Showing posts with label Handiwork for Orphans. Show all posts
Showing posts with label Handiwork for Orphans. Show all posts

Sunday, October 20, 2013

31 for 21 - Day 20

So I missed a few days due to being busy, sick, and tired. But, I'm back on track and will finish strong!

+++++++++

Before I get to today's two kids, I want to share about the craft sale Rachel and I did yesterday!
It was a large indoor (yay!) sale at a local school. One of those big ones you have to pay to get into. After a rough start with set up, we did so well, and ended the day with record sales!! We raised $374!! An all time sale record! God is soo good!!

+++++++++

This is beautiful Lanaya! She is 3 years old, has Down syndrome, a heart condition, and described as sweet and friendly.
She loves music, gets along well with other children, and plays with toys appropiately. She doesn't have any words or feed herself yet, but she can stand holding onto something.
She sounds like a sweet love bug who would do great in a family!!

+++++++++

And this is Aisha. Another beautiful girl with a beautiful name. But she is stuck in Russia, because of the adoption ban.

Please pray for her!

Saturday, October 12, 2013

31 for 21 - Craft Sale!

In my blogging hiatus over the summer, Rachel and I did several craft sales.

We had a tent in our town's yearly celebration festival thingy on July 20/21. It was two LONG hot days, but we made $252!!
Yes, that's Rebekah going under that table... this was the best picture we got.
Then we did the Farmer's Market twice. We made $219 on 7/29, because it was the end of July, but very chilly (we were wearing jeans and sweatshirts and still cold), therefore people bought lots of hats and scarves. And on 8/17, we made $129, probably because it was a bit warmer!

{Can't find a picture, not sure we took one at either sale...}

On 9/14, we did participated in an Applefest sale, making $116!

And today, we participated in the Oktoberfest sale. It was from 9am-5pm (most sales are until 12pm or 1pm), so very long, and I wasn't feeling well, but it's over and we made $176!

Roughly half of this money is going to the Hebbe family to help them bring home their precious boys!
They passed court, so I can finally share these sweet faces!

And the other half, brings me to today's waiting orphan with Down syndrome! Maria!

Rachel and I raising money for this sweet girl with Handiwork for Maria. She has (soon-to-be) over $16,000 in her account! Yes, SIXTEEN GRAND! That's almost all of the costs for a family to adopt her!
You wouldn't have to do much fundraising to go her and she is such a happy, joyful spirit, just waiting for you to go get her. So what are you waiting for??

++++

And I would feature Lilly for the child stuck in Russia, but since I already did, here's a beautiful girl who is in the same region/place as Lilly and also has Down syndrome, a heart condition, and strabismus - Anastasia.
 She also got a new picture the same time as Lilly... doesn't she look great?!?

Monday, September 23, 2013

Look what God has done! | 3 years

This past week we celebrated my little brother's 6th birthday! Who is that little brother? Elijah, as in handiworkforElijah.

Which means Handiwork for Orphans has been open for 3 years! THREE YEARS!

And during that three years God has blessed this ministry more than I can believe, and we're not done growing! 

Let's recap:
  • 3 years
  • Founded in Sept 2010 to help bring my little brother home from Ukraine
  • Added Rachel as the missing half of HFO in June 2011
  • Hundreds of hats made and sold
  • Hundreds of dishcloths and other items made and sold
  • 25+ craft sales
  • Several people inspired to start their own shops selling items to help orphans
  • Hundreds of people made aware of our cause and the plight of the orphan
  • Over $7000 raised (estimated)
  • 16+ orphans helped to find their families and come home
  • 6 of those have families working to get them!
  • and 8 are HOME with their forever families!

God is SO good! And we are so grateful to Him, and to everyone who made this possible.

Here's to another 3 years, to more money raised, to more children helped, to more families completed, to more love made.
Dude wasn't cooperating for pictures....
Thank you Elijah! For getting this party started!

++++++++++++++++++++

Our current child we are raising money for is Maria.

Check all the fun stuff we have fore sale including our newest item - these infinity scarves!

Plus we have LOTS of new cute hats you probably haven't seen! (Find them here!)

Thursday, September 12, 2013

A teachable moment.

Today an article popped up on my Facebook feed.

Intrigued, especially since it was posted by someone in one of my Lyme support groups instead of a by special needs adoptive mama, I clicked and started to read it.

It's worth the read and it teaches such an important lesson, for everyone, not just parents.

And it reminded me of something that happened a couple weeks ago.

But before I tell you that story you need to go read it.

When Your Kid Sees a Disabled Person at the Grocery Store

Done? Read it all the way through? No? Go finish.

Now are you all done? Okay.

So a couple weeks ago, I was at one of our local Farmer's Markets, selling the items Rachel and I have made to find Maria a family.

A lady came up with her son, who was probably 5 or 6 years old. They decided to buy a hat.

While she was standing there getting the money out of her wallet, her son was standing next to her, in front of the pile of business cards I had sitting on the table. He was looking at it.

