. Going to Stanford is a great idea, of course, they’re gold standard. From patients and advocates to medical professionals and vendors, the conference was a real who’s who of the lymphedema and lymphatic research world. 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. “Encourage every doctor you know as a therapist, or visit as a patient, to register for the new LE&RN CME Seminar for Physicians: Lymphatic-Vascular Disease: Diagnosis & Treatment. View 1 more reply. Juzo Canada, Ltd. What began as. We aim to close…Apply for the 2023 LE&RN/Lymph Notes U. Be sure to like our FB page Lymphie Strong. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. . Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021 YOUR WELLNESS REPORT. orIn this conversation. 3. VIDEO: To Dry Brush, or Not to Dry Brush? That is the Question. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. . . Veronica Seneriz is a patient, advocate and Founder of Lymphie Strong. At the heart of our photo is Ms. Be sure to like our FB page Lymphie Strong. 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. And now, that dream is becoming a reality with the…Thank you John Chuback, MD, FACS, Emily Iker, Monika Gloviczki and M. . 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. What began as. Nicole Faccio, known on social media as Facciolita, was born in Puerto Rico and. We are sponsored by the great. Hello Friends! Quick reminder on groups. Our community is where we discuss general lymphedema topics such as complete/complex. 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. The #movethatlymph challenge is $15 and includes these classes as well as a random prize drawing of 2 @juzocompression garments. Create new account. - Use code LymphieStrong for 2 Free Workouts. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. Founder Veronica Seneriz — a lymphedema patient and advocate herself — has a. Tune inSee more of Lymphie Strong on Facebook. 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. 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. There is a minimum of 31 required to print. . . . We are sponsored by the great. 🦋🎗Speaking of inspiration, the panel was joined by special guest Veronica Seneriz, a lymphedema patient and founder of the blog and online community Lymphie Strong. Whether you. Lymphie Strong, Katy, Texas. And if you are in your mid-career (35-50. Normally I do not do this, but Jann has been a member since March 2017. . This is a 10 minute, core and abdomen lymphatic exercise workout routine that is meant to stimulate the deep lymph nodes and lymphatic vessels, to help impro. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. 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. - Anyone can do it. We are different in our approach to lymphedema. - On your schedule, at your pace. 4 Reactions. Karen L. . Lets support our friend and fellow Lymphie, Tiffany Howe, by watching tonight. . #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. Roisin Laird If you find it, let me know. 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. It is in the pursuit of selfless acts and the unwavering dedication to making a positive impact that people find true fulfillment and purpose. June 25, 2018 Britta. 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. The swelling, the pain, the overwhelming sense of frustration can be so hard to bear at times. 2K members. The stretch allows the tissue to open the lymphatic gaps encouraging re. I love running at. 6,079 likes · 201 talking about this. m. Subscribe. Lymphedema CS_ 494625_8/20 siteman. The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. And now it's official here in New York thanks to the dedicated team from the Lymphatic Education and Research Network (LE&RN). What is the pelvic floor? "The pelvic floor is the base of the group of muscles referred to as your ‘core’. As someone who lives with lymphedema, I know firsthand how challenging it can be to manage the symptoms and maintain a positive outlook. ️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. You will find loads of good support and sharing of information on coping with LE. - Anyone can do it. Be sure to like our Facebook page Lymphie Strong. You are always one decision away from a totally different life. Nonprofit Organization. I watched it when it was on and thought he looks familiar! 2. When: Dec 21, 2021 07:00 PM Eastern Time (US. . This is the courageous story of our dear friend and fellow lymphedema advocate, Tiffany Howe. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. Whoever said “Never meet your heroes” obviously wasn’t a lymphie. Going to Stanford is a great idea, of course, they’re gold standard. As LE&RN’s executive director, Bill Repicci, says, “Although an estimated ten million Americans suffer from lymphedema, this disease remains in the shadows. S. Our groups are open to all living with lymphatic disease, their spouses, caregivers, families, clinicians, and others who support our community. Hello bbrinkley63. Stanford Medicine. Jun 14, 2021 - Discover (and save!) your own Pins on Pinterest. We are a very small but mighty group! One day lymphedema might be as. Lymphie Strong's Favorite Things. We are a global fitness group for people living with lymphedema by people living with lymphedema. March 2018 The State of Lymphedema Awareness. 5 Pt 1 & 2 were combined for the Lymphie Strong channel by Bisa Dobson, RMT. La Jolla Cosmetic Podcast Kathleen Helen Lisson. Launched in 2015 as a small Facebook group and a blog, Lymphie Strong has grown to include three Facebook support groups and numerous. Tressa Macaluso has been a member of Lymphie Strong since her teens alongside her mother Jennifer. Lymphie Strong hosts Kathleen Lisson, Author of the Southern California Plastic Surgery Cookbook. Be sure to like our FB page Lymphie Strong. 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. Welcome to our first ever Lymphie Strong Lymphatic Surgery Lightning Round Q&A featuring Dr. What began as. Me: I have lymphedema. When you are a lymphie, heat is a four letter word. 