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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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Maggie’s First Seizure

November 19, 2014November 19, 2014 ajtesler4 Comments

I posted this picture a few weeks ago on Facebook – what felt like a lazy Sunday.  This was at 9am.  She fell asleep right after this for about two and a half hours. Somewhere in the middle of that nap I Continue Reading

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Beauty Marks

November 12, 2014November 12, 2014 ajtesler2 Comments

Sorry to be overposting this week, but a lot is going on.  Our good friends Kate and Joey from Mr. Kate, a lifestyle brand, are just uber creative and smart and savvy and good looking.  And they’re launching a new Continue Reading

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Maggie on the news

November 11, 2014November 13, 2014 ajteslerLeave a comment

The news did a story on us back in August when we put out the video (bit.ly/magnoliashope).  It airs Wednesday, November 12th, on KCal9 at 10:00 PM.  If you’re not local, here’s the story: http://losangeles.cbslocal.com/2014/11/12/couple-determined-to-find-cure-for-daughters-rare-condition/ I’m not sure what we said at Continue Reading

Tagged maggie,news
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Birthday Celebration

November 10, 2014November 10, 2014 ajtesler8 Comments

Last year we were on the east coast for Maggie’s birthday and didn’t really have the opportunity to do a big party.  Plus at 3, would she really care?  This year, after a lot of uncertainty, we decided to give Continue Reading

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Halloween

November 5, 2014November 3, 2014 ajtesler6 Comments

We didn’t know how Halloween was going to go, this year.  It’s really only the second time she would have been  trick or treating since she’s been born.  It was too hectic last year.  And the year before we went, Continue Reading

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My email chain with the school district:

October 28, 2014October 27, 2014 ajtesler3 Comments

Names have been removed to protect everyone. I sent this first letter to the PT and OT assessor. Hi…, After some consideration, and in part, because I didn’t know I was supposed to have the discussion at the IEP, I Continue Reading

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Palm Springs

October 21, 2014October 18, 2014 ajteslerLeave a comment

A couple of weeks ago, we took a little weekend trip to the desert because nothing says relaxing like 109 degree temperatures.  It started out auspiciously with Maggie unable to calm her body, communicate her wants or regulate her body Continue Reading

Tagged #magnoliashope,#rettsyndrome,coping,cure,diagnosis,feeding tube,hope,Magnolia,rare disease,Rett syndrome,special needs,wheelchair
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IEP

October 18, 2014October 19, 2014 ajteslerLeave a comment

IEPs are dumb.  That’s the school district process whereby people who have never met Maggie spend 30 minutes with her and evaluate all of the things she can and cannot do and make recommendations about how she’s going to get Continue Reading

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Event Wrap Up Brings Us to…

October 14, 2014October 18, 2014 ajteslerLeave a comment

The auction I put together ended up raising over $30,000 and the event it was a part of raised over $700k – 96% of that goes directly to fund research. That’s a spectacular number and I’m so honored to be Continue Reading

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Traveling

October 7, 2014October 7, 2014 ajtesler1 Comment

Traveling is always harder than it needs to be, with more thought than should be required needing to go in to what to bring, how she’ll be comfortable, what will entertain her on the plane, how will we keep her 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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