughter. ‘Nuff said. But more importantly, puberty and autism can create a vicious cocktail that seems to bring on extremely magnified sensory issues, increased hyperactivity, regressive behaviors, and a whole lot of unexplained emotions. My boy just turned 12, but we started experiencing a profusion of puberty related issues as early as nine.

“The universe is incapable of hating, sweetie. What’s wrong?”

Evidently he had built a statue of his Minecraft skin in one of the game’s worlds and he told me that his friend destroyed it.  Minecraft is a unique multiplayer computer game where you learn survival skills and build custom worlds. The creative and building aspects of Minecraft allow players to build constructions out of textured cubes in a 3D world.

First and foremost, I was extremely proud of his ability to articulate to me that he was upset, the reason he was upset, and that he had worked very hard on the statue and it had taken him a long time. This is a HUGE milestone for us! But before we had a chance to begin talking about it, everything started going wrong for him. Everything he touched seemed to break or malfunction. He tried to pet the dogs and they ran away from him. His sister yelled at him for seemingly no reason.

I know from experience that when you have the “everything sucks” filter on, your experiences will follow suit. You know, like when you start out having a bad day it seems that your car won’t start, you spill coffee on yourself, you mess up a client proposal… have you ever had a day like that?

So the first thing I had to do was help diffuse his “universe hates me” perspective, starting with three deep and centering breaths together.

Delayed responses are another typical experience for Autistic children, and once I thought he was in a calmer place (about 30 minutes later), he started crying uncontrollably about the loss of his statue. It was that real guttural crying, too; I felt horrible. I consoled him and acknowledged that he felt upset that his statue was destroyed.

We then talked about choices. I told him he could either play one of his other favorite games (offline) to help get his mind off of it for now or he could choose to talk to his friend and tell him that his feelings were hurt. He could ask him why he destroyed the statue and open the lines of communication.

He had already removed his friend from his Skype list and blocked him from his server! His impulsivity coupled with an intensity of emotions he wasn’t accustomed to had caused him to overreact and shut down.

Once the tears were dry, we played a game called “5 Other Things”. I learned this gold nugget of a coping skill as a teenager and it’s never failed me. The idea is that it’s not what happens to us that causes emotional distress, rather our interpretation of it.  For instance, if a person doesn’t show up for a meeting with me I might immediately feel hurt and angry, assuming I had been blown off. This could rapidly lead to a barrage of negative thoughts: “Did they even INTEND to show up? Am I not good enough for a simple text or phone call letting me know? Who do they think they are?!” etc.

“5 Other Things” forces you to step outside of that neural pattern and look at some other possibilities for the event in question. Was there a family emergency? Are they simply running late? Car trouble? Did one of us write down the wrong day?

Naturally, if someone does this sort of thing to you regularly, “5 Other Things” is not the answer… getting a new friend is J

Being that my son didn’t SEE his statue being destroyed (it was simply gone when he logged back in to the server), we looked at some other possibilities:

  • Did another person playing on that server do it?
  • Did the game malfunction somehow?
  • Could his friend have accidentally done it?
  • Was the site hacked?
  • Did aliens land on earth and destroy all human forms of online entertainment? (Silly can be good if you’re trying to break neural patterns!)

“5 Other Things” worked! After some investigating (and a proven screenshot alibi of the suspect, ha!) he and his NOW UNBLOCKED friend discovered that the server crashed and the world was restored from an earlier version… before he had built the statue.

What a great learning opportunity this was for us! When puberty, autism and emotional shutdowns occur, we now have a blueprint:

  1. Take three deep breaths together
  2. Encourage him to share what is wrong, and praise him for being able to name it
  3. Help diffuse the “everything sucks” filter or mindset
  4. Acknowledge the feelings he is experiencing without judgment or criticism
  5. Play the “5 Other Things” game – without fear of getting a little silly!
spirit of autism sensory

It’s All About the Sensory

spirit of autism sensoryOkay, not ALL… but sensory issues play a bigger role in the daily lives of children with Autism than you might think.

