Dysautonomia Hacks and Facts Giveaway!

Dysautonomia Awareness Month Hacks And Facts From BrightLife Direct!

In honor of Dysautonomia Awareness Month this October, here’s your official spoonie guide, complete with tips and information to educate your friends, families and doctors. Plus, enter to win a $50 gift card in honor of Dysautonomia Awareness Month. See below for entry and details.


FACT: Dysautonomia symptoms can include lightheadedness, fatigue, fainting, blood pooling in the extremities, brain fog, chest pain, heart palpitations, nausea, migraines, shortness of breath and more.

HACK: Laying down or wearing compression socks can provide relief for some symptoms of dysautonomia. Many POTS patients have difficulty standing, so laying down can help your body improve the blood flow and reduce symptoms. A proper diet and exercise regimen can also help regulate symptoms.


FACT: Dysautonomia is an umbrella term for disorders of the Autonomic Nervous System (ANS), which helps to maintain the ideal blood pressure and body temperature, controls your heart rate, breathing, sleep cycles and digestion. Many dysautonomia patients look “normal” because their symptoms are invisible.

HACK: Educate others about the symptoms of dysautonomia and be aware of your own. The severity of symptoms varies between patients. Keep track of medications that work or don’t work, activities that provoke symptoms and note how your body reacts to different situations, so you can stay in control of your symptoms.


about dysautonomia


FACT: Over 70 million people worldwide have developed various forms of dysautonomia. A common form of dysautonomia is Postural Orthostatic Tachycardia Syndrome (POTS), which can be found in people of all ages and genders. POTS impacts an estimated 1-3 million Americans, and is most often found in women.

HACK: The most important thing to remember is that you are not alone. Get involved with a local support group or volunteer with an organization like Dysautonomia International or participate in Dysautonomia Awareness Month activities to help fundraise to find a cure.


FACT: Dysautonomia is a relatively unknown condition to doctors and patients.

HACK: Find a doctor or a specialist who is knowledgeable about Dysautonomia or autonomic disorders. It’s important to work with someone who can determine the most appropriate medications for you to effectively manage your symptoms, and who can answer any questions you may have. Finding a doctor who can create an individualized treatment plan is crucial. You can click here to find a doctor near you.


Spoon Theory - Dysautonomia Awareness Month


FACT: Although Postural Orthostatic Tachycardia Syndrome (POTS) is not a rare condition, it is frequently misdiagnosed. The average diagnosis can take almost six years.

HACK: Participate in Dysautonomia Awareness Month this October to educate patients, doctors, friends and family about this condition. Share your story or get involved with organizations like Dysautonomia International and support research to find a cure.


FACT: There is no cure for Dysautonomia.

HACK: Adapt your lifestyle to assure your symptoms do not get worse. Remember to wear compression socks to prevent blood from pooling in your legs and relieve the dizziness or lightheadedness from orthostatic hypotension. Get organized, fight off stress as much as possible, and eat lots of lean proteins, fibers, fruits and vegetables. A high sodium diet of about 2-4 grams of salt a day is recommended, along with increasing your fluid intake to about 2-3 liters of water each day. Refrain from consuming refined sugars and caffeine as much as possible. Make sure you are staying active as much as your symptoms allow and are getting a good night’s sleep. Most of all, stay positive!


Have some great tips and tricks of your own? Comment below to share!


ENTER TO WIN OUR DYSAUTONOMIA AWARENESS MONTH GIVEAWAY!

To win, follow the rules below and participate in Dysautonomia Awareness Month for your chance to win. Just comment on this post or share it on social media. Good luck!

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Breast Cancer Awareness Month Giveaway!

Breast Cancer Awareness Month Giveaway Contest

Here at BrightLife Direct, our customers are very important to us. Each day, we talk with people who have been diagnosed with lymphedema and hear not only their questions, but their struggles. Lymphedema is commonly overlooked by doctors and can go undiagnosed for a very long time. Many people battling breast cancer are unaware that lymphedema can be a side affect to treatment and are unprepared for managing this condition. It can also be hard to obtain the resources needed to manage lymphedema due to a lack of regional availability of therapists and the financial cost. Since there is no cure for lymphedema yet, patients must wear a compression armsleeve everyday which can be costly, especially depending on the severity of the swelling.

The BrightLife Direct Armsleeve Assistance Program

BrightLife Direct Komen Armsleeve Program for LymphedemaIn light of this, BrightLife has partnered with the Susan G. Komen Foundation to provide compression armsleeves to those who may not otherwise be able to afford it. We will be providing free compression sleeves to patients at six different Komen grantee organizations here in Washington, D.C. These awesome organizations will help the patient measure for the correct fit and find the best armsleeve to help manage their symptoms. They will then send this information to us, and we ship out the armsleeve free of charge the same day. Check out Francia, pictured on the left, happily showing off her new compression armsleeve!

