Does your child with autism spectrum disorder (ASD) experience sleep problems or gastrointestinal symptoms? Please help The Irish Centre for Autism and Neurodevelopmental Research


Irish Centre for Autism and Neurodevelopmental Research

Irish Centre for Autism and Neurodevelopmental Research

Does your child with autism spectrum disorder (ASD) experience sleep problems or gastrointestinal symptoms?

As you many of our readers will know we have been asking our readers to help The Irish Centre for Autism and Neurodevelopmental Research (ICAN) with various studies. They have contacted us to request our help with a new project.

They say “Some children with autism have both sleep problems and gastrointestinal symptoms, while other children have one of these issues or none at all. The Irish Centre for Autism and Neurodevelopmental Research (ICAN) in National University of Ireland, Galway is interested in hearing about your experiences with your child or adolescent aged 3 to 17 years with autism. We are interested in understanding how sleep problems and gastrointestinal symptoms affect both child and parent. Even if your child doesn’t have sleep or gastrointestinal problems, we can still learn a lot from your information on why some children have these issues and others do not. If you wish to participate, please use the link below.

http://bit.ly/1sYrzpp


A diagnosis of autism! What was your first reaction on hearing the diagnosis of autism?


Advice for autism parents

Advice for autism parents

When I started this blog a few years back I wrote a blog post describing our son’s autism diagnosis. You can read the story here.

In the five years which have passed so much has changed. Not always for the better.

But I still vividly recall the day of the diagnosis and the pain it caused. In fact it was the 70th anniversary of the German invasion of Poland if your interested. We got the diagnosis at around 11.30 in the morning. Again if you are interested.

My initial reaction was a bit of a surprise to me. Both my wife and I had expected it. In fact. looking back. I don’t suppose there was any other possible outcome. But hope springs eternal – as they say.

After the first few moments of bleak sadness my next reaction was anger. Not just at the way we were told. Though pretty inept I doubt it would have made a difference. It was as much the unfairness of it all. Why? Because in those days I really thought my son’s life was over before it had begun.


But it’s not. Not at all. Yes it is different sure and not always easy but we lead a full family life and John has developed in many ways.

But I still think about that day and wondered how typical I am.

So a couple of days ago I posted a question on our Facebook Page AutismTalk. The results were fascinating and I thought I would share some of them with you. The ones I’ve selected have been on the basis of being representative rather than anything else. Indeed at time of writing this post we have had over 320 comments.

It would be great if you would use the comments section below.

Jason was pretty relaxed “It wasn’t a big deal to me. I still love my daughter if she was autistic or not. Even though she is classified as special needs….i don’t see her that way. She is just Julie..my daughter…no more…no less. The world is a her doorstep!”

Another reader was similar to me “Broken.. Cried.. Blame my self… But he is still my little boy… And I’m proud of him.. Very proud of him….” said Silvia.

Angela shared ” Firstly it was relief…..not because my son has asd but because at least we had finally got some where and I knew I wasn’t going mad,….i had known from an early age that my son was autistic it has just taken a while to get anyone to listen…….but then the feelings of guilt,I couldn’t help feeling that it was my fault somehow….i still do get those feelings sometimes , but at least we can now fight for my son to get the correct help he needs…..i love my son with all my heart and wouldn’t change him for anything.”

” I held it together until I got in the car. Then quietly cried the hour drive home. My husband drove us in silence. We spent that day grieving normal, the loss of what we thought things should be like for our boy…only just 3 then. The next day we woke up ready to embrace everything with a positive and easy going attitude. We threw all expectations out the window. We accepted this challenge. We got educated, we embraced therapies, learned how to step inside him. Jonathan’s now 11. Doing great. He’s a happy, warm, loving, and brilliant boy. My gem ” said another reader.

Robert mentioned “Relief in the fact that I could tell family to back off that it wasn’t a discipline issues.”

Of course emotions are strong “I cried for like 2 hours in my car after my wife my son got back home . We went to the doc they told us she cried on the way home I ask God for stenght not to cry and be strong for her after we got home I told I had to return to work I got in my car and broke down and cried . I love my boy it more then 10 years for us to get pregnant . I never asked God why or have any bad feelings what I did tell God is that ok I love my boy and accept me with all my heart just please don’t let my do this on my own help me with your love if you do this with me I know I can see anything through . It been good my wife and are more like a team now with share all my son things therapies , doc visits were never alone on anything . There are the bad days really bad day but that’s why we’re a team if she feels she needs a brake or can’t go I’m like tag me I’m in ? But there are good day to and we both share them . He’s my boy ” I love you carlosmanuel I won’t change you for anything ”

Glorie told us “Relief in the fact that I could tell family to back off that it wasn’t a discipline issues.”