I have always tried to explain this to the adults, teachers, caretakers, and yes, even physicians in my son’s life, who insisted that my child needed to be medicated for hyperactive and impulsive behavior.

There were certainly quirky and challenging things about him, even from birth. But I also had a girl first; so many of his odd behaviors were instantly dismissed as “boy stuff.” The real trouble started when he went to Pre-K and had to transition to different activities, sit quietly in circle time, and interact with a group of peers.

I remember waiting months to see a highly-acclaimed pediatric neurologist before my son was officially diagnosed with Autism. He was four at the time. For our long-awaited appointment, we were in the waiting room for an hour and in the doctor’s office waiting for another hour. What four-year-old would NOT be climbing up the walls at that point?

The doctor came in and promptly spent 10 minutes with us.

“Write your name.”

“Stand on one foot and hop.”

“Copy this drawing of a tree.”

“Ma’am, your son has ADHD, fine motor dyspraxia, ODD (Oppositional Defiant Disorder), and maybe some sensory stuff going on. Here’s your prescription for Adderall. See you in six months.”

Whoa… wha? Oppositional DEFIANT Disorder? He’s FOUR! When my daughter was four I practically wanted to SELL her! (Kidding. Mostly.) Of COURSE he was hyper! We just waited TWO hours to see him! And what’s with the meds? No explanation of any of these “disorders”? No constructive suggestions? No support or help?

Nope.

I researched all of the labels that supposedly defined my baby boy. Yes, he was hyperactive, but the first one that really grabbed my attention was sensory processing disorder. I went through a checklist and instantly started understanding my son and the world he lives in. Many of those “quirks” were a direct stress-response to how he interprets all the sensory input from his day-to-day environment.

We had an entire sensory evaluation done with a different specialist, and eventually arrived at the Autism diagnosis.

Once I started to differentiate between “My body hurts, I’m exploding inside and need help” and “I’m being a boy and testing my boundaries” my whole world changed, and so did my son’s.

The school system did not follow suit, unfortunately. During our IEP (Individualized Education Program) meetings I provided all of his sensory triggers in a document, what calming methods worked for us, and physical toys and music that he could keep in his private break area at school. The Special Education Director for the district continued to try and strongly suggest he be medicated.

I was actually told in one of these meetings that I was the type of mother that would deny my child insulin if he had Diabetes just because I wouldn’t put him on Adderall or Ritalin. Unbelievable!

I calmly repeated, “We need to start here, with these sensory issues. It is tangible – you can SEE he is struggling in direct response to these triggers. Why not start with what we know and work out from there? Let’s see what behaviors are left after we address some of these root causes and we can re-evaluate from there.”

Although I finally began homeschooling my son after years of battling with the school, this information is still critical. Almost every outburst, meltdown, or seemingly “defiant” behavior can be traced down to a sensory problem my son is experiencing at the moment.

Recently I ran across Asperger Experts – two young men with Asperger’s Syndrome that have navigated their way through the roughest times of childhood and adolescence and are now helping parents and educators do the same.

They have a program called “Fundamentals For Thriving Bundle.” It’s been extremely helpful for me to continue to understand, teach and support my son in a way that he is most receptive.

They published a video called, “The Sensory Funnel.” It’s a MUST-SEE if you want to learn more about your child’s or student’s sensory issues, how they affect day-to-day living, and what you can do to help him or her succeed.

Watch the video below and let me know your thoughts! I’d love to hear if it clicked for you like it did for me, and any other comments, successes or struggles you’re going through right now!

SOA Siblings

5 Ways to Include Neurotypical Siblings

SOA Siblings“It’s not fair! You always talk about Autism, Autism, Autism! You always write about him on your Blog and put his pictures everywhere!”

My firstborn isn’t playing the favorites card, she’s a little sensitive about Autism. Especially since my website, training classes, workshops and marketing materials use stories and facts about her brother as their framework. Sure, I can remind her about all the special privileges she receives as the eldest and the times we go places together without her brother. But that isn’t what she wants to hear. She wants to know that she’s valued, unique, and most of all, heard.

