Listicles National Salsa Month 2022

<div class="listicle"><h2>5 Sizzling (and Saucy) Salsa Facts</h2><ol><li><div><h3>It's so spicy they named a dance after it</h3><p>Salsa, the dance, actually takes its name from the real thing in order to emphasize the spiciness of the moves. It's a robust mix of Hispanic, Caribbean, and African dance styles.</p></div></li><li><div><h3>Rooster beak salsa? Really?</h3><p>Yes, Pico de gallo literally means rooster beak salsa. Perhaps because this chunky salsa was eaten with the thumb and forefinger that resembled a pecking rooster!</p></div></li><li><div><h3>Holy Jalapeño!</h3><p>Every year Pace Foods uses 22 million pounds of fresh jalapeno. That's more than any other salsa company in the U.S!</p></div></li><li><div><h3>Get the right tools</h3><p>Traditionally, salsa is prepared with a mortar and pestle made from black volcanic rock. These are used to puree the tomatoes and chilies with other ingredients.</p></div></li><li><div><h3>Relish and salsa are sisters</h3><p>Relish, like salsa, is a condiment used to increase the flavor of foods and can be eaten cooked or raw. The difference is that the word 'relish' is French and 'salsa' is Spanish. European sisters!</p></div></li></ol></div><p>Tip: <a href="https://meongo.net/50-off-fabricville-promo-codes/">Fabricville discount codes</a>: Up to 50% Off Sitewide. Flyer Sale Now On - Get Up to 50% off online for all your fabric needs. #FabricvilleCoupons#FabricvillePromoCodes</p><p><a href="https://www.retailmenot.com/view/fabricville.com">Fabricville promo codes</a>: 50% Off Fabricville Promo Codes, Coupons May 2022</p><div class="content"><p>Here’s the spicy truth behind salsa. It’s no ordinary condiment. It’s an ancient Aztec recipe that was revealed to the world through the written word of a Franciscan missionary. One who had lived with the Aztecs and learned their ways. So let’s treat National Salsa Month, in May, with reverence. Bow to this ancient recipe and give in to our taste buds. Try out as many different types of salsa as you can. Trust us, the month will end but you will not run out of new and tasty recipes to try. That’s how hot salsa is all over the world.</p></div><p>Note: <a href="https://meongo.net/state-line-tack-promo-codes/">State Line Tack discount codes</a>: Lowest Prices of The Season During Spring Sale. Shop the Spring Sale for lowest prices of the season. No Code Necessary.#StateLineTackCoupons#StateLineTackPromoCodes</p><p><a href="https://capitaloneshopping.com/s/statelinetack.com/coupon">State Line Tack promo codes</a>: State Line Tack Promo Codes, Coupons May 2022</p>

Listicles National Salsa Month 2022

5 Sizzling (and Saucy) Salsa Facts It's so spicy they named a dance after it Salsa, the dance, actually takes its name from the real thi...

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Why Do We Celebrate National Taffy Day?

