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Fishing for Zebras: And the Merry Bells Keep Ringing (Mostly)
http://sophiespleen.blogspot.com/2008/12/and-merry-bells-keep-ringing-mostly.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Tuesday, December 23, 2008. And the Merry Bells Keep Ringing (Mostly). It is so much better though and despite little moments of pain I am really enjoying this holiday season (as my credit card bills will surely show in January!
Fishing for Zebras: September 2008
http://sophiespleen.blogspot.com/2008_09_01_archive.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Monday, September 22, 2008. Links to this post. Colorado newborn screening program. Subscribe to: Posts (Atom). Some Ways to Help a Grieving Person. Asplenia and Related Links. Another Asplenic Child (with an amazing Mom).
Fishing for Zebras: June 2008
http://sophiespleen.blogspot.com/2008_06_01_archive.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Sunday, June 29, 2008. A merry little weekend. We spent the weekend with my brother-in-law and my two neices- (and Tina is home too- yeah! Links to this post. Labels: coping with loss. Thursday, June 26, 2008. Heavy heart.heavy sigh.
Fishing for Zebras: March 2009
http://sophiespleen.blogspot.com/2009_03_01_archive.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Thursday, March 5, 2009. Too Good to be True. Links to this post. Subscribe to: Posts (Atom). Some Ways to Help a Grieving Person. Asplenia and Related Links. Another Asplenic Child (with an amazing Mom). Emedicine article on Asplenia.
Fishing for Zebras: Still Remember
http://sophiespleen.blogspot.com/2010/02/still-remember.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Thursday, February 25, 2010. I love you angel sophsoph. I was thinking of you the other day and was wondering how you are doing.You are always in my thoughts. February 25, 2010 at 8:34 PM. Subscribe to: Post Comments (Atom).
Fishing for Zebras: November 2008
http://sophiespleen.blogspot.com/2008_11_01_archive.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Thursday, November 27, 2008. Links to this post. I have so much good in my life, it didn't take Sophie's death to make me realize it, but you all really shined during this tragedy- we must be really good judges of character!
Fishing for Zebras: Too Good to be True
http://sophiespleen.blogspot.com/2009/03/too-good-to-be-true.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Thursday, March 5, 2009. Too Good to be True. Things happen in life that we have no control over. You are a good mom and your family is lucky to have you. March 20, 2009 at 7:22 PM. Just checking in to see how you are doing.
Fishing for Zebras: Happy Birthday Little Angel
http://sophiespleen.blogspot.com/2009/01/happy-birthday-little-angel.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Wednesday, January 7, 2009. Happy Birthday Little Angel. I do know that you would be so big.talking in full sentences, sleeping in a big girl bed, potty trained, playing with little friends.I really wish I could see you today. January ...
Fishing for Zebras: To EMC
http://sophiespleen.blogspot.com/2009/01/to-emc.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Tuesday, January 6, 2009. I know what you are going through right now, your grief is so fresh, it must seems sureal. Please email me when you feel like talking.it is gkate1@comcast.net. Subscribe to: Post Comments (Atom).
Fishing for Zebras: Waiting for Marble
http://sophiespleen.blogspot.com/2009/02/waiting-for-marble.html
A place for friends, family, and parents who have lost children to read about my experiences losing my 15 month old daughter to congential asplenia.how we are coping and what we are doing to help ensure this entirely preventable sort of death does not happen in the future. Saturday, February 28, 2009. Anyway, as it is getting closer to spring I am hoping that the owl (marble) might come back.I really felt that was some sort of sign. Sorry for the boring post- figured I'd better write something.
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Hetero Supremacy | noun: the belief, theory, or doctrine that the heterosexual is superior to all other sexual orientations, especially the homosexual orientation, and should therefore retain control in all relationships.