Enter Our Breast Cancer Awareness Giveaway!

You can win! In honor of Breast Cancer Awareness Month, BrightLife Direct wants to give back to the lymphedema community. To help others with the financial burden of lymphedema, we are offering a $100 gift card for one lucky winner to choose any armsleeve or compression stockings of their choice! See below for entry and details.

lymphedema fashion compression armsleeves and compression socks

Lymphedema Style Guide

BrightLife Direct offers tons of compression armsleeves in a variety of sizes, colors, patterns and fabrics so you can find the perfect sleeve for you. If beige isn’t your style, we have lots of fun patterned armsleeves like LympheDivas and the new Juzo Signature Prints. The Juzo Dream Collection offers armsleeves and lower extremity compression garments in fun seasonal colors and tie-dye patterns. If you’re looking for eye-catching patterned leggings, try the new Juzo Soft Print Leggings, available in a large variety of patterns. Check out our style guide below for our customer’s favorite lymphedema options:


Lymphedema Compression Garments for Fashionistas

Mild to Moderate Lymphedema Garments

Moderate to Severe Lymphedema Garments

Lymphedema Compression Wraps

Juzo Soft Fashion Compression Socks and Lymphedema Armsleeves

Sizing Help

If you’re shopping on your own and don’t know your size, check out our Size Machine! Just enter your measurements and we’ll tell you what fits you best in all of the major brands. If you still have questions or would like some help deciding, please contact our customer service team.

You Can Win!

The rules are simple – the more you share, the more likely you’ll win! You can comment on this blog post to share your experience with Breast Cancer or Lymphedema, or share this post on social media. For details, see the Rafflecopter Contest Box below. Good luck!

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Can I wear compression stockings swimming?

This blog was originally posted in July of 2014, but it’s a question we are asked often at this time of year, so we felt a refresh and re-post was in order.

It’s summertime, which means pools are open, and people are fleeing to the beach every weekend to escape the heat. For those of us that have to wear compression stockings from morning to night, this can be a difficult time of year.

beach sceneI was excited to see one of my favorite lymphedema bloggers, Monique at LymphedemaRunner.com, addressing the issue in a blog post.  Monique admits to being self conscious about wearing her stockings to the beach and pool at first, but found strength and inspiration in watching CrossFit Athlete Deborah Cordner Carsen proudly rocking her Elvarex stockings during a Triathlon.

Definitely check out the blog above to read more about Monique’s experience wearing compression to the beach and pool. Here are the basic FAQs on compression and water activities:

1. You CAN wear your compression stockings in the ocean, lake, pool or other water source. But, all of these environments will be hard on your stockings – causing them to deteriorate more quickly than regular daily use. We recommend setting aside a set of stockings or armsleeves specifically for water activities. These could be an older pair that you’re not worried about destroying, or a less expensive garment that won’t be a huge monetary loss (like Allegro).

2. If you will be submerged completely in water for most of your water excursion, you don’t need your stockings or sleeves. The pressure on your body under water actually replicates what your compression garment does outside of water. If you go without your compression garment, do make sure your affected limb will be under water and put the garment back on quickly after leaving the water. If your affected limb is not submerged in the water, you should be wearing your compression garments.

3. As always – stay hydrated. Being in the sun at the beach or pool may leave you dehydrated. Pack plenty of water!

Some additional information on water activities and lymphedema can be found on LymphNotes.

Lastly – a few product recommendations. If you have just one affected leg, you might try the Juzo Varin 3511 Thigh w/Hip Attachment and Open Toe – available in 20-30 or 30-40 or 40-50 mmHg. Sigvaris offers a similar option in 20-30 mmHg and 30-40 mmHg in the 862 line.

CrossFit superstar Deborah Cordner Carsen recommends the Jobst Elvarex, which is a custom order product.

And – if you’re looking for something that’s very durable and affordable, the Allegro Surgical Weight Line is a great option!

Do Compression Stockings Make Your Legs Itch?

Itching is universal.  Everyone, at some point, has to scratch an itch.

There are so many things that make us itch, besides wearing compression stockings, that determining and eliminating the cause is almost impossible.  Xerosis or dry skin makes us itch.  Allergies, fungal infections, and insect bites can make us itch.  Skin conditions like psoriasis and eczema can cause severe itching.  Even scratching can make us itch more.  Repetitive scratching produces a thick, often slightly darker area of skin, that itches even more.  A topical cream with capsaicin or corticosteroid may be required to break the itch-scratch-itch cycle.

