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Katelin’s Turn is HERE!!!, page-263

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    Rett Syndrome Awareness Month #2

    Every 90 minutes or so a baby girl is born with Rett syndrome. You go to the movie theater, get there a bit early, watch the pre-show, the previews, the movie… that’s two new Rett girls. Every two and a half days a new baby Rett boy is born. Just little drops in the bucket of new life; but to us, the people who love them, they are the glass full of joy, dreams, and hope. We watch them roll over, crawl, walk, babble, talk and then along comes Rett and dropperful by dropperful takes it away. Some days it feels like it just tipped the whole damn glass over all at once.

    We try to stop it. We watch it slip away toward the edge of the table, our hands cupped, trying to catch as much water as we can- through therapy upon therapy. Sometimes we put some back in the glass, other times we just have to sit there and watch it slip through our fingers. Such is this life we’ve all been given.

    There are times when the glass seems fuller, and we toast to a victory; other times it shakes so badly it seems it will shatter. We watch it… what does its reflection show today? A smile for the bus? A seizure? A giggle for grandpa? Or severe breath holding? Will there be a clock still ticking time? Or one with no time left? That’s our lives. Drops of this, drops of that; bubbles of laughter/bubbles in an IV bag; drops of kisses at night/kisses after drop seizures; splashes in pool therapy/splashes of tears on a hospital bed.

    It reminds me of a stanza from the “Rime of the Ancient Mariner” by Samuel T. Coleridge:

    Water, water, every where,

    And all the boards did shrink;

    Water, water, every where,

    Nor any drop to drink.


    So often we are adrift on that great ocean of the unknown, surrounded by all the things we need and, even still, Rett shrinks their hand use, their voice, their dreams whatever they may be. We can be completely engulfed and not one drop of anything will make it better.

    To live in America, right now, means that some of our children have access to Daybue and many are seeing their glasses filled again, drop by drop; that does not mean we still don’t see reflections of what could have been in that glass nor that we don’t still watch for the clock to stop.

    I’m never sure what will appear upon a page when I sit down to write during this month. Maybe it’s the hurricanes that made me think of Rett syndrome like water- swirling, flooding water causing so much destruction and yet even in the midst of devastation there are always pockets of joy, good will, a life saved, and there’s good water- good clean water brought in to help people survive, like Daybue and the constant research which will bring options around the world and one day a cure for some.


    Please keep those in the path of destruction in your thoughts and, if you can, be a drop of good for someone in need.





    Posted inAcadia,Daybue,Rett syndrome Awareness|Taggedcure,health,hope,hurricanes,Rett syndrome,Rett Syndrome,Rett syndrome research,Rett Syndrome Symptoms,Rime of the Ancient Mariner,Samuel T Coleridge,special-needs-parenting,Trail to a texas Trial|Leave a comment

    Rett Syndrome Awareness Month #1

    There are so many things I could choose from for my first post of the month, and I will get to all of them eventually- Acadia’sRettRevealed; the World Rett Conference, just held in Australia; the many events being held across the States. But I’ve chosen a topic that has reverberated across the US Rett Community this past week- the death ofSyndi Knowlton.

    Syndi was an inspiration to so many people, she startedUtah Kids’ Foundation; their mission”… is threefold: provide information and emotional support to our members, facilitate the sharing and distribution of medical supplies, and run programs and events to provide experiences for families with disabilities.” She served on the board of directors forEpilepsy Association of Utahand never tired of helping others, despite multiple challenges of her own.

    When Katelin and I visited her on our way out West, she was as gracious and as funny as could be. Her passion for helping others obvious as there were boxes upon boxes piled up ready to be filled or already filled with necessary items for families. Not once was there anything but a smile on her face and positivity just glowed off of her.

    Mine is but one teeny, tiny story in a life that touched thousands of others in the most positive of ways, often in their darkest times. She was a role model for humanity.

    There is a poem I think of often: The Dash Poem by Linda Ellis (the “dash” being the one between your birth and death). The final stanza goes like this:

    “So, when your eulogy is being read
    With your life’s actions to rehash…
    Would you be proud of the things they say
    About how you spent YOUR dash?”

    I know for a certainty Syndi should be very pleased with how she spent that dash-she helped selflessly, she tried tirelessly, she loved immensely.

    Please keep her children in your thoughts as they learn to navigate this life without her and especially, Izzy who lost the one person who understood her the most.




    Posted inRett Syndrome,Rett syndrome Awareness|TaggedRett Syndrome,special-needs-blogger,special-needs-parenting,special-needs-parenting,Syndi Knowlton,writing|Leave a comme


    That’s great Mel, have you and Katelin christened your new chariot yet? And apologies if I’m stealing your thunder by posting your latest two blog updates.


    Last edited by Kryptonite: 10/10/24
 
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