For Lymphedema Awareness Month, we are donating to the Lymphatic Education and Research Network (LE&RN) to support the education and research of lymphedema and lymphatic disease. We are working with blogger Britta Vander Linden to make a difference. During the month of March, you can help us donate 1% of the total purchase price to LE&RN by using the coupon code “DONATE” at checkout.
Britta Vander Linden writes an inspiring blog about her experience with lymphedema. She was diagnosed with primary lymphedema when she was 23 years old. Since then, she has juggled a demanding job and keeping up with her blog, Lymphedema Diary.com, in her spare time. She was inspired to start a blog to connect with others struggling with the same illness. Her blog serves as a network for her and her readers to support and comfort one another. “I felt it was time to share my experiences with others in an effort to try to make their life easier. I hoped to make Lymphedema Diary the resource I wish I had when I was first diagnosed.” Each month, thousands of readers spanning across over 100 countries read her blog. Check out her inspiring story and get tips on how to manage lymphedema.
Before she started Lymphedema Diary, Britta turned to local support groups for help, but they didn’t regularly meet and were located at inconvenient places. A lot of them were made up on breast cancer survivors, so she had a hard time connecting with them because she didn’t feel like they were going through the same thing. Once she got involved on social media, she was able to connect with people all around the world to share tips on anything from finding good therapists to lymphedema management.
Her most recent addition to Lymphedema Diary is a new blog series called “A Leg Up: Compression Stocking Tips–What the Doctors Don’t Tell You.” Those with lymphedema use compression garments every day to manage their condition. Britta says, “No matter the difference in type or severity of lymphedema from one person to another, all of us are struggling to deal with compression garments. I think that’s why the series has been so popular.”
Britta has been a customer with us for about a year because we have all “Four P’s,” or what she refers to as the four key things every stocking dealer should have: people, price, perks and policies. Juzo Soft Pantyhose in 30-40mmHg is her go-to compression garment because of how soft the fabric is, and because they don’t look like compression tights. According to her, the fabric is very susceptible to snags, however. Britta also suggests the Juzo Dynamic Pantyhose for exercising because they are much more durable. The downside is that they aren’t as fashion-friendly as the Juzo Soft pantyhose, and the thickness of the fabric makes it harder to get the stockings off.
Some other things that Britta has found that help her to manage her lymphedema are regular exercise, getting a healthy amount of sleep, eating a low-sodium diet and staying hydrated. “If I don’t keep up on any one of these habits, I feel it in my legs. For exercise, I prefer swimming, yoga and anything that gets me lifting the legs up and down. In the winter, I enjoy snowshoeing.” She developed a few techniques that help keep her legs stay happy and healthy during a long day at work.
Check out Britta snowshoeing! This is one of her favorite ways to keep lymph fluid flowing in the winter.
When she was first diagnosed, she underwent six weeks of complete decongestive therapy (CDT). Although she is happy that she did this therapy on both of her legs, the process was exhausting. Between waking up early in the morning and the long commute before work, it wasn’t a good long-term solution. Overall, it was beneficial because she learned a lot about lymphedema care. One thing she doesn’t believe helped her was the acupuncture treatments she tried at about the same time.
There are hundreds of millions of people around the world who are suffering from lymphedema, but there is no cure. LE&RN has done an amazing job over the years in the advocacy, research and education of this condition. You can become a member for only $5 a month and help support the cause year-round. March is a very important month for spreading the word about lymphedema. Many doctors and patients do not know what symptoms to look for in the early stages of lymphedema. LE&RN is working to change this through education. Many people are not aware that the most common cause of lymphedema is cancer treatment. The removal of lymph nodes significantly increases your risk, but there are a couple of things that you can do after cancer treatment that can reduce your risk of lymphedema.
Thanks for reading!