Your favorite Allegro compression products are getting a new look. The stockings will NOT change, but we are very excited to announce redesigned packaging for Allegro. The new packages include illustrated donning instructions, a size chart, care instructions and some easy to understand icons on the front, that tell you a little about the stockings inside. We’re also reorganizing the products into two groups, Essential and Premium, and making a few name changes so the products are easier to find online. Product item numbers will remain the same. Our new packaging will roll-out slowly over the next few months, and you’ll also see a few new products being added.
Here are a few more details on the changes:
New organization! With the addition of so many new socks, we’ve organized the Allegro lines into “Essential” and “Premium”. Essential socks are your favorite everyday, low-cost socks. They’re durable, comfortable and won’t strain your wallet. Allegro Premium Socks are made from more luxurious materials, like Italian Cotton, and are priced a bit higher.
The dance names sadly, are dancing away. The Jig, Swing, Samba, Jazz, and Paso Doble were fun, but they didn’t describe the products very well. New product names will now be more descriptive. For example, the Allegro Jig Cotton Sock will now be called the Allegro Essential – Unisex Cotton Compression Sock.
The item numbers will NOT change. If your favorite sock is the #100 – it will still be the #100 on the new packaging and online.
New products! We listened to your feedback, and went on a hunt to find the best compression products available. We found premium sheer stockings, wool knee highs, an open toe cotton sock, and a super soft sock made with milk fibers. Details on these exciting new products will be coming soon.
Check out some of our new packaging artwork below and let us know what you think!
For our final giveaway in honor of Breast Cancer Awareness Month, you can win a Solidea compression armsleeve of your choice! We hope that promoting awareness about lymphedema will help to educate both patients and doctors. Many people develop this condition after undergoing cancer treatment, and others are born with it. Lymphedema can affect many parts of the body, but most common are swollen arms and legs.
The Washington Post recently released an article about a newborn twin who was born with lymphedema. The doctor could not figure out what caused the twin’s badly swollen legs. The mother, Heather Ferguson, was simply told to keep an eye on it to see if the symptoms got worse. “That was the worst moment,” she recalled. “It’s so horrible to know that something’s wrong and to get the brushoff. I felt like we were on our own and that the medical system had just washed its hands of us.”
When a doctor figured out that the baby was suffering from lymphedema (thanks to searching the Internet), Ferguson was told to go back to the pediatric surgeon, not a lymphedema therapist. The surgeon again just advised to keep an eye on it. Without treatment, people with lymphedema are prone to infections and can develop complications. Going untreated can also make everyday tasks very difficult if not impossible. It is extremely important to educate medical professionals and patients who are at risk about this condition to catch it early on before symptoms get worse.
Many people are unaware that they have lymphedema until it is already moderate to severe due to the lack of awareness and education about the condition. Hundreds of millions of people around the world suffer from lymphedema, yet many doctors know nothing about it and just brush symptoms off. While there is no cure for lymphedema, compression garments are used to manage and provide relief for symptoms.
BrightLife Direct wants to help promote education and awareness about this condition to better the lives of people suffering lymphedema and to get patients the treatment they need. You may have seen people posting #LymphedemaOnEllen videos on YouTube to help build awareness. We hope to see lymphedema on Ellen soon! You can check out our video above. Comment on our blog to share your favorite #LymphedemaOnEllen videos.
Solidea compression garments and shapewear are designed in Italy with fashion and function in mind. Many Solidea products are uniquely made using 3D Micro Massage technology that helps to stimulate lymphatic system. The 3D wave knit fabric expands and contracts on the skin to moveup to 78% of sluggish lymph back into circulation. The unilateral and bilateral sleeves benefit those who have a hard time wearing a traditional armsleeve because of constricting the upper arm. Graduated compression increases circulation to reduce swelling and fatigue.These products are breathable and are infused with silver ions to reduce the risk of infection as well as bacteria and odor to keep you comfortable and cool. All Soldiea compression armsleeves and gauntlets are made latex free.
To enter, log in with your email address or Facebook information below. Then, choose how you would like to enter: You can answer a question, leave a comment about the blog post, follow us on Twitter or tweet a message. Good luck!! Remember, you can enter once (per entry type) each day. The contest for the Solidea compression armsleeve ends Tuesday, November 3rd at midnight. The winner will be announced the following week.
Lymphedema never looked this good! For Breast Cancer Awareness Month, this week we will be giving away a LympheDIVAS compression armsleeve of your choice! See the giveaway box below to enter.
Many breast cancer survivors develop lymphedema after the removal of lymph nodes and have to wear a compression armsleeve every day for the rest of their lives. However, not all armsleeves have to be boring beige. LympheDivas was founded by two breast cancer survivors, Rachel Troxell and Robin Miller, who were not fans of the typical armsleeve. These amazing ladies decided to make compression fashionable. Instead of heavy, hot, rough textured armsleeves, they decided to make fun, comfortable sleeves to inspire breast cancer survivors to feel beautiful, confident and strong.
