Welcome to the FG Syndrome Family Alliance, Inc., an organization for individuals and families touched by FG Syndrome and related conditions
Whether you are here as a friend, family member, medical professional, or have FG Syndrome yourself, we hope you find our website helpful in your quest to learn more about FG Syndrome or related conditions.
We also provide information on new research, etc. either through our Listserv or Facebook page. We also suggest family members or interested caretakers and medical professionals register with us to receive occasional news updates. (and rest assured we will only email when there is real news to share – we will not clutter your email box).
Thank you for visiting. Please come back often!
Thank you for supporting the FGSFA!
All information contained herein is for informational purposes only. Readers are encouraged to confirm the information contained herein with other sources. Readers should review the information carefully with their professional health care provider. The information is not intended to replace medical advice offered by physicians. The FG Syndrome Family Alliance, Inc. will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising herefrom.