Power Symposium 2019 in New Orleans

On Wednesday March 20th, I will be attending a Juzo USA event at Power Symposium 2019 in New Orleans as part of a patient panel on Lymphedema Advocacy. I am incredibly excited to share my story with this awesome team. Advocates Making a Positive Impact Pattie Cornute, Amy Rivera, Veronica “Vern” Seneriz, Lindsay Sosovec and […]

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Texas Strong: Lymphie Strong appears on Lymphedema Podcast

It’s Lymphedema Awareness Month, and we are full steam ahead with featuring all sorts of platforms where Lymphedema information is being shared across the world. One way is via the Lymphedema Podcast. Lymphedema Podcast featured Primary Lymphedema this week as a topic, and I was honored to be a guest on the show. Do you […]

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Lymphie Strong March Calendar

Hold on to your #compression! March is going to be busy this month!! Below is a list of events that Lymphie Strong is hosting or taking part in as a participant. Our mission is simple – To reach as many people who have little to no support in living with lymphedema. We aim to close […]

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Lymphie Strong Lymphedema Awareness Shirt

March is Lymphedema Awareness Month. Dozens of you reached out to me asking me why I didn’t do a shirt campaign, or when I was going to do the next one. Due to the demand, I created this campaign. Please share with others in the community that you think might be interested. Thank you for […]

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LRFC50 for 9th Annual NY LE&RN Run/Walk To Fight Lymphedema & Lymphatic Diseases

It is my honor to make this announcement. Since the Lymphie Strong fitness community known as, The Lymphedema Running & Fitness Club, virtually participated in the TX, DC, and CA Walks this year, I have managed to obtain an exclusive 50% off discount for NY registration by using the coupon code LRFC50 on the site […]

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Happy 3rd Anniversary, Lymphie Strong

This week the Lymphie Strong blog turned 3 years old. I was in shock when I saw the “Happy Anniversary” message from WordPress. I looked up and thought, “Daddy, we have come a long way.”  If you have never read why I actually started this blog, I encourage you to read My Daddy Had Lymphedema Too. […]

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Cellulitis Sucks!

This piece is dedicated to all the Cellulitis Warriors around the globe with lymphedema / lymphoedema. You know who you are. Those of you, like my father, that have been in the Intensive Care Unit maybe once, maybe multiple times from cellulitis. Whether you have survived 1 bout or 100, you know it is an […]

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2017 Year In Review – Lymph Science Advocacy Program and NLN Conference

This is the first blog post in a 2017 Year In Review Series. It’s going to be hard to encapsulate everything that has happened last year, but I will try my best. In mid-October, I attended one of the most life altering conferences in my life.  Sure, as an IT professional, I have been to […]

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#MOVETHATLYMPH 2018 New Year 30 Day Challenge

Hello New Year! Here’s to a New Year, New You! Exercise in any form is highly beneficial to the management of Lymphedema. Get moving, stay moving and commit to your lymphatic health! Sign up for the 2018 #MOVETHATLYMPH Challenge for Lymphedema & Lymphatic Heath and commit to doing something active, every day, for at least 10 […]

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Jingle Bell #MOVETHATLYMPH 5K Trot

We said we would finish the year out strong, and we will do it!   Look out December!! For those of you that missed out on the Summer and Fall Challenges, you can sign up for the final event of the 2017 #MOVETHATLYMPH Challenge for Lymphedema and Lymphatic Health year.  The final event of the year […]

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