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. It’s generally done on dry skin before bathing. Dec 24, 2020 - Explore Lymphie Strong's board "#MOVETHATLYMPH Cafe" on Pinterest. 2K members. hts and feelings that you have about your body, and lymphedema can be psychologically tough as much as it is physically. Standing up to Lymphedema with all of your faith, power, and might. Dhruv Singhal, MD, to be honored at the 2022 Global Run/Walk to Fight Lymphatic Diseases, Sunday, May 15! #LymphWalk Via Lymphatic Education & Research Network |. 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 opportunity will enable me to pursue my passion for lymphedema patient. Hugs, Catherine. 3. 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. 3. . 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. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. I have previously been misdiagnosed three times during this traumatic period. 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. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. 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. When you post include the sizes of your legs and waist piece or you’ll be flooded with loads of messages asking sizes. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. com and established in 2015. 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. Stine Sørensen posted images on LinkedInlymphie strong – standing up to lymphedema 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. Why? Because today is National Lymphedema Awareness Day. The pace of change is unreal. Forgot account? or. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. This creates better lymphatic flow, as well as keeping you cooler! Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. . - GIMS Group: The Demystifying Lymphedema, its Management, and. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. . There is no better time to. The original IGTV videos from ConversationlyTWL: The Interview Series Vol. 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. . It entails. Find out more! Starting at $129. Menu. Thanks for the suggestions and advise Lymphie Strong. . Whoever said “Never meet your heroes” obviously wasn’t a lymphie. I quickly. . Elaine is part of a tribe I refer to as. Battling lymphedema is all about arming yourself with the right weapons to fight the disease. a book for students and teachers. . 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. com) in 2017 and your lymphedema virtual workout community. . 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. 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. 6,079 likes · 76 talking about this. . Honored and thrilled to announce that the Lymphedema Treatment Act is now a formal collaborative partner of the Lymphie Strong #lymphiestrong community. This is. Home of the #MOVETHATLYMPH. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Premier Partners. Karen Bellows Bingham, of the Lymphedema Association of Nova Scotia, shared the following helpful Canadian FB links. Learn more about her and Lymphie Strong at staylymphiestrong. Thanks . 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. S. June 11, 2020Carolyn Shearlock. 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. ️ Gave my site a mini makeover. Lymphedema Awareness Month for March 2022 has ended. It all started when I discovered my childhood hero, Princess Diana. ♥️ #lymphedema #CureLE”“My right leg was 200% bigger than my left leg. 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. com and established in 2015. Sign this important petition on behalf of lymphatic disease worldwide. Lymphie Strong. . Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. 2y. 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. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. 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. It is available to view now in the group. Lymphedema - support awareness . 懶 李#lymphedemaawarenessmonth #lymphiestrong #movethatlymph #lymphedema #linfedema #lymphoedema #livingwithchronicillness #livingwithlymphedema. Coast Guard #Repost @lymphietriathlete with @get_repost ・・・ #movethatlymph 5k run complete. (Hairbrush microphone optional. 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. There are loads of lymphie support forums/groups/blogs on Insta, FB, You Tube. Home of the #MOVETHATLYMPH. Lymphie Strong. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. This was quietly relaunched based on requests from several members. I have been dealing with a few for months and recently I have had. Wear light, loose, non-constricting clothing. 501 subscribers. #lymphedema #movethatlymph #lymphiestrong. Lymphie Strong Amy Rivera 1y Aria Health Amy Rivera 1y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. Best wishes . com and established in 2015. What began as. FREE delivery Friday, November 3 on orders shipped by Amazon over $35. Veronica has also traveled to Washington DC on different occasions to lobby Congress both as a member of the TX. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. . . Thanks . 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. 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. Now she is launching a NEW Facebook group called Primary Youth Support Group specifically for. . org • • #brylansfeat. . That's why I've…Storming in I was diagnosed with congenital Lymphedema a year and a half ago. LYMPHEDEMA GARMENT PROGRAM FOR ADULTS. . com and established in 2015. . . Listen to Amy Rivera, founder of Ninjas Fighting Lymphedema Foundation, share her incredible story on the latest episode on Lymphedema Podcast. . 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. 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. com and established in 2015. This young man was Veronica Seneriz, the founder of Lymphie Strong son CJ. Lymphatic self-help from Anita Bakke (Certified Lymphatic Therapist), and Dr. August 31, 2021. . • 1100 Burloak Drive, Ste. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. I developed lymphedema in 2015 as a result of endometrial cancer. #lymphedemaawarenessmonth ️Some lymphedema challenges are not always visible. March is Lymphedema Awareness. Get virtually inspired — and encouraged — through online fitness groups like Lymphie Strong Running & Fitness Club for Lymphedema. com) in 2017 and your lymphedema virtual workout community. . Every day is a new day to try again. This opportunity will enable me to pursue my passion for lymphedema patient. “So proud and honored to be part of this amazing team! My ♥️is full. Beth Busacca Dziminowicz. 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. 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. • 3690 Zorn Drive • Cuyahoga Falls, OH 44223 • Call: 1-888-255-1300. ’As a lymphedema patient, my dream is to build a community that the #lymphedema population truly needs. Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021. Blogger. . 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. 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. Be part of the change you want to see in the world. What began as. It was a pleasure being a guest on the Lympha Press #Lymphedema Patient Roundtable. 2. What began as. My oasis. 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. . 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. Lymphie Strong. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. 350 views 2 years ago. Log In. LYMPHEDEMA RESEARCH, STUDIES, AND TRIALS. A retrospective analysis of 105 subjects with. . An occurrence that can be very uncomfortable and even painful. What began as. Autumn Moon Virtual 5K completed by lymphietriathlete, a Veteran of the U. The National Library of Medicine. 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. Ask A CLT Exclusive Q&A for Lymphie Strong. Fast'n Go has not only transformed my own life but also countless others. 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. See more ideas about weight loss blogs, lymphedema, sugar busters. When expanded it provides a list of search options that will switch the search inputs to match the current selection. 5. Aim for fifteen or thirty minutes a day while wearing your compression. 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. Veronica runs several social media platforms for lymphedema and lipedema thrivers, caregivers, physicians, therapists. The power we have as a #lymphedemacommunity and a #lymphedemafamily is so strong and honestly invaluable to me. Julius Zorn, Inc. The venue was buzzing all weekend with excited chatter and inspired conversations between attendees and faculty. Thank you for your support! Together we reached 57,000 (FB) during the month of March for Lymphedema Awareness Month 2022. 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. Lymphie Strong aka Vern. Ever since I was 8 years old, I knew that I wanted to help people. Lymphie Strong Amy Rivera 1y Aria Health Amy Rivera 2y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. Recent Posts. Per a recent report by PWC, 44% of workers’ SKILLS will be disrupted in the next 5 years. com and established in 2015. 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. We are sponsored by the great. 300 • Burlington, ON L7L 6B2 • Call: 1-888-255-1300. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. Imagine how this made me feel on top of…Lymphie Strong… May 28, 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. 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. Hopefully the wraps up to the knee stay in place and are easy to put on/take off. Oct 8, 2019 - Join our brand new group called the Lymphedema Sugar Busters Support Group! Sugar fuels inflammation which fuels lymphedema. Wei Chen, MD, FACS, Professor of Plastic Surgery, Head, Regional. Feel…Juzo #MOVETHATLYMPH Spotlight ⭐️ Congratulations Justine!! She completed the 10 mile 2018 Blue Cross Broad Street Run hosted by the Philadelphia Parks. These muscles are located in your pelvis and…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. The best rule of thumb for the. I’d like to share it too. google Lymphie Strong, The Lymphie Life, Lymphedema Diary to learn about self-care and so much more. 🦋🎗 Speaking of inspiration, the panel was joined by special guest Veronica Seneriz, a lymphedema patient and founder of the blog and online community Lymphie Strong. . 4 Reactions. “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. I was not aware of some of that information. Verified account Protected Tweets @; Suggested usersSurround yourself with positive like-minded people now and in the year to come. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Lymphedema Guru. Lymphie Strong Exercise Series Cancer Rehab PT 25 videos 10,165 views Last updated on Dec 9, 2022 Play all Shuffle 1 11:38 Seated Lymphatic Exercise Flow. A4BC is a 501(3)c non-profit corporation. Wishing you great lymphatic heath, and I hope that you are pain and cellulitis free. . Standing up to Lymphedema with all of your faith, power, and might. Just today 18 have been sold. 4,640 Followers, 929 Following, 192 Posts - See Instagram photos and videos from Lymphie Strong | lymphiestrong. . 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. Especially why it's important to wear compression garments in hot weather. . In fact, all the online chats and blogs are replete with comments from people just like me, with late. What began as. Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong ( lymphiestrong. You can't stop the disruption. 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. Thanks, Vern Seneriz /. . We are sponsored by the great. Beautiful cover photo via Brylan’s Feat FoundationLymphie Strong. She is an avid…Lymphie Strong Amy Rivera 1y Aria Health Amy Rivera 1y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong.