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Why give? Your contributions go directly to our outreach and awareness efforts, helping to keep youth, families, support group leaders, and professionals in touch through our network. We provide a way for warm, resourceful volunteers to connect with those who need their help. We discuss this in greater detail in our May 2003 fundraising letter.
How can you support us?
Your donation will help to cover the costs of the Pediatric Network for CFS, FM, and OI such as our web hosting fee, printing and mailing of brochures, and phone calls for Pediatric Network business. It will allow us to further our outreach and advocacy efforts to reach more students, families, and professionals concerned with CFS, FM, and OI. The Pediatric Network for CFS, FM, and OI is a project run by two volunteers: Mary Robinson, the mom of two kids who had CFS and POTS, and Rebecca Moore, a young adult who developed CFS and NMH/POTS as a teenager. We have funded this network ourselves in its first year, and continue to volunteer our time, but are ready to ask other concerned individuals to help us with the financial burden of maintaining this service. Please note that we are not a 501(c)3 non-profit organization, so your donation will not be tax deductible. How much of your donation will go to the Pediatric Network?
Where can you send donations? Mail checks made out to The Pediatric Network to The Pediatric Network c/o Mary Robinson, 507 Park Avenue, Medina, NY 14103-1519. Or, donate online through PayPal. How can you get more information? Mary Robinson and Rebecca Moore are available to answer your questions about our project and the ways you can contribute. E-mail us at mary@pediatricnetwork.org and rebecca@pediatricnetwork.org. You may also monitor our fundraising progress on our thank you page. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Disclaimer: The views in this website and forum are the feelings and opinions of the individual authors and do not necessarily reflect all of the current theories that are being explored and published. Ask your doctor or other health care provider about all medical information that you consider applying to your situation, including the information you read in our website and forum. We take no responsibility for the decisions you or your family members make about medical care. It is up to you to verify that the information you read is correct and applies to your unique situation. | |||||||||||||||||||