. I also have lymphatic swelling of my abdomen, pelvis, chest & upper legs, although I wouldn’t classify it as classic lymphedema (I do have complete lymphatic obstruction in abdomen). 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. The Lymphie Life—Wonderful blog and compilation of information about lymphedema, written by a lymphedema patient who has struggled with the disease since infancy. . I’ll be adding a couple of new sections to it and making updated corrections. 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. Honored and thrilled to announce that the Lymphedema Treatment Act is now a formal collaborative partner of the Lymphie Strong #lymphiestrong community. . There is nothing joyful about having lymphedema, but today there is reason to be glad. ” (Via irishtimes. S. I have previously been misdiagnosed three times during this traumatic period. For women with lymphedema, getting assembled for the day is even more challenging. Thank you Juzo for sharing the vision early on and your support for two awesome years. “In Canada, there are numerous. Didi Okoh, 20, was diagnosed with. a book for students and teachers. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Whether you. Vern Seneriz, founder Lymphie Strong. I have been dealing with a few for months and recently I have had. See more of Lymphie Strong on Facebook. . . . Find out more! Starting at $129. Nonprofit Organization. We are sponsored by the great. 6,079 likes · 201 talking about this. . Lipedema causes pain and swelling, resulting in decreased mobility. . com and established in 2015. 501 subscribers. Stanford Medicine. Allows…Apply for the 2023 LE&RN/Lymph Notes U. ) However you want to do it, just do it. When expanded it provides a list of search options that will switch the search inputs to match the current selection. Every meal is an opportunity to fight inflammation or feed it. 懶 李#lymphedemaawarenessmonth #lymphiestrong #movethatlymph #lymphedema #linfedema #lymphoedema #livingwithchronicillness #livingwithlymphedema. 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. would give even Idina Menzel pause. . Be sure to like our Facebook page Lymphie Strong. Amy Rivera posted images on LinkedIn757 221 9519 [email protected] recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. La Jolla Cosmetic Podcast Kathleen Helen Lisson. 322 views, 16 likes, 5 loves, 0 comments, 2 shares, Facebook Watch Videos from Lymphie Strong: The Book of Lymph has arrived. 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. . 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 is available to view now in the group. com. - No compression necessary as the water provides it. What began as. What began as. Add eighty-plus-degree-heat and a bucket of humidity, and we are ready to. • 3690 Zorn Drive • Cuyahoga Falls, OH 44223 • Call: 1-888-255-1300. The swelling, the pain, the overwhelming sense of frustration can be so hard to bear at times. Hello Friends! Quick reminder on groups. The open groups are not confidential/private , so I always recommend joining a private group. Especially why it's important to wear compression garments in hot weather. 645 views, 23 likes, 6 loves, 11 comments, 6 shares, Facebook Watch Videos from Lymphie Strong: #TRANSFORMATIONTUESDAY “Lymphedema does not take a day off. “A relaxing and gentle course in yoga for people living with lymphoedema begins on January 19th in Dublin. . What began as. ’As a lymphedema patient, my dream is to build a community that the #lymphedema population truly needs. Elaine is part of a tribe I refer to as. We are sponsored by the great. . . Whether you. 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. Veronica runs several social media platforms for lymphedema and lipedema thrivers, caregivers, physicians, therapists. This opportunity will enable me to pursue my passion for lymphedema patient. . What began as. Many people believe dry brushing works for lymphatic drainage. . Thanksgiving has always been one of my favorite holidays of the year. 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. We would like to show you a description here but the site won’t allow us. A4BC Founder's Blog . Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. . It all started when I discovered my childhood hero, Princess Diana. She serves as Chair for the LE&RN Texas Chapter and is a member of the National Lymphedema Network LSAP Class of 2017. This is the latest book by Kathleen. Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. And now it's official here in New York thanks to the dedicated team from the Lymphatic Education and Research Network (LE&RN). Amy Rivera posted images on LinkedIn. 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. . 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. “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. 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. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. Read Veronica's story. I watched it when it was on and thought he looks familiar! 2. RonK1 Sep 15, 2016 • 1:45 AM. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Full Interview: It is not uncommon to go years or even decades without a lymphedema diagnosis. What began as. Create new account. There is a minimum of 31 required to print. 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. 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. . This is a great, supportive community! There are others too on social media sites, such as Lymphie Strong Inspiration Group on Facebook. Lymphie Strong proudly presents a hands on live demo and discussion of diaphragmatic breathing in the Lymphie Strong Running & Fitness Club called Diaphragm. Also, have you watched the donning video - there are some tips for securing the thigh piece (at 2min20seconds). 