This campaign will be a fundraiser to assist in funding the different services that NOVA provides.The services include providing financial support to families, providing constant research updates,and locating physicians.
Subscribe to follow campaign updates!
13 days left and we have raised $725 of the $15,000 goal. Help make a difference in the life of a child or adult living with one of the many types of Vascular Anomalies. Donate today.
The National Organization of Vascular Anomalies is a Parent and Family Support and Education Reps, for those affected by vascular tumors and vascular malformations. This includes but is not limited to Infantile Hemangioma, Congenital hemangioma, Tufted Angioma, Pyogenic granuloma, Kaposiform hemangioendothelioma, Kaposi sarcoma, Angiosarcoma, Capilary Malformations, Lymphatic Malformations, Venous Malformations, Arteriovenous Malformations, Ateriovenous fistulas, Combined Malformations, Vascular Anomalies Associated with other anomalies such as Klippel Trenaunay syndrome, Parkes Weber Syndrome, Sturge Weber syndrome, Cloves syndrome, Proteus syndrome, and PHACE syndrome.
Traditionally these tumors and malformations have been called birthmarks.
Medicine and science today dictate that they are so much more.
THE NATIONAL ORGANIZATION OF VASCULAR ANOMALIES is a 501c3a organization and is eligible for tax deductible donations. NOVA is an all volunteer organization. No one affiliated with NOVA benefits financially from the association. NOVA provides this information as a resource. It is not intended to engage in the practice of medicine or to replace the physician. NOVA does not claim to have medical knowledge. NOVA does not endorse any particular physician, treating facility or treatment protocol. In all cases NOVA, the NOVA Board of Directors and associates recommends that you seek the opinion of a physician experienced in the diagnosis and treatment of hemangioma and vascular malformations. To Contact NOVA please email us at [email protected]
Please support this fundraiser, for NOVA to be able to continue providing support and education, to the families during this very stress journey of finding the proper treatment.
The tiers are a good example of what your donation will be able to supply. NOVA does understand that everyone may not be able to donate at the tiered level. We appreciate any donation that you feel comfortable with. Reminder as well many companies do offer matching programs for donations.
Lets join this battle together.
Sign in with your Facebook account or email.
13 days left and we have raised $725 of the $15,000 goal. Help make a difference in the life of a child or adult living with one of the many types of Vascular Anomalies. Donate today.
Sign in with your Facebook account or email.
13 days left and we have raised $725 of the $15,000 goal. Help make a difference in the life of a child or adult living with one of the many types of Vascular Anomalies. Donate today.
Sign in with your Facebook account or email.
29 days left and we have long way to go to meet our goal. Please support, you change a family's life.
Sign in with your Facebook account or email.
Thank you to everyone who has donated and supported the campaign, thus far. We raised $230 of $15,000, share the word to help us reach our goal.
Sign in with your Facebook account or email.
Thank you to our first donor Vicki & Dan Dezort. Your support is greatly appreciated.
Sign in with your Facebook account or email.
Jun 16
Jun 16
May 31
May 12
Apr 28