History of Meesha C. Saxton Fund
Meesha Chanell Saxton, was born October 17, 1995 with Sickle Cell Disease. Sickle Cell Disease (SCD) is a group of inherited red blood cell disorders. The main function of red blood cells is to carry oxygen from the lungs to all parts of the body and release the oxygen to the tissues of the body. Normal red cells are round with an indented center and very flexible, so they can move freely through the smallest blood vessels (capillaries). In Sickle Cell Anemia, due to the abnormal hemoglobin, red blood cells cannot carry oxygen very well. The cells become sickle shaped or pointed, rigid, sticky and brittle. These abnormal red cells cannot move freely through the blood vessels; they stick together and block the blood vessels. Therefore, Sickle Cells cannot supply oxygen to the tissues properly. The result is tissue damage and possibly tissue death (ischemia). This process causes extreme pain, called Sickle Cell Crisis.
Meesha's grandmother had sickle cell trait, and as her child Teresa received the sickle gene mutation from her. She did not have the disease, neither did her ex-husband, but not knowing that he had the trait also, they passed the defective gene on to their daughter Meesha. With that being said, due to complications and the miseducation of this disease, she passed away on December 24, 1996.
Teresa, Meesha's mother, has been a sickle cell advocate ever since. She started working with Cuyahoga County Sickle Cell Affected Families in 1997 with Kevin Jenkins and Glinda Dames – Fincher. Once the group dissolved she still had a passion to help and advocate for this devastating illness, but no group to support.
Then in 2004 she saw an ad in the Cleveland Calling Post Newspaper about a sickle cell anemia support group that Adrienne Kincaid was starting. She volunteered for years and served on the board of directors as Vice- President.
In December 2017 she resigned from the position, with hopes of starting a fund to help sickle cell affected individuals directly financially. Under the Kincaid's Kindred Spirits umbrella.
The Meesha C. Saxton (MCS~Fund) launched in June 2018. The MCS~Fund is governed by a fifteen-member Board of Advisors, with five officers (President, Executive Director, Vice President, Secretary and Treasurer) comprising the Executive Committee. Members of our board of advisors are:
Teresa S. McCurry, Founder, President
Lisa Workman, Executive Director
Kimberly E. Moss, Vice President
Jeannine Johnson Hogan, Treasurer
Joy Hayes McQuay, Secretary
Fatima Amaju, Board Member
Octavia Lucas, Board Member
Delicia Mayes, Board Member
Leah Legrone, Board Member
Gayle Anthony, Board Member
Our vision is to help Sickle Cell Anemia (SCD) affected individuals financially as part of KKS Sickle Cell Anemia Adult Community Outreach. We want to relieve the burden and be a blessing to the population we serve. Most SCD individuals are low-income and under-served, in need of various services. We serve by providing assistance with utilities, rent, food, medical supplies, transportation, and everyday basic needs.
Our generous private donors donate the unrestricted funds through personal gifts and by supporting our fundraising efforts.
We thank you in advance for your generous donation no matter how big or small, every dollar helps.
As a volunteer driven 501(c)(3) non-profit organization under the umbrella of KINCAID’S KINDRED SPIRITS, INC. (KKS) Citizens for Healthy Living: the MCS~FUNDs sole mission is to generate unrestricted funds for Sickle Cell Anemia affected individuals.
ANGELS HALL OF FAME
In 2018, the MCS~Fund established a special recognition for individuals in the community who make a difference for Sickle Cell affected individuals.
The following individuals have been inducted into the Angels Hall of Fame:
Adrienne Kincaid (Year: 2018)
Wanda Blount (Year: 2019)
Glinda Dames-Fincher (Year: 2020)
Please complete the form to receive an MCS~Fund Reward (Rewards are for SCD individuals in Cuyahoga County Only). Your Reward Application MUST be signed by a licensed social worker, case worker, medical professional, or agency director. You can email the completed Reward Application to : firstname.lastname@example.org
Please note that the Reward Application is not currently linked to the email address mcsaxton.funds@gmail
MCS ~ Fund was established to provide financial assistance to individuals affected by Sickle Cell Anemia. This year due to COVID 19 our fundraiser will be a Virtual GOSPEL EXTRAVAGANZA 2020, “FRIDAY JUNE 19, 2020” WORLD SICKLE CELL DAY CELEBRATION— The Gospel Extravaganza A Live Broadcast that will be showcase through several social media outlets. The live broadcast will begin at 6:30PM and will continue through to 8:30PM . The Live showcase will include several different preforming arts acts including skits, musical numbers, and dancers. During the GOSPEL EXTRAVAGANZA 2020, we will be highlighting several different ways to make a tax-deductible contribution to help support our cause.
Sickle cell anemia is one of the most deadly and unfortunately misunderstood diseases in the world, Sickle cell disease (SCD) affects millions of people throughout the world and is particularly common among those whose ancestors came from sub-Saharan Africa; Spanish-speaking regions in the Western Hemisphere (South America, the Caribbean, and Central America); Saudi Arabia; India; and Mediterranean countries such as Turkey, Greece, and Italy. In the United States
The exact number of people living with SCD in the U.S. is unknown. Working with partners, the CDC supports projects to learn about the number of people living with SCD to better understand how the disease impacts their health.
It is estimated that:
SCD affects approximately 100,000 Americans.
SCD occurs among about 1 out of every 365 Black or African-American births.
SCD occurs among about 1 out of every 16,300 Hispanic-American births.
About 1 in 13 Black or African-American babies is born with sickle cell trait (SCT).
While no readily available cure has been identified, patients require constant management of the condition to ensure they lead a happy and productive life. Unfortunately, managing sickle cell anemia can be expensive, complicated, and sometimes overwhelming for patients. This is where MCS ~ FUND is making a difference and aiming to help those individuals financially. We would appreciate you help with our efforts click the link below to make a taxes deductible donation.
MCS Fund is available in two categories:
A sustaining member agrees to make an annual donation of at least $250.00 and tries to support and attend MCS ~Fund events whenever possible.
Participating Member: Participating membership requires a voluntary time commitment. A Participating Member agrees to attend the quarterly membership meetings and to work at a minimum of two KKS event per year.
The kinds of tasks our participating members perform include:
Working on a committee to plan an event
Working at an event in various capacities
Selling raffle tickets
Soliciting donations of certificates and/or merchandise for auctions
Picking up donations
Soliciting financial support from event sponsors
Writing press releases
Working to “set-up” before an event
Working to “clean-up” after an event
Phoning members to schedule event participation
Preparing baskets for auctions
It is our goal to make participation in MCS~Fund fun. We strive to make involvement a guilt-free experience by following the edict that “No is an acceptable answer.” Explanations and excuses are never required.
JOIN MCS FUND
If you are interested in joining MCS Fund, sponsoring an event, or would like more information about the organization, please contact:
TERESA S. MCCURRY
Founder and President
Phone: (216) 466-3801
LISA M. WORKMAN
Phone: (980) 477-5047