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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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Its been awhile

Hi! Its been awhile. Life has been a rollercoaster. This past year we have had the exciting news that two different gene therapy trials have started. YAY! Magnolia is loving

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Words we have been waiting for….

                           US THEN 2016   , The words we have been waiting for... FDA approves Trofinetide for treatment

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How to turn your Iphone into an Eye Gaze Communication Device

So, a super cool new function of IPhone is head track switch control which allows any IPhone device to be turned into an eye gaze communication device, plus it allows

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I am happy Magnolia thinks I’m annoying

A week ago, we forgot Magnolia's eye gaze technology computer at home when we went to visit the grandparents for a night. Unfortunately, we remembered on the drive to their

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Surfer girl

A week of surf camp was not enough. What an unexpectedly amazing week we had in Long Beach, NY. Magnolia has always loved surfing, we have been getting adapted surf

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When Laughter Fills The Room

January 21, 2015January 21, 2015 ajtesler2 Comments

It’s amazing how much about Rett Syndrome I can forget when Maggie’s in a giggly mood.  Her laugh is literal music to my ears and it washes away all of the stress and pain of Rett Syndrome.  Knowing that she’s Continue Reading

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This was awesome…#mightymaggie

January 14, 2015January 14, 2015 ajteslerLeave a comment

 

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Diagnosis Anniversary

January 7, 2015January 7, 2015 ajtesler2 Comments

The anniversary of Maggie’s diagnosis was three weeks ago.  I had been reading about other families and how that day is indelibly marked in their minds.  Going through the day I didn’t think of it in the same way, in that Continue Reading

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Happy New Year

December 31, 2014December 30, 2014 ajtesler2 Comments

We spent the last week in Texas with Maggie where she, once again, was showered with love and affection from her cousins and Texas family.  Always nice to be in such a welcoming environment. We were scheduled to be in Continue Reading

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Happy Holidays

December 24, 2014December 23, 2014 ajtesler2 Comments

In honor of the holidays, I thought I would share Maggie’s holiday program from school.  I blurred out the other kids, because people get weird about that. This was a real treat for all of us.  We didn’t even know Continue Reading

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Art projects

December 17, 2014December 2, 2014 ajtesler2 Comments

Every time I pick up Maggie from school I inspect her art folder.  She has extremely limited use of her hands and she can’t draw or paint at this point.  We’re working on it, but she can’t.  So, every time Continue Reading

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Bike Riding

December 10, 2014November 26, 2014 ajtesler3 Comments

Maggie can’t pedal a bike – but Jenny’s mission has been to get her to experience bike riding one way or another.   There was a scooter she never quite got into.  We tried a tricycle that worked for a little Continue Reading

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Fender Bender and #givingtuesday

December 2, 2014December 2, 2014 Jenny Tesler4 Comments

Since Maggie’s diagnosis, we have gotten used to unwanted news and adapting our lives. So much so, news that would send most people into a panic, AJ and I tend to just say “It is what it is.” So getting in Continue Reading

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Finding things to be thankful for…

November 26, 2014November 26, 2014 ajtesler6 Comments

As the holidays roll around I realize it’s almost been a year since we got the diagnosis.  We’ve gone through a lot of emotion this year and hardship and change, but still, it’s easy to find things to be thankful Continue Reading

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NNZ trial press report released

November 21, 2014November 20, 2014 Jenny Tesler4 Comments

This past week has been a roller coaster of emotions. Last Tuesday November 12,2014, two days after Maggie’s 4th birthday. Neuren Pharmaceuticals released the information regarding the NNZ trial for Rett Syndrome. This is a big deal. There are several 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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