Lying Down…

… Have you ever tried lying down for a long time? i mean like for an extended period of time, just do nothing but lay down on a bed. Try it. Go lay down, fully awake, don’t go to sleep now. Lay there doing nothing for thirty minutes – that’s ok, in fact, you might feel rested. How about lying down, wide awake, doing nothing for two hours? Ok, maybe it was a little long but bearable – yes? Now go ahead and see how you feel after four hours or ten hours or an entire day and night? Then imagine that would be what your future holds, day in, day out, for the rest of your life…

i would be bored stiff within half a day. My heart breaks that there are children out there who have exactly that to look forward to in their futures, just because they have a disability and the orphanage or more likely the institution does not have the staff or the facilities to allow them to be outside of their cribs. In some places, children are left in their cribs all day because the society views that is all they can do. In other places, they do not know that these children can be helped or how to help them.

But we all know, we who live in places where medical facilities are available, we know that anyone with a disability if given the proper treatment, therapy and good, loving support, can thrive and live a fulfilling life.

A little girl needs a loving family to help her make the most of life.

Nastya is one of these many children who would have no future unless adopted. Ideally, adopted within her own country, but the reality is that in her country that would most likely not happen as disability is not widely accepted in their society. So international adoption would be the next option for her.

So today i am shouting out for her – she needs a family to love her, just as she is; a family to tell her she is worth their care and support, just because she is who she is. If she had a family who could give her the care she needs, then she can look forward to a future which would feature days outside, enjoying the sunshine, enjoying time interacting with her family and other people, and even a job when she is all grown up and maybe a family of her very own in the far future.

Nastya is already 7 years old and the future looks bleak. She has Spina Bifida and minor Hydrocephalus and is unable to walk. But this does not mean that she isn’t capable. In the right supportive environment, i believe she would grow into the beautiful flower i know she is, deep inside.

Do you see that in her? Do you think you could be her family? If yes, please contact Reece’s Rainbow for more details.

You don’t have to be her family to help. You can share her story so that more people will come to know her and increase her chances of finding a family.

You can give towards her adoption grant to ease the journey her forever family would have to bring her home. International adoptions cost an arm and a leg! Click on her picture or name to go to her profile page to donate.

You can most definitely pray for her. Pray for her daily needs, pray for a family to step up for her real soon.

Thank you.

syc

Just Like You…

… that’s the title of a video about children with Down Syndrome. It is very informative and i love how they point out the differences between everyone and that Down Syndrome does not definite who they are. This video really does cover lots of aspects of Down Syndrome and how a child with Downs needs help but they still want to do everything other kids do. They try their best.

The 3 kids with Down Syndrome in the video proudly show that they are indeed different but that doesn’t mean they aren’t awesome, just being who they are and live a full life with support from their family and friends. Their best friends share great testimony on their behalf.

Watch the video then read on:

My little Heath has Down Syndrome too. And as it is said in the video, ‘It’s just part of what makes me who i am.’ But it is only a part of it. He is much more than Down Syndrome.

But unfortunately, the society he was born into sees only his Down Syndrome and they only see it as a disability  Which is why Heath spends his days sitting in a wheelchair, doing nothing, absolutely nothing but stared at whatever happens to be before him. Because where he is from, being different from what is considered “normal” is unacceptable.

‘Once you learn what Down Syndrome is, you get use to it. Because when you have the knowledge and you understand, it’s easy to accept.’

12 year old Heath, is a cutie who needs his family asap.
12-year-old Heath, is a cutie who needs his family asap.

His only hope is to be adopted by a loving family who has the knowledge and understands that Down Syndrome is not a disability; a caring family who lives in a society which will accept him, just as he is; a little boy who just needs to be shown tender loving care, who will just thrive in such care. Could you be the one to give him such love?

‘She sees you for you, who you are on the inside.’

Please see my Heath for who he is, see that he is a little boy with much need but most of all, see his potential. Can you imagine what he could accomplish with a supportive family behind him?

‘I’m worth the wait…’

Indeed, he will be a blessing to the family who welcomes him with open arms and hearts.

My little Heath has a full grant! (We, his advocates, are so grateful to all the generous donors who made this possible.) Which means his forever family need only come up with the initial fees for commitment and home study and that is completely doable.

Money is now not a hurdle. We just need a family to step up. Are you his family? Please click on his name or picture to find out more or contact Reece’s Rainbow.

Will you share Heath‘s story far and wide so that his family maybe found? Do pray for him; for his daily needs and for a forever family to come for him.

syc

Looking Beyond…

Meet Angelina.

This sweetie needs a family. Would you be able to help?

She is an orphan in Eastern Europe. According to her file, she has the following health issues:

Congenital dysfunction, myelocele of lumbosacral part of spinal cord (had surgery); internal hydrocephalus, flail legs with dysfunction of pelvis/hips, delay of psychological development.

Sounds overwhelming?

But her medical conditions do not define her! She is not spina bifida and the dysfunctions it brings, she is not psychological delay. NO. She is simply a little kid who needs a loving mummy and daddy to help her work around and work with her health conditions and live a full life despite of these medical issues.

If we were defined by our problems, if God only saw our problems, none of us would be here today.

So please look beyond her various conditions and see the little girl who can blossom under the attentive, loving care of a wonderful family. Look into her eyes and see that she can have a great future with a family willing to support and encourage her.

Do you see her? Is she your little girl? Do you feel your heart beat a little faster? If so, do contact Reece’s Rainbow for details about adopting her.

Even if you can’t or don’t feel adopting is the way for you, you can still pray for her; for her daily needs and definitely for her forever family to step forward.

You can also help her by giving towards her adoption grant so that a lack of funds would not be the reason she can’t have  a family. You can click on her name or picture to go to her profile page to donate.

Thank you.

syc