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Loving Life With Full Trisomy 18 - Edwards Syndrome - Helping Families with Prenatal and Postnatal Diagnosis of Trisomy 18, 13, and Related Chromosome Disorders - Dealing with Ethics, Genetics, and Related Medical and Health Issues. Thursday, July 3, 2014. The Relationship Between Hot Weather and GI Issues. I also found this Huffington Post article about a medical study on the relationship between climate GI health. It states that prolonged heat exposure .
Last week I posted all the Medium articles. I have posted touching on communication from January and February. If you missed my reasons for doing so, you might like to know. I will then start sharing a roundup post each Friday, so the email list remains the best way to keep up with such posts. On Medium or look on Patreon. A tale of two trachs.
Conquering mommy-hood, two boys, two toddlers, special needs, and Trisomy while raising awareness. I recently read an amazing blog post by a fellow special needs mommy. To understand my following comments please read that blog post h e r e. Kaleb went back to St. Louis this week and while there we found out that this was going .
Click Logo for Support NOW! Before our son, Anthony Emmanuel Arritola. Of our Journey beyond the negative prenatal diagnosis. For those facing a similar walk of life. To the life of Anthony Emmanuel - co-founder of Emmanuels Foundation. Visitors close and far,.
Tuesday, August 6, 2013. I pray for may many more to come. Im so excised to say that Kayden is doing amazing this last year! I have been very busy with my advocating and co-founding Trisomy Families.
My day to day account with baby Mikayla. Trisomy 18 baby, and love of my life. Tuesday, May 8, 2012. Today you are two years old, and yet forever 16 months 2 days. And part of today is a remembrance of that, which brings with it immense sadness.
They each carry with them a message of hope, a message of courage and most of all they bring love. A love that will forever change the lives of all who hear their story. Help us bring you the information that you need most by completing our survey.
Life within our large family which includes three children with Down syndrome, Lily age 22 who we adopted, Noah aged 11 who was born to us and Isaac aged 5 who we adopted and who was tube fed for the first four years of his life and is now eating! Sunday, December 2, 2012. Sunday, October 21, 2012. Friday, August 10, 2012. Miserable, full of cold, kids. My study is not going well this.
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