Lympha Press is committed to telling the stories of patients with lipedema. We believe by sharing what these brave and resilient patients have learned as well as what leading medical professionals have discovered, many will be inspired to manage their condition and find hope in the process.
Many women are using the Lympha Press Optimal Plus and seeing great results like reduced pain, increased mobility, and in some cases, substantial reduction and even elimination of fat pads.
Best of all it’s so easy to use, as demonstrated by Lipedema Influencer @PaleGingerPear on Instagram. She is just one of the inspiring voices on our monthly Lipedema Patient Roundtables, which take place on the 3rd Wednesday of each month at 8 PM. Click below to register!
It can be the most stressful time of the year, but the women of the Lipedema Patient Roundtable are facing the seasonal challenges with healthy doses of fun.
This fascinating presentation highlights case studies and photos of patients with lipedema as well as those with Dercum's Disease. The unique markers of lipedema are revealed along with the results of an ultrasound study before and after Lympha Press therapy.
"Thank you for being a friend..." The Lipedema Patient Roundtable was a cornucopia of warmth and gratitude this month in celebration of Friendsgiving. We pulled up some extra chairs to the virtual table as our panelists each brought a special friend along to talk about life, lipedema, and friendship.
"Lip"-or-Treat! Panelists and attendees had a hauntingly good time at the Halloween-themed October Lipedema Patient Roundtable, complete with creative costumes and heartfelt conversations.
The Lipedema Foundation is a groundbreaking organization devoted to the lipedema community in meaningful ways. Chief Science Officer Guy Eakin talks about the Foundation's history, mission, and registry, which is key to the organization's goal of funding research that can lead to a cure.
Does lipedema affect fertility? How about the ability to sweat? And why does lipedema light up on airport scanners? These are just some of the questions that popped up during the September Lipedema Patient Roundtable for our panel of patients and medical professionals.
To learn that the condition that had plagued her for decades had a name was a relief for Amy Vasquez. For years she heard "calories in, calories out" and was even accused by medical professionals of eating more than she admitted to. She saw similar, big thighs among her family members and thought there wasn't anything that could be done to manage the symptoms, which had spiked at puberty.
Living with lipedema can be painful. But one of the beautiful things about living with lipedema is the community and the wealth of information and support it offers. A big theme during the August Roundtable was pain relief, with panelists and attendees discussing everything from cold laser therapy and far-infrared light therapy to flotation tanks and medicinal marijuana.
