CONGRATULATIONS KIM MEAGHER!!!!
We are a non-profit organization dedicated to providing lasting memories through the beautiful art of photography to the families with children who are facing life threatening illnesses. With the help of photographers worldwide, we are able to give a beautiful album that will carry the love, joy and everlasting memory of each individual family.
What an amazing two days. We flew out first thing Friday morning to Chicago where we met Gabi Heller, a 17 year old Hodgkin’s lymphoma survivor, and her friends who are all students at IMSA (the Illinois Mathematics and Science Academy).
https://www3.imsa.edu
Gabi’s friends Jamie, Dawna, and Matt are all co-founders of something called Shine On. The purpose of this event is to raise money and awareness about blood cancer through a multitude of school-wide events, culminating in head shaving. All money will be donated to the Leukemia and Lymphoma Society. Over 60+ students (boys and girls) and teachers came together as one to shave their heads in support of Gabi and they were able to raise over $7000 and we were there to capture this truly amazing event! What an inspiration these kids are…truly inspiring.
The Adventures of The Great Baldini
Gabi’s blog about her “whimsical life with cancer”.















We had the opportunity to meet and photograph Kelsey “girl” (as her mom calls her) and her wonderful family yesterday. Kelsey has a blog that her mom has kept up and it’s so amazing to read the stories and understand the strength that this family has. What an inspiration….
“Thursday, August 6th. This is the morning we found out our little baby Kelsey has Down Syndrome. It was devastating at first but the thought that she might also have Leukemia was even more devastating. Children with Down Syndrome are at risk for Leukemia plus heart problems and gastrointestinal problems. They were testing all of this ASAP. The morning was very emotional for us and everyone we told. But, then around 3:00 or 4:00 the Ped. Cardiologist came by to tell us the first piece of good news. Kelsey’s heart was great!!! She did have a small hole and something else I can’t remember the name of but that was normal for preemies and should fix themselves on there own. She also changed our attitude with her wonderful emotional and spiritual encouragement about Down Syndrome and most importantly a reminder of how God is in control and giving us Kelsey wasn’t a mistake but a blessing. She belongs to Him first and God entrusted her to us to take care of. God loves her more than we do!!! Later, several friends from church came by and prayed for us and our hearts were lifted and encouraged more and more. Several hours later, Kelsey’s doctor came to my room for more test results. The fact that he was coming to my room made us very anxious. We waited desperately wondering if our little girl also had Leukemia. He gave us an update but with no result of the test we wanted. We had to finally ask him about it and to our relieve she didn’t have Leukemia. So yet, another praise to end the last several days. This night we were so happy to have our little baby girl Kelsey and couldn’t wait to get to know her and love her.”











On a cold and wet Pacific Northwest January night, a group of women, all mothers, threw a fund raising potluck for Tiny Sparrow Foundation. Some of these women had been strangers to the cause of Tiny Sparrow until that very week, yet their generosity of spirit and heart is a blessing and an inspiration to go forward and provide families with precious mementos of their beautiful children battling illnesses no child should have to battle.
Amidst tears, laughter, and delicious food, we talked far into the night about our dreams for our children and how shattering it is when those dreams crumble in front of our eyes. And we came to the realization that in spite of it all, the memories remain, and the love is forevermore.
A very special thank you to all who were there that night. Your very generous donations, totaling in the amount of $1,950, will be used to provide beautiful coffee table books filled with memories to the families with these children battling these life-threatening illnesses.
Be sure to check out Angie Muresan’s blog post to see her interview with Lidia Boicu.
Many thanks Angie Muresan and Ani Campean for helping us spread awareness and for organizing this wonderful fundraiser.
Meet precious little Sherrlyne, who at just 21 months of age, is fighting Leukemia for a second time. I had the pleasure of meeting her last week. She was first diagnosed at just 3 months of age and has since relapsed.
She is such a beautiful little girl but in her little life she has been through so much that she doesn’t trust anybody so it was hard for me to get her to smile.. There is sooo much sadness behind those big brown eyes and I so wish I could take that sadness away from her.
She is a fighter and we ask that you keep her & her family in your prayers, as they continue to go through chemo.
If you want to get involved and help provide memorable pictures for other brave children like Sherrlyne please contact us at tinysparrow@me.com..
Meet little Zach…a happy and full of life 2 year old boy fighting a rare pediatric cancer called Rhabdomyosarcoma. A way too big and complicated disease name for a 2 year old to know and worry about.. but in plain and simple words it means that this is a fast-growing, highly malignant tumor. Little Zach has been fighting this since this summer and his little body has gone through a lot for this past couple of months.. To read more about his story please go to his caring bridge.
We ventured out for a little photo shoot with Zach and his family this past Saturday.. It was so cold but we still were able to capture some memorable pictures for Zach and his family.. Here are a few of the timeless memories we were able to capture for this sweet family…








I had the amazing opportunity this past weekend to be part of the Beads of Courage/ team and visit the Medical City Hospital here in Dallas as part of their annual holiday party for the kids on the oncology floor. Beads of courage is an amazing non profit organization, dedicated to helping children with serious illness record, tell and own their stories of survival through beads..
I got to meet some of the bravest kids out there that despite what they are going through, they are an inspiration for everyone. Their amazing spirit, their sad but courageous story will make you rethink your priorities in life and will really make you appreciate the littlest things in life.
As you can see from the pictures some of the kids have just started treatment, some are in the middle of treatment, some are just ending treatment and some are celebrating the few weeks or months that have past since they have finished the last round of chemo, the last radiation or the last surgery.. And there are those children that come to the party to remember their brother or sister that is no longer with them but was part of the oncology floor a few years ago..
I have been thought a lot myself but there were a few times when I could not hold back the tears while photographing these children.. One of the stories that brought tears to my eyes is when I met a little 3 month old baby boy (the one dressed in the little santa outfit). He is one of maybe 100 very rare cases world wide where his body can not process fats and his liver has pretty much gave up.. Unfortunately, there is no more treatment that he can go through and he will more than likely not make it till Christmas.. What a great, great opportunity as part of Tiny Sparrow Foundation that I was able to take a few pictures of this beautiful little baby and mail them out as a Christmas gift for his father. Priceless memories that will be sooo sooo cherished for the years to come..
If you are interested in helping create timeless and priceless memories for other children with similar stories please contact tinysparrow@me.com or you can donate to the Tiny Sparrow Foundation by clicking the donate button. Our goal for 2010 is to photograph 50 children facing life threatening illnesses and to provide each one of them with a very memorable professional album that will tell their story for years to come.




















Wow..what a success! We were able to raise almost $3000 from the auction. This money will go toward helping us finalize setting up the corporation and filing the proper paperwork to get this foundation up and running. Thank you to all of those individuals and companies who donated their time and goods to the auction. Without all of you and those who stopped by to place their bids it would not have been possible. We are thrilled beyond words the response we have gotten for Tiny Sparrow.








Another little fighter you can pray for… Meet little Walker… At just 7 months he has quite an amazing story.. He was diagnosed with a very rare and aggressive form of cancer. He had surgery to remove one of his kidneys and now is undergoing chemotherapy treatment hoping that the tumor will shrink. Please stop by their www.caringbridge.org/visit/walkerrainey and leave a word of encouragement…
I am so blessed to be able to share my gift and talent with this amazing family. Missy and Chad… I know we had all the odds against us today
(my car did not start, the storm was approaching rapidly) but we did manage to capture little Walker’s personality despite that.. Please enjoy these short preview.. You are in my prayers..










I am not even sure I can find the words for this blog… Little Kate… She is 5 years old battling brain cancer… Please read her story and leave a word of encouragement for her family here .. Pray for Kate
Kate lives in Phoenix, Arizona and I came across her story from a blog of another photographer. Myself being a cancer survivor her story touched my heart and I wanted to somehow share my gift of photography with Kate’s family. I flew to Arizona this past weekend to be able to capture some memories of Kate. It just so happened that the same day I flew in Kate and her family got a new addition to the family: Patrick.. the cutest little puppy.. I feel sooo blessed that I was able to be there to capture their first reaction when the puppy first came into their home…
Below are just a few pictures of Kate, her sister Olivia and her brother Will.. I had an amazing time with the kids and now I have a new name… Picture lady
… The kids called me that cause I probably had the camera in my hands 90% of the time I was with them. I just did not want to miss anything.
Holly and Aaron thank you so much for opening your home so I can capture a glimpse of what an amazing family you guys have.. And Stephanie.. you are such a blessing for Holly and a big thank you for helping me out with my heavy equipment
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Hugs to all of you…

Please click on the little arrow on the very first picture to view the slide show…
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