Stryders Fund

Stryder has an account at Mid Oregon Federal Credit Union under "Stryder Doescher".

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Visit Stryders List - Crafting for a Cause! A crafting directory with craft events, stores and reviews all in one place!
Tuesday, August 30, 2011

We finally got Stryders Speech therapy appointments scheduled for the Mayo Clinic. I am really nervous about going, but excited too. We will schedule the other visits that he needs as we are there. The system at the mayo is wonderful!

Stryder is doing great with his speech! I am so proud of him and I know that it is because of the prayers that everyone has sent us! He is able to speak many one and two word sentences, and clear at that. I am amazed at his progress! Miracles are happening abound here and I am amazed that God chose us to be a part of His Journey!

Also, Barbara, I call her our Angel, is getting a (or two) fundraiser going in our area. She has done so much work to get this thing going and words cannot express the gratitude that I have for her. Before she came along, I was so alone in all of this. I didn't know how to get money or help to get Stryder back to the Mayo or how to even get help for his therapy here. It's truly amazing what one person can do. (My sister-in-law Tera has been amazing too, a huge mental support, to say the least)

Here is a copy of the fundraising flier I designed with Barbara's help:

Sunday, August 21, 2011
Just click the picture to make it full size and print:

A lot of us with children who cannot speak will have to guess what our kids do at school or daycare. Someone on the Apraxia message board put a great link to a resource that will let us know what our kids did during the day,but unfortunately, the site got hacked and the image is no longer. I wasn't able to save it so I did one by memory for those interested.

Friday, August 19, 2011
Emily Perl Kingsley.

c1987 by Emily Perl Kingsley. All rights reserved

I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this......

When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."

"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."

And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

But... if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things ... about Holland.
Saturday, August 13, 2011
Our neighbors across the street came a couple weeks ago and said that they were having a garage sale to help raise money for the city, it was called "GeneroCity". It was the first time I met her and I was out making crafts to sell to raise money for Stryders Care, so I told her just a little about our journey so far. She came by last night and said that she asked her Pastor if we could set up a small table to raise some money for our cause and he said absolutley!

I met some tremendous people with big hearts. I sold the cards I made for $2 each and made close to $60 with very few cards. Neighbors in the area came by and one in particular, Barbara, came back and OMGosh, her heart was so generous. She wants to help us make some money by doing another garage sale, bake sale or handmade sale- something....She made me feel so good. I do not do these things for a handout, I don't want that. Yes, we really do need funds for Stryders treatment and ongoing medical issues, but I want to work for the money; I want to make things and sell them and I try very hard at that. My dream is to continue and make money for other people that have the same problems with their children and the medical help. We have great insurance and yet it still doesn't cover everything. The bill for the Mayo, for one week, was over $9,950- I can't imagine what someone without insurance, or even good insurance, has to pay. I want to help them and right now I want to help my little Stryder.

Crafting for a Cause! Let's join together and help people with our talents-
Friday, August 12, 2011

Yesterday my sister-in-law drove Stryder and I to the Shriners Hospital in Portland. It took us close to four hours, I think, but we stopped before the appointment and were able to have breakfast at Starbucks because my good online friend, Sam, sent me a Starbucks gift card- Thank you Sam!!!!!!!! It was a relief and a great break before a stressful day.

After our coffee and bagel, we went to Shriners. The people there were great! Poor little Stryder had been bent and fiddled with, but he did everything they asked. They were bending him all over and gasping at how flexible he is. They even tested me and said that I have some of the same flexible joints that most others don't have.

Stryder went in for an XRay of his hips because they seem to pop out all the time and the good news is that they look great! There is no damage or anything right now. The bad news: Stryder has the same physical problems that children with Downs Syndrome have, but as the DR. said "he obviously does not have Downs Syndrome." He said that they are the hardest children to work with because they can't do anything medically with them and things just get worse as they get older. The Dr. told us that after the age of 4 or 5, closer to 6, they start to show the problems in the hips, but again, can't do anything about it really. He said he calls them Gummy Bears and that is the perfect way to describe Stryder! I have always felt that he feels almost dead like the way he squishes, but gummy bears are so much more appealing (and squishy). My sister-in-law said that we will just call it the Gummy Bear Syndrome. How else do you explain to people that he has these problems?

I suppose that means he is a Shriners baby now :) We go back next year to check for anything that might be problematic and every year after and just pray that he doesn't get any worse and just stays flexible only.
Wednesday, August 3, 2011

Stryder fell the other day and got a HUGE bump on his head. This is the second time in a week that this happened. The next day it looked better and then yesterday he bumped heads with the dog and it came back. It's HUGE and makes my stomach turn whenever I look at it. It's really been a rough week. I'm not sure why he is not catching himself when he falls.

We got a call from a DR. the other day asking us about our family history. We were on the phone for close to 2 hours while she asked every question about every member of our family up to grandparents. It seems they think he may have a duplication of chromosome 7. I won't go into detail on it, but he does have all the symptoms such as short neck, hip dislocation, hypertonia and more. They say that children with this disorder can have a shortened lifespan, but I am choosing to not find out what this means until we know for sure that he does have it- they are sending a test kit soon.

We got a call from quota club yesterday and they want to pay for his therapy in MN when we go in October. It would have been $1500 just for therapy while there. Words cannot express how grateful I am for that. His medical bills from the last time that the insurance isn't covering were staggering and it will be so much more since we will be there for 6 weeks, so the $1500 for the speech therapy is a BIG help. They will send a check directly to Dr. Strand as soon as I get her address.

Stryder goes to Shriners next week. His hips and legs are getting worse. When he walks, his feet will often get caught in each other because of the way they twist; this is probably the reason he is falling so much. They may not be able to do anything for him, but we won't know until we go. I think this visit is just the consultation.

On a good note, Stryder is starting to say so many new words. I think his seizure medication is really helping him. He still is not able to combine two words together too well, but he tries. He can say Hershey now and will often say "Hershey NANA" which is Hershey, Kennel!" I am working on "I want that," but it's really hard for him. He is able to say the words individually, except "want" is hard, but put them together and it doesn't make any sense. He is trooper though and tries so hard.

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Angela Rozewski
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