Resources

We have assembled the following information that you may find useful. You are under no obligation to utilize any of the listed services nor is the listing of any information an endorsement or recommendation made by us. This information is merely intended to be convenient to you and the information is not intended to provide medical advice, diagnosis, or treatment.

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Links

The Ehlers-Danlos Society is a global community of individuals, caregivers, healthcare professionals, and supporters, dedicated to saving and improving the lives of those affected by EDS, HSD (hypermobility spectrum disorders), and related conditions. 

Georgia EDS Support Group - please contact them by emailing northatlanta.eds@gmail.com

MitoAction’s mission is to improve the quality of life for children, adults, and families living with mitochondrial disease through support, education, outreach, advocacy, clinical research initiatives, and by granting wishes for children affected by mitochondrial disease.

United Mitochondrial Disease Foundation mission is to promote research and education for the diagnosis, treatment, and cure of mitochondrial disorders and to provide support to affected individuals and families.

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Blog for Articles, Brochures, & Media

News and scientific papers containing Dr Fran Dougherty Kendall or Virtual Medical Practice plus VMP brochures and flyers - click here for more info.

Forms

Please click here to access our forms.

Remote Second Opinions

Click here for information on remote second opinions.

Testimonials

BlogWhom better to have than our patients share their perspectives on our services. Click here for the testimonial page.

Travel Tips

Helpful info if you are traveling to our clinic - click here for pdf