Lipedema News Corner
Support for Lipedema is on the rise.
Lipedema is underdiagnosed and has no magic cures
Patients can be frustrated and isolated by their disease. Support is needed from other patients and the medical community. Facebook, Web sights, Drs that take an interest in Lipedema are now with in the reach of Lipedema Women. Lets take a look at some of the support.
Fat Disorders Research Society
Revamped this past year, with newsletters, new web page, education at the NLN, Conference for patients, Networking physicians and therapists, Future goals of research and education. A small team, Consisting of Dr. Karen Herbst, Felicite Daftour, Yvonne Russell, Nancy Lazarus and Laura Baker. www.fatdisorders.org
Lipedema Education
Started two years ago by Lipedema Women. Offers education, support and is an ongoing community of over 1000 members.
Talk Lipedema
Located in the UK, has a web site and facebook support group. A wonderful group of very educated volunteers that started a non profit to give support to the Lipedema Community. http://www.talklipoedema.org
Here are more links for your patients
http://www.curelipedema.org/ started by Beau Dunn, an actress and model with lipedema
http://lipese.com/ women sharing their story
http://www.lass.org.au/ Australian women supporting each other
http://www.lipomadoc.org/ Dr. Karen Herbst.. leading Doctor for fat disorders.
Lipedema patient, nurse, therapist
Always looking for information for the Lipedema patient.
Please share these wonderful support.
Email: Lipedemaproducts@gmail.com
Website: www.lipedemaproducts.com
Location: Salt Lake City, UT, United States
Phone: 801 935 5483
Facebook: https://www.facebook.com/lipedemaproducts
Twitter: @lipedemaproducts
Text me for more information
801 935 5483
Lipedema gathering
Santa Barbara
Lipedema Conference
Az
Lipedema Conference and Fashion Show
Washington DC
Good things happening with the Lipedema Women