Here are some ways to make sure siblings feel included.

1. Don’t keep them in the dark.

The unknown is scary to children – especially when it’s surrounded by energy that may be tense and anxious. They are extremely sensitive to your feelings, so sugar coating or avoiding the subject of Autism in the home causes disharmony instead of protecting your child’s feelings.

Additionally, you should be open (in an age appropriate way) about what’s behind certain behaviors and that they are rarely, if ever intentional. Impulsivity and Sensory Processing issues can be hard to explain, but there are some amazing children’s books out on the subject of siblings and Autism. It’s a great place to start.

2. Consistent rewards.

It’s easy to get caught up in praising your child with Autism for every mark of progress and milestone. It is necessary. You may be missing the fact that the sibling is also counting every reward… and if the score isn’t evened they will remember.

Find a way to celebrate and recognize every achievement from all of your children.

This can also go the other way: many times my daughter will feel that her brother doesn’t get a just punishment for something she may have gotten in trouble for previously. Situations like that can indeed be a sticky-wicket, as your child with ASD rarely breaks rules intentionally. Unwanted behaviors still need to be addressed, and it helps to explain to siblings that discipline may be unique to each family member but no one is “getting away with it”.

3. Sibling-only time.

Often parenting our child with Autism requires an unequal amount time and energy for that child. It’s so important to schedule regular one-on-one time with your neurotypical child. Whether it’s a ritual of ten-minute blocks each night before bed or a once a week “girls night out” (in my case it’s my daughter), this time is to be treasured together.

4. Perspective and participation.

There are times when I’m truly stumped on one of my son’s behaviors that affect the entire family dynamic. Without sending her the message that I need her to solve the problem, sometimes I ask for my daughter’s perspective. She can throw some fresh ideas on the table that I may not have considered. Again, I never make her participate if she doesn’t want to or cause her to feel that she has to have the solution. She does appreciate that I value her opinion and viewpoint.

5. Support and expectations.

It’s important for siblings to feel that they are not alone in their experiences. There are many sibling support groups to share their struggles and feelings, but don’t force it. In our case, my daughter had a good time visiting one of our local groups but quickly discovered that being with people that focus on talking about her brother still makes her feel like the world revolves around him. She flourishes when involved in groups or classes that are uniquely hers, like her art community and comedy improve classes.

Equally as important, do not expect your child to be overly responsible for the child with Autism. Unrealistic expectations can lay an unbearable amount of pressure on siblings. This isn’t a free pass to skirt all family responsibility; check in often and encourage open communication throughout the journey.

What are some ways that you keep siblings out of the shadows and keep things “fair” in your house? Share by commenting  below or on the SOA Facebook page!

SOA Gifts of Autism

The Gifts of Autism

I was recently sent a tweet from Ryan McTavish, a brilliant and talented drummer who also happens to be Autistic. He asked me to watch his talent show performance video to raise positive awareness for Autism. Being a musician myself, I was beyond blown away by the gifts of this young man.

Before going any further with my thoughts and musings, here is the video he sent me:

Amazing, right?

This video made me think more about the gifts of Autism. Of course I see them in my son every day; I brag about him all the time!

He used to play online games, and then one day he was messing around and pulled up the code for the game. He changed some formulas and scripts and said, “Look, Mom! When I change this to <blah blah blah numbers and letters I don’t understand> the background of the game changes!”

This spawned a creative interest that resulted in him writing his own custom video games, filming his screen while showing custom “tips and tricks” and posting it all on his YouTube channel as a tutorial.

Gifts vs. Deficits

I currently train Emergency Responders and businesses how to recognize, respond to and best communicate with people with Autism. I love this career I’ve created for myself and am blessed to be doing something that truly makes a difference in people’s lives.

The part I don’t like as much is that I have to stay somewhat focused on the deficits and challenges faced every day by those on the Spectrum. I educate on Sensory Processing issues, communication struggles, missed social cues, muscle development issues, and more.

