Showing posts with label project ALS. Show all posts
Showing posts with label project ALS. Show all posts

Monday, October 27, 2014

2014 Annual Letter

What a difference 6 years makes. 

Six years ago, Laura Somerville Woodall had an  idea that her friends and family could make a real difference in a person’s life.  They were already making a difference in Laura’s  life through  their care, support, and love after her diagnosis with ALS.

Six years ago, Laura asked these friends and family to support her idea. She knew that women out there who have been given devastating news might not have the support system that she had.  These women - these mothers living in our community - would need help to get them through the hardest times.  They would need financial support to help pay for rent, mortgage, electricity bills, medical equipment, and medical bills.  They would need you.  They would need us. 

Six years ago, a seed was planted. 

What started out as a group of 25 friends is now a group of like-minded supporters over 700 strong.  And these are just the ones we know about.  Every dollar stuffed in our donation jar during Davidson Town Day, the Davidson Farmers Market, and other Awareness Month events by people learning of AGSF right at that moment means rent to a grant recipient.  We might not know their names, but they heard what AGSF does  and decided Laura’s idea was worth the investment.

Six years ago, two local mothers were given financial assistance and were able to focus on their health and their families instead of the mounting bills.  And since then, 22 mothers have been given that same opportunity.  In six years, over  $73,000 has helped these families do what Laura intended when she dreamt of this Foundation – focus on the family, focus on getting better and have relief from the financial stress and burden that comes with a debilitating disease.  In 2014, over $21,000 has gone toward mothers like Mrs. S of Charlotte.

Mrs. S., mother of a 14 year old, had already lost her car and home during her second round of breast cancer surgery.  She’s now in treatment for Lymphadema and the financial stress is taking a toll on her health in other ways as well. She has sleepless nights at the fear of losing her home.  Rent or treatment, that’s the choice so many face in situations like these. When she learned that AGSF would pay two months of her rent, she cried on the phone.

Mrs. S then wrote this to AGSF: “Words cannot express how thankful we are to all of you. Thanks for caring and being there for us during a great need in our life.  Thanks for giving us home for tomorrow.  Our hearts are forever grateful to you. God bless all.”

AGSF will continue to support research organizations until there is a cure for ALS. Nearly $10,000 has gone directly to these organizations since 2008, including over $2300 raised during the Shut Down for ALS challenge on May 18th and the amazing ALS Ice Bucket Challenge that overtook the world this August.  

Once again, we thank all of you who have nurtured the seed and been with us as it has grown and taken root. 2014 saw another successful AGSF Awareness Month, a community cookbook created by friends of AGSF for friends of AGSF, the Shut Down for ALS event, and the ALS Ice Bucket Challenge movement.

AGSF and Monkees of Lake Norman partnered for their own Wine Bucket challenge – all of the fun, none of the ice water – and the end result was a fun night out and many new pairs of Frye boots on the feet of Davidson residents!

In 2014 we introduced the AGSF Teen Council – a group of dedicated local teenagers who know the meaning of service and are intent on fulfilling the AGSF mission.  Their 24-hour Walk Around The Clock event raised over $10,000 that will go directly toward local mothers needing assistance when health issues impact the family financially.  A huge shout out to Chair Lexi Powers, Chair-Elect Daryl Konstandt and the entire AGSF Teen Council for their time and energy and dedication to AGSF!

And here we are, entering year seven.  We’re planning on continuing the good work started six years ago.  We’re planning on ensuring sustainability for the next six years and beyond.  Your support ensures that Laura’s vision continues to be a reality, helping those who need it most. 

How can you help?  Send your tax deductible donation today!


Sincerely,


A Giving Spirit Foundation Board of Trustees

Tuesday, June 17, 2014

The Shut Down for ALS




What would you do if you couldn't talk? Think about it.

On Sunday, May 18th, A Giving Spirit Foundation Board Members and supporters participated in The Shut Down.   Project A.L.S,  a leader in identifying and funding scientific research that will lead to effective treatment of ALS and, we all hope, a cure, created this campaign with the goal of showing support of those affected with ALS by taking a vow of silence.  All money donated to AGSF on May 18th will go toward our annual support of this amazing organization.

