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Tuesday, April 10, 2012

The Nameless One

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Everyone who has child with a named disease or syndrome has had to go through some sort of undiagnosed journey. We all start at the same place...the beginning, which can feel more like the end. From the moment you see or sense something is not the way it should be is the moment it all begins. There is the waiting for test results and thoughts of a bleak future that engulf all of the senses. These feelings are the same between the diagnosed and undiagnosed and yet the difference is so clear. The difference happens when you reach that proverbial Y in the road. At the point of a diagnosis there is a path for you. It might not be the expected path and it is usually overgrown with uncertainty but it is a direction. Without a diagnosis none of those paths are yours. You are stuck and alone except for the very few other people who get stopped at the same place. Like the island of misfit toys, all that we have holding us together is our struggle. Nobody knows what to say because we just have a list of symptoms and no known cause. We lack that one term that could sum it all up providing clarity and validation...not necessarily a term that describes the state at which you exist on the giant spectrum of possibilities...but a term that says ok you belong here...here is what you can expect. More than just a support group, it's going to doctors' appointments and knowing where to start the dialogue. With a name there wouldn't be the judgment that comes with the term undiagnosed syndrome; that it isn't a real thing or  just something you made up. It's the explanation to friends and families or a new parent at the park who looks at you with questions. I once had a person say to me that a friend of hers saw my daughter and with an element of disgust asked what was wrong with her. Not only was this a very hurtful comment but made me want to hide my child because I didn't know what to tell people. I don't want anyone thinking and absolutely not telling me anything hurtful about my sweet and innocent little baby girl who I LOVE no matter what. In my mind, if I had only had a name, strength would follow. I would say it loudly ...This is the card we were dealt and we are going to play this better than anyone else. I seek the label that shouldn't hold people back but rather help them to progress forward. A road map of what we know but an open end of hope for a positive direction.

9 comments:

  1. Brilliant post. So accurately describes my feelings about seeking out a diagnosis for our son. Ellie sounds a lot like our little boy, Lawrence. In fact they look quite similar too in some ways, facially. He's had a clear CGH array and nothing of note from any other tests. We are seeing a specialist geneticist now to see what else they might want to test for, using different methods. I don't know if we'll ever find out but we will keep trying. Ellie is a really beautiful little girl. Good luck on the journey to a diagnosis.

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    1. Thank you Mavis for taking the time to read and comment. I wish you all the best on your journey in finding answers. Feel free to email me if you want to connect more!

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  2. What an inner struggle you endure! It must be nice knowing you are not alone, however small that comfort may be. Here's to hoping answers come soon.

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  3. I hear you, I get it, and you're not alone. I invented the pretend awareness day for Undiagnosed Children and will do a much better job getting the word out next year so people know they're not alone. These are are very real issues. I'm putting up a post-awareness day blog post this friday and will be linking here. All the best on your journey. Heather

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    1. Thank you and to you as well! I have been to your blog wonderful blog several times and Aidan is so adorable. I would be happy to help promote Undiagnosed Children's day as much as possible so please let me know what I can do!

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  4. We are delighted to let you know that this post has been nominated in the ‘Best International' post category of the SWAN UK Blog Post Awards (aka The ‘SWANS’)

    Be sure to pop over to the SWAN UK website to grab some badges for these categories to encourage your other readers to also vote for you – make sure you let them know which specific posts have been nominated!

    If you tweet the SWAN UK twitter account using the #SWANS hashtag with the URL of your blog posts and the category you have been nominated for we will retweet it for you and hopefully get you some new readers.

    Good luck!

    http://www.undiagnosed.org.uk

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  5. So well put. I didn't realise, but our card of Down's Syndrome has been so very useful over the years.
    downs Side Up

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  6. A lovely post and you should be very proud that it is a finalist in the SWAN blog post awards. I thought you would want to know that the winners will be announced on 13th April at 2pm as part of our Undiagnosed Children's Awareness Day. Keep an eye on the SWAN UK blog or twitter where I will announce using @SWAN_UK and @RenataBplus3 ... GOOD LUCK!

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