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Trisomy 13 - Patau Snydrome - Photos, Support and Resources

  Embracing Life - One Moment at a TimeTM

LivingWithTrisomy13.org


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Prenatal Diagnosis & Birth Diagnosis of Trisomy 13
for Healthcare Professionals, Healthcare Workers,
Midwifes, Physical Therapists, Occupational Therapists

 

 

  To  all Physicians, Specialists, and Doctors  alike

   Now this patient has decided to carry her  baby to term. Her baby is born and she comes to you to “repair” or “fix” what’s wrong with her child. You are now medically inclined to say “it’s  trisomy 13” or “too many abnormalities”. Don’t think to yourself “what’s the  point, there’s no hope”. Rather, think of the other “normal” children that  face these different medical problems every day that you can  “fix”.

Please don’t think of this child any less than any  other child that may have a heart condition, cleft palate, or any other  problem. Please remember that this family has come to you at one of the most  vulnerable times of their life. Realizing that you as a doctor have been given  a wonderful gift of “fixing” people, aren’t all patients deserving of that  gift?
   
Instead of the mindset that these children are  not worth saving due to their chromosomal problem, stop and rethink things a  bit. Please don’t think of these children as a burden to the medical community, but rather as a true lesson in humanity and compassion. Please remember that no one will ever know what could have been if you never even gave the effort.
    
All this family asks is that  you at least try. Please do not give up on this child! Please do all you can  and know that the family will be eternally grateful, even if the outcome is  not what they had hoped for. Remember that these “abnormalities” show no mercy  to anyone. It doesn’t matter what age, race or social status you are. You may  also find yourself one day with someone you love with a chromosomal  problem.
    
Please remember that these issues  could affect any one at any time. Please remember this before you say “I will  not operate on this child”. If it was your own child, what would you do then?  Please take a moment to remember what drove you into this profession. Wasn’t  it the passion, love and need to help and heal people regardless of the  situation? Please try to never forget that no matter how long you’ve been  practicing medicine.
   
Please know that your kindness,  compassion and medical expertise when dealing with this family is greatly appreciated.
When you choose to help this family, you are giving back the  gift that was so generously given to you……….Life!!!
 
Thank you and  God Bless!
Samuel’s mom, Mary Mabeus
Click here for Samuel's page
 
 

 
"I believe that I have never seen the glory of God and the beauty of  humanity more than through the lives of these babies and children and  their parents."
E.H.T, MD
San Antonio, TX

Physician's Home

Not Compatible with Life, a diary of keeping Daniel
By Kylie Sheffield

Prenatal Diagnosis Information Package - Compiled by Kylie Sheffield (mum of Daniel, full Trisomy 13) in consultation with families on this web site

Articles on Eugenics, Ethics, Selective Abortion, Selective Induction and the killing of Disabled Children

Personal Qualms Don't Count: Hospital Forces Nurses To Participate In Genetic Terminations 
by MARNIE KO

 

Living with Trisomy 13
Focused on prayerful support and gifts of love to those touched by a Trisomy 13 child.
Inspired By An Angel
Attn: LivingWithTrisomy13
15802 Springdale St.. #68
Huntington Beach, CA  92649

info@LivingWithTrisomy13.org

 

 

All text and graphics © LivingWithTrisomy13.org 2005-2010 - all rights reserved
Use prohibited without permission
All information found on this site was submitted to us directly by the families
and used on this site with their permission.

Cover photo of Pamela Sullivan & her precious daughter Maria, copyright Pamela Sullivan 2004, used with permission.
If We Hold On Together  Song Copyright 2002 by Patricia Welch, Ltd. All rights reserved.   Used with permission.
 
*Disclaimer
All material on this site reflects our personal journey with raising a Trisomy 13 (Patau Syndrome) - child. It is not meant to replace any medical advise of a professional familiar with your specific condition. The personal journeys of any parents on this site are only their opinions and their own journey with having a Trisomy 13 child. You should consult with your own physician or other medical professional regarding the opinions or recommendations expressed within these pages as to your own child's symptoms and medical condition.
 
 

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