Joi Louise Talks Fashion & Shoes

It’s official! Fall is here in the United States, and I am excited to host a brand new guest and fellow Juzo Ambassador to Lymphie Strong. The very lovely Joi-Louise Hall “Talks Fall Fashion & Shoes” and will share some great advice for looking your best this season. You are invited to a Zoom meeting.When: […]

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My Interview With Conversationaly: Thriving With Lymphedema

Allow me to introduce you to two beautiful ladies who graciously invited me to be a guest on their Instagram IGTV channel and become part of their #ThursdayThriver program. For the purposes of this post, the original IGTV videos from ConversationlyTWL: The Interview Series Vol. 5 Pt 1 & 2 were combined for the Lymphie […]

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The Southern California Plastic Surgery Cookbook Drops By The Lymphie Strong Cafe

“Straight from when I was 9 years old and my mother was diagnosed with metastatic breast cancer, I understand that nausea is an issue and we can’t just push it aside.” Learned so much from this meeting and gained additional insight and perspective on some common post operative issues. I have had 9 surgeries in […]

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Podcast Interview with Lymph Logic

“We are different in our approach to lymphedema. We aim to provide hope and understanding of the lymphatic system through knowledge and experience.” – Lymph Logic Lymph Logic In early July before I was struck with an illness that took me offline for the better part of 8 weeks, I had the most incredible opportunity […]

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Happy 5th Anniversary Lymphie Strong

Not only happy to be alive but also grateful to celebrate 5 years of Lymphie Strong! It’s so hard to believe that in 2015, I started with a one post blog and 74 people in one group. Read on as I attempt to encapsulate 5 years of lymphedema advocacy and patient driven initiatives. Today the […]

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Massachusetts Advocate Lisa Palin Submits Lymphedema Abstract at Science and Technology Conference

Preface: It is my honor to share the following newsletter announcement excerpt praising the efforts of Lisa Palin, fierce lymphedema advocate from Massachusetts, my dear friend, and fellow LE&RN volunteer. Please join me in sending congratulations to Lisa on this outstanding achievement thus far and wishing her continued success in this endeavor. This is an […]

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Diaphragm Breathing for Lymph Flow led by Lisa Bergman Sylvestri, MSPT, CLT-LANA

Lymphie Strong proudly presents a hands on live demo and discussion of diaphragmatic breathing in the Lymphie Strong Running & Fitness Club called Diaphragm Breathing for Lymph Flow led by Lisa Bergman Sylvestri, MSPT, CLT-LANA (September 18th at 7 AM PST / 10 AM EST). This is a great way to #movethatlymph and part of […]

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Standing Up to Lymphedema Mask

Looking for a lymphedema awareness mask? Look no further. A few of our loyal members asked for a Lymphie Strong mask. This is a great opportunity to talk about our how our Lymphie Strong community creates awareness for lymphedema and tries to help end isolation for those who live with it. You have two options […]

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Turning Into A Mermaid – A Lymphie Journey

By Guest Blogger Pernille Henriksen Later as my lymphedema developed, I was aware of my leg that stood out. That people would stare at me. I struggled to deal with the stocking – on or off? Wondering how I could “discreetly” battle with putting the stocking on in the changing room at the pool while […]

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Founder of Lymphie Strong Faces Medical Challenges

The founder of Lymphie Strong, Veronica Seneriz, is offline facing medical challenges and her family is fundraising to help her defray medical expenses. Your support and prayers are a blessing and we wish you good health. We are stronger together. GoFundMe You can support the campaign directly at the below and share. God Bless. Help […]

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