Share And Care Cockayne Syndrome Network Inc

Organization Overview

Share And Care Cockayne Syndrome Network Inc is located in Watterford, VA. The organization was established in 2002. According to its NTEE Classification (G20) the organization is classified as: Birth Defects & Genetic Diseases, under the broad grouping of Voluntary Health Associations & Medical Disciplines and related organizations. This organization is an independent organization and not affiliated with a larger national or regional group of organizations. Share And Care Cockayne Syndrome Network Inc is a 501(c)(3) and as such, is described as a "Charitable or Religous organization or a private foundation" by the IRS.

For the year ending 12/2020, Share And Care Cockayne Syndrome Network Inc generated $17.5k in total revenue. This represents a relatively dramatic decline in revenue. Over the past 5 years, the organization has seen revenues fall by an average of (35.8%) each year. All expenses for the organization totaled $5.7k during the year ending 12/2020. As we would expect to see with falling revenues, expenses have declined by (44.4%) per year over the past 5 years. You can explore the organizations financials more deeply in the financial statements section below.

Mission & Program ActivityExcerpts From the 990EZ Filing

TAX YEAR

2020

Describe the Organization's Mission:

Part 3 - Line 1

SUPPORTING CHILDREN AND FAMILIES WITH COCKAYNE SYNDROME.

Describe the Organization's Program Activity:

Part 3

CS FAMILY SERVICES PROGRAM: THE PURPOSE OF THE SCCS FAMILY SERVICES PROGRAM IS TO CREATE AND FOSTER A CARING COMMUNITY THAT WILL OFFER EACH CS FAMILY INFORMATION, GUIDANCE AND EMOTIONAL SUPPORT AND MAINTAIN THE MOST COMPREHENSIVE MEMBERSHIP REGISTRY OF INDIVIDUALS AFFECTED BY COCKAYNE SYNDROME. SCCS MAINTAINS THE FOLLOWING RESOURCES FOR AFFECTED FAMILIES: THE CS WEBSITE WWW.COCKAYNESYNDROME.ORG AND THE FACEBOOK PRIVATE MEDICAL FORUM FOR COCKAYNE SYNDROME AS WELL AS THE FACEBOOK FAN PAGE. OUR INTERNATIONAL CS FAMILY CONFERENCE IS HELD EVERY YEAR IN WHICH THE LATEST INFORMATION IS DISCUSSED WITH FAMILIES. FREE MEDICAL CONSULTS ARE ALSO HELD ENABLING FAMILIES TO CONSULT WITH MEDICAL EXPERTS FROM AROUND THE WORLD. IN ADDITION THE CONSULTS OFFER FAMILIES THE OPPORTUNITY TO PARTICIPATE IN RESEARCH STUDIES, PROVIDING IMPORTANT INFORMATION AND BLOOD SAMPLES TO TEST. "CS SIBS" IS A SUPPORT PROGRAM FOR KIDS WHO HAVE SIBLINGS WITH COCKAYNE SYNDROME. THEY ARE SENT A BIRTHDAY PACKAGE EVERY YEAR THAT RECOGNIZES THEM AS A TERRIFIC SIBLING. WE ALSO HELP LOCATE SUMMER CAMPS FOR SIBLINGS TO ATTEND THAT WILL HELP THEM TO GROW. "GOOD GRIEF" IS A SUPPORT PROGRAM FOR BEREAVED PARENTS, IT IS A PRIVATE FACEBOOK GROUP FOR PARENTS TO PROVIDE PEER TO PEER SUPPORT AND THE DISCUSSION IS FACILITATED BY A BEREAVED CS PARENT WHO HAS TRAINING IN COUNSELING.


CS AWARENESS PROGRAM: AWARENESS IS THE COMMON THREAD WOVEN THROUGH ALL THE SCCS PROGRAMS. OUR GOAL IS TO RAISE AWARENESS AND TO REACH OUT TO THE MEDICAL AND RESEARCH COMMUNITIES FOR THEIR SUPPORT IN THE ADVANCEMENT OF RESEARCH AND CLINICAL CARE THAT WOULD BENEFIT INDIVIDUALS AFFECTED BY COCKAYNE SYNDROME. SCCS IS COMMITTED TO PROVIDING INFORMATION TO HELP PEOPLE UNDERSTAND CS. THROUGH THE USE OF EVENTS, PUBLICATIONS, WEBSITE, FACEBOOK, TWITTER, INSTAGRAM, THE NETWORK DISSEMINATED INFORMATION BEYOND FAMILIES, CREATING A GLOBAL COMMUNITY WITH FUNDERS, PHYSICIANS, AND RESEARCHERS. WE PROVIDE BROCHURES, BALLOONS, WRISTBANDS FOR THE BUTTERFLY WALK CS FAMILY FUN RAISERS WHICH HELP TO RAISE AWARENESS AND FUNDS TO HELP SUPPORT RESEARCH, SUPPORT PROGRAMS, AND THE ANNUAL FAMILY CONFERENCE.


CS RESEARCH PROGRAM:SCCS CONTINUES TO FOLLOW RESEARCH FOR CS AND CONNECTS FAMILIES WITH RESEARCHERS. OUR SCIENTIFIC MEETINGS ARE HELD EVERY-OTHER-YEAR AND ARE IN CONJUNCTION WITH OUR ANNUAL FAMILY CONFERENCES. SCIENTIFIC MEETINGS ARE HELD BI-ANNUALLY.


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Board, Officers & Key Employees

Name (title)Compensation
Jacqueline Arias Clark
President/ceo
$0
Haylee Carroll
Vice President
$0
Veronica Cuevas
Secretary
$0
Seth Zimmerman
Board Member
$0
Brent Smith
Board Member
$0

Financial Statements

Statement of Revenue
Total Revenue from Contributions, Gifts, Grants & Similar$17,512
Total Program Service Revenue$0
Membership dues$0
Investment income $0
Gain or Loss$0
Net Income from Gaming & Fundraising$0
Other Revenue$0
Total Revenue$17,512

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