And then he points to Owen's picture and says "Mom, he looks like an alien."
My heart hurt inside, but I pretended I didn't hear and waited to see what his mom would say.

I was disappointed, for the reasons stated so beautifully in the article above, when she only shushed him and whispered that wasn't very nice.

I couldn't let it go, so I used the opportunity, and spoke to the boy.

"His name is Owen. He's not an alien, God just made his head a little different than yours. When he was a baby he didn't have doctors to help fix the shape of his head, and now he's growing up with it still that shape."

His mom, seeming a little ashamed, jumped on board to help me explain. "Remember how your cousin Jacob had a head shaped a little different and had to wear a helmet so it would be the right shape again?"

Happy that she was helping instead of trying to get her son away from me and my "crazy ideas", I continued. "Owen doesn't have a mommy and daddy like Jacob does to bring him to the doctor and get him a helmet to fix his head."

He looked up to his mom, who nodded in agreement.

I kept going. "Some kids don't have a mommy or daddy to love them, to play with them, or give them hugs and kisses. Isn't that sad?"

He nodded his head and said "yeah", still trying to process what I had just told him. His mom smiled at me and they walked away.

++++++++++++++++

That exchange had me thinking the rest of the day. And I realized something else besides just what the article stated, and it's kinda off topic, but still wanted to add it.

The orphan crisis really is as simple as I explained it that boy. We need to see it through the eyes of a child, and be upset like a child would.

Children don't see the big picture, because they don't understand the numbers. They aren't hearing about the bad adoption experiences on the news, nor do they have firm views that they were taught growing up - their minds are open to new ideas much more easily than adults are.

They hear about the problem and do what they can to make a difference, one child at a time.

That's how we need to approach the orphan crisis. With the mind of a child.

++++++++++++++++

Something else, which kinda contradicting to the link I shared above.

I know several moms who it bothers big time when people stare at their children who look a little different.

So maybe if your child is staring, first redirect their gaze gently, but don't just tell them not to stare. Explain that God made that child or person a little bit different than everyone else, but they are should be treated like everyone else. If you know what their special need is, explain that.

Let your child ask questions and don't just tell them that's not nice. And if your child has questions you can't answer, go up to the person or parent of the person and ask respectfully. "My child is curious to know why she/he/your daughter/your son looks a little bit different than everyone else, would you mind explaining to them?"

And if there is an opportunity to lend a helping hand when they need it, by all means, do it, and let your child help too. Such as helping them up if they fall.

I think what bothers the moms who don't like people staring at their kids the most, is that the parents don't anything about it, not so much the fact the kids are doing it. That the parents didn't teach them when they were young and use every opportunity to reinforce it. If your kid stares and asks a question, but you use that opportunity to teach your child right then and there, they will appreciate that.

Monday, June 10, 2013

Grace's Benefit!

On Saturday night, our church held a benefit for us to help bring Grace home! We had such a fun time, and it went very well!
Ticket Table as you come in the door!
Raffle Baskets
A lot more raffle baskets
Going into the "dining room"
We told them to keep it simple. This look simple to you?? :)
There were about 4 6-foot tables jam packed full of baked sale items!
Handiwork for Orphans! We sold about $250 worth from our stuff alone!
The tshirt lady and the Handiwork girls - Ashley, Rachel and I
Time to eat!
Guest appearance by Toni Calzoni to draw the raffle tickets!
Grace's family and Toni! :)

The total raised as of Sunday morning was between $7000-$8000!!!! And over 50 tshirts were ordered from our t-shirt fundraiser!! THANK YOU JESUS!

Thank you so very much to everyone who made this event possible, and to everyone who came and donated! And to everyone who bought t-shirts! You helped bring my little sister home, and I am grateful!! ♥

Thursday, June 6, 2013

Saturday Night and T-shirts!

On Saturday night, our amazing church is holding another benefit for our family, this time to help us bring Grace home!

It will be a spaghetti dinner, and along with that, there will be a bake sale, auction items, and Rachel and I will be selling our items from Handiwork for Maria!

I know this is only for local people, but if you are not local (or even if you are!), you can still help! We have a t-shirt fundraiser going on right now as well selling these awesome t-shirts designed the talented Ashley Gibson!
Find all the details here - Love Makes a Family T-Shirt Fundraiser

Oh, and one more thing... :)

Wednesday, April 10, 2013

Ch-ch-changes! (WW: Maria)

As I'm sure you've heard, in late December, Russia closed to their adoption program to Americans.

The US government passed some legislation the Russian government didn't like, and in retaliation they closed adoptions, and the children are left to suffer. (I'm still not sure why that was a good retaliation tactic, as I'm not sure there are a lot of people in the US government who care about the orphans???) Anyways, they closed.

Some families who had court were allowed to bring their children home, but most in the process, even a lot of families who have already met their child, weren't able to bring them home. And of course, new families can't commit to a child or start the process to bring them home.

Many, many people were affected by this ban, all the advocates for Russian orphans, all the families, and all the children who are now stuck in orphanages and institutions. PLEASE PLEASE pray that this ban is lifted soon, or that a special needs waiver is passed so special needs adoptions can continue. The lives of many children hang in the balance.

