Here is a list of Veronica's top compression garments and accessories to manage lymphedema. . 2y. . Repost from. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. Launched in 2015 by a father and daughter from Texas initially hoping to spread awareness about multigenerational hereditary lymphedema with a blog and a small Facebook group, Lymphie Strong has grown into a global patient support and advocacy community with thousands of members who live with lymphedema and. Whether you. I lived feeling alone for a long time. t’s Winning Wednesday! We want to close out #LymphedemaAwarenessMonth with a lymphedema nighttime garment giveaway! 拾朗 Pure Medical is a Move That Lymph partner and they are happy to provide a. On World Lymphedema Day 2022, the Lymphie Strong community stands together with our group members from over 100 countries and others like us who live with lymphedema and lymphatic disorders of all. 1. Roisin Laird If you find it, let me know. Lymphie Strong, Katy, Texas. On World Lymphedema Day 2023, the Lymphie Strong community stands together with our group members from over 100 countries and others like us who live with lymphedema and lymphatic disorders of all. . An occurrence that can be very uncomfortable and even painful. RonK1 Sep 15, 2016 • 1:45 AM. #LymphedemaAwarenessMonth 露 ♀️ ♀️ Hey Friends! It’s Workout Wednesday and time to #movethatlymph with cardio and leg例 strength! Check out this month’s new FREE video from Cancer Rehab PT. Huge thanks and love to my garment fitter and dear friend, Sophie Long, for her excellent care at my appointment. ” (Via NBC Bay. You have been dealing with LE for. As parents, we all strive to give our children the best foundation for a successful future. Cruising Stories are little snippets of the cruising life, telling about the ups and downs, triumphs and challenges of this life. It seems hard to believe there aren’t more LE specialists or therapists in the Bay Area. What began as. I have a "water scarf" and will give it try. . Breakthrough tissue engineering study, combining CelGro® with lymphatic and blood vessel cells to create functional lymphatic tissue, has been. . VOTE FOR THE EURORDIS Social Media Award 2023 Let’s help one of our own put LYMPHEDEMA on the map in Brussels. Veronica Seneriz is a patient, advocate and Founder of Lymphie Strong. 317K subscribers Subscribe 22K views 1 year ago Lymphie Strong Exercise Series This is a 15 minute, aerobic and strength lymphatic exercise workout routine for. Nonprofit Organization. Join Catherine Seo, PhD & Co-Director of The Lipedema Project for our next Facebook Group Livestream in the Official Lymphie Strong Inspiration Group. Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. This button displays the currently selected search type. . I have previously been misdiagnosed three times during this traumatic period. . . What is the pelvic floor? "The pelvic floor is the base of the group of muscles referred to as your ‘core’. Hope it. My oasis. Aim for fifteen or thirty minutes a day while wearing your compression. From patients and advocates to medical professionals and vendors, the conference was a real who’s who of the lymphedema and lymphatic research world. . I developed lymphedema in 2015 as a result of endometrial cancer. Mary Al-Saleh (CLT, BS, MS, NP, PhD Nursing). We are different in our approach to lymphedema. The marker is not found in obesity. She may be a good resource too. . There are 8 #MOVETHATLYMPH fitness. March 7 at 3:56 AM # lymphedemaawarenessmonth Body image is a combination of the thoug. Chronic Wound Care: Reading The Weep (Via Lymphedema Guru) #lymphedema #lymphedemaawareness #wounds #weeping #leakingfluidOh snap! We are kicking off 2022 in style with @juzocompression this year and changing things up! In lieu of our normal #movethatlymph challenges, we invite you to share your compression fashion. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. Also, have you watched the donning video - there are some tips for securing the thigh piece (at 2min20seconds). Be sure to like our FB page Lymphie Strong. Welcome to the Lymphie Strong Running & Fitness Club for Lymphedema We are a global fitness group for people living with lymphedema by people living with lymphedema. At any time. Lymphie Strong. Order within 6 hrs 38 mins. . Lymphie Strong Amy Rivera 2y Explore topics Sales Marketing Public Administration Business Administration HR Management. Whether you. It entails videos on the major components of lymphedema treatment, including lymphatic draina. Home of the #MOVETHATLYMPH. Vern Seneriz, founder Lymphie Strong. Oct 8, 2019 - Discover (and save!) your own Pins on Pinterest. This is the courageous story of our dear friend and fellow lymphedema advocate, Tiffany Howe. But I wonder what else there might be? There’s a FB group – the Official Lymphie Strong Inspiration Group – that has a lot of members, and somebody on there might be able to help. Ever since I was 8 years old, I knew that I wanted to help people. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. Please. Wei Chen, MD, FACS, Professor of Plastic Surgery, Head, Regional. Also, excellent websites for education about Lymphoedema which also have links to great blogs: Lymphatic Education and Research Network (their library of web symposiums is brilliant and. Hope it. This young man was Veronica Seneriz, the founder of Lymphie Strong son CJ. BrightLife Direct 10% off lymphedema products using code LYMPHIESTRONG2023. Being bullied or teased about abnormal swelling, regardless of severity, can lead to depression, anxiety,. 2K members. There’s no reason I can’t stay fly and relatively active like others who are fighting the good fight. 317K subscribers Subscribe 22K views 1 year ago Lymphie Strong Exercise Series This is a 15 minute, aerobic and strength lymphatic exercise workout routine for lymphedema and lymphatic drainage. Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong ( lymphiestrong. . One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. . - Anyone can do it. Congratulations #pickmypumpkin2021 Winners 朗拾 Our contest was the biggest one yet in our 6 year history!! This year 28 great entries made us smile. June 25, 2018 Britta. com) in 2017 and your lymphedema virtual workout community. Author. . ”. We are sponsored by the great. Donations go straight to the Lymphatic Education & Research Network. - Use code LymphieStrong for 2 Free Workouts. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Slow, deliberate exercise can often be more beneficial than going "hard" in the long run - especially for lymphedema. Happy Veterans Day To all who have served and their families, we thank you for your service. For the. “Amy realized that this community needed a voice and. Thanks for sharing. It is in the pursuit of selfless acts and the unwavering dedication to making a positive impact that people find true fulfillment and purpose. 6,031 likes · 14 talking about this. com (@lymphiestrong)Welcome to the first Move That Lymph @movethatlymph Challenge for 2023! Let's Go! Let's Go! We begin 2023 with our RISE Challenge, a focus on yoga, sleep, and. 4 Reactions. Lymphie Strong is an online resource for people living with lymphedema by people living with lymphedema who know from firsthand experience how challenging living with chronic swelling can be and. . Thanksgiving has always been one of my favorite holidays of the year. . . Congratulations to All!!! Rise Challenge Winner - Leslie J Hero Challenge Winner - Ramona K 5th Annual Lymphie Strong Winners - Lori H, Becca A, Karen J, and Lianne M Each. It’s a salt water pool located five minutes from my home – close enough that I can make it without compression stockings on the drive to and from. Cheers to us ️ We did it. Forgot account? or. Be sure to like our Facebook page Lymphie Strong. We are proud to announce that BrightLife has teamed up with Veronica, founder of Lymphie Strong! We are working together to promote lymphedema education and share resources among the community. The knowledge provided in these online communities – including Lympha Press’ Roundtables and interviews – has empowered Jenny to advocate for her health and implement an effective self-care. Autumn Moon Virtual 5K completed by lymphietriathlete, a Veteran of the U. . Lymphie Strong. We want a better future for our children and generations to come. Lymphie Strong, Katy, Texas. Many people believe dry brushing works for lymphatic drainage. What began as. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Amy Rivera posted images on LinkedIn757 221 9519 [email protected] recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Dry brushing involves using a brush with stiff bristles to rub the skin. This opportunity will enable me to pursue my passion for lymphedema patient. At first my leg only swelled a little after running, especially after a longer run or after intervals but now after 12 bouts of cellulitis my left leg is about 25% larger in. Log In. . Especially why it's important to wear compression garments in hot weather. 4 Reactions. “Lymphie Strong Live Q&A with the BIDMC Lymphatic Center” Dr. Full Interview: It is not uncommon to go years or even decades without a lymphedema diagnosis. We are sponsored by the great. Little Miss Lucia's Lymphoedema Life. . . 4,640 Followers, 929 Following, 192 Posts - See Instagram photos and videos from Lymphie Strong | lymphiestrong. Lymphie Strong is a closed group so just request to join. Lymphie Strong, Katy, TX. Shana Grantham is a Medical Advisor for Essity in Northern California and is a lipedema patient who was diagnosed with lipedema in her mid-40s, even though she noticed at 13-14 years old that as she was trying to find clothing to wear and that fit her, she could not find clothes that fit. My new Lymphie friend brought 4 friends to the presentation tonight, who DID NOT have Lymphedema, to help educate and spread the word THANK YOU ⭐️ #amazing #advocacy #lymphedema. Lets support our friend and fellow Lymphie, Tiffany Howe, by watching tonight. Little Lymphie’s struggle to find appropriate care- our children’s size & the complexity that comes with Primary Lymphedema and it’s diagnosis make fantastic adult tools hard to obtain for our children. Hugs, Catherine. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. . Check out her favorite things below: See more of Lymphie Strong on Facebook. Beautiful cover photo via Brylan’s Feat Foundation Lymphie Strong. - On your schedule, at your pace. What began as. What began as. . An athlete diagnosed with the same rare condition as Kerry Katona refuses to let it hold her back and has her sights set on competing at the 2024 Paralympics. I have been dealing with a few for months and recently I have had. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. “#FollowFriday Inviting our Lymphedema Clinics, Certified Lymphedema Therapists, & Physiotherapists around the world to share their sites in the. From fellow lymphedema bloggers to treatment providers, patient advocacy groups, and medical suppliers, the internet is a fantastic resource for lymphies. ️Shout out to Mo Samuels, a young man from the UK advocating for #primarylymphedema ♂️ #lymphedema #lymphedemaawareness #compression #lymphaticsystem #chronicedema #lymphiestrong #movethatlymphClick the link to join our support group for people living with lymphedema by people living with lymphedema. It now has 2500 members world wide but mostly American Lymphies. . It’s a closed group (easy to request membership) but very well administered and hugely supportive practically and emotionally. org • • #brylansfeat. Skip to content. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021 YOUR WELLNESS REPORT. Two upcoming events in AUSTIN, TX ️ Here are the links to register ⭐️. . . Lose toxicity. Compression therapy by Lft. Menu. #StayElevated Hello! 👋 The Lymphie Life is currently undergoing updates, so you may see some funky formatting in the meantime. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Lymphedema Information · September 21, 2020 · September 21, 2020 ·Overcoming Lymphedema: Embracing Life's Challenges and Creating My Own Path. . com. Whether you. Let us come together on World…Lymphie Strong March 6 · On World Lymphedema Day 2022, the Lymphie Strong community stands together with our group members from over 100 countries and others like us who live with lymphedema and lymphatic disorders of all types. “Standing Up To Lymphedema with all of our faith, power, and might. 5 Pt 1 & 2 were combined for the Lymphie Strong channel by Bisa Dobson, RMT. ️ Gave my site a mini makeover. Jul 2, 2021 - Explore Lymphie Strong's board "The Lymphedema Running & Fitness Club" on Pinterest. Shelley Smith DiCecco of LymphEd. Juzo Canada, Ltd. The stretch allows the tissue to open the lymphatic gaps encouraging re. Beth Busacca Dziminowicz. Sign up here before March 5 to participate: Welcome to the first #MOVETHATLYMPH Virtual Race for 2020!! We are so proud to present the 2nd Annual Lymphie Strong Virtual Half Marathon/10K/5K for 2020. ♥️ #lymphedema #CureLE”“My right leg was 200% bigger than my left leg. Lymphie Strong Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management Engineering Soft Skills. I watched it when it was on and thought he looks familiar! 2. (Hairbrush microphone optional. 350 views 2 years ago. This is a great, supportive community! There are others too on social media sites, such as Lymphie Strong Inspiration Group on Facebook. . We want a better future for our children and generations to come. . . The Lymphie Life—Wonderful blog and compilation of information about lymphedema, written by a lymphedema patient who has struggled with the disease since infancy. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. jaz sem čisto v stilu . See more of Lymphie Strong on Facebook. Standing up to Lymphedema with all of your faith, power, and might. Every day is a new day to try again. Me: I have lymphedema. We will be doing a special ride on Monday March 6th for the 2023 WORLD LYMPHEDEMA DAY and coach will be joining us for that one! Check out LE&RN for more lymphedema awareness events!ACT Lymphoedema Support Group · November 16, 2017 · November 16, 2017 ·Next Friday night at a fundraising dinner the Lymphatic Education and Research Network (LE&RN) is honoring me for raising awareness of lymphedema. Never stop asking questions. There is no better time to. We are sponsored by the great. . Wear light, loose, non-constricting clothing. Lymphie Strong Amy Rivera 2y Explore topics Sales Marketing Public Administration Business Administration HR Management. This playlist was created in collaboration with Lymphie Strong. Welcome to the Lymphie Strong Running & Fitness Club for Lymphedema We are a global fitness group for people living with lymphedema by people living with. Oct 8, 2019 - Last week Lymphie Strong was proud to present "Deep Water Running by Jennifer Conroyd, CEO of Fluid Running" on Thursday June 20, 2019 at 12:00 PM CST. On Facebook there are good support groups, the best in my opinion is called Lymphie Strong Inspiration Group which is led by Vern who has Primary life long bilateral LE. The only prerequisite is having LE. Joy and I were so incredibly thankful to participate in the Networking & Educational Seminar for Lymphedema Therapists Memorial Hermann Greater Heights Hospital TIRR Memorial Hermann Houston, TX as. . This is. This was quietly relaunched based on requests from several members. . 