Completely eliminating the itch from compression stockings may not be possible, but you may be able to reduce the severity by moisturizing.  We sell several creams and gels that do a great job of moisturizing your skin, and there are many dermatologist recommended pharmacy brand lotions that do a good job too.  I have very dry and sensitive skin, plus eczema and psoriasis, and have found Cerave lotion does the best job of keeping my skin type moisturized.  I slather it on from head to toe in the morning after I shower, and at night before bed.  In the morning, I try to moisture at least 15-20 minutes before donning my stockings so the lotion has time to be absorbed.  Consistency is important.  If I miss a day or two, my skin starts to itch again, with or without compression stockings.

This regimen won’t work for everyone, but if your legs itch when you wear compression socks, give it a try for a few days to see if it helps you.

The First World Lymphedema Day!

BrightLife Direct Supports World Lymphedema Day

We are so excited to share the highlights from the very first annual World Lymphedema Day. March 6 is dedicated to honor lymphedema patients and this year, this great day was made official by the US Government. World Lymphedema Day is meant to promote awareness to this condition and show appreciation to everyone who is affected by lymphedema. More than 150 million people suffer from lymphedema worldwide and it is time that we find a cure.

One of the leaders in lymphedema advocacy, the Lymphatic Education & Research Network (LE&RN), led the effort to officially dedicate March 6th as World Lymphedema Day. This organization strives to raise awareness and educate people about this condition and has worked side by side with Kathy Bates to get the voices of lymphedema patients heard.

Senators Chuck Schumer and Chuck Grassley introduced a Resolution to the US Senate to recognize March 6th as World Lymphedema Day. Many lymphedema patients shared their stories and talked about how they were celebrating the day, urging others to spread the message.

Many people are aware of the fight against cancer, but few know that many breast cancer survivors develop lymphedema as a result of treatment. Others are born with it. Lymphedema can develop in the arms or legs and symptoms range from mild to severe. With so many people suffering from this condition, it is surprising that so few doctors are aware of it. This results in many patients going un-diagnosed for much of their life, and their symptoms worsening without proper treatment.

March is Lymphedema Awareness Month. We urge you to take some time to learn more about lymphedema, talk about it with your friends and family, and see how you can help make a difference this month. To show our support, we are giving away one Juzo Soft compression garment of your choice! The winner can choose one of the following in any size, color and compression level: knee highs, thigh highs, pantyhose, leggings, gauntlet, glove or armsleeve.

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Relief for Ankle Pain!

If you experience pain or swelling in your ankles, we have some great tips and products to help you feel better, fast. Ankle pain is most often caused from a sprain, osteoarthritis, tendinitis, gout, stress fracture or an injury. Symptoms of ankle pain can include numbness or tingling, swelling, redness, weakness and stiffness.

TREATMENT

Rest:

Try to stay off your feet for a while. The less stress you put on your ankle, the better. With most pain and injury, giving your body a break and a little TLC is all it needs to heal. For more serious injuries or ongoing pain, you may want to look into daily or weekly regimens to help manage and treat your pain.

Ice and Elevation:

At the end of the day or when you have the time, prop your ankle up above heart level with pillows or on the back of the couch. Putting ice on your ankle for about 20-30 minutes a few times a day will help reduce the swelling and pain. For an injury, the swelling should go down in a couple of days and depending on the severity, the pain should subside within a week or two at the most.

Ankle Braces:

If you are experiencing pain, it is important not to push yourself. The more stress you put on your ankle, the longer it will take to heal and you will increase your chances of it becoming a more serious complication. It is important to support your ankle with an ankle brace or wrap to help it heal, prevent injury and get relief.

MalleoTrain Ankle Brace by Bauerfeind

MalleoTrain Ankle Brace by Bauerfeind

To reduce ankle pain and swelling, try out the MalleoTrain ankle brace. It has won several awards for design and functionality.

This knit brace has two cushions on the inner and outer ankle bones that massages the ankle joint as you walk and helps to support and stabilize your ankle.

If you are injured, have osteoarthritis or recently had surgery, this brace will help you get relief. The MalleoTrain ankle brace is available in three different colors and is great for everyday wear.

 

PREVENTION

Make sure you are wearing comfortable and supportive shoes, especially when you are exercising or plan on doing a lot of walking.  If you notice tenderness in your ankle or you have been more active than usual, take a couple of minutes to stretch.
Orthosleeve FS6 Compression Foot SleeveIf you have suffered from an ankle injury in the past, it is extremely important to make sure your ankle is supported. If you are exercising, try wearing a foot sleeve or an ankle brace to protect and prevent injury.

If you’re looking for a foot sleeve to wear everyday or while exercising that isn’t bulky, check out the OrthoSleeve FS6 Compression Foot Sleeve. It can be worn under your normal socks or shoes and is safe to wear overnight. It is made from a lightweight, moisture-wicking fabric and helps to relieve symptoms of Plantar Fasciitis, Achilles Tendonitis, swollen feet, heel spurs and chronic arch or heel pain.