Not everyone was positive “Sad. Confused. Frustrated. Lost. Hopeless. I didn’t cry, I just developed severe anxiety and depression. I’m pretty sure I have no clue what I’m doing. God help us all.”

Pauline movingly said “pride and love and knowing i was right a mother knows her child best xxxx” and another said “My husband and I sat in our car in shock and said that no one would just slap a label on our son..we expected the same for him as our other son. We had to make adjustments over the years, it was not always easy, but he is now 21 and is an amazing young man.”

The view from people with ASD was interesting. Katheryn shares “Finally I have a reason why I was different and that I’m not alone ”

Anna was upbeat “My son and I heard the news together. He was not diagnosed (with Aspergers) until he was 17. We both looked at each other with that sudden dawning of understanding. Suddenly we knew the reason for all our struggles. We hugged and talked well into the night. And had many conversations about all of it.”

So what about you? What was your reaction?

DesireeNicole Relieved, Camren is my third son and I learned not to compare my children after my second cause I seen first hand all kids were different and they developed on their own time. But I knew something was different or special I call it about Cam. My older boys threw temper tantrums but camren has episodes and when we got his diagnosis our life became easier, his and mine because we learned how to communicate and compromise with each other and his therapy’s and teachers I am forever grateful for.
MichelleBarger When I first got my son’s diagnosis I thought of my pregnancy, I ate lots of sea food. Then thought of the delivery, his umbilical cord was wrapped around his neck when he was born and he also swallowed merconium before he came out. Then I thought about his development when he was growing up. I saw signs but no one would listen. Finally got a Dr to listen but only after he was hospitalized with RSV at 15 months old and I got mad at the hospital staff.
BevLeroux Asperger’s – My Story
September 5, 2010 –
November 5, 2014
I had been researching
autism since 2005 when my young granddaughter was identified with
‘developmental delays’. I
lived my whole life not knowing I was on the autism spectrum, struggling to fit
in and hold down a job as a single parent. Managed to do this by the skin of my
teeth and retired in December 2010 at 65, just two months after my diagnosis.
SELF-IDENTFICATION,
FIRST!
In September 2010, I came across a local Asperger’s
group on Meetup.com that provided a list of websites, articles, videos and
books. I really connected with Michael John Carley’s “Asperger’s from the Inside
Out”. That very day, between videos and books I filled 30+ pages in a notebook:
“Yes, that’s the way I think. Yes, I do that. Yes, that’s what it feels like.
Yes, yes, yes, yes, yes!” Watershed
moment.

Receiving an Asperger’s diagnosis, in October 2010, was a powerful
experience and a huge breakthrough for me. I had always known I was different,
from earliest childhood, and now I understood why. And I’d found others who are
like me! What a relief to view my life in retrospect and no longer blame myself
for being weak, flawed or wrong… but simply wired differently and experiencing
life from a different perspective than most people.

In addition, I realize now I had been self-medicating
most of my life as a way of coping with depression and anxiety resulting from
living life on the spectrum… being different and yet seeming to be ‘normal’…
struggling to fit in and meet high expectations both in school and at work, day
after day. That, and some pretty traumatic life experiences, made for a very
bumpy ride. I like to call it ‘high-functioning hell’.
Neurodiversity.Autism is a genetic neurodevelopmental condition. I
believe that undiagnosed and untreated it can well lead to mental illness and
addiction.I’m willing to bet that
thousands of people with ADD/ADHD and autism-spectrum disorders—particularly
the high-functioning ones—go through years of suffering undiagnosed or
misdiagnosed. They end up alcoholics or drug addicts and mentally ill—with
their lives derailed… a loss to themselves and society. Who knows how many suicides result from this kind of suffering?
Yes, I retired two months after my diagnosis in
November 2010 (after working 45 years in 20+ jobs) and life has never been
better. Enjoying every moment of my freedom to do what I love each and every
day. Helping others who are travelling
a similar road, especially young people on the spectrum who are just beginning
to make their way in the world. I
spend my social time with these mostly 20-somethings… mentoring, encouraging
and learning from them. I made these wonderful connections through social media
over the last four years.
I am very grateful for
this breakthrough. It has given me a wonderful opportunity to serve the adult
autism community.
On the creative side, I’m
an avid knitter, soon to attempt jewellery making, drumming and guitar. My dog
Lily and I travel as a team. Having the time of my life!
Bev Leroux

Autism and animals. We are looking for parents of children with autism to help with some research for Warwickshire College


Autism and dogs

Autism and dogs

As you may know PatientTalk.Org has been interested in the use of animals as a therapy for people with Autism. You can check out a blog post I wrote on autism and service dogs here.

