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Category Archives: Thankful

Provision

21 Wednesday Sep 2016

Posted by Ann Kilter in Autism, cancer, faith, Health Crisis, Miracles, Thankful

≈ 2 Comments

Tags

autism, cancer, faith, miracles, provision

On June 10, 2016, Ralph received the diagnosis of myelodysplastic syndrome (a rare bone marrow cancer). He started on chemotherapy the next week. We were told that his prognosis was six months to two years to live. Before he started the chemo, we were told that any fever of 100.5 and above was a reason to call the doctor, day or night due to his significantly impaired immune system.

Someone said to me on a support group Facebook page “dust will be your husband’s enemy.” That shook me. We need to move, I thought. I remember going downstairs to do laundry and looking up at the rafters in the basement with dust all over them. I stood at the washer and I prayed, ” Lord, what am I going to do?”

God heard that prayer. Wrapped up in that prayer was the thought, How will I care for my husband in this house?

And it was as if he said, ” Now you will see what I am going to do.”

Saturday morning, July 2nd, I suggested to Ralph that he could take some money out of his 401(k) to help Erin with a down payment on a condo. He agreed. The next morning, he said to me, “I’m sorry to disappoint you, but don’t think we are going to be able to find a condo.”

“I think God will provide a place for us,” I said. “Look how He has provided for us in the past. He provided a way for you to go to college and graduate with no debt. He directed us to move into this school district where our kids got the help they needed for their autism. He provided a job for me before the kids went to college. He provided the money our kids needed to go to college, graduate, and kept us safe during that time of taking them back and forth to school. Don’t you think that if God provided all those things, He will provide a place for us to live in our time of need.”

Ralph went to the computer. “I’ll look, but I don’t think I’ll find a place.”

“Well, here’s a place. Two bedrooms, two baths. Maybe we can go over and look at the outside of it. To see where it is located.”

I then sent an email to a real estate agent that we have been working with to find a condominium for Erin close to her job. I told her about Ralph’s cancer. She replied that she didn’t think we would be able to find a place. 45 minutes later, she called me and told me about the place that Ralph had found and we all went over to look at the inside of it.

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In a market so hot our real estate agent told us condominiums were getting 20 offers, God found us a condominium within 4 days of that prayer. On July 5th, Marie made an offer on a condominium in Kentwood, only two miles from the job that God provided for her a year and a half ago. At 6:30 the next morning, we received a call from the seller that her offer was accepted.

On August 11, Marie signed the mortgage papers for her own condominium.

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Then God also supplied the help that we needed tomove. Many from our church came to help us, sacrificing two Saturday mornings, one to help us move to the condo, and the second to clean out the house to get it ready to sell. Our backyard was a jungle.  The youth group came to cut down the brush and clean up the back yard.

What a testimony this has been to our neighbors and my coworkers. They say they were amazed at how this all happened so quickly.

I sat in church the Sunday morning after we moved, thinking about what God had done. It was stunning. God’s hand was clearly evident in all of this. Praising God through the tears.

Ann and Ralph.

 

 

A Little Christmas Magic – Courtesy Local Cops

10 Wednesday Dec 2014

Posted by Ann Kilter in Thankful

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Tags

asperger's, autism, Christmas, Police, traffic stop

A little something to warm your heart….

A video of a different kind of traffic stop. 🙂

Transition Update

16 Monday Dec 2013

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

≈ 2 Comments

Tags

asperger, autism, independence, transition

“A ship is safest in the harbor, but that is not what ships are built for.” John Shedd. This was my the quote my friend Sharon had under her senior photo in our high school year book. As my children’s IEPs began to reference transition in their later years of high school, I remembered it and it became my motto. At the time, I put this quotation in my email signature lines both at home and at work to remind myself on a daily basis that my kids could not stay in the harbor. It was not healthy for them or for Ralph and me.

As a result, I began taking concrete steps to move our whole family toward transition. When my youngest daughter, Patty, was 12 years old, I went back to school to become a legal secretary. When she was 14, I graduated and started working. I told my kids, “I need to have something to do when you don’t need me anymore.” This type of language combined with concrete action (going back to school), helped all of us to move toward transitioning to independence.

Transition is the theme of this blog, so I thought I would update you on how transition is working out in our household.

Mary is living at home. She is working at a homeless shelter as a part-time accounting assistant in the accounting department. This fall, she also worked part-time at Habitat for Humanity for three months, but due to personnel changes, her position was eliminated. She is actively looking for full-time work. She says that when she finds a permanent position, and she has saved enough money, she will find her own place. Her brother’s transition to independent living has spurred her on. I have some reservations regarding how this will happen; however, at some point, she must live on her own separate from us. She has amazed us before; she will again.

