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I finally did it — I hid the gross, disgusting, ugly ,worn-out, fake crocs that Alex has been wearing every day for 2 1/2 years. It took a lot of guts – but I am proud of myself (at least for now).
When my kids were little, I thought it was sort of cute if they wanted to wear the same pair of jeans or shirt for more than two days in a row. However, Alex is 16 and these dreadful blue shoes have got to go. She should not have even worn them for two weeks in a row.
Many people I know with down syndrome have flat, wide feet. I am not sure exactly why that is – but as a result Alex has a funny step and walks with her feet pointed outwards. As with everything in her life, Alex has learned to compensate, and walking or even running – as evidenced by the fact we are going to participate in track and field at the National Olympic Games – is not a problem for her…
On Aug 12th, a new journey began for our family. Micah Mitchell Ward was born at St.Joseph’s hospital. He joined the other three M &M’s, Macie, Mason, and Merrick. Micah was supposed to be born Sept. 16th, but decided he wanted to get out early and meet his new family. He was delivered by c-section and whisked off to the NICU unit where he would under go test which were normal for preemie babies. A few hours later, I was greeted by a team of medical staff standing at the foot of my bed. The news they brought me was that the journey I had experienced before with my other children, wouldn’t be the the same journey I would be taking with Micah. Shock and fear raced through my every being when they told me that Micah had Down Syndrome. I wasn’t prepared for this journey! I wasn’t strong enough for this journey! Why me for this journey? I’m so scared to make this journey.
Donna Sauer and Mom after a cardiac procedure
Go DONNA GO…
Our friend Laura Sauer just posted on her blog that her daughter came through her PDA with flying colors. I know many of you were sending …
A few months ago I received a letter from a woman named Linda who just found out that her sister’s new baby has down syndrome. I receive a few of these letters occasionally from confused people that don’t know where to turn and have more questions than answers. The fact that I run this website makes some people think that in some way I have more answers and understanding than my peer group who also have children and family that have had this shared experience. I do not. The support groups that work in your respective communities are infinitely more qualified than I to answer your questions about the condition and how to best provide advice and services to help your child achieve all they can be.
What I can speak to is the raw emotion that came over my when I found out that my son would have Down Syndrome. This was the day that we all have shared in the past; the day that we all asked ourselves, “Why me?”.
Below is the exchange between me and Linda (name changed of course).
Technicality
This is a little technicality, but since I was made aware of it, I like to make others aware of it also. I used to say it this way, until a friend of mine made …
Anybody out there?
January 22nd, 2009
Hey is anybody out there reading this stuff? Please let me know! Anyway, I took my daughter to the endocrinologist for a routine check up today and everything looks …
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