Drew Goodman

At 4
years old Drew was diagnosed with a highly aggressive, adult brain
tumor, rarely seen in children. The name of this beast is a
Glioblastoma Multiforme. His parents were
told to go home and enjoy their time of 5 – 12 months. I am happy to say it has
been 4 years and Drew is doing well. Drew is a very loving and fun
child. He has never met a stranger. Drew loves everyone he meets. He is
known to shower everyone with his love, hugs and kisses.
On
In April 2007, Drew started presenting symptoms of tumor recurrence. An
emergency MRI performed, showed a new area of concern. This area was not
in the tumor bed and it was not in the form of a mass, but more like a
coating. After much deliberation, it was decided that the area was
probably radiation necrosis (damage from the radiation). The only known
treatment was steroids (Decadron) to manage his symptoms and the
contraversial Hyperbaric Oxygen Treatments.
Drew started 60 Hyperbaric Oxygen Treatments at
Unfortunately, the MRI on
Gunner is 7 years old from Marshall County, Kentucky in the first grade at Central Elementary in Mary Morgan's first grade class. He has a wonderful little sister, Garlynn (4 yrs), who is his best friend. His mommy and daddy, Janna & Gus, love him so very much.
Gunner was diagnosed on November 30, 2007 with an inoperable tumor on his brain stem. The type of tumor he has is called a pontine glioma and is very aggressive, highly malignant, treatment resistant and recurrent. This is a rare form of terminal brain cancer that mostly affects children between the ages of 4-10 years old.Gunner began radiation treatments in Nashville, TN at Vanderbilt's Children's Hospital on Monday,December 10, 2007. He received 30 treatments 5 days a week for a total of 6 weeks.
This is the only treatment available for Gunner. Although there is a very small chance the radiation will help, the prognosis remains poor. There are only about 200 cases diagnosed each year. Due to the diffuse nature of the cancer there are no surgical options, and current chemotherapies have been found to be ineffective. With treatment, the median survival rate is less than 12 months. Please keep Gunner in your prayers for complete healing. Please, Please say prayers to move Gunner's mountain.
Gunner is collecting post cards from around the world. If you know of someone that can send postcards, please have them send to:
Gunner Gillespie-109 Lakeside Drive-Benton, KY 42025
Brookelynn Hunt

Brookelynn was born July 29, 2006, a happy wonderful little girl. She is the daughter of RJ and Christy Hunt from Ohio. Brookelynn has a very large family and they have been there for her and her parents every step of the way.
The week of August 25, 2007, Brooke starting throwing up. After a kick visit to her pediatrician, they were assured she had a viral infection. After she became worse, her parents took her to the local emergency room, where they told her it was an ear infection.
The following evening, while Christy was working and RJ was taking care of Brooke, she began to have a seizure. After calling 911, she was taken by ambulance to the Toledo Children's Hospital. She received a cat scan and blood was discovered in her head. After assuring the doctors, she had not fell or been dropped on her head, a MRI was ordered. The results were devastating, she had a massive brain tumor.
Brooke was air lifted at 2:00 am to Cleveland's Rainbow Babies and Children's Hospital. On Friday, August 31, Brooke underwent brain tumor surgery to remove a golf ball size tumor. The doctors were able to remove it all, but more bad news was delivered from the pathology report. She was diagnosed with AT/RT, the rarest and most difficult type of brain cancer. Survival rate is less than 10 percent.
Brooke started chemo and radiation at St. Jude's on September 29, 2007. She is receiving high dose chemo and needs 30 radiation treatments. Her journey at St. Jude's is coming to a close and they all hope to be back home in Ohio by the middle of April.
Brooke will continue with low dose chemo from her home and require weekly lab tests to keep check on her counts. She will return to St. Jude's every two months for scans.
Please keep Brookelynn and her family in your thoughts and prayers. This little one is a fighter and we believe she will kick this cancer.

