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Written by lori on Mar. 12, 2015
Yvonne,

Thanks so much for your blog! My daughter is 4 and was recently diagnosed with atypical Baraister-Winter syndrome. My daughter is 4 and sounds like your daughter; she is happy and loving, loves to read and meeting people and has speech delays. We live in South Carolina.
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Written by Hutch on Mar. 1, 2015
Hi Yvonne
I am hopeful we can make a positive change for Erin and I can connect you with a host of people to assist with your challenges. Let us give it a go and if we succeed share the information with others!
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Written by Kristen W. on Feb. 3, 2015
Hi Yvonne,
Thank you for posting Erin's story! My son C, who just turned 2, was just diagnosed with Baraitser-Winter last month. We live in Northern Ohio. So much of Erin's story sounds just like C (who I think is the happiest baby on the planet)! I'd love to hear from you via email, or even meet one day!
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Written by Laurie Huset on Oct. 26, 2014
Hi. This is going to be a short message for now.Just heading out the door.I am the mother of Ryan Huset who also has the same syndrome as your beautiful daughter.I was so surprised when I found this site and read about your daughter and I saw her picture.Our children are so much alike it was overwhelming to say the least. I would love to talk to you sometime soon.My son is now 22 and he walks and talks and he knows a lot compared to the children with lissencephaly.Hope to talk to you in the near future.My number is 715-418-2060. If you could call in the evening sometime .That would be great. Thanks.
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Written by Cameron on Sep. 30, 2014
I am A Speech Language Pathologist in Texas and just received a new student with this diagnosis. I am researching his syndrome so I may better serve him. Thanks!
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Written by Monica reina on Sep. 8, 2014
I am Brazilian and I have a friend that has a daughter with the same diagnosis as yours I'm going to tell her to get in contact with you I just found out there is only 50 cases in the world thank you for sharing your story you have a beautiful family god bless
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Written by Juana Luisa Morales on Mar. 12, 2014
Hello to read your blog. The Last Monday Of The Far visiting my sister, I was very concerned that Alexis would not be enrolled in and What do neurologist Special Request School teacher and diagnosis Baraitser WINTER SYNDROME. In this note I saw reflected my sister and her son, thanks to center reabilitacion, and never under the arms, speech and walking.
May God fill you with blessings and Erin Whole Family! Affections!
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Written by juanaluisa.morales on Mar. 12, 2014
Hola he leido tu Blog. El lunes pasado pase de visita por la casa de mi hermana ,estaba muy preocupada porque a Alexis no seria matriculado en la escuela ya que su neurologo solicito una maestra especial y diagnostico BARAITSER WINTER SYNDROME. En esta nota vi reflejada la lucha que lleva mi hermana con su hijo ,gracias al centro de reabilitacion, a que jamas bajo los brazos, el habla y camina.
Que Dios llene de bendiciones a Erin y a toda la familia!! Cariños!!!
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Written by juanaluisa.morales on Mar. 12, 2014
Hola he leido tu Blog. El lunes pasado pase de visita por la casa de mi hermana ,estaba muy preocupada porque a Alexis no seria matriculado en la escuela ya que su neurologo solicito una maestra especial y diagnostico BARAITSER WINTER SYNDROME. En esta nota vi reflejada la lucha que lleva mi hermana con su hijo ,gracias al centro de reabilitacion, a que jamas bajo los brazos, el habla y camina.
Que Dios llene de bendiciones a Erin y a toda la familia!! Cariños!!!
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Written by Alayne Burge on Jan. 18, 2014
You are officially my hero!!!!
Written by Lisa Maxwell for Rayna on Jan. 5, 2014
Good Morning Yvonne,

I love your blog - it's amazing. I'm writing on behalf of a friend, whose son was just diagnosed. I am going to share your site with her, so she can hear of your journey. May Erin be continually blessed to have you as her mom.

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Written by Linda Dietrich on Oct. 16, 2013
Well done Yvonne. I like to check in on Erin's progress every once in a while on your block via Christine. I think you are an amazing family and I was fortunate to meet Erin at Paris fair and was very taken with her.
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Written by chelsea Asbury on Aug. 23, 2013
Helo everyone my son callum has this syndrome he's is 5 Dec 1st we liven in England and would love meat and get more info x bless x all the kids
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Written by Cindy Mels on Aug. 4, 2013
Thank you so much for letting me glimpse through the window of your world. Your words are so eloquently put together. I feel like I am sitting right beside you and partaking in your journey. I especially loved your "mimbit" story and had to wipe the tears from my eyes. Thanks for sharing. Your family is truly an inspiration and a blessing.
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Written by BillRosie Cromer-Brodie's Grands on Jun. 30, 2013
Will be thinking and praying for Erin and all of you on July 3rd. Know this is a new journey you are taking and hoping only the best for Erin. Thank you for sharing this with all of us. Please keep us posted on her adjustment to this new area of her life.