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. google Lymphie Strong, The Lymphie Life, Lymphedema Diary to learn about self-care and so much more. Lymphie Strong on Facebook is US based and has a huge membership. The power we have as a #lymphedemacommunity and a #lymphedemafamily is so strong and honestly invaluable to me. We are a very small but mighty group! One day lymphedema might be as. Aim for fifteen or thirty minutes a day while wearing your compression. In fact, all the online chats and blogs are replete with comments from people just like me, with late. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Lgarcia Oct 26, 2018 • 4:27 AM. 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. . Jul 2, 2021 - Explore Lymphie Strong's board "The Lymphedema Running & Fitness Club" on Pinterest. Stay positive. 2y. Herbst. Hope it. Log In. Lymphedema Awareness Month for March 2022 has ended. Log In. 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. We are different in our approach to lymphedema. 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. Be sure to like our FB page Lymphie Strong. Even in the face of adversity, those with lymphedema continue to persevere and inspire others with their strength and resilience. . Feelings of heaviness, tingling, numbness, skin tightness, pain, limited range of motion, and fatigue are common. Ask A CLT Exclusive Q&A for Lymphie Strong. ”. Shop recommended products from Lymphie Strong on Learn more about Lymphie Strong's favorite products. Little Miss Lucia's Lymphoedema Life. 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. com and established in 2015. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. 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. March 2018 The State of Lymphedema Awareness. It entails. Autumn Moon Virtual 5K completed by lymphietriathlete, a Veteran of the U. “Amy realized that this community needed a voice and. Causes less inflammation. Jennifer Conroyd is the founder of Fluid Running, a nationally recognized deep water exercise program. . #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. . 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. Nonprofit Organization. Sign this important petition on behalf of lymphatic disease worldwide. Shout out to all CLTs during #LymphedemaAwarenessMonth #lymphiestrong #movethatlymph #lymphedema #linfedema #lymphoedema #livingwithchronicillness #livingwithlymphedema. View 1 more reply. Ask A CLT Exclusive Q&A for Lymphie Strong sponsored by Monarch Continuing Education January 2020 – Truncal, Abdomen, & Genital Lymphedema TopicsThis video w. Whether you. com and established in 2015. The Lymphie Life. . Here is a list of Veronica's top compression garments and accessories to manage lymphedema. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. . Lymphedema Therapist Scholarship before August 14! Scholarships are awarded annually in memory of writer and lymphedema (LE) advocate Ann Ehrlich, who. Lymphatic Education & Research Network. 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. Home of the #MOVETHATLYMPH. . If you get overheated, elevate your affected limb and place a cold, wet towel over it. Be sure to like our Facebook page Lymphie Strong. . Lymphie Strong's Favorite Things. 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. 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. . 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. 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. com. Lymphie Strong, Katy, Texas. Hvala za darilce Medi. Me: I have lymphedema. Brylan’s Feat Foundation. 2y. There is no better time to. Follow #lipedemafitness on the #peloton leaderboard. Additional Media. For the. Be sure to like our FB page Lymphie Strong. . Be sure to like our Facebook page Lymphie Strong. Thank you for your support! Together we reached 57,000 (FB) during the month of March for Lymphedema Awareness Month 2022. - Use code LymphieStrong for 2 Free Workouts. LYMPHEDEMA RESEARCH, STUDIES, AND TRIALS. Lymphedema Awareness Month for March 2022 has ended. 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. 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. 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. I even wear them to the office. . 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. 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. Lymphie Strong Lymphedema 101 Cancer Rehab PT 51 videos 2,723 views Updated yesterday This playlist was created in collaboration with Lymphie Strong. Lymphie Strong. In reply to LymphieStrong's comment. com and established in 2015. 癩 Exclusive for Official Lymphie Strong Inspiration Group for Lymphedema. PODCASTS. Through lifelong adversity with my disability, I developed an activist mindset as I feverishly fought to better. . We are a global fitness group for people living with lymphedema by people living with lymphedema. Log In. I have been dealing with a few for months and recently I have had. 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. When: Dec 21, 2021 07:00 PM Eastern Time (US. “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. Make the decision to move forward and…The 2nd Annual Lymphie Strong Virtual Half Marathon begins March 1. 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. “Lymphie Strong Live Q&A with the BIDMC Lymphatic Center” Dr. Two. Be sure to like our Facebook page Lymphie Strong. As posted and shared yesterday, I have been working extremely hard behind the scenes on expanding Lymphie Strong this year. Fluid Running. And you’ll feel less isolated in having this disease. You have been dealing with LE for. We are sponsored by the great. 4 Reactions. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. When you post include the sizes of your legs and waist piece or you’ll be flooded with loads of messages asking sizes. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. 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. - No compression necessary as the water provides it. Be sure to like our Facebook page Lymphie Strong. The #LymphedemaAwarenessMonth celebration continues with the 5th Annual Lymphie Strong Virtual Half Marathon/10K/5K Race REGISTER NOW: Details from Lymphie Strong are. All of the makeup, hair and costume acrobatics performed on a daily basis before 7 a. It now has 2500 members world wide but mostly American Lymphies. . Home of the #MOVETHATLYMPH. . Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. 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. #StayElevated Hello! 👋 The Lymphie Life is currently undergoing updates, so you may see some funky formatting in the meantime. Juzo Canada, Ltd. 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. Cancel Call or Text Support 1. 3. . From the time my alarm clock goes off in the morning to the moment I shut my eyes at night, I am constantly. Whether you. One thing that makes me truly IRATE is the lack of options, tools or support in trying to change this. Check it out and let me know what you think. This was quietly relaunched based on requests from several members. Thanks, Vern Seneriz /. Fast'n Go has not only transformed my own life but also countless others. 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. See more of Lymphie Strong on Facebook. 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 Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management Engineering Soft 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. 🦋🎗 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. Be sure to like our Facebook page Lymphie Strong. Going to Stanford is a great idea, of course, they’re gold standard. Putting on and then wearing thick, tight compression stockings all day, every day is challenging enough. Our community is where we discuss general lymphedema topics such as complete/complex. Our aim to provide hope and understanding of the lymphatic system through knowledge and experience. Shelley Smith DiCecco of LymphEd. . Links and Resources. 2. 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. Welcome to our global patient advocacy and support group for lymphedema which belongs to lymphiestrong. Beth Busacca Dziminowicz. com and established in 2015. Thank you Juzo for sharing the vision early on and your support for two awesome years. Putting on and then wearing thick, tight compression stockings all day, every day is challenging enough. Amy Rivera posted images on LinkedInAre you always worried about what others think about you? Do you often find yourself stuck in the opinions and expectations of others? Well, it's time you…17 million Americans are estimated to be living with lipedema. . Be sure to like our FB page Lymphie Strong. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. m. How many of you have coexisting conditions that you battle along with lymphedema? I do. Post on a USA Lymphie page as this is UK based. Especially why it's important to wear compression garments in hot weather. Thanks for the suggestions and advise Lymphie Strong. Hugs, Catherine. . Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. Happy Veterans Day To all who have served and their families, we thank you for your service. Learn more about her and Lymphie Strong at staylymphiestrong. Learn more about her and Lymphie Strong at staylymphiestrong. I lived feeling alone for a long time. Beautiful cover photo via Brylan’s Feat FoundationLymphie Strong. There are 8 #MOVETHATLYMPH fitness. . 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. Karen L. 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. I quickly. We are so excited to be sponsoring the 2nd Annual Fluid Running® for Lymph Flow Challenge in August. • 1100 Burloak Drive, Ste. Ninjas Fighting Lymphedema Foundation . Almost all people living with lipedema are women. 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. Avoid salty foods for sane reason. edu 800-600-3606 NATIONAL LEADERS IN CANCER PATIENT EDUCATION How do you treat lymphedema? The goal of treatment is to reduce swelling and pain, toThe TREAT program is “Leading the Fight Against Lipedema” at the University of Arizona Health Sciences and led by Dr. Mar 12, 2021 Juzo Mar 8, 2021 Xpandasox Mar 6, 2021. 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. “Standing Up To Lymphedema with all of our faith, power, and might. 📚 Passing the Torch of Inspiration to My Team 🚀 Over 8 years ago, I was working at an unfulfilling 9-5 job. Thanks again. Lymphie Strong Amy Rivera 2y Aria Health Amy Rivera 2y Explore topics Sales Marketing Business Administration HR Management Content Management. Great workout for those with Lymphedema! - No impact. Want to feel like you don’t have lymphedema? September 12, 2013 Britta. Never stop asking questions. 2. 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. . #lymphiestrong #movethatlymph. 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. 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 am humbled beyond words to have been given such amazing opportunities by my Juzo family. I am proud and happy to announce the launch of the newest group. 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. Whether you have Lymphedema, or support someone that does, whether you can run, walk, do yoga, or Fluid Running (which you likely can), this is a great event, from Lymphie Strong and it’s amazing founder, Vern Seneriz. Lymphie Strong Mar 25, 2021 Aria Health Mar 18, 2021 Courage is telling your story. Welcome! Discussions around food, diet, recipes, grocery shopping, dining out, beverages, and supplements are welcomed. 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. 1 Reactions. You have been dealing with LE for quite a while and known many of the consequences. Order within 6 hrs 38 mins. . . . “Lymphedema is a common condition with global impact and a multitude of complications, however, only a few professionals specialize in its management. 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. 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. Per a recent report by PWC, 44% of workers’ SKILLS will be disrupted in the next 5 years. My shirt says “Don’t make me flip my witch 慄♀️ switch. . 6,079 likes · 76 talking about this. You’re always going places -physically, emotionally and spiritually. #MyFeetAreKillingMe #Lymphedema #LymphedemaCommunityThen I found the phenomenal Veronica of Lymphie Strong, a blog about not giving in.