The stretch allows the tissue to open the lymphatic gaps encouraging re. This weekend I followed the Live Tweets of The Lymphie Life at the Fat Disorders Research Society, Inc. . We are sponsored by the great. I am forever grateful for those there as well as there in spirit (the lovely @lymphiestrong & @camronayala ) as well as throughout the world!!!! A post shared by 🦋 The Little Lymphie 🦋 (@thelittlelymphie) on Aug 26, 2019 at 10. Be sure to like our Facebook page Lymphie Strong. ” — By. . Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. . Be sure to like our FB page Lymphie Strong. com) in 2017 and your lymphedema virtual workout community. Welcome to the page if you just found us this year!! 朗 Many of you are new to Lymphie Strong while others have been following the page for over. ) However you want to do it, just do it. Be sure to like our FB page Lymphie Strong. Through lifelong adversity with my disability, I developed an activist mindset as I feverishly fought to better. 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 to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Feel…Juzo #MOVETHATLYMPH Spotlight ⭐️ Congratulations Justine!! She completed the 10 mile 2018 Blue Cross Broad Street Run hosted by the Philadelphia Parks. We are a support group for reducing it as much as we can in our lives. 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. SamLymphie 4 months ago. 797 views, 7 likes, 0 loves, 1 comments, 87 shares, Facebook Watch Videos from Geriatrics Infolinks Management Strategies Inc. Founder of the Lymphie Strong Social Channels and Blog. Premier Partners. 300 • Burlington, ON L7L 6B2 • Call: 1-888-255-1300. 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. Home of the #MOVETHATLYMPH. #lymphedemaawarenessmonth ️Some lymphedema challenges are not always visible. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. Whether you. 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. . org. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Mrs Kathleen Helen Lisson Swollen, Bloated and Puffy: A manual lymphatic drainage therapist's guide to reducing swelling in the face and body $2999. 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. 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). Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Just today 18 have been sold. . . Lymphie Strong Amy Rivera 1y Aria Health Amy Rivera 1y Explore topics Workplace Job Search Careers Interviewing Salary and Compensation. 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 |. Thanks for your support in following. “In Canada, there are numerous. 3. This entailed visits to various medical specialists at the same time accumulating an exorbitant amount of medical bills for my parents. If we don’t make the 31, your money will. Ask A CLT Exclusive Q&A for Lymphie Strong. Together we can find a cure. . Lymphedema Awareness Month for March 2022 has ended. Help us break a record. 645 views, 23 likes, 6 loves, 11 comments, 6 shares, Facebook Watch Videos from Lymphie Strong: #TRANSFORMATIONTUESDAY “Lymphedema does not take a day off. When you are a lymphie, heat is a four letter word. Luis López Montoya The positive affirmations on the wall read: Risk To Win Follow Your Passion Know Your Skills. 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. The Doctor's TV Show interview part 1. Healthy Habits for Patients at Risk for Lymphedema - NLN Position Paper • Healthy Lifestyle • Skin Care • Medical Check-ups • Infection Education • Avoid Possible Triggers Battle Your Lymphedema with Toe Caps. 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’d like to share it too. or I am humbled and honored to announce that I have accepted the role of National Lymphedema Network Social Media Manager. Lymphie Strong March 7 at 3:56 AM # lymphedemaawarenessmonth Body image is a combination of the thoug. Additional Media. Be sure to like our Facebook page Lymphie Strong. When you are a lymphie, heat is a four letter word. . Lymphie Strong is a closed group so just request to join. 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. Lymphedema Guru. “Amy realized that this community needed a voice and. The Lymphie Life is a patient-run blog that aims to educate, connect, and support fellow lymphedema patients and. orI am humbled and honored to announce that I have accepted the role of National Lymphedema Network Social Media Manager. RonK1 Sep 15, 2016 • 1:45 AM. 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. Especially why it's important to wear compression garments in hot weather. 322 views, 16 likes, 5 loves, 0 comments, 2 shares, Facebook Watch Videos from Lymphie Strong: The Book of Lymph has arrived. We are sponsored by the great. 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. Whether you. That's why I've…Storming in I was diagnosed with congenital Lymphedema a year and a half ago. If you get overheated, elevate your affected limb and place a cold, wet towel over it. Lymphie Strong aka Vern. Cheers to us ️ We did it. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. . Follow #lipedemafitness on the #peloton leaderboard. The venue was buzzing all weekend with excited chatter and inspired conversations between attendees and faculty. Log In. 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. Read Veronica's story. As posted and shared yesterday, I have been working extremely hard behind the scenes on expanding Lymphie Strong this year. Now she is launching a NEW Facebook group called Primary Youth Support Group specifically for. We prioritize their education, both academically and socially. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. Learn more about her and Lymphie Strong at staylymphiestrong. There is a minimum of 31 required to print. jaz sem čisto v stilu . 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. #TrainingTuesday 露 ♀️ ♀️ Hey Friends! It’s Training Tuesday and time to #movethatlymph with cardio! Check out this month’s new FREE video from Cancer Rehab PT YouTube! @cancerrehabpt. 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 |. - Anyone can do it. So take a look around, check ’em out — you’re sure to find a wealth of information, experiences, and support within the online lymphedema community! Vern Seneriz, founder Lymphie Strong. 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. Verified account Protected Tweets @; Suggested usersResearch Roundup: Summer 2021 Edition. . It now has 2500 members world wide but mostly American Lymphies. Find out more! Starting at $129. Hopefully the wraps up to the knee stay in place and are easy to put on/take off. Thanks for the suggestions and advise Lymphie Strong. Battling lymphedema is all about arming yourself with the right weapons to fight the disease. Two. Thanks . The best rule of thumb for the. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. Welcome to the page if you just found us this year!! 朗 Many of you are new to Lymphie Strong while others have been following the page for over. Check out her favorite things below: See more of Lymphie Strong on Facebook. She may be a good resource too. . Hope others offer better advice than I can. I am proud and happy to announce the launch of the newest group. Join us every Wednesday through Nov 3, 2021. June 11, 2020Carolyn Shearlock. What began as. Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong ( lymphiestrong. Welcome to our first ever Lymphie Strong Lymphatic Surgery Lightning Round Q&A featuring Dr. Best wishes . At the heart of our photo is Ms. 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. It seems hard to believe there aren’t more LE specialists or therapists in the Bay Area. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Whoever said “Never meet your heroes” obviously wasn’t a lymphie. . ” Via. This is the latest book by Kathleen. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. Our traveler! Great to see you Ramon. Many people believe dry brushing works for lymphatic drainage. Whether you. I love running at. Wei Chen, MD, FACS, Professor of Plastic Surgery, Head, Regional. . The venue was buzzing all weekend with excited chatter and inspired conversations between attendees and faculty. The only prerequisite is having LE. 懶 李#lymphedemaawarenessmonth #lymphiestrong #movethatlymph #lymphedema #linfedema #lymphoedema #livingwithchronicillness #livingwithlymphedema. Normally I do not do this, but Jann has been a member since March 2017. 300 • Burlington, ON L7L 6B2 • Call: 1-888-255-1300. The Lymphie Life is a patient-run blog that aims to educate, connect, and support fellow lymphedema patients and advocates across the globe. March is Lymphedema Awareness. VOTE FOR THE EURORDIS Social Media Award 2023 Let’s help one of our own put LYMPHEDEMA on the map in Brussels. Skip to content. My shirt says “Don’t make me flip my witch 慄♀️ switch. . Check it out and let me know what you think. Thanksgiving has always been one of my favorite. What began as. This free zoom webinar is a great opportunity to learn more about the pelvic floor hosted by Lymphie Strong and Dr. . March is around the corner! Are you ready for World Lymphedema Day and Lymphedema Awareness Month 2023 ⭐️拾朗. . A4BC is a 501(3)c non-profit corporation. 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. Order within 6 hrs 38 mins. Post on a USA Lymphie page as this is UK based. Our groups are open to all living with lymphatic disease, their spouses, caregivers, families, clinicians, and others who support our community. 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. Light refreshments and snacks are provided. Aim for fifteen or thirty minutes a day while wearing your compression. We would like to show you a description here but the site won’t allow us. Conversationaly: Thriving w/ 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. There are loads of lymphie support forums/groups/blogs on Insta, FB, You Tube. Ninjas Fighting Lymphedema Foundation. Lymphie Strong on Facebook is US based and has a huge membership. Thanks for sharing. Great workout for those with Lymphedema! - No impact. “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. ” (Via NBC Bay. Whoever said “Never meet your heroes” obviously wasn’t a lymphie. “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. 