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Category Archives: diagnosis

Comorbidity – Rodgers

26 Monday May 2014

Posted by Ann Kilter in Achievement, Asperger's syndrome, Autism, diagnosis, Disability, Not autism

≈ 7 Comments

Tags

asperger's syndrome, Elliot Rodgers, Lanza, mental illness

I was alarmed when I heard that Elliot Rodgers had been diagnosed with Asperger’s Syndrome. That was one of the first things I heard about Adam Lanza after he killed 26 at an elementary school in Connecticut.

The media gloms onto a diagnosis in an effort to make sense of the unexplainable, the incomprehensible. Unfortunately, it has the effect of casting others with the diagnosis in a very negative light. When unenlightened people hear a child has Asperger’s syndrome, or a future school, or employer, the word may cast aspersions on those who have the diagnosis. Accommodations? Why might you be needing accommodations?

When I saw the videos of Rodgers, I said to my kids, “He can’t have Asperger’s syndrome. He doesn’t strike me as a person with Autism.” He does strike me as a person who is very seriously mentally disturbed.

I could be wrong, this could just be Asperger’s in its worst form, but I don’t think so. If he did have Asperger’s syndrome, it almost certain that it is comorbid with other conditions. When my daughter was placed in an autism classroom, I became aware that having autism does not insulate you from other insults to the brain and body. Mary had classmates who were also blind, also epileptic, and/or mentally impaired. Mary has very mild cerebral palsy and severe learning disabilities, along with autism. When two or more conditions are present, they are said to be comorbid. My daughter had autism and the comorbid conditions of learning disabilities and cerebral palsy.

Adam Lanza’s father said that he doesn’t believe that Asperger’s Syndrome was the cause, that other mental problems were the issue. (http://time.com/19957/adam-lanzas-violence-wasnt-typical-of-aspergers/).

Elliott Rodgers may have Asperger’s Syndrome, but in my opinion it is very clearly comorbid with severe mental illness. We may find out that he was misdiagnosed, as some claim about Adam Lanza.

 

 

 

 

Courage is Contagious

31 Monday Mar 2014

Posted by Ann Kilter in Asperger's syndrome, Autism, diagnosis, Disability, high functioning autism, Support

≈ 5 Comments

Tags

ASD, aspergers's, autism, Autistic spectrum disorder, courage, disability

Courage.

Some days, some months, some years, it takes courage to get out of bed and do the job of raising our children with special needs.

The Merriam Webster Dictionary defines courage as “mental or moral strength to venture, persevere, and withstand danger, fear, or difficulty.”

That pretty much sums it up.

Some days it takes courage just to get dressed, get our kids dressed, and get everyone where they need to go. Sometimes it takes courage to face special education committees to advocate for your child. Sometimes takes courage to advocate for our kids to the youth group leader, Sunday school teachers, summer camp leaders, neighbors, family, school, etc. Etc. Etc.

Sometimes it takes courage when a day has been a complete and utter mess, exhausting everyone, to get up the next day and start again.

But, when you live your life with courage, others are encouraged.

When my children were young, sometimes tears would slip down my cheeks when discussing my children’s difficulties. I am sometimes an overly emotional person. I can’t always keep smiling in the face of difficulties. Actually, I can rarely keep smiling in the face of difficulties. That’s not me. During these meetings sometimes my kids’ teacher consultant or social worker would tell me that they would bring me up as an example to other parents. I didn’t really believe them. I thought they were just saying that because of their discomfort with my emotions.

I was reminded of those meetings when I visited with my parents at my brother’s house this weekend. My sister also showed up from the other side of the state. She is a nurse, with wildly varying hours, so it is not easy to see her, or even talk to her on the phone these days. (She ended up having to leave early because she is on call for two weeks). While we were talking about her youngest son, she mentioned that she knew how to advocate for him because of our many conversations when my kids were young and watching how I handled my kids. She told me that he has some autistic features. “He has autism?” I said. She nodded. Thinking back on it, I can see it in him. He is in his third year of college planning to go into computer programming. He is on the high end of the spectrum, so they didn’t realize what they were dealing with until much later in his education.

