Open your heart and diaphragm in Feb by joining our @movethatlymph Lymphie Strong Valentines Day ♥️ yoga 律 ♀️ challenge sponsored by Absoyogalutely and the great people at Luna Medical, Inc. What began as. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. 350 views 2 years ago. Forgot account? or. What began as. Veronica has also traveled to Washington DC on different occasions to lobby Congress both as a member of the TX. Wear light, loose, non-constricting clothing. Aim for fifteen or thirty minutes a day while wearing your compression. 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 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 meditation which helps increased. 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. Per a recent report by PWC, 44% of workers’ SKILLS will be disrupted in the next 5 years. Lymphie Strong Amy Rivera 1y Aria Health Amy Rivera 1y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. com and established in 2015. . Two. 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. A reminder of why we advocate so hard. What began as. VOTE FOR THE EURORDIS Social Media Award 2023 Let’s help one of our own put LYMPHEDEMA on the map in Brussels. This is a 12-minute, core lymphatic exercise workout routine meant to exercise routine to stimulate the lymphatics and get the lymphatic system moving. BrightLife Direct 10% off lymphedema products using code LYMPHIESTRONG2023. . Cheers to us ️ We did it. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. 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. What began as. Learn more about her and Lymphie Strong at staylymphiestrong. Be sure to like our FB page Lymphie Strong. The power we have as a #lymphedemacommunity and a #lymphedemafamily is so strong and honestly invaluable to me. 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. Also, have you watched the donning video - there are some tips for securing the thigh piece (at 2min20seconds). Visit the Women's Health Boutique-Memorial and ask for Sophie if you are in Houston. Lymphie Strong aka Vern. Want to feel like you don’t have lymphedema? September 12, 2013 Britta. Light refreshments and snacks are provided. . Normally I do not do this, but Jann has been a member since March 2017. . Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. If we don’t make the 31, your money will. org. #lymphiestrong #movethatlymph. Lymphedema CS_ 494625_8/20 siteman. Certainly, it's becoming increasingly evident that the prevalence of primary lymphedema with central lymphatic dysfunction might be higher than initially…Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. . “A relaxing and gentle course in yoga for people living with lymphoedema begins on January 19th in Dublin. This young man was Veronica Seneriz, the founder of Lymphie Strong son CJ. Lymphie Strong. You showed great creativity and imagination and. Through lifelong adversity with my disability, I developed an activist mindset as I feverishly fought to better. This is. 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. ” No truer words have been spoken. Lymphie Strong proudly presents a hands on live demo and discussion of diaphragmatic breathing in the Lymphie Strong Running & Fitness Club called Diaphragm. Lymphie Strong. Lymphedema Awareness Month for March 2022 has ended. Seeing the impact that…Salon RX - Post-Surgical Fitting Services · August 31, 2018 · August 31, 2018 ·Guide to Blogs About Lymphedema and Lymphatic Diseases LE&RN486 © 2019 261 Madison Avenue,9th Floor, New York, NY 10016 • 516-625-9675 info@LymphaticNetwork. - GIMS Group: The Demystifying Lymphedema, its Management, and. Karen L. Lymphie Strong. 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. 13K views, 120 likes, 12 loves, 3 comments, 27 shares, Facebook Watch Videos from Brylan’s Feat Foundation: Spread Awareness by Liking, Following, and Sharing brylansfeat. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. 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. 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. 4,640 Followers, 929 Following, 192 Posts - See Instagram photos and videos from Lymphie Strong | lymphiestrong. We have never met, and I don’t have the resources to help for housing, but she gave me permission to share on my page. . Lymphie Strong hosts Kathleen Lisson, Author of the Southern California Plastic Surgery Cookbook. Whether you. Lymphie Strong. would give even Idina Menzel pause. 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. Nonprofit Organization. . 📚 Passing the Torch of Inspiration to My Team 🚀 Over 8 years ago, I was working at an unfulfilling 9-5 job. You can't stop the disruption. Lgarcia Oct 26, 2018 • 4:27 AM. 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. Slow, deliberate exercise can often be more beneficial than going "hard" in the long run - especially for lymphedema. 1. Hopefully the wraps up to the knee stay in place and are easy to put on/take off. com and established in 2015. . Nonprofit Organization. Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong ( lymphiestrong. 