Orphans with Arthrogryposis
There are kids with Arthrogryposis all over the world who wait for a family to call their own. Every child should have a Mama and Papa to love them. Sadly many kids will never know the love of a family as they will live out their shortened lives in institutions. The children posted here are from Reecesrainbow.com If you can't adopt, you can donate to their grants on reecesrainbow.com Don't leave them to die in institutions.
Sunday, June 12, 2011
Saturday, June 11, 2011

A generous person has offered to match every donation made to baby Joel's (his RR profile: tinyurl.com/4z9h4qe) adopting fund up to $2000!! & if we get to $2000 by the 13th the donor will throw in another $500! So even if you only have $5 PLEASE give bc it will $10! Joel is only 8 mons old! The more $$ in his account the more likely he'll be adopted! & we all no the sooner treatment for AMC starts the better! PLEASE SHARE THIS!!!!
Donate Here: tinyurl.com/4z9h4qe
Here is the blog post with more details! http://www.laeliasky.com/2011/06/09/my-thats-generous/
Monday, June 6, 2011
Understanding Arthrogryposis
This video gives a superb and easy to understand explanation of what arthrogryposis is.
http://vimeo.com/24626314
Its an interview of Dr. Harold van Bosse from Shriners Hospitals for Children in Philadelphia, PA. He specializes in arthrogryposis and treats many of the former Reece's Rainbow kids who have AMC.
This video was done by Margarget Chaidez. She is making a documentary about AMC called The Sweetest Gift: Living with Arthrogryposis
Arthrogryposis Awareness Day is June 30th!! Wear blue that day!
http://vimeo.com/24626314
Its an interview of Dr. Harold van Bosse from Shriners Hospitals for Children in Philadelphia, PA. He specializes in arthrogryposis and treats many of the former Reece's Rainbow kids who have AMC.
This video was done by Margarget Chaidez. She is making a documentary about AMC called The Sweetest Gift: Living with Arthrogryposis
Arthrogryposis Awareness Day is June 30th!! Wear blue that day!
They met their families!!
The three kiddos who I talked about in the previous have all met their families!!
Moira meets her Mom and Dad!
http://wronginalltherightways-travcat.blogspot.com/2011/05/chosen-ones.html

Please say a few extra prayers for Moira she shows very little emotion because of the conditions she has endured in the orphanage.
Ember meets her Mom and Dad!
http://addingasenti.blogspot.com/2011/05/big-day.html

Ethan (Gage) meets his Mom and Dad!
http://hebrewselevevone.blogspot.com/2011/06/celebration-day.html
Moira meets her Mom and Dad!
http://wronginalltherightways-travcat.blogspot.com/2011/05/chosen-ones.html

Please say a few extra prayers for Moira she shows very little emotion because of the conditions she has endured in the orphanage.
Ember meets her Mom and Dad!
http://addingasenti.blogspot.com/2011/05/big-day.html

Ethan (Gage) meets his Mom and Dad!
http://hebrewselevevone.blogspot.com/2011/06/celebration-day.html
Wednesday, May 4, 2011
Rainbow Kids
Rainbow Kids has a special needs section which can be found here!
They have about eight kids with Arthrogryposis (or other similar joint disorders) listed.
Here is their section on Arthrogryposis: http://specialneedsadoption.rainbowkids.com/Arthrogryposis_-_Joint_Disorders.aspx
Click "waiting children with Arthrogryposis" on that page and you'll be taken to their listings. You have to register and login before you'll able to see the listings
They have about eight kids with Arthrogryposis (or other similar joint disorders) listed.
Here is their section on Arthrogryposis: http://specialneedsadoption.rainbowkids.com/Arthrogryposis_-_Joint_Disorders.aspx
Click "waiting children with Arthrogryposis" on that page and you'll be taken to their listings. You have to register and login before you'll able to see the listings
3 families Traveling in May!!!
Three families who are adopting kids with various forms of Arthrogryposis are traveling to meet their kids in May!
First up is the Ferrone's! Appointment on May 17th!
They're adopting this sweety and another little girl with a different diagnosis

You can follow their journey here: www.wronginalltherightways-travcat.blogspot.com
Then The Senti's appointment is May 24th!
They're adopting this cutie pie!

You can follow their journey here: http://addingasenti.blogspot.com/
And last but not least is the DeVowe Family! Their appointment is May 30th
They're adopting this handsome young man!

You can follow their journey here: http://www.hebrewselevevone.blogspot.com/
First up is the Ferrone's! Appointment on May 17th!
They're adopting this sweety and another little girl with a different diagnosis

You can follow their journey here: www.wronginalltherightways-travcat.blogspot.com
Then The Senti's appointment is May 24th!
They're adopting this cutie pie!

You can follow their journey here: http://addingasenti.blogspot.com/
And last but not least is the DeVowe Family! Their appointment is May 30th
They're adopting this handsome young man!

You can follow their journey here: http://www.hebrewselevevone.blogspot.com/
Tuesday, May 3, 2011
The Ferrone Family
The Ferrone Family are adopting these two cutie from Eastern Europe! Moira has Arthrogryposis. They leave in less then TWO weeks!!!
Moira

Nastya

They could really use your help to fund the rest of this adoption. They still need a good deal of money before they leave to go meet the girls!
Click here for their Family Sponsorship Page on Reece's Rainbow!!!
Remember no amount is too small!!!!!!!
Moira

Nastya

They could really use your help to fund the rest of this adoption. They still need a good deal of money before they leave to go meet the girls!
Click here for their Family Sponsorship Page on Reece's Rainbow!!!
Remember no amount is too small!!!!!!!
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