“ASHLEY’S ANGELS”
HELPING TO FUND LUNG TRANSPLANT!

Sunbury native Ashley Spotts is like a lot of 19 year-olds
– she likes riding her horse, Flicka,
shopping, swimming, and hanging out with her friends.
She also enjoys working out on the trampoline
and driving four-wheelers, dirt bikes, or go-karts.
And close to her heart are her two nephews, Allen, 2,
and one year-old Jayden. As a 2009 high school graduate, she should
have a full life ahead of her.
But unlike a lot of teenagers her age, Ashley has to
deal with cystic fibrosis (CF), diabetes, and asthma.
Recently, her CF physician at Hershey Medical Center
suggested that she go on the list for a lung transplant
due to her deteriorating lung condition. CF is the most common genetic
disease among children and young adults,
and it primarily impacts the respiratory and digestive systems. People
with CF have to take digestive enzymes
to help their body absorb food and most do three times daily nebulizer/chest
percussion treatments to loosen
the thick mucus in their lungs. Progressive research has increased the
life span to a median of 37 years,
but thirty years ago it was only about 15 years.
Enter Joshua Richard, founder of Walk On Foundation (see
www.walkonfoundation.com) in Milton.
The Walk On Foundation is a nonprofit organization that aligns the resources
of individuals and corporations
to impact the lives of community members by providing assistance with
medical equipment, safety devices,
and financial assistance related to medical hospitalization.
“We really wanted to do something to help this family,”
Richard said. He contacted Kingdom Kidz Puppet Ministry
(see www.hiskingdomkidz.org)
in Milton and they responded favorably. Donna Bridge, the director,
noted that the organization began as an outreach ministry
of St. Andrew’s UMC in Milton
in December of 2000. Since then, the ministry team has traveled over
11,000 miles through four states
in presenting over 200 programs in churches, nursing homes, block parties,
schools, malls, and private events.
Richard also contacted Pennsylvania Cystic Fibrosis, Inc.,
an independent, nonprofit, all volunteer 501 (c)(3) organization that
provides services
and supports for families affected by CF and raises funds for CF research.
“We’re always willing to help with CF transplant funds,”
Betty Hollenbach, current PACFI president, said.
“And we’ve been working with the Spotts family for several
years in helping them get
what’s needed for Ashley’s health care.”
Walk On Foundation arranged for a fundraiser to be held at the New Hope
Baptist Church
in Middleburg on Saturday, November 21, from 6-8 PM. The public is invited
to attend and the event
will feature a bake sale and an hour long puppet show by Kingdom Kidz.
With the approval of Ashley and her family, the many fundraisers being
planned will benefit
the newly formed Ashley’s Angels Transplant Fund. According to
Ashley’s mother, Christine,
Ashley liked the sound of Ashley’s Angels because it included
her brother, George,
who died due to CF in 2004 at 12 years-old. “Ashley’s Angels”
will include anyone who helps
with fundraisers or donates to the transplant fund. PACFI has already
donated $1000 to the fund.
“We’re going to meet with the transplant staff at Children’s
Hospital of Pittsburgh
on Monday, November 9th,” Christine said. The Hospital is one
of the leading transplant centers
in the United States. She noted that Ashley wants to keep in touch with
her friends and meet new people,
so Ashley invites people to email her at ashlinn17@aol.com.
Ashley has been hospitalized
at Hershey Medical Center for most of the past month.
Lung transplants cost around $550,000, and the Hospital staff will tell
the Spotts family how much
will be paid by their insurance and how much remains to be paid by other
means.
Many times insurance will pay 80% or more of the costs, and that leaves
about $110,000
to be paid by other means. Each transplant candidate is given a “lung
allocation score”
that is based on several health related items listed by the United Network
for Organ Sharing (UNOS).
UNOS determines a person’s standing on the transplant list based
on the severity of their condition.
According the national Cystic Fibrosis Foundation, lung transplants
were first performed in the United States
in the early 1980’s. Today, with progressive improvements, about
90% of people with CF
are alive one year after a lung transplant, and 50% survive at least
five years or more.
Anyone who wants to donate to Ashley’s Angels Transplant Fund
can make a check out to
‘PACFI’ and mail it to PACFI, c/o Ashley’s Angels,
P.O. Box 29, Mifflinburg, PA 17844.
For those who want to donate online, click
the 'Donate' button on this website and do the following:
* Click on the 'Guidestar' icon
* Type in "Pennsylvania Cystic Fibrosis, Inc." where it says
'Start Your Search'
* Click 'donate' under the name 'Pennsylvania Cystic Fibrosis, Inc.'
on the Organization Name Chart
* Type in the amount, donation preference, and what information you
want to share.
Under 'Designation,' type in Ashley's Angels Transplant Fund.
* Follow remaining instructions
We're working with Walk On Foundation and Kingdom Kidz puppet ministry
to raise needed funds.
