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Elaine Hall

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Living With Autism: You Are Not Alone

Posted: 03/19/2012 11:17 am

I am haunted by the headline: Mother killed 22-year-old autistic son, then herself.

"He used a voice-output device that allowed him to communicate on a limited basis," reads the article written by Lisa Fernandez and Julie Prodis Sulek in the Mercury News. "He was delightful," a neighbor said about the son. "He was nonverbal but very physically active. He loved walking and hiking."

This description of George Hodgins reminds me eerily of my own son, Neal. I can't stop thinking, "There by the grace of G-d go I." I have definitely had dark days and felt helpless. But fortunately, I have had friends and family to pull me out of it. Or as my friend Christina says, "We all have our dark days, but then our kids do something that causes us to laugh and we see the sunshine again. I guess Mrs. Hodgins just didn't have enough of the sunshine days."

My Facebook is flooded by comments to the article:

A father writes: "So many of us parents are lost, alone and unsupported; All I want is to know that when I am not here that my son is ok and taken care of, but I cry everyday wondering what will happen to him."

A single mom adds to the conversation: "Sadly, my surprise is that we don't see more cases like this ... Despite community 'awareness,' there remains a lack of support and educational opportunities for young adults on the spectrum. As parents age, their energy decreases and the stress of who will care for their child after they are gone can simply be too much to shoulder.
It seems clear that she felt that ending her life and that of her child was preferable to the torment both were experiencing.
 There is clearly a need for more meaningful support for families in this situation. Research is all well and good but shouldn't we be focused on where and how our young adults will live?"

Fortunately, through The Miracle Project, and the Nes Gadol Religious Education Program, I have been blessed with an incredible community of parents. Lots of sunshine days to share, and whenever one of us falls into that "rabbit hole," there is always someone to pull us up, yank us out, take us out for coffee, and remind us that we are not alone. Obviously, Mrs. Hodgins felt very much alone.

The 24/7 challenges of parenting a child with special needs can be daunting. Raising any child with a disability or illness can be difficult to say the least. But for many reasons, and for many people, parenting a child with autism can be especially overwhelming.

If you see a physically-disabled child in a wheelchair or blind child with a cane, you immediately have compassion and understanding. Autism on the other hand, can be an invisible disability. At first glance, many children with autism appear "normal" (whatever that means). Autistics who are highly verbal, but lack in social skills, can be called "weird" and bullied. Those with fewer verbal abilities may act out in frustration, needing to be understood. Parents can be embarrassed by their child's behaviors when others look at them with fear, judgment, and disapproval.

Parents with children who have autism are often "forced" by lack of school programs to be the "experts" on their child. The emphasis on "curing" their child prevails. So if a child is not "cured" by adulthood, the parents may feel like failures. This sense of responsibility is not uncommon with many families. Although every child with autism benefits from early intervention, only a small percentage of diagnosed children are actually "cured." Accepting a child's "differences" and creating lifelong supports are paramount to ease the intense stresses that many families experience.

This feeling of helplessness and aloneness when raising a child with autism is not just limited to the U.S. It is global. I was recently invited to the ReelAbilities Film Festival in NYC. While there, I watched two films on autism: one from China, Oceans Heaven, and the other from Israel, Mabul.

Ocean's Heaven opens on a small boat in the middle of the sea with a dad and son. Dad is tying a weight to his and his son's legs and pushing them both overboard. At first I thought this was a dream sequence only to learn in the next scenes that the father had terminal cancer and he didn't want to leave his autistic son without him. For the remainder of the film, the father teaches his son independent living skills. It is a beautiful story of love and letting go.

The Israeli film, Mabul focuses on the intense challenges a family endures when they are forced to take their older autistic son out of the institution where he lives. Both movies convey the desperate need for community support.

In the film, Autism: The Musical, one of the parents states that nothing will change until people "value" our kids with disabilities. To me, this stands out as how we need to value those who perceive the world differently, to listen to the child who doesn't speak, to enjoy slowing down, to cherish the many gifts of wonder that those with disabilities have, to channel their abilities and preferred interests, and to embrace our children for the resource they are for all of us.

Perhaps we can let the tragic events of last week be a call to action. An action for the "typical world" to reach out to those who are isolated, to take care to help out that parent in the grocery store who is having a rough day, not with dirty looks but with compassion and understanding. And to offer a shout out to those of us families in the "other world," the autistic world, that we are never alone. We have all felt helpless, we have all felt isolated, and it does get better. Let us bring hope to those who are in despair and compassion to those who feel overwhelmed. Let no family again believe their only choice is to leave the planet. And may Elizabeth and George Hodgins rest in peace.

Need help? In the U.S., call 1-800-273-8255 for the National Suicide Prevention Lifeline.

For more by Elaine Hall, click here.

For more on autism, click here.

This post has been updated since its original publication.