Noun: the belief, theory, or doctrine that the heterosexual is superior to all other sexual orientations, especially the homosexual orientation, and should therefore retain control in all relationships. Sen Stacey Campfield thinks only gays get AIDs. Filed under Stacey Campfield. On August 22, 2012 at 7:34 am. Currently making the social media rounds again is a January 26th, 2012 article from Raw Story. Personally, I’m sure that Campfield actually knows the truth, he just knows that he has a follow...
heterotalia-pairings.deviantart.com
HETEROtalia-Pairings | DeviantArt
Window.devicePixelRatio*screen.width 'x' window.devicePixelRatio*screen.height) :(screen.width 'x' screen.height) ; this.removeAttribute('onclick')". Founded 7 Years ago. A group to support the non-Yaoi/Yuri/Poly pairings of Hetalia. Welcome to HETEROtalia! A group to support the non-Yaoi/Yuri/Poly pairings of Hetalia. Welcome to HETEROtalia! Founded 7 Years ago. Jun 14, 2011. Div div.gmbutton2town a:hidden').clone().appendTo('#super-secret-buttons .gmbutton2town').css('float', 'none'...Beer and Tea Week.
Heterotalia | DeviantArt
Window.devicePixelRatio*screen.width 'x' window.devicePixelRatio*screen.height) :(screen.width 'x' screen.height) ; this.removeAttribute('onclick')". Founded 7 Years ago. THIS GROUP IS NOT TO HATE AGAINST YAOI/YURI FANS, FAN MADE PAIRINGS, OR HOMOSEXUALS. THIS GROUP IS TO PROMOTE STRAIGHT PAIRINGS AND OC FEM CHARACTERS. Everyone is equal and we all should have our say. Ours is showing our OC fems, favorite straight pairings, and favorite fem chars. Love! Founded 7 Years ago. Jul 23, 2011. Div div.gmb...
Heterotaxy Foundation
Skip to main content. The Heterotaxy Foundation is a non-profit organization created to raise funds for research and promote awareness of a rare disease called Heterotaxy Syndrome and is managed by Keegan's Spirit Foundation,. 100% volunteer, 501(c)(3) tax-exempt organization centered on providing hope to those with congenital heart disease. Please click on one of the links above to learn more about the rare disease of Heterotaxy Syndrome, our organization, and how to help.
Heterotaxy Syndrome | The Story of a little boy born with Heterotaxy Syndrome
The Story of a little boy born with Heterotaxy Syndrome. I wear red for Logan. February 2, 2013 by kristenspyker. The Month of February is Congenital Heart Disease Awareness Month. Today had me thinking about the last 3 years and everything we have been thru. Honestly, I don’t know how I got thru it. From getting the devastating diagnosis that kept getting worse every single time we saw a new doctor, to having to rock him in […]. Continue reading →. Birth and NICU Stay. Children's Hospital of Boston.
heterotaxyconnection
Find a Group on Facebook. Regional Coordinators and Facebook Team. Complex Congenital Heart Defects. Isomerism – Asplenia and Polysplenia. Welcome to Heterotaxy Connection! We are so happy you found us! We are constantly trying to find ways to improve our website, find up to date resources, and connect more families affected by Heterotaxy Syndrome. We know that this journey is a difficult one, but we hope that we can partner with you in making your journey a little less scary and much more hopeful.
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heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Tuesday, May 14, 2013. A mother's love helps others - The Sun Chronicle : Local News. A mother's love helps others - The Sun Chronicle : Local News. Links to this post. Tuesday, December 4, 2012. Alexander's Fight - Baubles for Boston. A dear friend of mine is making hand-crafted Christmas ornaments. Even then, there...
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Heterotaxy Syndrome | The Story of a little boy born with Heterotaxy Syndrome
The Story of a little boy born with Heterotaxy Syndrome. I wear red for Logan. February 2, 2013 by kristenspyker. The Month of February is Congenital Heart Disease Awareness Month. Today had me thinking about the last 3 years and everything we have been thru. Honestly, I don’t know how I got thru it. From getting the devastating diagnosis that kept getting worse every single time we saw a new doctor, to having to rock him in […]. Continue reading →. Birth and NICU Stay. Children's Hospital of Boston.
