Surviving with Thanatophoric Dysplasia- A Very Happy little kid-
Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 6 years old
Samuel is my nephew his mom is my sister-in-law Evelyn. Our husbands are brothers.
Samuel's Mom now has her own blog at:
http://hopeseed.wordpress.com/
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 6 years old!
This is Samuel and one of his teachers.
Update Samuel Turned 6 on Aug 2, 2011 and is still doing awesome things. He now is in school, well the teacher comes to him, but still really cool. He uses switches to operate his computer and toys.
Other More Recent Pictures from about 2009 to present (11/2010) not in any order.
This is Samuel and his mom Evelyn (Evelyn is my sister-in-law and Samuel is my nephew)
Isn't he Darling!!
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8/1/2008 Update on Baby Samuel
He was born a Thanatophoric Dwarf. It is Also called Thanatophoric Dysplasia. It is a condition considered incompatible with life. Only 3 have ever been known to survive into early childhood. Well Samuel is going to make number 4. Samuel Turns 3 years old on Saturday and miracle of miracles he is breathing on his own off the vetillator for short periods of time. Another thing, according to doctors he was never suppose to be able to do. Check out his website where his mom keeps a journal. Feel Free to Sign his guest book and wish him a very happy 3rd Birthday. I know he and his family will appreciate it greatly and please keep them in your prayers.
Yeah to Samuel and his Family.
This is Samuel.
Hope you enjoy it and laugh along!!
Surviving Well on a ventilator, Surviving Thanatophoric Dysplasia, Surviving with Ventilator not painful, Thanatophoric Dwarf, Living With Thanatophic Dysplasia
Thanatophoric images, Thanatophoric pictures, Children living with Thanatophoric Dysplasia, thanatophoric dysplasia type 1 survivors
Tuesday, November 10, 2009
Chose Life Story, Samuel living with Thanatophoric Dysplasia
As most of you know my nephew Samuel was born with a condition called Thanatophoric Dysplasia which is a condition that is considered incompatible with life. My Sister-in-law and brother-in-law went against Doctors wishes and did not have a therapeutic abortion. A few weeks ago Spirit FM 90.5 aired their story This is an audio file of that story that aired on Spirit FM.
Here is the audio Story/ Interview that aired
Here is a link to some pictures of my nephew Samuel
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 4 years old!
Samuel's Caring Bridge Website
Tags: long-term thanatophoric survival, living thanatophoric dwarf, thanatophoric dwarf turns 3, laughing and happy child with thanatophoric dysplasia, Living with thanatophoric dysplasia, surviving thanatophoric dysplasia, living on a ventilator
Here is the audio Story/ Interview that aired
Here is a link to some pictures of my nephew Samuel
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 4 years old!
Samuel's Caring Bridge Website
Tags: long-term thanatophoric survival, living thanatophoric dwarf, thanatophoric dwarf turns 3, laughing and happy child with thanatophoric dysplasia, Living with thanatophoric dysplasia, surviving thanatophoric dysplasia, living on a ventilator
Friday, January 16, 2009
Update: Sam a Surviving 3 1/2 year old Thanatophoric Dwarf has Fun at Sea World & Disney
Update: 1/16/09
Hi Everyone,
This is another Update on the wonderful and amazing life of Samuel who was born with Thanatophoric Dysplasia. He is surviving, thriving, full of life and doing fantastic. Here he is in his shades on his trip to Disney & Sea World. The wonderful Make A Wish foundation granted this wish for Samuel and his family. I want to let families know that if they ever have to face the choice of whether to put their child on a ventilator that these children do not live in pain and do have a very wonderful quality of life. I don't always think doctors give parents all the information necessary to make an informed decision. I think doctors in many cases scare people away from life saving procedures especially when they feel there is supposedly no hope. I want to let parents know they do have options. Choose life.
He is a giggly, happy toddler who does interact with his environment.
Samuel and His Mom at Disney & Sea World in Orlando Florida
A Wish Granted to Him By The Make A Wish Foundation
A Wish Granted to Him By The Make A Wish Foundation
Samuel's Website
Sign his Guest book
Sign his Guest book
Tags: long-term thanatophoric survival, living thanatophoric dwarf, thanatophoric dwarf turns 3, laughing and happy child with thanatophoric dysplasia, Living with thanatophoric dysplasia, surviving thanatophoric dysplasia, living on a ventilator
Saturday, September 18, 2010
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 5 years old!
Update Samuel Turned 5 on Aug 2, 2010 and is still doing awesome things. He now is in school, well the teacher comes to him, but still really cool. He uses switches to operate his computer and toys.
Other More Recent Pictures from about 2009 to present (11/2010) not in any order.