 
 
 

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12:36 PM on 03/30/2012
Elaine - you are not living with Autism - you are living with a HUMAN BEING who has autism. I'm sure Mrs. Hodgins did indeed feel alone. But let us not forget how equally alone it must feel to be a child staring down the the barrel of a gun that your own mother is pointing at you. In your effort to voice compassion for parents, you seem to leave little space for the voices and experiences of the children that they are parenting. George was a human being. He was murdered. Compassion for his mother yes, and an equal measure of compassion for George, and for every child who experiences neglect, resentment, and hatred from the one person who is supposed to love them without condition.
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09:33 PM on 03/21/2012
I made this video a few years back called "You're Not Alone" basically for our one twin son that has autism (dx'd at age 4 years old) I struggled & fought with hubby was in denial, and more, but wanted to give our son love, support & understanding. We (as a family) needed that support & understanding from our friends & family. When they saw my video , some reached out to give support, others cried and shied away and are less heard from. But our family is there for our son Cameron- always. It has been a very long lonely roller coast road for all of us. But now 4 years LATER after putting that video up, I am so glad we pulled together, (and constantly do!) because Cameron has really done so well. At first, I really wanted to give it all up.. my life, my family & kids.. but I know now that I needed Cameron in my life: before Cameron, we REALLY had NO idea what Autism really was.
Yes, it's been hell but also a blessing: http://www.youtube.com/watch?v=AJHTOy-tHQA Don't just watch the video, but hear the words of the song played to this video.. (Don't Give up)

We must never give up no matter what we face.. in your darkest hour, believe me YOU ARE NOT ALONE! (ps: Yes, Cameron STILL loves Thomas & Friends to this day)
11:14 PM on 03/20/2012
I have a 26 year old son who as autism, and I agree that we must take action to change the lonely and strife - filled lives we lead, worrying about "What happens when they grow up?" I believe that we cannot expect adults to truly understand our situations when they don't live with the same struggles. The only way is to start teaching about this huge social problem at a much younger age... people have to grow up with the awareness. The action that I took was to create a doll program called My Sibling dolls that would teach children about others who learn and grow differently than they do. I tell the stories, from the perspective of the typical brother or sister,about what life is like when you have a sibling with a disability. I also have a My Pal for Autism Awareness doll and bear that come with a booklet in which children can write about what they do to make more people understand about life with autism. The best part about my project is the Work Experience Program in which I provide job sampling experiences for people with disabilities.
09:55 AM on 03/20/2012
Thank you so much Elaine for speaking out for so many autism parents and the utter anguish they feel about letting go. As a mother to a teenage son with autism, severe learning difficulties and epilepsy we have found over the years that people do not 'rush' to help him, we find ourselves reaching out and trying to bring people to our son who is so vulnerable and challenging in such complex ways. It is a total minefield and we find ourselves constantly being the voice for our son, with form filling for benefit claims and social care here in the UK. The list is endless and exhausting, and yes, we are getting older and feeling older. At the end of the day you are right, it is about people and the patience, love and care they can bring to our children. Even though no one has come knocking on our door to want to help our son, I just can't lose faith in human kindness otherwise I would be the same as this tragic mother and son case. I just can't afford to let my guard down. I can't afford to stop believing that there is help out there for my son.
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Kibblet
.This is it, that's the end of the joke.
08:28 AM on 03/20/2012
We can't die. No parent wants to outlive their child, we hear that all the time, but for those of us with children like ours, we simply cannot die. And that's a really scary thought.
11:55 PM on 03/19/2012
Beautifully worded, Elaine.
10:35 PM on 03/19/2012
I am in nearly the same situation as the mother in the opening story. I feel abandoned by friends, live too far away from family, and it seems as though our son's condition is slowly killing us. My husband and I are exhausted and psychologically devastated. We are hanging on with some paid help, for a few hours a week and with a bit of therapy. But it is the lack of help from my friends or anyone else in the community that is really killing us. And your article doesn't actually provide any help. No organizations to call, no support groups.
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Chantal Sicile-Kira
Author, Advocate, Founder of AutismCollege.com
08:20 PM on 03/19/2012
Thank you for this post, Elaine. The situation of Georges and his mother with a tragic end illustrates the strain parents feel as their children reach adulthood. Options are few and far between and parents feel more isolated when their now adult children leave the school district. It is harder as your child gets older. This is the reason why Jeremy and I wrote our book A Full Life With Autism. We have to create connections and options when there are none.
Thanks, Elaine, for all you do.
Best,
Chantal
12:40 PM on 03/19/2012
Elaine, you have a talent for bringing heart to all these issues concerning autism. There are certainly challenges for many in the community, but choosing to see the beauty in diversity is a daily journey. Having focused professionals in the community who infuse intellect with the qualities of the heart.....is a gift. Thank you.