During the 24 period of time, participants stayed silent for 2 hours.  While we all had the luxury of knowing that we could get back to our normal lives at the end of the shift, simply concentrating on staying silent brought a new understanding to the disease that we may not have had before


AGSF Board Member Monica Galloway (and husband): "Awareness of this horrible disease."


AGSF Board Member Steve Bragg (and daughters): "A Giving Spirit Foundation."


AGSF Board Member Carly Schiano: "The Woodalls."




AGSF Board Member Erica Felthaus: "Laura Woodall."
.

AGSF Teen Council Member Abigail Woodall: "My Mom, Laura Woodall."

AGSF Teen Council member Amelia Woodall: "Not only my mother, but so I can know how difficult and frustrating not being able to speak is. Keep fighting. You're strong. "

AGSF Teen Council Co-Chair Lexi Powers: "ALS Awareness."


AGSF Board Chairman Lisa Bynum: "All those that do not get to choose to NOT shut down."



AGSF Teen Council Co-Chair Daryl Konstandt: "Awareness."

AGSF Board Member David Stewart: "Laura and AGSF."

AGSF Board Member Temple Day (and daugher): "Our friend Laura Woodall."

AGSF Board Member Lori Tate: "Laura Woodall."


AGSF Supporter Lesley Swartz: "ALS Awareness, Laura Woodall and those making a difference like A Giving Spirit Foundation."

AGSF Board Member Teri Brooks (and daughter): "ALS Awareness."

AGSF supporters: "ALS Awareness."



It's never too young to learn. How would you _____ if you couldn't talk? Teri Brooks' K/1 Multiage class at Davidson Elementary encourages us to "think about it."  Watch her students answer this question and begin to understand just a little bit how ALS impacts lives.   http://vimeo.com/95465605 

Wednesday, May 14, 2014

The Shut Down: Stop ALS




"More than 30,000 of our husbands and wives, mothers and fathers, sisters and brothers, grandparents and friends are losing everything to Amyotrophic Lateral Sclerosis or ALS, also known as Lou Gehrig's disease. It takes away the simple things—holding a pencil… thumbing a text message… screaming at the TV. It also steals the big things—walking… breathing… talking.

Well, we say: Enough! It's time to shut this thing down. So on May 18, 2014, from 1-4pm, Project A.L.S. is asking you to join The Shutdown. By taking a vow of silence that day, we’ll show our support for our loved ones with ALS.

You can give your silence to save lives, donate, or inspire others to join this movement to find a cure for ALS. However you participate, you'll be making a difference in the fight against this devastating disease. ALS may silence those affected, but together we can raise our voices—and some dollars—to stop ALS in its tracks." - www.projectals.org 

On May 18th, A Giving Spirit Foundation Board Members and supporters will be taking a vow of silence to raise awareness of this disease that takes a voice, and much more.

Support us by vowing silence with us or making a donation to AGSF.   All funds raised on May 18th - whether donations, cookbook or tote sales - will go directly toward Project ALS to assist in their efforts to end this disease.

Learn more: www.projectals.org

Sunday, April 14, 2013

Get Ready for AGSF Awareness Month!

We're gearing up for our 2nd Annual A Giving Spirit Awareness Month to be held in May, 2013!  Last year was a success and local businesses showed their support throughout the month by hosting events and donating proceeds from sales.


AGSF Awareness month is planned for the month of May to coincide with ALS Awareness month, Mother’s Day and Laura Somerville Woodall's  birthday.  

A Giving Spirit Foundation (AGSF) provides financial assistance to deserving mothers in the Davidson and greater Charlotte, NC area who are suffering from a debilitating disease or other unforeseen health challenge.  AGSF also supports research organizations searching for a cure for Amyotrophic lateral sclerosis (ALS), like Project ALS and The ALS Association.  AGSF is a 501(c)(3) charitable organization.

AGSF was founded in 2008, soon after Laura Woodall was diagnosed with ALS. Laura quickly realized that one of the most challenging parts of living with disease is the toll it can take on the family, mainly due to the new financial pressures that come with ongoing  health issues. That realization prompted her to take action and ask friends to form A Giving Spirit Foundation.

Local businesses that will be holding events this year are Carrburitos, The Village Store, Davidson Farmers Market, Raeford's Barber Shop, Ben & Jerry's and Flat Iron Grill.   We're in discussions with more businesses and anticipate a full month!  The May events calendar will be published as soon as details are finalized.