It’s great that I’m bringing awareness and action into businesses and public safety. But what they don’t get to see are all the gifts I experience on a daily basis from raising my son.  They don’t know how kind and good-natured he is, or how innocently he views the world. He marches to his own beat and knows what is in his best alignment.

He sings and hums all day long. He gets on Skype and teaches new friends how to play and build in Minecraft. He hugs the dogs and tells them they’re beautiful. He always kills spiders for his terrified older sister, no matter how much she teased him or yelled at him minutes earlier. He offers the last cookie before taking it. He delights in taking walks and gets excited about Nutella sandwiches.

He sees the world so differently than I do, and I am grateful that I get to go into his world and catch glimpses of his perspective as often as I do.

Yes, I want to help him with his challenges. Yes, I want to help him be more independent. Yes, I want to support and teach him about making it in the world. And I do all of these things. But most of all, I am the one learning from him. And that’s the greatest gift of all.

What gifts of Autism are you most thankful for? Share by commenting below or posting to the SOA Facebook page or on Twitter using #GiftsOfAutism!

autism bullying

How Safe Is Your Autistic Child from Being Bullied?

Going through the school system today is harder than ever for our children, especially with the increased pressures of test scores, the lack of recess or gym in many schools, and the barrage of ridiculous standards that seem to be set by social media.

As parent of a child on the Autism Spectrum, I want my son to have the best possible experiences – academically, developmentally, and socially.  But when it comes to making friends and fitting in, bullying can be a real threat for him. Especially since he is so sweet and kind by nature and is quick to believe everything at face value.

SIDE NOTE: It is this innocence that also makes your child with Autism a vulnerable target for online predators! Read about our experience with an internet hacker here.

Bullying doesn’t always mean getting beat up for  lunch money. It could show up in the form of manipulating my son to perform an action or say something that will get them in trouble in class. It could look like another child coercing him to hand over his dessert every day in exchange for letting him sit next to him. And it most certainly can rear its ugly head with any words that make my child feel like he is somehow less than the other kids around him.

In the first few grades of elementary school, it was easy to explain my son’s differences to his peers. When he covered his ears to block out the painful school bell sound I simply told his classmates that he had super-sonic hearing! When he jumped up and down and couldn’t sit still in circle time I exclaimed that he was exercising his special springy legs for some Mario power jumps later on. Little tricks like that were accepted.

Now my child is 11, wears men’s medium clothes and sports a mustache.  It’s not as easy to step in and offer plausible explanations for some of his quirks. He needs real tools and strategies that can help, not a helicopter mom following him around :)

What does work?

In Growing Up on the Spectrum: A Guide to Life, Love, and Learning for Teens and Young Adults with Autism and Asperger’s, Dr. Lynn Kern Koegel and Claire LaZebnik offer some practical suggestions for helping your child on the spectrum feel safe in every environment. Here are a few of our favorites:

Checking in. If your child is at the age when he doesn’t want a parent around at school, making a point of dropping off that missed homework or forgotten lunch at a social time of day (such as lunch) will help you understand how your child is faring in his social interactions and may give you some hints about what social skills you need to work on at home.

After school clubbing. Help your child get involved in a club, even if you have to start it yourself. It will give your child the opportunity to interact with peers who have similar interests. What is your child really good at? Can he teach or demonstrate those gifts to his peers? Make it happen!

Party time. Have short get-togethers or parties that are structured around an activity. We have had tons of fun with a short “Make Your Own Pizza Bagel” party (I cut out sliced cheeses in the shape of Super Mario characters to go on top of the mozzarella) or “Design Your Own Pokemon” party with simple index cards and markers. Now that he is older we have Minecraft and Wii-U gatherings.

Buddy system. Find a peer buddy who will help your child safely get to classes. Recruit some kind-hearted kids to be a buddy to your child and accompany him through the hallways.

Educate them. Teach the students at your child’s school about disabilities. Even with a special needs department and inclusion programs in many schools, there is still a staggering lack of training and understanding. It shouldn’t stop with the teachers and staff. If peers are made aware of your child’s challenges and how he’s struggling to overcome them, they’ll be far more likely to lend him a hand.