So were are delighted to be able to give some help to Jenna Lauder, a student at Warwickshire College, who is studying companion animals and the effect they have on autistic children. She needs the help with some research from parents of children with ASD.

Ms Lauder writes” My name is Jenna Lauder; I am currently a 3rd year student studying a BSc Hons in Animal Science and Health at Warwickshire College. This year I am undertaking a dissertation based on the subject of companion animals and the effect they have on autistic children. As part of my research, I am required to distribute a questionnaire.

I am looking for parents of children particularly between the ages of 4-11 who have a companion animal, but also would like those who do not have a companion animal to respond for an equal comparison.
It would be great if you have a few minutes to complete my anonymous online survey, which should take no more than 5 minutes.

Your time and contribution is much appreciated!

Please click on the following link if you DO have a pet: http://goo.gl/forms/rhBnfPujBz

Please click on the following link if you DO NOT have a pet: http://goo.gl/forms/TZoDF5Z5WE


“Understanding Family Role Play in Second Life”. The University of Alberta are looking for people who do NOT use Second Life to take part in some research.


University of Alberta

University of Alberta

Laura Gilmore, a PhD student the University of Alberta, has asked us to help locate people to participate in some research.

She is looking for people with autism and without ASD who do not use Second Life.

She writes “I am a first year PhD student at the University of Alberta and am continuing work from my Master’s Thesis. Seeking participants for graduate student research survey on second life participation for individuals with autism spectrum disorders (ASD) and those who do not have ASD. Interested in both users of Second Life and Individuals who do not use Second Life. The link below will take you to the survey. Thank you for considering my survey.”

You can take the survey here.

Background.

Previous research has suggested that people can learn social skills from participating in 3D replicas of real life situations. However, there has been little research about potential of these 3D replicas of real life situations to be socially beneficial for those who participate in them.

Study Procedures

Participants will be invited to click on a hyperlink and be given the opportunity to complete an online survey. In this survey, there are no right or wrong answers, we simply want to know how participants solve social problems and how they perceive their own well being. The survey should take less than 10 minutes to complete.

Benefits

If this study finds a positive association between participation in family role play and social problem solving skills and well-being among adults it will be used as a basis for future studies that may support the use of virtual environments in therapy.


Risk

The risks involved in participating in this study are no more than what would be experienced in a normal day.

Voluntary Participation

You are under no obligation to participate in this study and can exit the survey at any time. As surveys will be anonymous upon submission, you will not be able to withdraw your data once the survey is submitted.

Confidentiality & Anonymity

This research will be used for completion of a thesis by Laura Gilmour and a potential publication of a research paper. Addresses and Second Life usernames which will be deleted immediately after data has been collected. The only individuals who will have access to the survey data will be Laura Gilmour and her research supervisor Dr. Veronica Smith. The data will be stored on an encrypted, password-protected computer in for five years before being destroyed.

The plan for this study has been reviewed for its adherence to ethical guidelines by a Research Ethics Board at the University of Alberta. For questions regarding participant rights and ethical conduct of research, contact the Research Ethics Office at (780) 492-2615.

World Autism Awareness Day 2015 – find out how you can take part!


Autism Awareness Month

Autism Awareness Month

As you may know 2nd April each year sees World Autism Awareness Day.

Throughout the globe the autism community comes together to raise both awareness and acceptance of autism, Asperger’s and autism spectrum disorder (ASD).

So we thought it would be useful if we helped promote a new Facebook event entitled, unoriginally, World Autism Awareness Day. It would be great if you could join us here.

So why are we running this event rather than just providing you links to other peoples?

Well there are a few reasons.

Firstly we actually believe that the autism community should be doing our own stuff rather than being told what to do by governments and NGOs.

Secondly we think “small really is beautiful”. The little events all put together beat the massive PR lead stunts.

So what would we like you to do. Well obviously join the event and invite all your friends and family to do so as well!

Secondly we would love it if you used the comments section below to provide any information , pictures or links to stuff you are doing around the day.

So please help us spread the word.

And do remember that autism awareness does not end at the end of April. Every day should be World Autism Awareness Day .