+++++

I have advocated for many children in Russia, and while I will still keep praying for them, I will not be advocating for them anymore until they are adoptable. You can find them all at the bottom of my sidebar where it's split into two columns. Please take a moment to pray for their precious lives.

+++++

Lilly and Owen are two children you will find in that section of the sidebar, as they are in Russia, and I have advocated, a lot, for them here.


Rachel and I were fundraising for them over at Handiwork for Orphans, and of course we were and still are devastated about the situation and the fact they, and all the other children can't have the loving family they deserve. Both actually had pretty interested families right before the shut-down.

Since their grants closed on RR (please note all grants for Russian children are currently on hold and will be saved for that child), we had no place to send people to pay for our items. So we needed a new child to advocate and raise money for.

After many prayers, we found our new child (who is not in Russia). While it hurts so much to not be able to help all the ones we want to help, we feel this child needs it most right now.

+++++

Meet Miss Maria:

This precious girl will be 11 years old this year, but is the size of a toddler. She has Down syndrome, and needs a family quickly because she is already living at an institution. 


(Two fun facts about her institution - I visited there while in Ukraine, but only for an afternoon and didn't see her. And also, she is at the same place, and even the same grouppa that Maxim and Ryan were in (who are both now home and thriving in their awesome loving families, both of whom I've met!)! 

She is described as spunky and a bit of a drama queen, and even though she has been living at a bad institution for quite awhile, she still has so much life.


Here's some more about her from her profile:
Girl, born 2002
Down syndrome
Maria is a bundle of sweetness and pure energy! She lives her life sort of like a game of bumper kids, not afraid of crawling over, through, or into other children to get where she wants to go. She is otherwise all girl, giggly and sweet, loving to blow kisses or play with dolls.
She is not speaking, but uses some sign language she may have made up to communicate her basic needs, such as thirst or needing to go to the bathroom. She also makes some of the most hilariously adorable facial expressions. She is not able to stand or walk, and she appears to have problems with her hips. She is very flexible, and often sits with one foot above her head. She can get around quite well in a very unique way of holding her feet and scooting along on her bottom, she moves at a very fast pace. She is a sweet girl who does not know about personal boundaries (such as crawling around instead of over the other children) but is nonetheless very loving and would probably do great in a family where she was the youngest.

We are so excited to be raising money for her... go check out the things we have up for sale! 100% of the proceeds go to her adoption fund which will help her find a family and pay for her adoption when she has a family. Come visit us at Handiwork for Maria!

Friday, November 2, 2012

Angel Tree 2012

It has started. Angel Tree 2012.

Reece's Rainbow's biggest fundraiser of the year, with the goal raise $1000 for all the AT children from November 1st to December 31st.

Near the end of day 2, there are two AT kids with FAMILIES, one child at $500 (half his goal!), one child over $300, 11 children with over $100, 16 children over $50, and 91 children under $50 but over $0. What a GREAT start to the season!

Unfortunately, there are still 93 kids at $0, but I'm sure it won't be that way for long!


This year, I am a warrior for the first time. And I'm actually sort of a double warrior. Rachel is a warrior for Lilly, and I'm a warrior for Owen. And we are teaming up to raise $1000 for each of them, with the ultimate goal to find each of them a family.
Lilly and Owen
We have fundraisers in the works, and I will let you know as soon as they start. But the main one will be our blog, Handiwork for Lilly. Which during the AT season will be Handiwork for Lilly & Owen. Any funds will be split between the two of them, and go toward their AT goals.

Both Owen and Lilly are in the same region. Both of them turn 5 this year - Lilly did in February, and Owen will in December). Lilly has Down syndrome, Owen has Saethre-Crotzen syndrome (cranial facial). And they both need families.

Thank you for joining with us this Christmas season to help raise money and find families for these angels!! We have a big job ahead of us, but with God, ALL THINGS ARE POSSIBLE!

Saturday, October 27, 2012

Jimmy's Benefit

Tonight was Jimmy's benefit. I blogged about the benefit/him here. There was a great turnout, but no total yet!

Rachel and I had a table of our stuff, including some Ghana flag themed items. :) The donation basket on our table (we did prices labeled as suggested donation, not actually sold it) $166 for Jimmy!! Praise God! Ironic thing is, that's the same amount as our farmers market last weekend for  Lilly! :)


The tables all set up, ready for lots of people to eat lots of pie!

And the pies.... yes, I'm being cruel and making you hungry. Bwahaha (evil laugh)! ;]



All the people watching the groups that played tonight...


In Harmony...

Con Brio...





Don Shire...

And the Ott Family led several songs at the end, one of which I will share when my ridiculously SLOW internet finally finishes the 1 min 30 sec video after 2 hours. No, I'm not joking.

And then there's the fun in the nursery! :) My little 3 sibs - Elijah, Rachel, Jonathan, my mom, "big" Rachel, and half of the Prevost family, including Caleb! :)


It was an awesome night to bring an awesome little boy home!!