Lessons about how to be a friend. There are a lot of ways that you can teach your child to make and maintain friendships. Sharing is one. Asking questions is another. Good phone and electronic etiquette are essential. If your child is on the spectrum, she may need help with these areas. I know mine does!

Multiple choice responses. There are times when the best response to a bully is ignoring them and there are other times when standing up to a bully may be the only option. Many schools have mediators who can tackle the situation from both sides. Use social stories to teach your child how to differentiate appropriate responses based on the situation at hand. My son responds to code systems when it comes to choosing appropriate responses. We have code words and numbers for almost every emotion and typical responses to certain situations.

How about you? What strategies do you use to avoid or address bullying with your child?

Share by commenting below or posting your thoughts on our Facebook page!

autism visual strategies

Two Simple Visual Strategies You’ll Use All The Time – via Behavior Communicates

I recently ran across a brilliant video from Carla Butorac with BehaviorCommunicates.com that teaches two simple visual strategies that help remind us as parents and teachers to cut the verbal and go visual with our children.

If you find yourself telling a child to do something over and over and over (my son) and they don’t comply, you need to go visual and SHOW them!

This video illustrates two simple examples of visuals you can use in the classroom or at home. The first is called FIRST and THEN; the second visual is called a token board.

Take a look at the video to see what this looks like!

I can’t wait to employ these ASAP to help Justin stay on track, especially since I homeschool. Give them a try and let me know how it goes by commenting below or posting to the SOA Facebook page!

You’ll also want to head over to Carla’s website, BehaviorCommunicates.com, to learn some more amazing tips like how to teach a child with Autism to play!

autism wandering child

7 Vital Tips for Autism Wandering Prevention

My son was 18 months old. He was standing next to my bed, humming, as I was folding laundry and separating the piles. Then he walked out. In the time it took me to fold a pair of jeans, the child had walked to the other end of the house, found my keys, figured out which one was the car key (!), went outside, opened the trunk, and climbed in.

When he was in First Grade, I dropped him off at school, walked halfway to his class with him, then went on my merry way after kisses and high fives like usual. It just so happened that I forgot something from the house that day. Coincidentally, I also needed gas and went left instead of right, passing the school once again. About four blocks from the school, in a direction I normally never would have traveled, was my son, walking with his backpack and singing, without a care in the world. He apparently walked right out of the building after we parted in the hallway, and the teacher assumed he was absent that day. No one knew! Imagine what could have happened if I had turned right like I always did!

Here are 7 tips if your child is prone to wandering

  1. Safety-proof your home. Home should be a safe haven. In addition to traditional childproofing for small children, you will have to take some extra measures for your child with Autism.
  2. Install door alarms. Many children with Autism are prone to wandering. Alarms offer great back up protection.
  3. Arm your child with a form of communication. Whether your child is verbal or non-verbal, communication is a challenge. Create a visual safety book for your child with key questions and answers he or she may be asked in an emergency situation. Practice, practice, practice!
  4. Get to know your neighbors. It’s a good idea to introduce yourself and your child to your neighbors. You can explain what Autism is, along with some of your child’s behaviors that would strike other people as odd. This way they will call you instead of the police, or help direct your child home if found wandering.
  5. Register your child with public safety. Contact your local police precinct, fire department, and hospital and register your child with their database of special needs families.
  6. Use social stories. Teach your child how to handle emergency situations like fire, burglary, strangers at the door, when someone is hurt, and calling 911.
  7. Get QR Code iD apparel for your child and subscribe to their website.

What is QR Code iD?

People who have Autism, cognitive disabilities or other special needs or health issues may be unable to state personal information such as name, phone number, address, medications taken, where Mom and Dad work, issues peculiar to that day, the hotel where the family is staying on vacation, etc.

If your child is lost or wanders, rescuers need to know who to call, and how to help.