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. orIn this conversation. Amy Rivera posted images on LinkedIn. You’re always going places -physically, emotionally and spiritually. The National Library of Medicine. Be sure to like our Facebook page Lymphie Strong. Our routines include more than. - Anyone can do it. 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. 🦋🎗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. . I’ll be adding a couple of new sections to it and making updated corrections. Create new account. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. 4,640 Followers, 929 Following, 192 Posts - See Instagram photos and videos from Lymphie Strong | lymphiestrong. . com and established in 2015. Log In. My Lymph Node. Stay positive. It is available to view now in the group. Jun 14, 2021 - Discover (and save!) your own Pins on Pinterest. Book Reviews:World Cancer Day reminds us all that we all are together in this fight against cancer and we must conquer it together. 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. . THIS! Something magical happens when you BELIEVE!I had the privilege to work with ResMed on a #lymphedema project a few years ago. . . You will find loads of good support and sharing of information on coping with LE. 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. Hugs, Catherine. . It’s generally done on dry skin before bathing. Related Pages. Not all heroes wear capes. What began as. LE&RN's Chapter Chairs & Special Projects Director who advocate for fighting lymphatic diseases across the country and globally. . Home of the #MOVETHATLYMPH Challenges founded by Lymphie Strong (lymphiestrong. Lymphatic Education & Research Network. From the time my alarm clock goes off in the morning to the moment I shut my eyes at night, I am constantly. 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. I even wear them to the office. Cathleen Donovan. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. 4 Reactions. . “So proud and honored to be part of this amazing team! My ♥️is full. Whether you. Welcome to our first ever Lymphie Strong Lymphatic Surgery Lightning Round Q&A featuring Dr. What began as. Get Fast, Free Shipping with Amazon Prime. Be part of the change you want to see in the world. Be sure to like our Facebook page Lymphie Strong. Happy Veterans Day To all who have served and their families, we thank you for your service. The Lymphie Strong Running & Fitness Club has reached a milestone 2,500 members from 80 countries thanks to the support of Juzo for our 2020. com and established in 2015. Advertisement. The Lymphie Life. My supervisor at the time handed me a book that…🚀 Fast'n Go: Remarkable Post-Surgical Results! 🚀 Discover the game-changing bandage that's revolutionizing post-surgical outcomes and volume reduction in lymphedema management!Lymphie Strong Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management Engineering Soft Skills. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. An international share via group Limfedem Slovenija. Learn more about her and Lymphie Strong at staylymphiestrong. com. This opportunity will enable me to pursue my passion for lymphedema patient. We are different in our approach to lymphedema. We are proud to announce that BrightLife has teamed up with Veronica, founder of Lymphie Strong! We are working together to promote. . Big hugs to my Dad in heaven who gave his blessing to start this blog which became an entire platform that reaches 25K and 176 countries around the world. It entails videos on the major components of lymphedema treatment, including lymphatic draina. Thank you for your support! Together we reached 57,000 (FB) during the month of March for Lymphedema Awareness Month 2022. We are a global fitness group for people living with lymphedema by people living with lymphedema. What began as. Veronica runs several social media platforms for lymphedema and lipedema thrivers, caregivers, physicians, therapists. Menu. 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. 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. . #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. 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. Juzo Canada, Ltd. 1 Reactions. Founder Veronica Seneriz — a lymphedema patient and advocate herself — has a. 