Partnering with FPA connects you to a community of over 55,000 patients. If you provide services to people with neuropathic facial pain, we have many opportunities for you to partner with us:
FPA’s Professional Membership Program connects the facial pain community with specialists diagnosing and treating neuropathic facial pain and related health care conditions. Connect with the worldwide facial pain community through an annual individual or center FPA professional membership.
Contact Brandi Underwood at firstname.lastname@example.org.
The FPA promotes and supports medical research that is relevant to the neuropathic facial pain community. While FPA does not provide funding, we support research in a number of ways for the betterment of the lives of people affected by facial pain. Contact Melissa Baumbick at email@example.com.
Our national network of virtual and in-person support groups welcomes you to share your expert knowledge on any number of relevant topics. Contact Regina Gore at firstname.lastname@example.org.
The FPA has been publishing this popular news digest for many years. The FPA Quarterly print edition is mailed to several thousands of our members and the digital version is sent to approximately 30,000 four times per year. If you would like to contribute an article or purchase advertising space, contact Brandi Underwood at email@example.com.
Medical centers and experts in the field can support the facial pain community with an FPA annual sponsorship. This popular new program provides tremendous benefits and exposure to tens of thousands in the U.S. and internationally. Join the FPA annual sponsorship program and add your company or center as a valued sponsor. Contact Brandi Underwood at firstname.lastname@example.org.
By filling out the form below, you will receive a free FPA Patient Guide and periodic updates on the management and treatment of facial pain conditions. We do not share this information with any outside sources.