Tonight as I was checking my facebook before bed, I saw that a friend had joined a group against child abuse and the photo for that group was a picture of a little girl around the same age as Nicholas with her face all scratched and beat up with a black eye sucking on a pacifier.
It made me cry.
It made me angry. REALLY angry.
I saw a video several months back on the same website about a 6 month-old baby girl who suffered horrendous abuse before dying at the hands of her abusive parents.
The images have never left my mind. Not a day has passed that I have not thought about and prayed for these little angels who don't know love. It truly breaks my heart that children suffer so much when they are so vulnerable.
It is intolerable.
It is cruel.
It is heartless.
I know that I am being called to do something for these kids, but I don't know what it is. I have been praying and contemplating what it is that I can do to help these innocent lives but I don't have any answers. All I know is that my heart breaks every single time I think about this and I just feel as if I want to scream. I want to hurt the child abusers and make them suffer the way these children have.
If anyone has any suggestions of ways I can help (big or small) please let me know. At this point I feel so helpless that this injustice is going on in a world where I live and I just know I have to do something. Here I am trying to save my little boy from an incurable disease while perfectly healthy, beautiful children are being tortured at the hands of their abusers. It's not okay and I will not tolerate it.
skip to main |
skip to sidebar
Donate to Nicholas' Memorial Fund
Information about Spinal Muscular Atrophy (SMA)
Click HERE to learn about Spinal Muscular Atrophy.
About Me
- Jessica
- Washington, United States
- We are the Gustafsons: Daddy Jeff, Mommy Jessica, Big Brother Nicholas and Little Sister Elizabeth. We started our blog in 2008 when our son was born as a way to document our life. Jeff and I feel so blessed to be parents to two amazing kids. Our oldest, Nicholas, was diagnosed with a terminal condition called Spinal Muscular Atrophy. We are praying for a cure for Nicholas and all children who suffer from this physically limiting diagnosis. We are also parents to a little girl who who brings us sunshine and laughter everyday. We treasure every moment with our sweet kiddos. Please let us know you visited our blog by leaving us comment. May God bless you today and always.
Popular Posts
-
I took this photo one year ago, yesterday. The day Nicholas died. I didn't know in the hours to come that our son would pass away...
-
It is with profound sadness and utter disbelief that I write this blog entry... Nicholas, the light of our world and joy of our hearts, wa...
-
GUESS WHAT?! A cure for Nicholas and other babies with SMA is right around the corner... literally, like 2010, around the corner ! Can you ...
-
Many people have been asking us questions about how Nicholas is doing and where he is in terms of SMA right now, so I thought I would share...
-
On Thursday, January 21st, I took a test that would change our lives forever. I had been feeling more tired than usual, napping in the after...
-
Any mother will tell you she worries about her children, but the worries of a mother who has a child with a terminal illness are profound . ...
-
Elizabeth Rose Gustafson was born five days early on Wednesday, September 15, 2010 at 11:58 a.m. She was 7 lbs 6 oz and 21 inches long. As...
-
We have been going to Shriner's weekly this past month to give Nicholas more practice on the power chair . Since he will be turning two...
-
I am so behind on blogging. With this being my first year back to classroom teaching after seven years, I will admit that the majority of my...
-
Jeff was home for a few days recently and we tried to cram in as much fun into four days as possible. We started with our neices' thirt...
Falling In Love
Our Wedding Day

Brother & Sister Love

Motherhood

Nicholas's Story
Click HERE to read Nicholas's story from birth to his diagnosis with SMA at 10 months-old.
All About Nicholas
sweet. easy-going. smiley. happy. fighter. playful. courageous. loving. joyful. amazing. gift. wise. strong. handsome. kind. brave. Heaven-sent.
Nicholas's Birthday
Nicholas at 1 Year

Nicholas at 2 Years

Nicholas at 3 Years
Nicholas at 4 Years
Nicholas at 5 Years
Nicholas at 6 Years
All About Ella
loving. cuddly. toddler. curious. explorer. walker. silly. happy. sleeper. blessing. fearless. adventurous. kisser. sassy. dancing queen. spirited.
Ity Bitty Baby Ella

Ella at 1 Year

Ella at 2 Years
Ella at 3 Years
Ella at 4 Years
Ella at 5 Years
Blog Archive
Followers
Friends
Other Kiddos With SMA
Blogs We Like To Read
Visitors
Translate
Powered by Blogger.
3 comments:
I have the same feelings. It sickens me. And children with special needs are especially susceptible to abuse from parents who blame them for their disabilities. And somehow, because the children aren't "perfect", these criminals think they are justified. No abuse of a child is okay. None. These people are monsters. I hope you find what a way to give back. I am still searching my heart, too.
Great post Jess. Check this out. I had a simiar inspiration a few years ago and found lots of volunteer groups such as this:
http://www.casahelpskids.org/
Love you and your passion!
xo
L
Our good friends adopted a beautiful baby girl who had been hospitalized at 6 weeks old with a fractured skull and brain damage, done by her parents. She and her siblings were taken into loving homes and maybe that's some consolation. The police, the social workers, foster parents and later the adoptive parents all cared for the kids in different ways. Maybe there's something there for you?
Post a Comment