My courage encouraged her. Your courage will encourage others…even if you can’t see how.

courage-to-continue-mcounts

 

Battling Isolation

05 Wednesday Mar 2014

Posted by Ann Kilter in Asperger's syndrome, Autism, diagnosis, Disability, high functioning autism, Independence, Transition issues

≈ 9 Comments

Tags

autism, disability, finding work, friendship, growing up, isolation, Loneliness, making friends

I haven’t been writing as much lately or going to meetings. It’s hard to find the time when somebody needs you.

Last month, Mary, my 27-year-old daughter with autism, mentioned she was feeling lonely, bored, and discouraged about her job prospects (It has been 3 years since graduation without landing a full time or half time job in her field). My mother instinct revved up and I sprung into action or inaction, that is. So I have dropped some of my writing, quilting, and scrapbooking nights in order to spend some time with her after work watching The Voice, and American Idol. We’ve gone out from breakfast on some Saturdays.

When my children were young, before we knew about the diagnosis of autism, I thought by this time in my life, my children would be out on their own. Not that they wouldn’t need me anymore, just that their need for my help would diminish and our relationship would change. After the diagnosis, I realized that my plans for my retirement would need some adjustment. I might be caring for one or more of my children for the rest of my life.

We began a life filled with therapy, IEP meetings, medication decisions, searching for answers, repeating the same instructions and promptings to our children, going to conferences, etc. As those of you who have read this blog for any length of time know, our children have made remarkable progress.

Then, when Mary, our most impaired child, graduated from college, I thought I might have some time after all, to pursue my own hobbies and develop more friendships with other adults my age. When my siblings and I left home, my parents enjoyed spending more time with people their own age, playing cards, going out to eat, taking long trips and vacations.

Despite his diagnosis with autism, Will has now lived in his own apartment for almost two years. He has a good job with a large corporation. Patty, Mary’s younger sister, is about to graduate from college, and in a year or two expects to move away and attend graduate school. Her mentoring professor has called her one of his most brilliant students, which embarrasses Patty.

But Mary works one day a week at the homeless shelter, for which I am grateful. Other than that, she is home with the dog, five cats and her computer. Her sister attends school five days a week. Her father and I work full time.

I am struggling with my own reaction to this turn of events, wondering why I feel so selfish and trapped.  When I think about going on a long vacation to Washington DC or Mt. Rushmore, I think about getting Mary a ticket so she can come with us. She would be interested in a trip to those locations. I would like to go to a week-long writers conference in another city. I think my husband would enjoy going with me. But Mary is not interested in writing. Therefore, my angst.

Then I read this wonderful blog post from a young mother of three young children, struggling with her desire to write and her responsibility to her children.

http://yourbestnestindy.com/2014/02/27/mommy-somebody-needs-you/

And my struggle came into focus. I am not free to do what I want. When I had young children, I had these same thoughts. However, like many parents of adult children with disabilities, the future is here and the plan to resume my young dream of writing the great American novel is still on hold.

When our kids were young, we struggled with isolation. We weren’t doing the same activities with our kids that other parents were doing. Instead of little league and girl scouts, we took our kids to therapy. Senior class trips were not an option for our kids because they would have needed their own chaperone, and the spots were limited to other sponsors because our kids would have needed more attention, more watching. It wasn’t worth the fight. The road less traveled meant isolation by default.

Wondering what to do about this has been waking me up at night. As older adults, we are battling  isolation both for ourselves and for our Mary. One of my reasons for encouraging Mary to attend college was that “at least she would have something to do.”  Then college ended.

The search for work has been ongoing. Mary is hindered by her inability to drive and her autism. Even though she dresses well and has a good resume, she can’t find competitive employment. I suspect it is her autism showing. If she says up front that she has autism, interviewers will politely dismiss her as soon as possible. If she stays quiet regarding her disability, interviewers still know something is not quite right, though they might suspect mild cerebral palsy. Either way, there has been no job. She is beginning to be willing to do anything (but not able due to her physical disability).

Mary will be 28 this summer. I think about her at 30, 40, 50…. I just turned 55 and Ralph is 62. We take her to church with us where she has a very good Sunday School class with people her own age. Someday we won’t be able to take her. Church is seven miles away and there is no bus to church. We won’t always be around to take her to church, plays, concerts, and vacations. She will have to find her own way.