If you have tried numerous remedies to reduce the pain and swelling and have had no luck, make sure you see a doctor immediately, especially if you can’t put much weight on your ankle.

BROWSE ANKLE BRACES AND WRAPS

If you have tips on relieving ankle pain or have questions about prevention or treatment, comment below!

Lymphedema on Ellen + Armsleeve Giveaway!

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.

solidea-blog-giveaway

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.

CMYK baseSolidea 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.

SHOP SOLIDEA

New Lymphedema Therapist Scholarship Program

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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 scholarship@brightlifedirect.com. 

Click Here To Apply Now

 

Lymphedema Treatment Act Update + 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.

How can you help? Contact your members of Congress to make sure they support the bill. Learn more here: http://lymphedematreatmentact.org/

Win A Prize Every Week!

juzo-soft-bc-giveaway

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.

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RESOURCES

Breast Cancer Navigator

Shop Lymphedema Products

Managing Lymphedema

Kathy Bates – Life With Lymphedema

March is Lymphedema Awareness Month

Sigvaris Supports the Lymphedema Treatment Act

Congressman Reichert’s Involvement in Reintroducing the Bill

Invisible Illness Awareness Week 2015

Dysautonomia and POTS – Invisible Illness Awareness Week

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Dysautonomia refers to a number of conditions that describe the breakdown or failure of the autonomic nervous system (ANS). The ANS regulates unconscious or involuntary body functions, including the cardiovascular system, metabolic system and more. To diagnose Dysautonomia, a tilt-table test is used to evaluate how the patient regulates blood pressure regarding stressful events.

Some of the most common Dysautonomia symptoms include blood pressure changes, fast heart rates, anxiety, dizziness, lightheadedness, stomach pain, mood swings, migraines and insomnia. For some people with Dysautonomia, getting out of bed can even be a struggle. For others, travel may be limited or nonexistent. These symptoms can be mild or severe and may even seem “invisible” to someone who doesn’t know what to look for. Patients with Dysautonomia may have symptoms that come and go, some caused or enhanced by stress.

Over a million Americans suffer from a primary autonomic system disorder. One of the most common conditions is Postural Orthostatic Tachycardia Syndrome (POTS). Others include Neurocardiogenic Syncope (NCS), Orthostatic Intolerance (OI), Vasovagal Syncope, Neurally Mediated Hypotension (NMH), Multiple Systems Atrophy (MSA), Post-Viral Dysautonomia, Pure Autonomic Failure (PAF), Familial Dysautonomia (FD), Non-Familial Dysautonomia and Generalized Dysautonomia.

With so many people affected by this condition, you would think that there would be tons of information on it. However, there is not. After researching POTS and Dysautonomia resources, some of the most helpful information was found on personal blogs. The biggest thing to take away here is that your voice matters. With limited information and scientific research, personal experiences and advice are sometimes the best things to rely on. That is why Invisible Illness Awareness Week is so important. It builds and strengthens a community of people who are fighting to be heard.

As of now, there is no cure for Dysautonomia. To relieve symptoms, many patients turn to physical therapy, drinking lots of fluids, increasing sodium intake as well as limiting the amount of caffeine and sugary drinks that consumed. You can check with your doctor about getting medication to relieve more severe symptoms and determine what the best option would be for you. There is also a new treatment called TVAM, or Transvascular Autonomic Modulation, to improve the autonomic function in patients.

Wearing compression socks can also help alleviate symptoms to improve circulation in the body which helps to decrease lightheadedness, dizziness and normalize the heart rate and blood pressure. Compression socks also help to reduce the amount of pooling blood, swelling and fatigue and to prevent blood clots and varicose veins. Compression socks are also recommended for exercise and traveling, especially if you’re flying. If you have Dysautonomia and have a hard time traveling, wearing compression socks could be your secret weapon to getting back on the road or in the gym. Compression garments are available in knee high, thigh high and waist high options in a variety of compression levels, colors and sizes.

The most important thing to remember is that you are not alone. There are tons of people who are suffering from an invisible illness too. With the help of bloggers, support groups and organizations, together we can bring awareness to these conditions. Share your story and join the #invisiblefight today.

Invisible Illness Awareness Week is extremely important to share the unheard voices of so many people who are suffering. Many people struggle with undiagnosed or rare conditions that many medical practitioners are unaware of. The good news is, you can help make a difference. Starting September 28 – October 4th, share your stories or those of loved ones to promote awareness about rare conditions. You can also spread the word by participating on social media by including #InvisibleIllness in your posts. What do you fight for?

Additional Resources:

Invisible Illness Awareness Week

October is Dysautonomia Awareness Month

Lauren Stiles – Dysautonomia 101

Best POTS and Dysautonomia Blogs

Compression Socks

Dysautonomia Symptoms

Lifestyle Adaptions for POTS