To stay up to date on the May events, please  like the AGSF Facebook page.

If you would like to know more about AGSF, be a volunteer or request a grant application, please contact agsf@agivingspirit.org.

Friday, September 30, 2011

"They made me feel like somebody."

September 26, 2011

Dear Friends of A Giving Spirit Foundation,

“What do you say to a mother battling life-threatening cancer when she says ‘We will be homeless, me and my kids’ as she shares the journey of her darkest hour. With eviction looming overhead and not a resource in sight, my patient thought the situation was hopeless. She was ready to give up. Until A Giving Spirit Foundation stepped in to shine their light. To say thank you to what I consider a group of angels on Earth is not enough and I wish I could capture the tears of joy and expression of gratitude that patients share upon receiving news they have been blessed by a grant from A Giving Spirit. It’s like having the front row to watch a miracle take place. One particular mom exclaimed ‘they made me feel like somebody.’ What can you say to that? To all the angels of A Giving Spirit Foundation, my deepest gratitude for shining your light, making miracles happen and giving my patients the precious gift of hope.” Mellisa Wheeler, Blumenthal Cancer Center

Mellisa Wheeler understands all too well the stress that families feel when the mother has been diagnosed with a debilitating disease and the family does not have the financial resources to pay for healthcare and choices need to be made between the mother’s health and the basics like rent and groceries. As the American Cancer Society Patient Resource Navigator for the Blumenthal Cancer Center in Charlotte, NC, she sees this pain and struggle every day. Fortunately, A Giving Spirit has been able to ease the burden for three of her patients this year and the gratitude that these mothers have expressed make it clear that there is a need for A Giving Spirit Foundation in the greater Charlotte community.

Every person receiving this letter deserves some of this gratitude. Without your support, AGSF would have been unable to bring relief to the many families that have received grants over the last three years. In the past year, AGSF has awarded over $13,000 in grants to these deserving families.

Operating under the vision of Laura Woodall, A Giving Spirit Foundation strives to lend a helping hand to deserving mothers in the Davidson and greater Charlotte, NC communities suffering from a debilitating disease or other unforeseen major health challenges. Of equal importance is supporting research organizations who are searching for a cure for Amyotrophic lateral sclerosis (ALS). Organizations like Project

ALS, The ALS Association and the ALS division of MDA do fantastic work and are making advances every day. AGSF is proud to support them. AGSF donated $1500 to these organizations over the past year to go directly toward ALS research.

Laura says it best: “It was the invitation from friends and my opportunity to give back that embarked a journey which has proven worthy. A Giving Spirit Foundation (just three years young) has given to individuals who needed assistance, has given to research, has created a board to guide the mission, and has successfully hosted three fundraisers. It is my and my family's hope that this foundation continues to give back. My vision is that A Giving Spirit Foundation will persevere for years to come. Your support will drive that vision. If you find yourself in a position, when you can give or want to give... I strongly encourage you to give to A Giving Spirit Foundation. My wish is that you become a giving spirit.”

For the past several years, AGSF has raised the majority of our funds through the annual Autumn Fest event. Last year’s event raised over $12,000 from attendees, silent auction bidding and donations from supporters unable to attend the event. Again, we thank you all for your contributions last year! A big special thank you goes to Kelly and Steve Gentry, who hosted the event at their beautiful home, local bands Sunday Union and Billy Jones who kept everyone entertained, and especially to the many wonderful women and men on the AGSF volunteer committee (led by Kim Fleming and Melissa Reddick). These people spent countless hours organizing this phenomenal event and it could not have gone more smoothly.

So, we’re giving our volunteers a year off this year from planning the big event. Instead, we’re going to treat this as a building year. We’re working on strengthening relationships in the community and learn how to build a stronger organization that can raise money year round and not be dependent on one large annual event. We’re here for the long haul so that we can realize Laura Woodall’s vision by continuing to make the lives of deserving mothers in the community facing a health challenge a little bit easier.

If you have fundraising ideas or experience and would like to become more involved, please email us at agsf@agivingspirit.org.

“They made me feel like somebody.” And that, my friends, is why we do this.


Sincerely,


The AGSF Board of Trustees

Tuesday, August 9, 2011

Buy a Book, Support ALS Research!