<div class="whyhow"><h2>National Taffy Day Activities</h2><ol><li><div><h3>See it get made</h3><p>Watching taffy being made is not to be missed! Most taffy factories offer guided tours so that you can see how taffy is heated in huge copper kettles, and then slowly cooled by hand on cold marble slabs and then put on a machine that now does the pulling.</p></div></li><li><div><h3>Indulge in a taffy binge</h3><p>Gorging on candy for National Taffy Day might not seem like the best advice, but then again it is the custom for other holidays (not naming any names)… so having a few taffies is a great way to celebrate!</p></div></li><li><div><h3>Make your own</h3><p>The best way to celebrate National Taffy Day is to actually make your own! Not only is this a fun activity, but it also means that you will have a good supply of taffy to give out to your friends and family. Look up a recipe on the web and get cooking (and pulling.)</p></div></li></ol></div><div class="whyhow"><h2>Why We Love National Taffy Day</h2><ol><li><div><h3>We love to watch it get made</h3><p>Not only is taffy a delicious candy, enjoyed by all ages, but making it is also a real upper body workout! Nowadays taffy is made by machines, but in the past, or if you are making it at home, you use the ‘taffy pull’ to add air to the taffy mixture. This is what gives taffy its distinctive texture.</p></div></li><li><div><h3>It makes us nostalgic</h3><p>We love that tasting taffy takes most Americans back to childhood memories of blissful summers by the sea. As taffy is traditionally sold at boardwalks, it has been a staple of American seaside resort towns for over one hundred years.</p></div></li><li><div><h3>The flavors are endless</h3><p>Taffy has survived the test of time because of its unique texture, which comes in almost every flavor imaginable; from vanilla, maple, mint and watermelon, to raspberry, banana and licorice… or anything else you can think of!</p></div></li></ol></div><p>Tip: <a href="https://stcouponcodes.com/closet-clothing-coupon-codes/">Closet Clothing coupon codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Closet Clothing Coupon Code: PINK (59 People Used)</p><p><a href="https://www.retailmenot.com/view/closetlondon.com">Closet Clothing coupon codes</a>: Closet Clothing 20% Off Pink Edit</p><div class="content"><p>On May 23, we celebrate our favorite sweet and chewy treat on National Taffy Day. Taffy has a long history as one of America’s native sweets. Common lore has it that in the 1880s, a Jersey Shore candy shop got flooded, soaking the shop’s taffy stock with Atlantic salt water. On a lark, the owner sold the candy as “saltwater taffy” and an American delicacy was born! Today it’s sold on boardwalks up and down the Eastern seaboard of the U.S. and has even found its way to landlocked candyshops. National Taffy Day is a day to indulge in the sweet pastime of unwrapping that twisty wax paper and popping a chewy bit of taffy into your mouth. Yum!</p></div><p>Note: <a href="https://stcouponcodes.com/the-tool-nut-coupon-codes/">The Tool Nut discount codes</a>: No coupon code needed. Tap to shop the sale now.</p><p><a href="https://capitaloneshopping.com/s/toolnut.com/coupon">The Tool Nut discount codes</a>: The Tool Nut $20 Off $100 Select Bosch Products</p>

Why Do We Celebrate National Taffy Day?

National Taffy Day Activities See it get made Watching taffy being made is not to be missed! Most taffy factories offer guided tours so that...

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Cystic Fibrosis Awareness Month 2022

<p>Tip: <a href="https://9promocodes.net/allen-brothers-promo-codes/">Allen Brothers promo codes</a>: Get Free Prime Steakburgers With $179+ Purchase.. Allen Brothers Promo Code: FRIDAY15 (-1 People Used Today)</p><p><a href="https://www.retailmenot.com/view/allenbrothers.com">Allen Brothers promo codes</a>: Allen Brothers Today Only! Free Prime Steakburgers With $179+ Purchase</p><p>May is Cystic Fibrosis Awareness Month. Across the world, thousands of volunteers will come together to raise awareness about this devastating disease and tell our story of hope and progress.</p><p>You can join them. Take time this month to share your CF story and encourage people in your community to join the search for a cure.</p><h2>Consider these facts:</h2><ul><li>Approximately 30,000 children and adults in the United States have CF.</li><li>More than 10 million Americans are symptomless carriers of the defective CF gene.</li><li>CF used to be considered exclusively a childhood disease. Thanks to advancements in CF research and care, people with the disease are living into their 30s, 40s and beyond.</li><li>The life expectancy for someone with CF has doubled in the last 30 years, but people still lose their lives to this devastating disease every day.</li><li>The CF Foundation will not rest until we find a cure for all people with cystic fibrosis.</li></ul><h2>What you can do:</h2><p><strong><br></strong>As someone who is interested in advocating on behalf of people with cystic fibrosis, you have a powerful voice. Here’s what you can do to help support the CF community.</p><ul><li>Check out the official “<a>CF Awareness Toolkit</a>” to get tips, tools, and language that you can use to help spread the word.</li></ul><h2>Learn more about:</h2><ul><li>Participating in <a>Great Strides</a>;</li><li><a>Becoming an advocate</a> and contacting members of Congress on behalf of people with CF; and</li><li>Talking about CF in your social networks, including <a>Facebook</a>, <a>Twitter</a> and <a>Instagram</a>.</li></ul><p>Take some time this month to educate someone about CF or encourage people in your community to get involved. It only takes a few minutes to make a difference.</p><p>Note: <a href="https://9promocodes.net/franklin-planner-promo-codes/">Franklin Planner discount codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Franklin Planner Promo Code: BUYSELLPLAN (24 People Used Today)</p><p><a href="https://capitaloneshopping.com/s/franklinplanner.com/coupon">Franklin Planner coupon codes</a>: Franklin Planner 15% Off Select Items</p>