6,079 likes · 76 talking about this. Didi Okoh, 20, was diagnosed with. We would like to show you a description here but the site won’t allow us. Thank you for having me! 懶Memorial Hermann Cancer Centers Support Groups will host its monthly Lymphedema Support Group meeting on Tuesday November 6, 2018 from 6-7:30 p. ) However you want to do it, just do it. Lymphatic self-help from Anita Bakke (Certified Lymphatic Therapist), and Dr. Home of the #MOVETHATLYMPH. We have received inquiries and your holiday cards are welcome! Please send to our business address: Lymphie Strong 20180 Park Row #6047 Katy, TX 77491 USA Happy Holidays to all!Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. An exciting new article just published that talks about the role of micronized purified flavonoid fraction (MPFF) as part of a treatment paradigm in total. Great workout for those with Lymphedema! - No impact. Her post on The Tights Lady resonated deeply with me. Just today 18 have been sold. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021 YOUR WELLNESS REPORT May 24, 2019 I WILL NO LONGER HIDE MY LYMPHEDEMA SO I CAN HELP OTHERS. Join our friends JOBST USA in Boston at Artesani Park on May 15th for #LymphWalk 2022! We invite you to join in person or virtually to walk/run to fight lymphatic diseases with LE&RN (Lymphedema. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. com and established in 2015. . - No compression necessary as the water provides it. A Lymphedema Online Support Community. You showed great creativity and imagination and. “Our first VASCERN Spotlights interview of 2020 is with no other than Pernille Henriksen, our European Patient Advocacy Group (ePAG) co-chair for the Primary and Pediatric Lymphedema Working Group. . 📚 Passing the Torch of Inspiration to My Team 🚀 Over 8 years ago, I was working at an unfulfilling 9-5 job. Read Veronica's story. Log In. Lymphie Strong… Feb 5, 2022 - Launched in 2015 by a father and daughter from Texas initially hoping to spread awareness about multigenerational hereditary lymphedema with a blog and a small Facebook group, Lymphie Strong has grown into a global patient support and advocacy community with thousands of members who live with lymphedema and. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. a book for students and teachers. Whoever said “Never meet your heroes” obviously wasn’t a lymphie. orIn this conversation. . Light refreshments and snacks are provided. Little Lymphie’s struggle to find appropriate care- our children’s size & the complexity that comes with Primary Lymphedema and it’s diagnosis make fantastic adult tools hard to obtain for our children. Call To Action: Let's all click on this New York Post link and comment under Conversation about how not "rare" lymphedema is in 2022! “People will often stop and stare at my legs,” Okoh told South. Welcome to the Lymphie Strong Running & Fitness Club for Lymphedema We are a global fitness group for people living with lymphedema by people living with lymphedema. Lymphie Strong March 7 at 3:56 AM # lymphedemaawarenessmonth Body image is a combination of the thoug. LymphaPress Leadership Series, Kathleen Helen Lisson. Visit the Women's Health Boutique-Memorial and ask for Sophie if you are in Houston. Lgarcia Oct 26, 2018 • 4:27 AM. We are a very small but mighty group! One day lymphedema might be as. Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. Every meal is an opportunity to fight inflammation or feed it. Stay strong. Our community. What began as. . The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. Julius Zorn, Inc. com and established in 2015. . Lgarcia Oct 26, 2018 • 4:27 AM. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. Lymphedema Podcast. Founder Veronica Seneriz — a lymphedema patient and advocate herself — has a. Whether you. Be sure to like our FB page Lymphie Strong. Mrs Kathleen Helen Lisson Swollen, Bloated and Puffy: A manual lymphatic drainage therapist's guide to reducing swelling in the face and body $2999. com and established in 2015. Welcome to the Lymphie Strong Running & Fitness Club for Lymphedema. Just choose a no/low sodium sparkling water as salt/sodium increases lymphie swelling. What began as. Juzo Canada, Ltd. Lymphie Strong Lymphedema 101 Cancer Rehab PT 51 videos 2,723 views Updated yesterday This playlist was created in collaboration with Lymphie Strong. Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. Great workout for those with Lymphedema! - No impact. With its innovative approach and powerful impact, we are changing lives, one step at…Lifelines for her have been the social groups focusing on Lipedema and Food Sensitivities, Lipedema Fitness, Lymphie Strong, and Dances with Fat. Welcome to the Lymphie Strong Running & Fitness Club for Lymphedema We are a global fitness group for people living with lymphedema by people living with lymphedema. Lymphie Strong is an online resource for people living with lymphedema by people living with lymphedema who know from firsthand experience how challenging living with chronic swelling can be and. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Thanksgiving has always been one of my favorite. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. “In Canada, there are numerous. Be sure to like our Facebook page Lymphie Strong. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. Whether you. Putting on and then wearing thick, tight compression stockings all day, every day is challenging enough. - GIMS Group: The Demystifying Lymphedema, its Management, and. Subscribe. In reply to LymphieStrong's comment. Honored and thrilled to announce that the Lymphedema Treatment Act is now a formal collaborative partner of the Lymphie Strong #lymphiestrong community. Be sure to like our FB page Lymphie Strong. 7K views, 44 likes, 16 loves, 3 comments, 134 shares, Facebook Watch Videos from Lymphie Strong: Congratulations to this phenomenal team for building the manifesto!! @the_lympha is part of the. “A relaxing and gentle course in yoga for people living with lymphoedema begins on January 19th in Dublin. . I love running at. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. Thank you Juzo for sharing the vision early on and your support for two awesome years. We are proud to announce that BrightLife has teamed up with Veronica, founder of Lymphie Strong! Check out her list of top lymphedema compression garments and accessories. Elaine is part of a tribe I refer to as. SamLymphie 4 months ago. S. Lymphie Strong is an online resource for people living with lymphedema by people living with lymphedema who know from firsthand experience how challenging living with chronic swelling can be and. Lymphie Strong on Facebook is US based and has a huge membership. Lymphie Strong has created a team to join the fight and help LE&RN continue its mission by walking on behalf of the estimated 10 million Americans and 250 million worldwide who are fighting lymphatic. Veronica “Vern” Seneriz has lymphedema and founded the Lymphie Strong social channels and blog as a way to motivate herself and others to get and stay moving. . For most women, getting ready for work is like preparing for opening night on the Broadway stage. . Lymphie Strong—An insightful blog on living with lymphedema, written by a strong advocate. Whether you. . But I wonder what else there might be? There’s a FB group – the Official Lymphie Strong Inspiration Group – that has a lot of members, and somebody on there might be able to help. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Lymphie Strong's Favorite Things. Get Fast, Free Shipping with Amazon Prime. Verified account Protected Tweets @; Suggested usersSurround yourself with positive like-minded people now and in the year to come. Put on some of your favorite tunes and dance around your bedroom. See more of Lymphie Strong on Facebook. The Lymphie Life. Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. . . Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. Jennifer Conroyd is the founder of Fluid Running, a nationally recognized deep water exercise program. VIDEO: To Dry Brush, or Not to Dry Brush? That is the Question. Veronica has also traveled to Washington DC on different occasions to lobby Congress both as a member of the TX. 3. Reply (0) Report. Fast'n Go has not only transformed my own life but also countless others. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. . We are a global fitness group for people living with lymphedema by people living with lymphedema. 曆 懶At this time, I’d love to thank Arizona based Fluid Factor Lymphedema - Lipedema Care for their recent bulk order of Lymphie Strong t-shirts. . What began as. Lymphedema Awareness Month for March 2022 has ended. . Join Zoom Meeting Alexa launched The Lymphie Life in 2011, having felt frustrated with the lack of online resources for young adults living with lymphedema. “They realised the special needs of children with lymphedema but also at the same time supporting the families who were seeking answers and reduce their feelings of isolation and helplessness. Launched in 2015 as a small Facebook group and a blog, Lymphie Strong has grown to include three Facebook support groups and numerous. Every now and then you meet someone who inspires you and leaves a lasting impression from their passion to change the world and make it a better place. Fluid Running. This free zoom webinar is a great opportunity to learn more about the pelvic floor hosted by Lymphie Strong and Dr. S.