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. If you get overheated, elevate your affected limb and place a cold, wet towel over it. 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. What began as. There’s no reason I can’t stay fly and relatively active like others who are fighting the good fight. Lymphie Strong. Let’s Get Physical Move That Lymph Challenge! ♀️ Continuing on with our 80’s theme for 2022, Let’s Get Physical by Olivia Newton-John was a number one song in 1982. . And now it's official here in New York thanks to the dedicated team from the Lymphatic Education and Research Network (LE&RN). . 2019 Conference and here she sums all of them up‼️ FANTASTICYou are invited to hear my patient story at the 3rd Annual Patient Lymphedema Symposium hosted by BIDMC/Harvard Medical School on Saturday, September 28, 2019 along with BSN Medical / JOBST. 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. Thank you Juzo for sharing the vision early on and your support for two awesome years. A Lymphedema Online Support Community. Standing up to Lymphedema with all of your faith, power, and might. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. What began as. PODCASTS. Now she is launching a NEW Facebook group called Primary Youth Support Group specifically for. Normally I do not do this, but Jann has been a member since March 2017. June 25, 2018 Britta. Wishing you great lymphatic heath, and I hope that you are pain and cellulitis free. . Apply for the 2023 LE&RN/Lymph Notes U. Verified account Protected Tweets @; Suggested usersResearch Roundup: Summer 2021 Edition. 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. Be sure to like our FB page Lymphie Strong. Ninjas Fighting Lymphedema Foundation . 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. Recent Posts. Repeated dismissal of symptoms can cause distrust. Drink plenty of water! Staying well hydrated makes it easier for your body to regulate its temperature. “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. 797 views, 7 likes, 0 loves, 1 comments, 87 shares, Facebook Watch Videos from Geriatrics Infolinks Management Strategies Inc. . com. com and established in 2015. I watched it when it was on and thought he looks familiar! 2. Verified account Protected Tweets @; Suggested usersSurround yourself with positive like-minded people now and in the year to come. 300 • Burlington, ON L7L 6B2 • Call: 1-888-255-1300. Veronica runs several social media platforms for lymphedema and lipedema thrivers, caregivers, physicians, therapists. What began as. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. Lymphie Strong Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management Engineering Soft Skills. 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. Lymphedema Guru. “Lymphie Strong Live Q&A with the BIDMC Lymphatic Center” Dr. Home of the #MOVETHATLYMPH. Whether you. Advertisement. Dhruv Singhal and his multidisciplinary team from Beth Israel Deaconess Medical Center Lymphatic Center answer questions about lymphatic surgery & more in this webinar with Veronica Seneriz of Lymphie Strong. 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. . Home of the #MOVETHATLYMPH. . com and established in 2015. Lymphedema Awareness Month for March 2022 has ended. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Feelings of heaviness, tingling, numbness, skin tightness, pain, limited range of motion, and fatigue are common. . We want a better future for our children and generations to come. Battling lymphedema is all about arming yourself with the right weapons to fight the disease. ” (Via irishtimes. google Lymphie Strong, The Lymphie Life, Lymphedema Diary to learn about self-care and so much more. Lymphie Strong is a closed group so just request to join. Dry brushing involves using a brush with stiff bristles to rub the skin. Log In. . If you are thinking about giving a charitable donation before the end of the year, I recommend considering the Lymphatic Education & Research Network (LE&RN). Find out more! Starting at $129. ” Via. There is no better time to. . Author. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. Thanks . The venue was buzzing all weekend with excited chatter and inspired conversations between attendees and faculty. Conversationaly: Thriving w/ Lymphedema. When you are a lymphie, heat is a four letter word. 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. We want to tell the world that it is not just a little swelling! ️🩹 💙 Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Multiple Authors (See Below) In an effort to raise awareness of lymphedema, Juzo invited some of our medical partners and thought leaders in the lymphedema community to share how far they feel we’ve come in helping those battling this disease and ideas for educating others. 