Cystic Fibrosis Awareness Month 2022

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Ehlers-Danlos Syndrome Awareness Month 2022

<p>Tip: <a href="https://top1promocodes.com/smocked-auctions-promo-codes/">Smocked Auctions coupon codes</a>: Free Shipping on Your Order. Smocked Auctions Promo Code: SATREAT. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#SmockedAuctionsCoupons#SmockedAuctionsPromoCodes</p><p><a href="https://www.retailmenot.com/view/smockedauctions.com">Smocked Auctions discount codes</a>: Smocked Auctions Promo Codes, Discount Codes May 2022</p><p>Are you living with Ehlers-Danlos syndrome? Do you know someone who is? If so, then it’s time to get ready for the eponymous month, raising awareness for people across the globe with this rare and difficult-to-diagnose condition.</p><p>For years, the medical community has struggled to identify patients with this set of syndromes correctly. There’s a drive to highlight the symptoms of the condition, raise money, educate the public, and fundraise for those affected. </p><p>Ehlers-Danlos syndromes are a collection of more than thirteen hereditary disorders that affect the connective tissue throughout the body. People with the condition have mutations of specific genes that affect the ability of cells to create proteins to construct joints in the usual way. These syndromes, therefore, result in symptoms such as chronic pain, fragile skin, the ability to flex joints beyond the normal range, and rupturing of internal organs. While many of the effects of the disorder are mild, some can be life-threatening and require immediate hospitalization. </p><p>People with Ehlers-Danlos syndrome historically struggled to obtain accurate diagnoses. Many of the symptoms closely resemble those of other more common diseases, causing doctors to make incorrect diagnoses. At root, Ehlers-Danlos syndromes are genetically heritable. So in an era marked by a lack of DNA testing, an accurate diagnosis was difficult. </p><p>Recently, however, there has been substantial progress towards classifying and identifying the conditions. In 2017, researchers published more than eighteen papers in the Journal of Medical Genetics, clarifying the different varieties of the disease and better characterizing their properties. The Ehlers-Danlos Society added to the body of research and publicly-available information by releasing a review of the research materials, backed by more than ninety experts. It was the first significant update for more than twenty years. </p><p>The result of this effort is a considerably improved understanding of the syndrome at the scientific level. The challenge is to filter the information out to medics, schools, and the public at large. </p><h2>History of Ehlers-Danlos Syndrome Awareness Month </h2><p>Before 1997, researchers classified Ehlers-Danlos Syndrome into ten specific types, based on specific genetic mutations associated with symptoms (such as connective tissue issues). As genetic testing improved, however, the number of Ehlers-Danlos-type syndromes began to expand, with more than thirteen currently classified. </p><p>The rationale for Ehlers-Danlos Syndrome Awareness Month, however, isn’t as straightforward as calling for more accurate DNA tests. Many researchers believe that medical science is only just scratching the surface of syndromes related to the original set. Genetic testing, therefore, may not detect all instances of the disease. Some mutations may be so rare that there are just a handful of people affected by them throughout the world. In some cases, a person presenting with Ehlers-Danlos-like symptoms may be the only example. </p><p>There is a need, therefore, to pay close attention to the clinical manifestations of the condition, not just testing. Individual patients may present with all the hallmarks of the syndrome, but DNA procedures for the most common varieties of Ehlers-Danlos may not provide confirmation. </p><p>The Ehlers-Danlos Society ran the first Ehlers-Danlos awareness month in 2006. Since then, the organization has worked tirelessly to improve the public consciousness of the condition by supporting people around the world with the syndrome. In 2017, the society attempted some branding and social media outreach under the “Dazzle Together” hashtag. </p><p>The story behind the name for the campaign is interesting. Traditionally, medics called patients presenting with Ehlers-Danlos syndromes “zebras,” a reference to the medical school mantra “when the hoofbeats, think horses, not zebras.” The original saying inculcated trainee doctors in the idea that they should proceed with the most obvious diagnosis first – the horse – and only investigate less clear-cut symptoms afterwards – the zebra.</p><p>The problem for Ehlers-Danlos patients is that <em>they are zebras</em> – they have a rare disease. So applying the standard medical school wisdom doesn’t help them. In fact, it is counterproductive. </p><p>The “dazzle” part of the hashtag comes from the traditional way of referring to a group of zebras as a dazzle. Thus, the “Dazzle Together” campaign was born. And now, the community works together to improve awareness of the condition, raise funds for research, and reach out to the public over social media. </p><p>There are a lot of different people involved in Ehlers-Danlos Syndrome Month. Patients, health professionals, charities, donors, and caregivers all work to get the critical message discussed here out to the public. The Ehlers-Danlos Society provides brochures, posters, digital presentations, and instructions for members for how to best make use of their time. </p><h2>How to celebrate Ehlers-Danlos Syndrome Awareness Month </h2><p>So how do you get involved and show your support for the people who must currently live with Ehlers-Danlos Syndrome? It turns out that there are loads of things that you can do. </p><p>The first thing that you can do is join forces with the Ehlers-Danlos Society. Most years, the organization runs so-called “challenges” where people engage in various community events to raise money. Many of these events are fun and designed to suit individual interests. Some of the official events organized by the charity include things like dressing up as zebras, lectures, and coffee mornings. </p><p>Of course, you don’t need to join in with the official events to celebrate the month. There are plenty of things that you can do as an individual to do your bit for the EDS community. </p><p>Perhaps the best way to show your support is to donate money. Currently, there is a massive research effort underway to understand the condition better and find treatments. With further research, it may be possible to undo the genetic mutations that cause the syndrome and help people take back control of their health. We will have to wait and see.</p><p>There’s also a need for further education of the general public, people who work in schools, and the medical community. Rare genetic diseases tend not to get the same level of attention or support as more common conditions, so they require outreach. </p><p>Failing that, you can always dress up as a zebra!</p><p>Note: <a href="https://top1promocodes.com/free-people-promo-codes/">Free People coupon codes</a>: Free Express Shipping. Free People Promo Code: N838DYZ3MM6. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#FreePeopleCoupons#FreePeoplePromoCodes</p><p><a href="https://capitaloneshopping.com/s/freepeople.com/coupon">Free People discount codes</a>: Free People Promo Codes, Discount Codes May 2022</p>