QR Code iD creates a way to put this information in one place. This information is accessed from any computer browser, either by entering the URL manually with the computer keyboard, or by scanning a QR code printed directly on the child’s clothing, both of which will take you to the client’s non-secure homepage. This page displays all the information that a loved one wants someone to know when finding the child. This information can be updated REAL TIME!

QR Code iD commissioned Special Needs Artists to create beautiful artwork to put on shirts, buttons, key chains and other products that have QR codes on them. These talented Special Needs Artists will be discovered and contracted to contribute original artwork for our products.

Membership is only $29.00 a year for this invaluable service. I highly recommend it!

Use “spirit 15″ when you check out for 15% discount through July 4!

Do you have any stories of your child wandering that really frightened you? What did you do? Share your comments below or post them to the SOA Facebook page!

ssi

Guest Post: How to Apply for Disability Benefits for an Autistic Child

Image courtesy of ssa.gov

The Social Security Administration (SSA) does recognize autism as a potentially disabling condition; however, your child must be severely autistic in order to meet the SSA’s eligibility requirements. This is because many children who suffer from more mild forms of autism are able to function at a nearly “normal” level socially and academically.

Children with more severe forms however, do require significant supportive care, which can leave you financially strapped. Social Security Disability (SSD) benefits can give you the financial resources you need to ensure your child receives the consistent support and attention he or she needs and deserves.

Supplemental Security Income

Children who meet the SSA’s eligibility requirements receive benefits through the Supplemental Security Income (SSI) program. SSI is a need-based program, which means it has strict criteria regarding financial status for children to qualify. In other words, even if your child suffers from severe autism and meets the SSA’s definition of disability, he or she may not meet the financial eligibility requirements for getting SSI benefits.

The income and other financial resources you and your child have available will be thoroughly reviewed by the SSA, and must be very limited in order for your child to receive SSI benefits. The calculation of income and resources is fairly complex, with some sources counting and others not. To learn more about SSI financial criteria, visit: http://www.socialsecurity.gov/pgm/ssi.htm.

Medical Eligibility for SSI

For your child to be found medically eligible to receive SSI benefits, he or she must be severely impaired. To prove severe developmental impairment, you must have substantial medical records documenting specific information, including:

  • Severe limitations in interacting socially
  • Pronounced communication deficits
  • Inability to engage in age appropriate activities that require imagination
  • Very limited involvement in a broader range of interests and/or activities

You must also have the following information well documented in his or her medical records:

  • For children between 1 and 3 years of age, a pronounced limitation in at least one of the following areas:
    • Fine motor skills
    • Communication and/or cognitive abilities
    • Age appropriate social functioning
  • For children between the ages of 3 and 18, severe limitation in at least two of the following areas is necessary:
    • Communication and/or cognitive function
    • Age appropriate social functioning
    • Inability to provide age appropriate self care in everyday activities
    • Pronounced difficulties with concentrating, remaining focused and on task, or in completing tasks at a reasonable/normal pace

Medical Evidence and SSI Eligibility

The documentation in your child’s medical records must meet certain standards in order to prove the criteria listed above. You must work closely with your child’s doctor to ensure the right tests have been completed to satisfy the SSA’s evidentiary requirements. You may also want to consider seeking assistance from a Social Security advocate or attorney who is familiar with handling autism disability claims.

The Application Process

You can begin the application process by contacting your local SSA office and obtaining a copy of the Child Disability Starter Kit. You can also get the kit from the SSA’s website.

The kit will tell you how the application and review processes work and what information you will need to complete the SSA’s application for benefits. Required information includes your child’s medical history and school records. Additionally, as SSI is a need-based program, you must present the SSA with financial records as well.

To finalize an application for SSI benefits on behalf of a child, you must participate in an interview with an SSA representative. If you have a caseworker from family and social services with whom you work, he or she can arrange the SSA interview appointment for you, or you can contact your local SSA office directly to make an appointment.

Article by Ram Meyyappan
Social Security Disability Help

For more information on Autism and Disability, please visit: http://www.disability-benefits-help.org/disabling-conditions/autism-and-social-security-disability