Will has been living in his own apartment in another city for a year and a half now. He became a regular employee (rather than a long-term supplemental employee) in October. Now he has vacation time, a 401(k), and salary. He drives his beat up old car around his community. This Sunday, he will be singing in a cantata at his church. We are looking forward to seeing him at Christmas. My husband talks to him a little bit every weekday morning on the phone. I talk to him a couple times a week. He would like to meet a girl and get married. It could happen.

Patty is finishing up her senior year in college. We are pushing her to learn how to drive. Like many millennials, she is afraid of driving, but in order for her to transition to studying for her Masters/PhD, she must learn to drive. One more semester, and the Kilter College Taxi Service will cease to operate.

As for Ralph and me, we are beginning the process of transitioning to retirement. Ralph is by some miracle and perseverance and prayer, still working. (He has gone through six months of harassment at work – his employer would like him to quit). He is 62 and would like to work until 65, or at least get close. I am 54 and hope to work until I am 65. But the process of thinking about living with far less income has us thinking seriously about downsizing. Maybe we’ll have more time for volunteering. Have more time for fun activities.

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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.

Rejoice, Pray, Give Thanks

19 Tuesday Nov 2013

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

≈ 12 Comments

Tags

asperger's, autism, Depression, thankful, thanksgiving

Thessalonians 5:16-18

16 Rejoice always, 17 pray continually, 18 give thanks in all circumstances; for this is God’s will for you in Christ Jesus.

If I have a life verse, this is it. Practicing thankfulness was the way out of darkness, out of depression, out of despair.

We were thrust into the world of special education when my oldest daughter was five years old. At the young fives qualification testing, she tested at 2.5 years in reading and math readiness. Instead of thinking about young fives placement, we were offered placement in a pre-primary impaired program. Instead of thinking about the academic achievements of my children, the sports achievements; we began thinking about slow, steady progress, two steps forward, one step back. I dreaded the beginning of the school year. And I mourned the sudden loss of dreams for my daughter. I questioned everything we had done up to that point in raising her. I wondered if something was wrong with me and/or my husband.

Within that year all three of our kids qualified for special education placement. In hindsight, we should have been able to figure out that something was wrong. There were clues.

After our oldest daughter had been in her pre-primary impaired class for a while, I mentioned my concerns about my son. He was very easily distracted. He turned the lights on and off, constantly. He opened and shut doors to the extent that we had to put spring locks high up on all the doors to keep him from shutting the doors on his sisters’ fingers. He was a screamer who insisted on sameness. Everything he possessed had to be green if there was a choice. He had to have his sandwiches cut in triangles. We should have known. We should have known.

My daughter’s teacher also felt that my son should be tested. So an appointment was made for my son. After two tests, which was all he needed to qualify for special education placement, the teachers, social workers, psychologists, and therapists felt that he should be tested more. In all, he went through eight evaluations. It was emotionally draining. My husband and I, along with our local school representative met with all the evaluators in one big meeting to go over the meaning of the tests. My husband did not want to go because he felt that all they were going to talk about was what was wrong with his little boy. They said he was mentally impaired, had a mild speech impairment, and had autistic traits. But one of the testers told us we should not get involved in the local autism society. (We received some less than stellar advice along the way).

Toward the end of my son’s evaluations, the testers suggested that my youngest daughter also be tested. At this point, I was weary of testing. I told them that they could only perform two evaluations; they could  only do what it took to know if she qualified for special education services. She also qualified for special education placement. At this point, my older daughter and son were in opposite sessions of preprimary impaired preschool; one in the morning and one in the afternoon. The teachers wanted me to bring my youngest daughter to the special school for her therapy. I said no. I cannot be stretched that much.So they had a speech therapist come to my house for my youngest daughter once a week.

The first two years of dealing with all the meetings and special education therapy homework from the school took a toll on my emotional health. I was depressed and crying all the time. We became isolated from parents with normal children, even my siblings. Part of that was our withdrawal – I could only stand so much bragging about how advanced their children were.

When I thought of the future, there was a wall before me. I couldn’t visualize the future. I couldn’t see the light at the end of the tunnel. There was so much fog, I wasn’t even sure there was a tunnel.

Then God gave me this verse.”Rejoice always, pray continually, give thanks in all circumstances for this is God’s will for you in Jesus Christ.” (I Thessalonians 5:16-18)

I decided that even though I couldn’t see the future laid out before me, I could give thanks. Every day. I could do God’s will. I could obey God in doing this.

As for praying continually, that was easy. I was doing that already, every day. Some of the the praying was questioning God’s wisdom in choosing me for this job (James 1:5)  Some of it was crying out to God. Some of it was seeking wisdom, because God says that he will not upbraid a person for asking for wisdom.

But rejoicing? That was a bit much to ask of a person. I found that to be very difficult for a long time. So I practiced what I could do, and waited  for God to tell me how I could rejoice. Eventually, I began to sing songs of rejoicing. Just by singing those songs, I could rejoice.

As I began to practice purposeful, intentional thankfulness, my depression began to lift.

Give thanks

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