A Giving Spirit Foundation proudly supports the work done by Project A.L.S. - they are committed like no other organization to finding a cure for this disease.   The actor Rob Morrow is a dedicated Project A.L.S. Board Member and has written a short story about his adventures playing golf in the AT&T Pebble Beach Pro-Am and proceeds will go to Project A.L.S.

In his words:
My friends, A year and a half ago I played golf in the AT&T Pebble Beach Pro-Am.  It was an extraordinary and inspirational odyssey.  I've written a short story about it that is now available on Kindle Shorts. All items on the Amazon Kindle Store can be downloaded and read using the free Kindle app on a PC, Mac, iPhone, iPad, BlackBerry, Android and Windows Phone 7.  The proceeds are going to Project ALS, which has been making significant breakthroughs toward eradicating not only ALS, but Alzheimer's, Parkinson's and spinal injuries.  The day is coming when these afflictions will be a thing of the past.  Please make the small donation of $2.99 and get An Actors Nightmare (Redux) for yourself or anyone you know interested in golf and the creative process.  We are going to put these diseases behind us, it's just a question of when. 

Hope you are all having a great summer and are not being tortured by the golf gods as I am...

Many thanks, 
Rob Morrow


So, if you were a fan of Northern Exposure, golf, books, reading funny tales of an actor or just want an easy way to donate money to a wonderful organization searching for a cure to a terrible disease, you'll want to buy Rob Morrow's short "The Actor's Nightmare: Redux" today!

Tuesday, July 27, 2010

Catalina Channel Swim for ALS



On August 5th, three brave people will swim 21 miles across the Catalina Channel in California.  Why?  To raise funds and awareness for ALS.   Please support the team and Project ALS by visiting the crowdrise page:


Cliff says: "Help propel us across the Catalina Channel by donating to the fight against ALS."

Monday, May 10, 2010

May is ALS Awareness Month



If you ask someone if they know anything about ALS (Amyotrophic Lateral Sclerosis), most will ask if that's the disease Lou Gehrig had.  The answer is Yes, but there's much more to know about this disease:
  • Approximately every 90 minutes, ALS  claims the life of one American.
  • 5600 people in the US are diagnosed with ALS each year.
  • ALS affects 2 per 10,000 people.
  • As many as 30,000 Americans may have the disease at any given time.
  • ALS occurs throughout the world, with no racial, ethnic or socioeconomic boundaries.

To learn more about how ALS affects people just like you, read "ALS - Anyone's Life Story" on www.als-mda.org. 


There are many wonderful organizations fighting for a cure, a few are listed below.  Please, help raise funds and awareness in May or any other month of the year.

Wednesday, March 24, 2010

Move for ALS - 3600 miles, 2 bikes, 1 cause



Augustin Quancard says it best: "ALS is a terrible disease: no one deserves to suffer it. But with your help I believe we can make a significant impact on the search to find a cure."


That's why events like Move For ALS are so important.  These are just two guys who have decided to make a difference by cycling across the United States while raising money for a cure and awareness of this disease.


The journey starts on May 15 but you don't have to wait until then to show them you support what they're doing.  Go to www.moveforals.com to learn more about them, Tony Judt (the inspiration for the ride) and to lend your support - either moral or monetary.



Saturday, October 11, 2008

Introducing... A Giving Spirit Foundation

This foundation is guided by the vision of Laura Woodall and her family. It will primarily support families of Mothers experiencing adversity in the face of an unforeseen health challenge, as well as Project ALS and the ALS Division of the Muscular Dystrophy Association.

In 2006, Laura was diagnosed with a motor neuron disease which falls under the realm of ALS. Under the shadow of this diagnosis, Laura formed a team of her closest friends and fellow mothers. "Laura's League" proceeded to reaise over $100,000 for the MDA Stride N'Ride event in March 2007. For leading this remarkable effort, Laura was named Honoree at the MDA's 2008 Black & Blue Gala. And once again, Laura's League played a part in a record-breaking ALS fundraising effort for this Charlotte Chapter MDA event.

We are so pround of Laura and all that she has done to promote awareness and funding for ALS research. She is an inspiration to us all. A Giving Spirit Foundation will strive to continue the momentum generated by Laura's League and to inspire others along the way.