Max, Oh Max!

Max, Oh Max!
Waiting for my Forever family!

Wednesday, September 14, 2011

BETHANY!!!

Bethany needs a family NOW.


Regardless of what her profile says, more importantly, she is SMART, she is BRILIANT, and she needs medical help, but it will NOT LIMIT her options.

See for yourself:

Here are some translated parts of the conversation:
-          The journalist is calling her “Sweet little dove”, she says seriously “ Why you are calling me Dove? I am not a dove, my name is Rita”
-          The journalist is asking her “ Do you like to sit in a armchair?”, she responds “ Of course, I like it. It is very convenient in general. You just need to put an extra roller for the back in order your back not to be curved”
-          The journalist is telling to the camera about Rita’s medical condition and she comments “ Oh…I understand everything what you are saying here about me…yes…it is truth!” 
- When being asked to introduce herself, she is saying " My name is Rita and I am very smart" 
- The journalist is asking her " Are your eyes being bothered by the camera's light?", she responds " No, because the light is pointing directly to my nose".   




 Here is her profile:

December 2006
Osteogenesis Imperfecta
melx-15
From volunteers who met her:  This radiant girl lives in a Russian orphanage. She suffers from OI, Group 3. She was bedridden for the most of her life; until she was almost 4 years old she could not sit and could not turn over. She had multiple bones broken by simply moving around in bed. Only one year ago volunteers found her in a cast from head to toe. They have begun raising money for her rehabilitation in the American Medical Center in Moscow. As a result, she is now sitting vertically first time in her life. The first time she was able to look out the window, she saw the bleak Moscow landscape of late November and there was no limit for her joy! She takes such pleasure in being able to see that the street cleaning guy has a “soft” hat and that birds are “fuzzy .” Despite having such a handicapped childhood, Bethany is unbelievably bright. At three and a half she knew all colors, 1 to 10 numbers, could recite many children rhymes, and she has a perfect music pitch! According to the nurses, Bethany radiates positivism and humor to such degree that children from the hospital gather in her room for a good laugh, a song, or a story. When it was time for her to leave the hospital and to part with the nurses, she broke down crying for the first time, despite all the physical pain of the hospital procedures. She desperately wants to belong, to be part of a family.

Update Sept 2011:  Bethany is extremely bright child…despite of the orphanage environment, her mental development is far beyond her age group. You should see how she responds to the questions and how she comments…she is so funny and so cheerful. She can sit without a help, but she is still not walking.
More information and a video from June 2011 is available for interested families.  More pictures available.  Potential families must have good medical coverage and be comfortable financially.
A new video of Bethany:

Wednesday, September 7, 2011

Time keeps ticking...

This is just down right painful. I have fallen in love with so many many children, Bethany, Samual, Shaun, Nick, Darby, where is mommy and daddy????


I am asking a very simple request. Pass this blog to ANYONE who might help carry the torch for one of these children!!!!

Kelly

Monday, August 22, 2011

Help Nick find a home!

This little boy needs to find a home fast, as he has a rare skin disorder (EB) and needs treatment as soon as possible.  He is a beautiful little boy who needs a mommy and daddy who will be willing to take care of him, take the time to bath and wash his skin, and wrap bandages on a daily basis.  Help spread the word and HELP him find a 'forever' family!!


Thursday, July 21, 2011

THIS WEEK- Conference on Trisomy 18/13 in Chicago!

As we speak, there is a conference going on in Chicago for Trisomy 18. I have begged a family to pass out flyers about Shaun, who has Trisomy 18.  He is just adorable, but sadly, because of a label, he has been forgotten.   However, I have NOT forgotten, and I will NOT give up until he has found his forever family.

Won't you please donate just $18 to his fund, as a symbol for his genetic disorder? 

http://reecesrainbow.org/shaun-etkf-region-3
Won't you please just pass this blog to 18 more people, in hopes we can spread the word?

Won't you please just post this on Facebook or send to 18 more friends?

Won't you just please????

Tuesday, July 12, 2011

Another month has passed!

Ok, so I am going to try this again!  My last fundraiser- well, didn't do so well.  However, doesn't EVERYONE want a coach purse?  I am going to RAFFLE this one off- and I am going to try to find a WINNER this time!   Take a look at this almost- brand new purse- it could be yours for- ANY PRICE YOU MIGHT OFFER!  Best offer will be the taker- and all proceeds will go to Shaun's account through Reece's Rainbow.  On the home front, my advocacy team is trying to find out more information about Shaun for several families that are interested in finding out more about Shaun!  I am SO hopeful we can find a family for Shaun- SOON!  I think about you often Shaun, please hang on!!!



Also, many of you do NOT know what I look like, so I have included a picture below (not so pretty), but it is a picture of my son Ryan and myself at a park several months ago- look how my little one is riding his very first bike!!




Also, one does NOT realize, but I JUST learned how to garden this year- CHECK THIS OUT! CAN YOU GUESS WHAT IT IS???
Need I say more???

Tuesday, June 14, 2011

I have not forgotten you!

Each day I read new notices about so many children that need homes.  This is just a note to Shaun that I have not forgotten him, and that I think of him each day.   Although I am busy with some course work, my heart is getting ready to plan a bigger fundraiser for him.  No bites yet on this nice leather toiletry kit- but I am not giving up yet.  If not this fundraiser, I will think of something else!  Keep on spreading the word for Shaun's sake!!!

Thursday, June 9, 2011

Heavy Day!

Today has been a LONG day.   I just had to write a short note and say that I had the opportunity to speak with Victoria Miller from the Trisomy 18 Foundation and she has graciously indicated she will advocate for Shaun.  However, I am SAD.   I am impatient and I want to find a family that will commit to him NOW.  Where is his family!  Come get Shaun now!!!