srps.net
the srps family networkSRPS Family Network, a support and information network for individuals and families with a history of, or interest in, Short Rib Polydactyly Syndrome
http://www.srps.net/
SRPS Family Network, a support and information network for individuals and families with a history of, or interest in, Short Rib Polydactyly Syndrome
http://www.srps.net/
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Teresa Tauchi
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Teresa Tauchi
6107 Roc●●●●●●●●vd South
Oa●●nd , California, 94618
United States
View this contact
Teresa Tauchi
6107 Roc●●●●●●●●vd South
Oa●●nd , California, 94618
United States
View this contact
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the srps family network | srps.net Reviews
https://srps.net
SRPS Family Network, a support and information network for individuals and families with a history of, or interest in, Short Rib Polydactyly Syndrome
Loving Leah, Tommy, Nic and Kenny: Out of the Ashes
http://lovinglittleleah.blogspot.com/2009/11/out-of-ashes.html
Tuesday, 24 November 2009. Out of the Ashes. A friend and counselor of mine during our long walk through Leah's death and Tommy's adoption recently asked to share our story during a devotional she was preparing. She asked for some pictures of both Leah and Tommy, so I made a little slideshow. I used music from Steven Curtis Chapman's newest album Beauty Will Rise. This album rocks my world. Which helps hundreds of families bring home kids every year (including us! A few weeks ago I saw an article on CNN&...
Loving Leah, Tommy, Nic and Kenny: Seven Years
http://lovinglittleleah.blogspot.com/2015/06/seven-years.html
Wednesday, 24 June 2015. So sad. So beautiful. Your growing family is just beautiful. Thank you for sharing these pictures. 3 July 2015 at 16:46. Subscribe to: Post Comments (Atom). As our lives moved forward we continued to blog about the adoption of our precious son Tommy from Uganda, his homecoming, and the everyday moments that now compose our lives. Now we find ourselves on yet another adoption journey to bring home another son from Africa. Thank you for reading and walking this road with us. The Lu...
Loving Leah, Tommy, Nic and Kenny: Our Prayer for Our Baby
http://lovinglittleleah.blogspot.com/2008/07/our-prayer-for-our-baby.html
Wednesday, 23 July 2008. Our Prayer for Our Baby. After we received Leah’s diagnosis, our prayers changed. We prayed for a miracle, we prayed for comfort and peace, for wisdom in our decision making process, and that our baby would survive labor and have some time to spend with us. But our number one prayer remained the same, that God would use our baby’s life to bring glory to His name. Thank you for doing this blog! 24 July 2008 at 00:18. You help sharpen on MY faith! 24 July 2008 at 21:49. I was just ...
Loving Leah, Tommy, Nic and Kenny: The Second Ultrasound
http://lovinglittleleah.blogspot.com/2008/07/second-ultrasound.html
Thursday, 31 July 2008. Labels: Potters Syndrome and Oligohydramnios. Again, thank you for sharing your story. Your love for Leah, for God, and for each other is so obvious and inspirational. My prayers for you continue. 31 July 2008 at 11:21. Subscribe to: Post Comments (Atom). Please feel free to contact us at lovinglittleleah@gmail.com. Subscribe to Loving Leah. Our Prayer for Our Baby. Labor and Delivery, Part One. Labor and Delivery, Part Two. Out of the Ashes. Worth a Thousand Words. Some Much Need...
Loving Leah, Tommy, Nic and Kenny: Cub Scout Fun
http://lovinglittleleah.blogspot.com/2015/04/cub-scout-fun.html
Saturday, 4 April 2015. Tommy has really been loving cub scouting. It has been fun to try so many new things, and the while family has been enjoying the outings and pack meetings. Here are some pictures from the Pinewood Derby. He and Jeff crafted his car to look like Jeff's "cool car." It didn't win, but it sure was fun to watch! It does look like a lot of fun. 4 April 2015 at 21:47. Subscribe to: Post Comments (Atom). Please feel free to contact us at lovinglittleleah@gmail.com. Subscribe to Loving Leah.
Loving Leah, Tommy, Nic and Kenny: Happy Birthday Tommy!
http://lovinglittleleah.blogspot.com/2015/04/happy-birthday-tommy.html
Friday, 24 April 2015. Sometimes I'm not sure how we got here, but we now officially have a seven year old! Speaking of socializing, Tommy had a friend birthday party too. He loves his birthday, and starts discussing his party and invite lists months in advance (which is nice because it usually starts with "I want to invite the entire school! We are so proud of you and are blessed to be your parents! I cannot and will not believe it! But the proof is in the pictures:) What a mature guy 3. As our lives mo...
Loving Leah, Tommy, Nic and Kenny: Catching Up Pt. 1: Easter
http://lovinglittleleah.blogspot.com/2015/04/catching-up-pt-1-easter.html
Tuesday, 21 April 2015. Catching Up Pt. 1: Easter. Here are a few pictures from our Easter festivities - the egg hunt after church, our impromptu backyard picnic (because it was such a beautiful day that the kids begged to eat outside), and our neighborhood egg hunt in the park. It was a wonderful day! Subscribe to: Post Comments (Atom). Please feel free to contact us at lovinglittleleah@gmail.com. Subscribe to Loving Leah. Our Prayer for Our Baby. Labor and Delivery, Part One. Out of the Ashes. Resistin...
Loving Leah, Tommy, Nic and Kenny: The First Ultrasound
http://lovinglittleleah.blogspot.com/2008/07/first-ultrasound.html
Saturday, 26 July 2008. We knew that we were not going to make any decisions without a second opinion and the best diagnostic assessment possible, and lots of time to weigh our options and pray. We also knew there was no way we would deliver prior to 24 weeks, the standard time when doctors consider babies able to survive labor and viable outside the womb. We would not deliver if no chance of survival existed. Labels: Potters Syndrome and Oligohydramnios. 28 July 2008 at 00:21. 3 November 2009 at 19:13.
Loving Leah, Tommy, Nic and Kenny: Whale Carrot vs. Pink Mustache
http://lovinglittleleah.blogspot.com/2015/04/whale-carrot-vs-pink-mustache.html
Saturday, 25 April 2015. Whale Carrot vs. Pink Mustache. Followed by The Time Kenny Rubbed His Upper Lip So Raw That He Gave Himself a Mustache Which He Wore Proudly For About a Week. I have a pink mustache. Subscribe to: Post Comments (Atom). Please feel free to contact us at lovinglittleleah@gmail.com. Subscribe to Loving Leah. Our Prayer for Our Baby. Labor and Delivery, Part One. Labor and Delivery, Part Two. Out of the Ashes. Worth a Thousand Words. The One in Our Arms. Waiting, Waiting, Waiting.
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the srps family network
We are a support and information network for individuals and families with a history of, or interest in, Short Rib Polydactyly Syndrome. The SRPS Family Network was founded in the fall of 2000 as a volunteer effort by families whose lives have been touched by the syndrome. Our mission is twofold:. The primary activities of the SRPS Family Network are to maintain this web site, to conduct mailings, and to moderate a Yahoo e-mail discussion group for SRPS Family Network members. New members will be sen...
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