When I am told something I often feel that I must DO something about this, even if I am just given bare facts. To make the right decision is often difficult for me.
So I start too many things, barely manage to finish a few of them, and feel absolutely beaten when I think about the many things I still have to do.
I am working on a kind of filter that helps me focus on the really important things. Right now, this filter doesn’t work as good as I need it to be.
Each time someone stands up for an ideal, or acts to improve the lot of others, or strikes out against injustice, he sends forth a tiny ripple of hope. ~ Robert F. Kennedy ~
This is one thing I really believe in. A small ripple does not stay insignificant: It spreads out, and so it reaches many people while getting farther and farther away from its starting point. It touches people. It can carry them along. So, be the one who starts another ripple of hope. You don’t know how many will be encouraged to do the same because YOUR ripple nudged them.
This quote made me relax immediately! Happiness is nothing that is far away and out of reach, I can just sit down and find it in my mind. No long and exhausting journey ahead of me, happiness is right where I am. Nobody can keep it from me.
Have a wonderful week!
I read a german post yesterday in which a foster mother tells about her struggle finding a place in kindergarten for a child with special needs. It reminds me of the challenges my family faced in the 1970s.
Today, children in Germany are monitored closely to detect problems as early as possible. Back then, we saw our pediatrician for vaccinations and when we were ill. In my case, nobody noticed that I was dear on the left ear. Delayed speech development was explained with my premature birth.
After a infection of my right middle ear in my last year of kindergarten, my mother noticed that something was seriously wrong with my hearing, and that I didn’t react when she called me. This started an odyssey.
I remember the following tests very clearly. Doctors and hearing aids technicans were not prepared to deal with children. My mother was not allowed to be in the same room with me during the tests, even though I made it clear through crying and screaming that I didn’t want her to leave. Nobody even tried to tell me what was going on. I was a clever child, I would have understood an explanation suitable for children. I was expected to behave compliant and calm, as an adult would do. Of course I couldn’t do that, and many unpleasant experiences piled up. I became anxious and shy and regressed. My mother had to be near me all the time. It was a hard time for my mother, too. She just could stand there and watch everything.
Finally the results came in. Not only had the middle ear infection affected the hearing in the right ear, but I apparently was completely deaf in the right ear, too. This, too, was explained with my premature birth. A hearing aid was adjusted for my right ear, and we were sent our way. A hearing aid technican told me a few years ago, that some of her colleagues now have special training to treat children. I hope there are many of them.
Then I was tested for school readiness. I refused to participate. I knew the answer to all of the questions, but I was way too nervous. I kept squirming around on the chair and wanted to leave the room, because I knew my mother waited outside. At this time, children were given the oppurtunity to have a special year of preschool between kindergarten and school. This really saved me. We were a small group of ten children, all with special needs. We had a teacher and an assistant teacher. It was a lot like school, we learned to sit at our desk and started writing and counting. I slowly got used to my hearing aid.
Then I started “really” going to school, at a special school for deaf children. Teachers used sign language and spoken language simultaneously. All of my classmates were using sign language. I didn’t know anything about sign language, so I wasn’t able to really talk to them.
At this point, I could read fluently and was well into learning how to write. The classes bored me. What I didn’t know then, pupils at this school were given two years to learn what was thaught in one year at the normal primary schools. The teachers quickly noticed I was bored, and told my parents I would be better off at a regular primary school. And my parents somehow made it happen.
I was very glad because many of my new classmates were living in my neighborhood, and I knew them. It took me some time to catch up with them, but that was easy. To orient myself in a large group of 25 people was hard, especially during the breaks or physical education with lots of noise.
Meanwhile, my speach had been affected by my poor hearing. I slurred words and it was difficult to understand what I said. I started logotherapy. Hopefully it is more fun for children today. We were shown posters with many objects drawn on them, the therapist pointed at one of those objects and we had to say what it was. Once again, no explanations what we were doing, or why. This training was continued at home, we had a book with pictures in it and I had to say what was in those pictures. The practice payed off, though, I learned to speak quite well. I still slurr the “S”-sounds, my husbands says it sounds like lisping. But apart from that, my pronounciation is similar to that of a person with normal hearing.
So far, so good? I am aware of the fact that I was very lucky.
1.) My mother fought like a lioness that I get adequate therapies and help. She tirelessly worked with me, so
a) what I didn’t hear in class, I would learn later at home, so I didn’t fall behind,
b) my pronounciation was good, and I wasn’t picked on by classmates.
2.) My father was a high school teacher. So
a) money wasn’t an issue. I always got the therapies and expensive hearing aids I needed,
b) my mother could be a stay-at-home-mum and had the time to work with me,
c) being a techer himself, he was able to talk with other teachers and principals eye to eye. This gave me opportunities others don’t have.
My parents motto was: Demand and encourage. I was expected to adapt completely to the hearing world. This was no problem as my intelligence was concerned, but it took years for me to admit that some things are, and always will be, impossible for me. This is not my fault, and I can’t change it, either. Period.
What made our situation even more difficult was the fact that we didn’t know any families facing the same problems, or advice centres. And we didn’t have something like the internet back then. We fought this battle on our own, as well as we could.
English is not my first language, so please be patient with me and forgive my mistakes. I love the english language and follow english blogs from all over the world, the purpose of this blog is to keep in touch with non-german bloggers. Constructive criticism and feedback are always welcome of course!