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. . This is a great, supportive community! There are others too on social media sites, such as Lymphie Strong Inspiration Group on Facebook. The Lymphie Life. Nicole Faccio, known on social media as Facciolita, was born in Puerto Rico and. 2K members. Thanks again. As the meeting’s keynote speaker, actress Kathy Bates, put it, “Because ‘you’re’ successful, ‘we’re’ surviving, and now we need your help, to educate not. Be sure to like our Facebook page Lymphie Strong. La Jolla Cosmetic Podcast Kathleen Helen Lisson. Beth Busacca Dziminowicz. Our aim to provide hope and understanding of the lymphatic system through knowledge and experience. VIDEO: To Dry Brush, or Not to Dry Brush? That is the Question. 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. August 31, 2021. Mark Melin for having me on LymphCast! I'm truly blessed to have the opportunity to share…As you probably know, not every garment you buy for lymphedema will work. 癩 Exclusive for Official Lymphie Strong Inspiration Group for Lymphedema. Mary Al-Saleh (CLT, BS, MS, NP, PhD Nursing). This young man was Veronica Seneriz, the founder of Lymphie Strong son CJ. 2. - On your schedule, at your pace. If you’re on Facebook an excellent support group is Lymphie Strong Inspiration Group. Lymphie Strong hosts Kathleen Lisson, Author of the Southern California Plastic Surgery Cookbook. “Standing Up To Lymphedema with all of our faith, power, and might. Herbst. Jul 2, 2021 - Explore Lymphie Strong's board "The Lymphedema Running & Fitness Club" on Pinterest. Be sure to like our FB page Lymphie Strong. Thanksgiving has always been one of my favorite holidays of the year. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. The pace of change is unreal. . 📚 Passing the Torch of Inspiration to My Team 🚀 Over 8 years ago, I was working at an unfulfilling 9-5 job. #lymphiestrong #movethatlymph. It’s a closed group (easy to request membership) but very well administered and hugely supportive practically and emotionally. Slow, deliberate exercise can often be more beneficial than going "hard" in the long run - especially for lymphedema. The marker is not found in obesity. 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 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. . There are 8 #MOVETHATLYMPH fitness. . Whether you. Be sure to like our Facebook page Lymphie Strong. 350 views 2 years ago. What began as. What began as. . 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. Wishing you great lymphatic heath, and I hope that you are pain and cellulitis free. 5. And you’ll feel less isolated in having this disease. com and established in 2015. This opportunity will enable me to pursue my passion for lymphedema patient. It entails. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. . Never stop asking questions. You are always one decision away from a totally different life. 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. Allows…Apply for the 2023 LE&RN/Lymph Notes U. . 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. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. 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. . . Also, the knee piece is put on last in this video. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. . Two of my favorite ladies, Peggy Warny & Kathleen Lisson talk about the Lipedema Treatment Guide. - Use code LymphieStrong for 2 Free Workouts. Our goal is to provide guida…When lymphedema goes unmanaged, tissues become more fibrotic—or thick—due to a buildup of protein-rich fluid. S. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. This organization recently changed its name from the Lymphatic Research Foundation and expanded its mission after 15 years of providing hope, inspiration and progress to the. Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021. . WELCOME TO THE LYMPHIE STRONG MOVE THAT LYMPH CHALLENGE SERIES FOR 2023 sponsored by JUZO USA & CANADA Next is our Hero Challenge - For the first time ever…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. A4BC Founder's Blog . ” Happy Halloween everyone Be safe. 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. Dry brushing involves using a brush with stiff bristles to rub the skin. We are sponsored by the great. Log In. Beth Busacca Dziminowicz. The swelling, the pain, the overwhelming sense of frustration can be so hard to bear at times. 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. It has Loads of excellent info and links to Lymphie blogs as well as web symposiums. Lose toxicity. 2y. . FREE delivery Friday, November 3 on orders shipped by Amazon over $35. Add eighty-plus-degree-heat and a bucket of humidity, and we are ready to. The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. 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. At any time. . This is. ” No truer words have been spoken. Lymphedema - support awareness . 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. 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. Verified account Protected Tweets @; Suggested usersSurround yourself with positive like-minded people now and in the year to come. m. Stanford Medicine. Learn more about her and Lymphie Strong at staylymphiestrong.