1 person found this review helpful
Brain Tumor Foundation for Children, Inc.
Invite reviews
Invite friends and colleagues to share their experiences with this nonprofit
November 26, 2012
1 person found this review helpful
My daughter was diagnosed with a brain tumor at 19 y/o on 29 Jul 12. They do not know how long she's had it. She had two surgeries to remove the tumor and she is currently going through radiation therapy then on to chemotherapy. She has an 11 month old son. Through my social worker the foundation has provided us with $350 in gas cards as we have had to travel back and forth at least once every two weeks for two hours for her doctor appts. Without the foundation we would be hurting as I nor my daughter are currently working; since I have exhausted all of my leave from work being by her side. We also are struggling to get her disability approved so the foundation is truly a God sent organization. They are willing to help with bills, car repairs, etc. if you just ask. We are truly grateful and thankful for God and him providing donors with such caring hearts. I am sure other families are just as grateful.
More feedback...
How would you describe the help you got from this organization?
Some
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 22, 2012
This past year out daughter was diagnosed with a rare brain tumor. Immediately the foundation reached out to us offering support in a number of ways. It was assuring to know we were not alone in this battle. Our daughter is admist receiving treatment and the foundation has reached out to our family and older daughter.
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 20, 2012
December of 2007 i received a call while my child and i were at st jude.The lady i spoke to was so kind sweet and thoughtful was as if a family member had called to offer help.Was a great burden lifted the finacial support was just the begining , they would call and check on us regularley they even sent my other child a gift for the holidays .And when i lost my son they send a gift i keep it in a special place so thankful for all they have done an do each day may god bless the btfc and as long as i walk this earth you'll have my support thank you.
More feedback...
How would you describe the help you got from this organization?
A lot
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2008
November 14, 2012
My 9 year old daughter Zoe was diagnosed with Glioblastoma Multiforme (GBM) brain tumor and had to have immediate resection surgery at OU Children's Hospital in April 2009. According to protocol she would also need radiation and chemotherapy treatment so in order to be closer to family we decided to relocate and continue her care at Miami Children's Hospital, Florida. For over a year Zoe did very well but the tumor came back and she had to have a second surgery in October 2010. It was then, through the staff at MCH that we learned of BTFC. BTFC stepped in and helped us when we didn't even realize that we needed help! They assisted us in paying several bills and travel expenses, which was well needed since we lived 2 hours away from the hospital and had other children. Their help allowed my husband and I to focus on Zoe's recovery as this time she also needed occupational, physical and speech therapy. When we returned home from the hospital, our mail man delivered huge box to our doorstep. Inside we found all sorts of goodies for not only Zoe but enough to share with her siblings. We were all excited, I only wish you could have seen her dimple filled smile which lit up the room! Since then BTFC kept in touch with us through emails and cards. Sadly Zoe passed away on December 11, 2011 at age 12 due to a third occurrence. Again, BTFC was there to assist us with several of our living expenses and also Zoe's final expenses. This time we focused on our broken hearts and those of our other children. You see, when you no longer have to go back and forth to the hospital for check-ups and treatments, when you no longer have to make appointments and fill prescriptions, when doctors no longer call and your extended family goes home it intensifies the fact that your child is gone. Then one day when our world had stopped, I heard the doorbell ring and looked to see our mailman holding a small box. Inside was a beautiful angel that was sent to our family from BTFC. It made our day, as was a gentle reminder that someone still remembered us, that someone still cared and that there are many other families like ours still fighting for their kids battling brain cancer.
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 11, 2012
The Brain Tumor Foundation for Children have been there for use over the last 10 years and we are so thankful for this organization. My son, Blake Carpenter, was diagnosed in January of 2003 with a craniopharyngioma. He has been fighting this brain tumor and the side effects for the last 10 years. Sherry Samuels and Mary Moore along with other volunteers from BTFC have been emotional and financial support for us over the years. There have been times when we needed a hug, smile, listening ear, surprise, or help with gas throughout the years and they have always been here for our family. Also, the BTFC has provided just simple FAMILY FUN for us and so many other families and provided us with an opportunity to meet other families that are also living a roller coaster life. I am thankful for BTFC and so happy to be blessed to be a part of this heartfelt organization!
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 11, 2012
What a wonderful organization! We are so thankful for all the support from initial diagnosis to relapse and eventual death of our son. Mary Moore and her team mean so much to our family! Sincerely, Jacque Porter
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 10, 2012
The Brain Tumor Foundation for Children is a godsend for families of children with brain/spinal cord tumors. Our son was diagnosed at the age of 8 with a large brain tumor. Thankfully the resection surgery was very successful but he endured many post-surgery complications. The BTFC was very helpful in connecting us with other families who were in the same situation, as well as providing information and support to help us through the entire ordeal. I'm happy to report that my son is now 18 years old and is a freshman in college. Life is not without its challenges but the BTFC is still there to help us.
More feedback...
How would you describe the help you got from this organization?
A lot
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 9, 2012
Evan Carswell, my son, was diagnosed at 15 with a rare aggressive brain cancer he died at 16, with his sweetheart Faith (diagnosed with a brain tumor). They were certainly not their disease however BTFC is definitely part of our families. Here’s partly why.
The financial burden of the disease is monumental for families. It is an easy choice between paying $400 for an electric bill and buying two doses of medicine. (or $30,000 for 60 shots) The medicine came first – Evan’s health came first – and our electricity was cut off. Thanks to BTFC’s wonderful Butterfly Fund, our utilities were restored – not once, but twice. And when I called to get donation envelops for the funeral they asked for Evan’s funeral expenses. It felt too much and I protested… but so grateful again for their donation….
Once the treatment starts you realize that in a few short weeks your child will not feel well. About one month into treatment, Evan gave us a ‘bucket list’ – the things he wanted to do in life. As I read it, I prayed that he didn’t see the disappointment and despair in my face as I realized there was no money for fun…no money for making great memories. Having BTFC pay a $30 water bill may seem insignificant to you, but for our family it provided a night at the movies…a night to make memories. BTFC enables families of children with brain cancer a few moments to devote making life somewhat ’normal’ during a period of time that may be the remainder of their life.
Research is vital and my son felt so strongly he donated his brain tissue and BTFC donates too! It is important to know its not that our son died, but that he lived and lived well - with laughter, love, courage, a little romance and faith….he lived his best. Cancer does not change these children…it reveals them.
We are forever grateful for the Brain Tumor Foundation for Children and those who support them! You would need a whole other nomination for the staff there… we are forever joined by my sons illness and death… Ed and I are proud to be their friend.. The staff are just incredible. I just don‘t see how they do so much.
Any words we could think of really mean nothing. We pray the Holy Spirit will translate those feelings we hold in our hearts … but are unable to verbally express “Evan’s Proud Mom and Dad” Jennifer and Ed Carswell
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 9, 2012
My daughter was diagnosed with a brain tumor that was discovered to be medulloblastoma brain cancer at 11 months old. Being a single parent, I had to leave everything, including my other 4 children, to be with my baby and care for her at the hospital. BTFC came into our lives and offered caring, compassion, and support that you rarely find. It wasn't just financial. It was emotional. They weren't just there for my daughter. They were there for my other children as well. They know that cancer affects the entire family. They are concerned about "their" kids. They are special people who go above and beyond for complete strangers. I will forever be thankful for them. They shined a light in the midst of all our darkness. Their purpose and cause couldn't be more perfect!
More feedback...
How would you describe the help you got from this organization?
A lot
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012
November 9, 2012
My 18 month old daughter was diagnosed with a brain tumor September 2011. It was the most devastating news any parent could ever hear. She underwent a 9 hour surgery and yak fully the sergeon fully resected the tumor. Our family then had to go to Jacksonville for 6 weeks of radation treatment. The brain tumor foundation helped our family tremendously during this time helping us pay for our bills back at home. It was a super easy process and they made everything simple of us...which is a big deal because nothing was simple anymore. I am happy to say that our daughter is doing very well 1 year later. The brain tumor foundation helped is in a way that we couldn't even imagine. To top it off they still send Anabella cards and letters during holidays and her birthday just to say hello and to let us know they are thinking of us! We love the brain tumor foundation, greatest non profit out there!! Xoxo -Spadaro Family
More feedback...
How would you describe the help you got from this organization?
Life-changing
How likely are you to recommend this organization to a friend?
Definitely
How do you feel you were treated by this organization?
Very Well
When was your last experience with this nonprofit?
2012