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. Thank you for your support! Together we reached 57,000 (FB) during the month of March for Lymphedema Awareness Month 2022. Beautiful cover photo via Brylan’s Feat FoundationLymphie Strong. It was a pleasure being a guest on the Lympha Press #Lymphedema Patient Roundtable. All My BestOur team in the 2020 #MOVETHATLYMPH Lymphie Strong Kick Start Your Lymph 30 Day Challenge are crushing week 2 with the Butts & Guts circuit or outside snow activities! ⛄️ ️@juzocompression. Brylan’s Feat Foundation. I lived feeling alone for a long time. Beth Busacca Dziminowicz. . One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. 6,079 likes · 76 talking about this. . com and established in 2015. Happy Veterans Day To all who have served and their families, we thank you for your service. . Cam Ayala Opens Up About Life as an Amputee: 'The Biggest Challenge Is Letting Go of Who I Used to Be' (Exclusive)Feb 26, 2021 - Discover (and save!) your own Pins on Pinterest. 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. Related Pages. 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. Hvala za darilce Medi. Them: What’s that Me: A disease of the lymphatic system. Especially why it's important to wear compression garments in hot weather. . Whether you. I encountered several doctors who were stuck in their dogmatic thinking about movement causing our #lymphedema to exabrate over the years. 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. 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. (Hairbrush microphone optional. . . The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. Join us every Wednesday through Nov 3, 2021. Vern Seneriz, founder Lymphie Strong. Add eighty-plus-degree-heat and a bucket of humidity, and we are ready to volunteer for the crew of ‘ Ultimate Survival Alaska . A4BC is a 501(3)c non-profit corporation. Here is a list of Veronica's top compression garments and accessories to manage lymphedema. This free zoom webinar is a great opportunity to learn more about the pelvic floor hosted by Lymphie Strong and Dr. 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. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. See her full bio in the Event link posted in. . We are sponsored by the great. Huge thanks and love to my garment fitter and dear friend, Sophie Long, for her excellent care at my appointment. See more of Lymphie Strong on Facebook. Launched in 2015 as a small Facebook group and a blog, Lymphie Strong has grown to include three Facebook support groups and numerous awareness initiatives, bringing together thousands of lymphedema patients and advocates from across the globe. Lymphie Strong proudly presents a hands on live demo and discussion of diaphragmatic breathing in the Lymphie Strong Running & Fitness Club called Diaphragm. . Not now. com (@lymphiestrong)Let’s do it‼️ ️ Repost from @lymphfitness VIRTUAL MOVEMENT + LYMPHIESTRONG WEDNESDAYS in OCTOBER 6:30PM CST with Andrew @iamyogandy This is a very exclusive virtual class collaboration. Welcome to our first ever Lymphie Strong Lymphatic Surgery Lightning Round Q&A featuring Dr. Vern Seneriz, founder Lymphie Strong. . In this conversation. Oct 8, 2019 - 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. An occurrence that can be very uncomfortable and even painful. Please. . Feel free to share. The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. Jennifer Conroyd is the founder of Fluid Running, a nationally recognized deep water exercise program. Blogger. As LE&RN’s executive director, Bill Repicci, says, “Although an estimated ten million Americans suffer from lymphedema, this disease remains in the shadows. 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. Amy Rivera posted images on LinkedIn. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. wustl. This is a great, supportive community! There are others too on social media sites, such as Lymphie Strong Inspiration Group on Facebook. . When expanded it provides a list of search options that will switch the search inputs to match the current selection. Be sure to like our Facebook page Lymphie Strong. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. #lymphedema #movethatlymph #lymphiestrong. Just today 18 have been sold. Fast'n Go has not only transformed my own life but also countless others. Get Fast, Free Shipping with Amazon Prime. Be sure to like our Facebook page Lymphie Strong. Roisin Laird If you find it, let me know. Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021. . . Check it out and let me know what you think. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. . . Be sure to like our FB page Lymphie Strong. But no scientific research yet supports this claim. Putting on and then wearing thick, tight compression stockings all day, every day is challenging enough. Just choose a no/low sodium sparkling water as salt/sodium increases lymphie swelling. It’s generally done on dry skin before bathing. 300 • Burlington, ON L7L 6B2 • Call: 1-888-255-1300. . Thank you Juzo for sharing the vision early on and your support for two awesome years. 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. Our aim to provide hope and understanding of the lymphatic system through knowledge and experience. Thanks for the suggestions and advise Lymphie Strong. Thanks for your support in following. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Follow #lipedemafitness on the #peloton leaderboard. From fellow lymphedema bloggers to treatment providers, patient advocacy groups, and medical suppliers, the internet is a fantastic resource for lymphies. You have been dealing with LE for. Cathleen Donovan. . We are sponsored by the great. 1 Reactions. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. . 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. I developed lymphedema in 2015 as a result of endometrial cancer. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. 3. We aim to close…Apply for the 2023 LE&RN/Lymph Notes U. You’re always going places -physically, emotionally and spiritually. Especially why it's important to wear compression garments in hot weather. . - Use code LymphieStrong for 2 Free Workouts. 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. . This was quietly relaunched based on requests from several members. ” Happy Halloween everyone Be safe. Panelist Kelly Bell was one of the first members of Lymphie Strong when it began years ago, and there wasn’t a dry eye on the Zoom call as he shared just how much the group had. Whoever said “Never meet your heroes” obviously wasn’t a lymphie. 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. . Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Not all heroes wear capes. Hope it. orI am humbled and honored to announce that I have accepted the role of National Lymphedema Network Social Media Manager. Whether you. Lymphie Strong Lymphie Strong. Home of the #MOVETHATLYMPH. Veronica Seneriz of Lymphie Strong has developed a dynamic calendar of events for the month of March, including the 3rd Annual Lymphie Strong Virtual Half Marathon/10K/5K, a fundraiser to support Texas lymphies affected by Winter Storm Uri (apply for support here), educational webinars featuring medical professionals, and more. Whether you. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. Launched in 2015 as a small Facebook group and a blog, Lymphie Strong has grown to include three Facebook support groups and numerous. ♥️ #lymphedema #CureLE”“My right leg was 200% bigger than my left leg. I was not aware of some of that information. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. It seems hard to believe there aren’t more LE specialists or therapists in the Bay Area. It all started when I discovered my childhood hero, Princess Diana. Thanksgiving has always been one of my favorite holidays of the year. ”. The only prerequisite is having LE. Be sure to like our Facebook page Lymphie Strong. . And now, that dream is becoming a reality with the…Thank you John Chuback, MD, FACS, Emily Iker, Monika Gloviczki and M. Oct 8, 2019 - Join our brand new group called the Lymphedema Sugar Busters Support Group! Sugar fuels inflammation which fuels lymphedema. LYMPHEDEMA RESEARCH, STUDIES, AND TRIALS. Help us break a record. 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. . Beautiful cover photo via Brylan’s Feat Foundation Lymphie Strong. . 322 views, 16 likes, 5 loves, 0 comments, 2 shares, Facebook Watch Videos from Lymphie Strong: The Book of Lymph has arrived. There are 8 #MOVETHATLYMPH fitness. 2y. 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. This opportunity will enable me to pursue my passion for lymphedema patient. Didi Okoh, 20, was diagnosed with. . A retrospective analysis of 105 subjects with. orIn this conversation. m. 2. It is available to view now in the group. The National Library of Medicine. ” — By. In this episode, Michele Watson tells of the challenges of cruising with lymphedema and her personal triumph, with a heavy emphasis on “you can do anything you set your sights on. Our goal is to provide guida…When lymphedema goes unmanaged, tissues become more fibrotic—or thick—due to a buildup of protein-rich fluid. . . Because of Fluid Factor, we were able to reach a recent. We are a global fitness group for people living with lymphedema by people living with lymphedema. Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong (lymphiestrong. From the time my alarm clock goes off in the morning to the moment I shut my eyes at night, I am constantly. Lymphie Strong, Katy, Texas. Hope others offer better advice than I can. Thanks to the unique structure, Fast'n Go bandage is the only hybrid bandage to use a patented technology that combines the respective benefits of inelastic…"The foam channels apply bidirectional or directional compression to the limb, creating localized stretch and pressure. “Lymphedema is a common condition with global impact and a multitude of complications, however, only a few professionals specialize in its management. Book Reviews:World Cancer Day reminds us all that we all are together in this fight against cancer and we must conquer it together. - No compression necessary as the water provides it. 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. March 2018 The State of Lymphedema Awareness. . 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. . . jaz sem čisto v stilu .