_______________________________________________________________________
8/1/2008 Update on Baby Samuel
He was born a Thanatophoric Dwarf. It is Also called Thanatophoric Dysplasia. It is a condition considered incompatible with life. Only 3 have ever been known to survive into early childhood. Well Samuel is going to make number 4. Samuel Turns 3 years old on Saturday and miracle of miracles he is breathing on his own off the vetillator for short periods of time. Another thing, according to doctors he was never suppose to be able to do. Check out his website where his mom keeps a journal. Feel Free to Sign his guest book and wish him a very happy 3rd Birthday. I know he and his family will appreciate it greatly and please keep them in your prayers.
Yeah to Samuel and his Family.
This is Samuel.
Hope you enjoy it and laugh along!!
Tags: long-term thanatophoric survival, living thanatophoric dwarf, thanatophoric dwarf turns 3, laughing and happy child with thanatophoric dysplasia
Saturday, August 1, 2009
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 4 years old!
Samuel is my nephew his mom is my sister-in-law Evelyn. Our husbands are brothers. This was an old post. Samuel Turned 6 in 2011 and his mom now has her own blog.
Samuel's Mom now has her own blog at:
http://hopeseed.wordpress.com/
(new update: of 11/10/2009 A few weeks ago Spirit FM 90.5 aired their story. Here is the audio Story/ Interview that aired)
Yeah! Another Birthday- I can't believe it has been another whole year!!
For anybody new-- here is a little information about Samuel :
He was born a Thanatophoric Dwarf. It is Also called Thanatophoric Dysplasia. It is a condition considered incompatible with life. Only very few have ever been known to survive into early childhood. Samuel will turn 4 years old this Sunday and miracle of miracles he is breathing on his own off the ventilator for short periods of time. According to doctors he was never suppose to be able to do that. Check out his website where his mom keeps a journal. Feel Free to Sign his guest book and wish him a very happy 4th Birthday. I know he and his family will appreciate it greatly and please keep them in your prayers.
Yeah to Samuel and his Family.
Samuel's Website
Welcome to Samuel's WORLD PREMIER YOUTUBE Video!!
http://www.youtube.com/watch?v=R_Q92MC8plU
Hope you enjoy it and laugh along!!
Welcome to Samuel's WORLD PREMIER YOUTUBE Video!!
http://www.youtube.com/watch?v=R_Q92MC8plU
Hope you enjoy it and laugh along!!
Tags: long-term thanatophoric survival, living thanatophoric dwarf, thanatophoric dwarf turns 3, laughing and happy child with thanatophoric dysplasia
Boy I'm tuckered out. Just too much excitement!
Hey you-- get down on the floor and play with me.
Monday, July 28, 2008
Update: On Miracle Baby Samuel Born With Thanatophoric Dysplasia, Turns 3 years old!
Samuel is now 6 years old as of August 2011
Samuel is my nephew his mom is my sister-in-law Evelyn. Our husbands are brothers.
Here is a link to my Sister-In-Law's New blog as of March 2012
Samuel's Mom now has her own blog at:
http://hopeseed.wordpress.com/
Update Samuel Turned 5 Years Old on Aug 2, 2010 and is still doing awesome things. He now is in school, well the teacher comes to him, but still really cool. He uses switches to operate his computer and toys.
More Updated Pictures: From 2009 to present 11/2010 not in any order
(new update: of 11/10/2009 A few weeks ago Spirit FM 90.5 aired their story. Here is the audio Story/ Interview that aired)
Hey it has been a year now since I wrote this. Samuel turns 4 tomorrow Click here to see my new post and new pictures
Click Here to Read A News Article on Samuel and Watch A video done by Catholic News Agency
Checkout Samuel's Newest Update 1/16/09 His Trip to Disney & Sea World
Update on Baby Samuel
He was born a Thanatophoric Dwarf. It is Also called Thanatophoric Dysplasia. It is a condition considered incompatible with life. Only 3 have ever been known to survive into early childhood. Well Samuel is going to make number 4. Samuel Turns 3 years old on Saturday and miracle of miracles he is breathing on his own off the vetillator for short periods of time. Another thing, according to doctors he was never suppose to be able to do. Check out his website where his mom keeps a journal. Feel Free to Sign his guest book and wish him a very happy 3rd Birthday. I know he and his family will appreciate it greatly and please keep them in your prayers.
Yeah to Samuel and his Family.
This is Samuel.
Samuel's Website
Welcome to Samuel's WORLD PREMIER YOUTUBE Video!!
http://www.youtube.com/watch?v=R_Q92MC8plU
Hope you enjoy it and laugh along!!
Samuel's Website
Welcome to Samuel's WORLD PREMIER YOUTUBE Video!!
http://www.youtube.com/watch?v=R_Q92MC8plU
Hope you enjoy it and laugh along!!
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