If you’re feeling crafty, you can make your own “designer” armsleeve too! Pick up a pair of girl’s patterned tights. Just cut off the tops and bottoms and slide them over the armsleeve. They’re a great, affordable way to spice up any outfit. Check out the video below for instructions. Have ideas of your own? Comment on this blog post to share how you express your style.
LympheDivas compression armsleeves are available in 15-20mmHg and 20-30mmHg compression levels. These seamless, lightweight garments feel like a “second skin” and provide 360° stretch to keep you comfortable. LympheDiva armsleeves are made with state-of-the-art moisture-wicking fabric to keep you cool and dry, as well as an infusion of unscented aloe vera to moisturize and soften skin. All sleeves come with the option to include the DIVA Diamond Band to help keep the garment in place. These gorgeous armsleeves are machine washable – just place them in a garment bag and use warm water and gentle detergent. Washing your sleeve frequently helps to sustain the effectiveness of the garment and prolong its lifespan. All LympheDiva armsleeves are made latex and silicone free in the U.S.A.
Here are some of our favorite sleeves inspired by Breast Cancer Awareness Month. This adorable Breast Cancer Awareness shirt is available from New York and Company for $9.95 and is made of 100% cotton. NY&C will donate $2 of each shirt to the Breast Cancer Research Foundation.
This week’s winner can choose any LympheDivas pattern, compression level and the optional DIVA Diamond Band. To enter, log in with your email address or Facebook information below. Then, choose how you would like to enter: You can answer a question, leave a comment about the blog post, follow us on Twitter or tweet a message. Click here for more help. Good luck!! Remember, you can enter once (per entry type) every day. The contest for the LympheDivas armsleeve ends Sunday, October 25th at midnight. The winner will be announced the following week. Don’t forget to check back next week for our last giveaway! a Rafflecopter giveaway
BrightLife Direct is excited to announce a new scholarship program for aspiring Lymphedema Therapists. Our staff wants to help lymphedema patients get the help and medical guidance that they need. With so few practicing lymphedema therapists available in the U.S., we understand this can be quite a challenge. This new scholarship program is designed to help aspiring students to meet their goals of becoming practicing lymphedema therapists and thus helping the customers we work with every day.
BrightLife Direct will provide $500.00 directly to the course tuition for any complete Lymphedema Certification Course that is listed on National Lymphedema Network. The deadline to enter this year’s scholarship is January, 31, 2016. Winners will be announced in February 2016. Scholarships will be awarded based on financial need, personal references and a personal essay.
To apply, you will need a completed application, a resume or curriculum vitae, official high school and/or college transcript as well as one or more letters of recommendation. You can get the details on the application process and eligibility requirements here. For more information, please contact us at 877-545-8585 at firstname.lastname@example.org.
Academy Award winner Kathy Bates has earned 40 wins and 68 nominations including Emmys, Golden Globes and an Oscar. Over the past year, Kathy has taken on a new project – becoming the Lymphatic Education & Research Network’s (LE&RN) National Spokesperson. After being diagnosed with ovarian and breast cancer, Kathy Bates underwent a bilateral mastectomy to remove 19 lymph nodes from her left armpit and three from right. She developed lymphedema shortly after and has to wear a compression armsleeve for the rest of her life unless a cure is found.
To help spread awareness of breast cancer and lymphedema this month, we are giving away an armsleeve each week. Check out the giveaway at the end of this post to enter for your chance to win.
Every day, Kathy connects with others suffering from lymphedema and their families by writing letters to thank them and comfort them. She has made great strides in building awareness and education. She recently spoke at a two-day NIH symposium that took place on September 29-30. Bill Repicci, Executive Director of LE&RN, believes that this conference is a turning point in the field of lymphatics.
In her speech, “Lymphedema: The Human Side,” Bates explains that she was shocked to find out that millions of people suffer from lymphatic diseases, not just breast cancer survivors. Many people are born with it or develop it later in life. With about 10 million Americans and hundreds of millions worldwide, it is surprising that most primary physicians haven’t heard of this condition. To make matters worse, many people are not even aware they have lymphedema and suffer in silence. Without treatment, lymphedema symptoms can get worse and infection may occur, which can cause serious complications.
Many doctors who are aware of lymphedema don’t understand the severity of the condition, brushing it off as a “cosmetic issue” or blame symptoms on obesity or other causes. One woman suffered for eight years before being diagnosed with stage 3 lymphedema. Another patient, Marie Apodaca, was told by her doctor that she had to lose weight. She wasn’t diagnosed until she was accidentally hit with a cardboard box on her leg, which caused a clear liquid to drain out of her leg instead of blood. After months of therapy, Marie was able to remove 35 lbs of lymph from her legs.
Managing symptoms is no walk in the park either. Finding a lymphedema therapist isn’t easy. Since there aren’t many, it can be hard to find one that’s available or is located in your area. This can result in long commutes, which can aggravate symptoms. Zalee Harris who suffers from severely swollen arms can’t get regular treatments because of a long waiting list, causing her to be in more pain.