My idea of a successful launch for her is to earn her own living, have an apartment, along with social activities, and her own church. I don’t know if this will be possible for her. If she always lives with someone in the family, maybe that is best. It is a hedge against complete isolation. Not what she wants, but maybe she can find contentment. Maybe I can find contentment. I want to make sure she is taken care of, at the least.

The apostle Paul wrote to Timothy in the first century, “but godliness with contentment is great gain.” (I Timothy 6:6).

And I turn to God for wisdom. The apostle James wrote, “5 If any of you lacks wisdom, you should ask God, who gives generously to all without finding fault, and it will be given to you.” (James 1:5). I have come to God many times asking for wisdom regarding my children…and He has met my needs many times.

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This is a heavy topic,  but isolation is a common problem for individuals with disabilities and those who care for them. I am praying that Mary will come up with some of her own ideas.

Giving Thanks versus Being Thankful

21 Saturday Dec 2013

Posted by Ann Kilter in Asperger's syndrome, Autism, diagnosis, Disability, faith, Miracles

≈ 2 Comments

Tags

faith, give thanks, joni earekson tada, thankfulness

“AS a matter of fact, God isn’t asking you to be thankful. He’s asking you to give thanks. There’s a big difference. One response involves emotions, the other your choices, your decisions about a situation, your intent, your ‘step of faith.”
― Joni Eareckson Tada, A Place of Healing: Wrestling with the Mysteries of Suffering, Pain, and God’s Sovereignty

Joni is one of the world’s longest surviving quadriplegics. She has been in her wheelchair since 1967, when she had a diving accident as a teenager. Despite this, or maybe because of this, God has used this event in her life to bless millions of people. Her paintings, her books, and her ministry to provide wheelchairs around the world to disabled people are just a few of the ways God has used her to bless the lives of others.

http://www.joniandfriends.org/jonis-corner/

I have read her devotional, Diamonds in the Dust, over and over since the 1990s. It has been a rich source of encouragement and faith building challenge.

Shortly after Will was diagnosed with autism, I wrote a letter to her regarding one of my favorite passages from the Bible, I Thessalonians 5:16-18*, which she read on the air during one of her radio broadcasts in the early 1990s.

Giving thanks is an act of faith.

Don’t beat yourself up because you don’t feel thankful.

20 “for whenever our heart condemns us, God is greater than our heart, and he knows everything.” I John 3:20.

He knows our struggles, he knows that we are dust. Jesus says, “28 “Come to me, all you who are weary and burdened, and I will give you rest. 29 Take my yoke upon you and learn from me, for I am gentle and humble in heart, and you will find rest for your souls. 30 For my yoke is easy and my burden is light.”” Matthew 11:28-30.

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*(16 Rejoice always, 17 pray without ceasing, 18 give thanks in all circumstances; for this is the will of God in Christ Jesus for you.)

Tiger, Tiger – Apologies to William Blake

02 Monday Dec 2013

Posted by Ann Kilter in Achievement, Asperger's syndrome, Autism, diagnosis, Disability, faith, high functioning autism, labels, Thankful

≈ 2 Comments

Tags

autism, high functioning autism, Merry Christmas, Tyger, William Blake

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Tiger, tiger in our tree. I see him looking out at me. Who knew, when kitten found that he….Would make his home a Christmas tree?

When first he shimmied up the tree…He was a kit, 2 oz, pound three,…Now 15 pounds, give or take…His climb doth cause the tree to quake.

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He is the smartest cat of all…and with his polydactyl claws..He knocks ornaments off with fury…Picking them up makes me weary.

Tiger coos with delight…As he climbs up past the lights…Then hubby cries out with a mighty shout…Tiger, from the tree get out!

Then Mr. Tiger takes a flight…Over all the Christmas lights…Like a sparrow, like a robin…He just makes those lights go wobblin’

Mr. Tiger, in our tree…Why did you climb up so high? Did you think you are a bird? Did you think that you could fly?

Tiger, tiger, in our tree…Again I see him look out at me…Who knew, when kitten found, that he…Would make his home a Christmas tree?

*****

This is a parody/take-off of a famous poem by William Blake, Tyger, Tyger. Some of you may have read this work in High School or college. I published this last year as well, but I am so taken with its silliness that I am reposting it.

Merry Christmas to all. Ann.

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