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Magnolia's Hope

They thought they would teach their daughter about the world Instead they have to teach the world about their daughter

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Author: ajtesler

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The End of Summer

September 8, 2015September 8, 2015 ajtesler7 Comments

Labor day has always signified the end of Summer for me.  Though Maggie started school two weeks ago, it’s still Summer to me until Labor day.  Looking back on it, I think we did a good job this summer – Continue Reading

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DIY Supplements

September 1, 2015September 1, 2015 ajteslerLeave a comment

In order to keep Maggie at equilibrium, she needs to take a swath of supplements.  Currently she’s on 300 MG of Magnesium 5MG B12 Calcium Chewable Kids Chewable Pro Biotic 100 MG Iso-Phos 1100 MG of L-Carnitine 1600 MG Norwegian Continue Reading

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Hope for Hannah & Gaby – REVERSE RETT LA

August 25, 2015August 24, 2015 ajteslerLeave a comment

Last year when I reflected on the amount of money we raised collectively, I was proud to have been a part of Maggie’s solution, her hope.  This event, which takes place in LA on October 29th this year, is a Continue Reading

Tagged gaby,hannah,hope,la,rett,reverse
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An upswing

August 18, 2015August 18, 2015 ajtesler2 Comments

When Maggie had pneumonia a few months ago I actually thought it wasn’t that bad.  She was sick for a month but the pneumonia part only lasted a few days. But soon after the pneumonia was gone, she started experiencing Continue Reading

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Science updates

August 11, 2015August 12, 2015 ajtesler2 Comments

The past couple of weeks have brought some fairly promising news in the Rett Syndrome community.  I’ll share it here with links so you can become an amateur geneticist too. 1) Trofenitide – one of the drugs currently in trials Continue Reading

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Special Olympics

August 5, 2015August 12, 2015 ajtesler3 Comments

The Special Olympics were in LA last week.  I’d never been; though I have oft times considered volunteering.  When we first heard about Rett Syndrome, my dreams of Maggie someday competing in the Olympics quickly faded.  I mean, the daughter Continue Reading

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The Letter S

July 28, 2015August 12, 2015 ajteslerLeave a comment

For the longest time the letter s was important.  It was how she said yes with a long extended “s”.  It was how she hissed like a snake.  It was how she responded to Brown Bear Brown Bear what do Continue Reading

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Bad Night – the movie

July 21, 2015August 12, 2015 ajtesler1 Comment

I produced a movie that comes out today.  It’s called Bad Night. I guess, if I had thought about it at the time, I’d realize the title has some relation to Rett Syndrome and all the bad nights Rett has Continue Reading

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4th Installment

July 14, 2015August 12, 2015 ajteslerLeave a comment
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Idle Hands

July 7, 2015August 12, 2015 ajteslerLeave a comment

I wish she had idle hands.  She doesn’t  She has hands that won’t stop moving.  At times, like now, they won’t stop moving extremely violently.  Right now she can’t control them at all.  I watch as she stares at them Continue Reading

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AJ and Jenny Tesler

When their daughter was diagnosed with rare neurological disease, Rett Syndrome, they promised her they would do everything they could to find a cure and help her live the best life she could. It was then that Magnolia's Hope was born.

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