With permission, I have copied the following from a woman's blog I enjoy visiting (http://www.thevoiceofadventure.blogspot.com/). I think what cuts to my heart the most is that she is three. So is our son. I can't imagine anything like this happening to Seth. I wept when I saw the pictures and read about this little girl's situation. I know there are people suffering all around the world. I wish I could do something tangible for all of them....I'm thankful some thoughtful people have organized ways for me (or any of you who feel led) to help Abby. To find out more, continue to read. You can also see Abby's family's blog at http://www.riggsfamilyblog.com/. Most importantly, please take some time to pray for Abby and her family.
This precious little girl is Abby, and she needs your prayers. Abby is so many wonderful things. She is part of an amazing family. There are 7 wonderful kiddos in her family. 3 of those sweeties- including Abby came by way of adoption. Abby is a bouncing, happy, funny princess of a 3 year old....Now she is also a dear little warrior fighting for her life. She was diagnosed with Leukemia and life suddenly took a radical turn for this amazing family. Her concerns of which princess dress she should wear have turned to whether she will get poked or be able to keep her food down today.
OPERATION PRINCESS HAIR BEGINS!
There are so many battle scars she has right now in her fight against cancer...
Just one of the MANY things she has been forced to give up is her GORGEOUS princess hair and it makes her very sad.... What is it like to be the mommy that has to tell your 3 year old that she has to take medicine that will give her horrible sores, make her throw up constantly, and cause her to lose her hair? What is that like? What is it like to watch tears slide down your sweet baby's cheeks even in her sleep cause that's how much it hurts.
THIS is not OK with me. If I could I would make this go away. If I could I would change this- I wish there was a way. I know there are so many of us who wish that. We CAN'T MAKE IT GO AWAY! We just can't.
What we can do is give Abby back her princess hair. It's expensive and not something this family needs to worry about during this stressful financial time of paying for medicine and gas and hospital bills. We can not make this all go away but we can give Abby back her hair and make her smile.
SOOOOOO TODAY WE BEGIN....
OPERATION PRINCESS HAIR! This is your mission, should you choose to accept it...
OPERATION PRINCESS HAIR BEGINS!
There are so many battle scars she has right now in her fight against cancer...
Just one of the MANY things she has been forced to give up is her GORGEOUS princess hair and it makes her very sad.... What is it like to be the mommy that has to tell your 3 year old that she has to take medicine that will give her horrible sores, make her throw up constantly, and cause her to lose her hair? What is that like? What is it like to watch tears slide down your sweet baby's cheeks even in her sleep cause that's how much it hurts.
THIS is not OK with me. If I could I would make this go away. If I could I would change this- I wish there was a way. I know there are so many of us who wish that. We CAN'T MAKE IT GO AWAY! We just can't.
What we can do is give Abby back her princess hair. It's expensive and not something this family needs to worry about during this stressful financial time of paying for medicine and gas and hospital bills. We can not make this all go away but we can give Abby back her hair and make her smile.
SOOOOOO TODAY WE BEGIN....
OPERATION PRINCESS HAIR! This is your mission, should you choose to accept it...
1. I want us to buy sweet Abby one of the hats with hair pictured above- http://www.hatswithhair.com/
It's called a pony sport. It costs $228. It's made with real human hair. It's very comfortable and can be worn with any baseball type cap that Abby prefers.
After visiting with her mommy we feel this would be very comfortable and fun for everyday use at home and the hospital.
2. We will flood Abby and the other kiddos in the family with care packages that let her and her family know they are loved. If you feel you would like to send Abby or her family a present please e-mail me at angelweir@gmail.com
We can all send Abby fun presents AND ALL SEND an ADORABLE BASEBALL CAP to wear with her new hair. Then everytime she is having a hard day her momma can bust out a new care package to give her something to smile about.
3. We are also going to buy Abby a custom made wig! Check it out here....
http://www.celebritystylewigs.com/shop/index.php?act=viewProd&productId=493
I am so excited about this! It is going to be custom made to look a lot like her hair did before she needed to start chemo. So when Abby wants to dress up nice and look like the Abby she remembers she will have this. This wig will cost about $450. It is made of real hair and created just for her little head.
4. If there are donations exceeding the needed amount for the princess hair we will invite the family to use this money to help with whatever extra expenses they are facing during this difficult time.
It's hard for me to fathom what this family is facing. I want to do whatever I can to support them.
They are full of faith and strong. Cancer FEARS this little fighter! Let's do whatever we can to love and walk with this family during this time. I can't begin to imagine what they are facing but I PRAY that people would be there for me if we ever did walk this path.
It's called a pony sport. It costs $228. It's made with real human hair. It's very comfortable and can be worn with any baseball type cap that Abby prefers.
After visiting with her mommy we feel this would be very comfortable and fun for everyday use at home and the hospital.
2. We will flood Abby and the other kiddos in the family with care packages that let her and her family know they are loved. If you feel you would like to send Abby or her family a present please e-mail me at angelweir@gmail.com
We can all send Abby fun presents AND ALL SEND an ADORABLE BASEBALL CAP to wear with her new hair. Then everytime she is having a hard day her momma can bust out a new care package to give her something to smile about.
3. We are also going to buy Abby a custom made wig! Check it out here....
http://www.celebritystylewigs.com/shop/index.php?act=viewProd&productId=493
I am so excited about this! It is going to be custom made to look a lot like her hair did before she needed to start chemo. So when Abby wants to dress up nice and look like the Abby she remembers she will have this. This wig will cost about $450. It is made of real hair and created just for her little head.
4. If there are donations exceeding the needed amount for the princess hair we will invite the family to use this money to help with whatever extra expenses they are facing during this difficult time.
It's hard for me to fathom what this family is facing. I want to do whatever I can to support them.
They are full of faith and strong. Cancer FEARS this little fighter! Let's do whatever we can to love and walk with this family during this time. I can't begin to imagine what they are facing but I PRAY that people would be there for me if we ever did walk this path.
TO HELP ABBY GET HER PRINCESS HAIR YOU JUST NEED TO GO TO www.thevoiceofadventure.blogspot.com. CLICK ON THE PAY PAL BUTTON ON THE TOP RIGHT HAND CORNER THAT SAYS "OPERATION PRINCESS HAIR."
IF YOU WANT TO SEND ABBY A CARE PACKAGE INCLUDING A CUTSIE NEW BASEBALL CAP PLEASE E-MAIL ME AT angelweir@gmail.com
Thank you from the BOTTOM of my little ol' Texas heart for taking care of a little girl named Abby. What we do matters. What we do makes life better or worse for those around us EVERY SINGLE DAY. Let's take time to stop and care. Hugs, Angel
PS If you would like to spread the word on your blog PLEASE do it!! Feel free to take this whole post or part of it.
IF YOU WANT TO SEND ABBY A CARE PACKAGE INCLUDING A CUTSIE NEW BASEBALL CAP PLEASE E-MAIL ME AT angelweir@gmail.com
Thank you from the BOTTOM of my little ol' Texas heart for taking care of a little girl named Abby. What we do matters. What we do makes life better or worse for those around us EVERY SINGLE DAY. Let's take time to stop and care. Hugs, Angel
PS If you would like to spread the word on your blog PLEASE do it!! Feel free to take this whole post or part of it.
1 comment:
I am so happy that you are able to spread the word about Abby. I too have been following her blog and feel exactly the same way and try to contribute in everyway possible. Glad to see you are still following the website I sent you:)
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