LE&RN focuses on raising awareness and education, but even more so, encouraging people to stop hiding their condition and share their story. Kathy took the Face of Lymphedema Challenge to inspire people to find comfort by sharing stories and to know they’re not alone. Dancer Pearl-Ann Hinds developed LE and decided to choreograph a dance dedicated to lymphedema called “Hello World.” She says “If I continued to hide the reality, the power to change the legs of future generations would be lost.”
Seven-year-old Emma Detlefsen was born with lymphedema in both legs and often battles infections that cause her to be hospitalized. This inspiring seven-year-old appeared before the NY State Legislator last year and convinced lawmakers to pass a bill for research funding that had been languishing for 12 years. She was awarded with the LE&RN Youth Ambassador Award on September 19th at the 5K Walk to Fight Lymphedema & Lymphatic Diseases on the Brooklyn Bridge. Kathy hopes that by bringing Emma’s message to us, it can inspire “even one of us” to accomplish her challenge and hopes you will join the fight for education and research.
Mediven Harmony Armsleeve Giveaway
For Breast Cancer Awareness Month, each week we will be giving away a compression armsleeve. Every week, we will feature a different brand. This week, you can win a Mediven Harmony armsleeve in your choice of compression level, size and color. To enter, log in with your email address or Facebook information below. Then, choose how you would like to enter: You can answer a question, leave a comment about the blog post, follow us on Twitter or tweet a message. To tweet the message, click the “Tweet” button then go to your profile. Click on the timestamp on the tweet and paste the url in the box below. Click here for more help. Good luck!! Remember, you can enter once (per entry type) every day. The contest for the Mediven Harmony armsleeve ends Friday, October 16th at midnight. The winner will be announced the following Monday. Don’t forget to check back next week for our next giveaway!
October is Breast Cancer Awareness Month. This month, BrightLife Direct will be spreading awareness about a condition that many breast cancer survivors face after a mastectomy – lymphedema. This condition refers to mild, moderate or severe swelling (edema), and is often caused by the removal of lymph nodes during cancer treatment. Blockage in the lymphatic system results in the buildup of lymph fluid, which is why swelling occurs.
Lymphedema can develop in the legs, arms and other parts of the body. Some people are born with this condition and others develop it. Approximately 10 million Americans suffer from lymphedema. Breast cancer survivors who develop lymphedema have to wear compression garments over their arms and hand everyday to increase circulation to help manage their condition.
In addition to sharing information on lymphedema this month, we will be doing a weekly giveaway in honor of the many brave Breast Cancer survivors. See below for more information and your chance to win!
Today we want to share information and updates on the Lymphedema Treatment Act.
According to lymphedema specialist, Sue Enerson, many of her patients who are covered by Medicare are only allowed one visit after being diagnosed with lymphedema and more often than not, compression garments are not covered. The financial burden on lymphedema patients is huge. Patients often require frequent visits to doctors and lymphedema therapists to receive treatment and also to learn how to manage lymphedema at home. Patients must also purchase a supply of compression garments to wear continuously, for the rest of their lives, which comes at no small cost.
The Lymphedema Treatment Act is a federal bill that will improve insurance coverage for treatment, mandating that insurance companies provide the medical supplies to patients that are required to manage lymphedema symptoms (including compression garments, bandages, etc.). This in turn will reduce the total healthcare costs associated with lymphedema by reducing the number of complications and disabilities that result from poor treatment of lymphedema symptoms. Currently, most insurance policies including Medicare do not cover lymphedema treatment.
Seniors who suffer from lymphedema should not be punished for taking the necessary steps to treat their condition,” said Reichert. “By rectifying Medicare’s failure to cover compression garments we give seniors their best chance and real hope to fight back against this chronic disease. I am pleased to be joined by my colleagues from both sides of the aisle in this fight against lymphedema. – Congressman Reichert
On March 26, 2015, the Lymphedema Treatment Act was introduced to the current Congress, including a “Findings” section to explain the need for medical coverage. Treatment for lymphedema includes manual lymphatic drainage, wearing compression garments and Complete Decongestive Therapy (CDT), which the bill will make the standard of care for lymphedema.
The Lymphedema Treatment Act currently has over 100 cosponsors. BrightLife Direct as well as many other compression garment companies are showing their support for the Lymphedema Treatment Act. Compression garment makers Sigvaris, Jobst, Medi, Juzo, Solaris and LympheDIVAS also support the bill.
While there is no cure for lymphedema yet, compression garments help to provide relief. Every Friday during the month of October, we will be hosting a giveaway to win the featured armsleeve of the week. To kick of Breast Cancer Awareness Month, this week we are offering a Juzo Soft Compression Armsleeve. Juzo Soft is available in six different colors as well as a variety of new colors for fall and winter. Juzo Soft Armsleeves are available in three compression levels and in a variety of sizing options. Winners can choose the color, compression level and size. Don’t forget to keep checking our blog for your chance to win!
You can enter below by logging in with an email address or through Facebook and following BrightLife Direct on Twitter, answering a question, commenting on the blog post or by tweeting a message in the giveaway box below. To tweet the message, click the “Tweet” button, then go to your profile. Next, click on the timestamp on the tweet and paste the url in the box below. Click here for more help.