Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God...there is so much to say about Our Life With Raymond.
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Our Life With Raymond | ourlifewithraymond.blogspot.com Reviews
https://ourlifewithraymond.blogspot.com
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God...there is so much to say about Our Life With Raymond.
ourlifewithraymond.blogspot.com
Our Life With Raymond: Wow Raymond!
http://ourlifewithraymond.blogspot.com/2014/07/wow-raymond.html
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Thursday, July 3, 2014. But today was an exceptional day! So in our first appointment...
Our Life With Raymond: February 2014
http://ourlifewithraymond.blogspot.com/2014_02_01_archive.html
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Wednesday, February 12, 2014. Say What, Ray? Sometimes he just looks at me as if to s...
Our Life With Raymond: Vote for Ray if you want to Partay!
http://ourlifewithraymond.blogspot.com/2014/10/vote-for-ray-if-you-want-to-partay.html
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Thursday, October 9, 2014. Vote for Ray if you want to Partay! So, Matt and Raymond p...
Our Life With Raymond: March 2013
http://ourlifewithraymond.blogspot.com/2013_03_01_archive.html
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Monday, March 4, 2013. Life can really be stressful, right? Today in Physical Therapy...
Our Life With Raymond: January 2014
http://ourlifewithraymond.blogspot.com/2014_01_01_archive.html
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Sunday, January 5, 2014. Out with 2013.In with 2014. Struggle No.1…Seizures. With eve...
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Our life without a Car
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ourlifewithpeanut
Subscribe to: Posts (Atom). View my complete profile. Simple theme. Powered by Blogger.
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Our Life with Pip and Squeek
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Our Life with props | the moon in our eyes
Our Life with props. The moon in our eyes. The moon in our eyes. BENNY HILL – ‘A cherub sent by the Devil’. Michael Caine. August 12, 2015. August 12, 2015. Maybe rose coloured specs would have been better. The music that ended his show, with him being chased by an assortment of girls and other characters that he had upset in various ways. He was often the loser, the fall guy, the one chased. And have a good giggle as you head down to hades. Plum pudding on a chain. Maybe with a file inside? Or ‘we can d...
ourlifewithraymond.blogspot.com
Our Life With Raymond
Hi, we are the Lara Family. Our younger son Raymond has Cerebral Palsy, Mitochondrial Disease (a very complex disorder), is profoundly deaf, but hearing since age 6 with a Cochlear Implant, he is feed through a tube and is very medically fragile. We hope that this blog can be a way to share the beautiful blessings from God.there is so much to say about Our Life With Raymond. Our Life With Raymond. Our Life With Raymond. Wednesday, October 29, 2014. Is it almost Halloween already? Raymond was in the corne...
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Our Life With RyLeigh Joy | This blog is about our journey with RyLeigh and how a Down Syndrome diagnosis made our life a more beautiful place.
Our Life With RyLeigh Joy. This blog is about our journey with RyLeigh and how a Down Syndrome diagnosis made our life a more beautiful place. What Does Low Tone Mean? Posted by Our Life With RyLeigh Joy. Asymp; Leave a comment. This right here…. Generally kiddos with low tone seem to be squishable because they melt right into you when you hug or hold them. This is great for cuddling but if you are carrying a baby or kiddo around that. Posted by Our Life With RyLeigh Joy. Asymp; Leave a comment. Having h...
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Our Life with the Boy
Our Life with the Boy. September 4, 2013. First Day – No Tears. At 5:43 pm by ourlifewiththeboy. Today was Matthew’s first day of Pre-K 4. He is now at the school where his sister attends and the school where he will remain through 8. If you have been reading my blogs over the past few years, you know how much I struggle with worry (control). Finally, finally, finally, I am starting to feel a shift. Could it be perhaps that I am learning not to worry so much? April 30, 2013. Dear NICU Mom,. So watching t...
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Our Life With the Littles
Our Life With the Littles. Friday, April 14, 2017. Little did I know this is the last time I would hug and kiss Hazel with her being my youngest babe. Our midwives finished some laundry and picking up and were out the door after hugs were shared. Were hollered out. ;) She is so beautiful and we are all so blessed by her, our sweet Ruby Ophelia. Thursday, February 5, 2015. After I got all cleaned up I got back into bed for another short monitoring session. (I hate those monitors! It was around this time t...
Blog de OurLifeWithThem - Nos Amis, Nos Amours, Nos Emmerdes ... OuLifeWithThem - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. Plus d'actions ▼. S'abonner à mon blog. Nos Amis, Nos Amours, Nos Emmerdes . OuLifeWithThem. Photographie : Avatar Randy Orton, ne touche pas :). Propriétaire du blog : xBloodyPast and xStooryWwe. D-GENERATION X , THE LEGACY ♥. THE RATED R SUPERSTARS EDGE ♥. MISSING YOU ♥. Création : 21/12/2010 à 19:01. Mise à jour : 15/11/2011 à 09:13. Ou poster avec :. Retape dans le champ ci-dessous la suite de chiffres et de lettres qui apparaissent dans le cadre ci-contre.