Ehlers-Danlos Syndrome Awareness Month 2022

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Asian Pacific Heritage Month 2022

<p>Tip: <a href="https://zonecouponcodes.com/15-off-photojannic-coupons/">Photojannic coupon codes</a>: 15% Off Your Restoration Order. Photojannic Coupon Code: APRO. Get 15% Off your restoration order. Expires on 04/30/2015.#PhotojannicCoupons#PhotojannicPromoCodes</p><p><a href="https://www.retailmenot.com/view/photojaanic.com">Photojannic discount codes</a>: 15% Off Photojannic Coupons & Promo Codes May 2022</p><p>May is Asian/Pacific American Heritage Month – a celebration of Asians and Pacific Islanders in the United States. A rather broad term, Asian/Pacific encompasses all of the Asian continent and the Pacific islands of Melanesia (New Guinea, New Caledonia, Vanuatu, Fiji and the Solomon Islands), Micronesia (Marianas, Guam, Wake Island, Palau, Marshall Islands, Kiribati, Nauru and the Federated States of Micronesia) and Polynesia (New Zealand, Hawaiian Islands, Rotuma, Midway Islands, Samoa, American Samoa, Tonga, Tuvalu, Cook Islands, French Polynesia and Easter Island).</p><p>Like most commemorative months, Asian/Pacific American Heritage Month originated with Congress. In 1977 Reps. Frank Horton of New York introduced House Joint Resolution 540 to proclaim the first ten days in May as Pacific/Asian American Heritage Week.</p><p>In the same year, Senator Daniel Inouye introduced a similar resolution, Senate Joint Resolution 72. Neither of these resolutions passed, so in June 1978, Rep. Horton introduced House Joint Resolution 1007. This resolution proposed that the President should “proclaim a week, which is to include the seventh and tenth of the month, during the first ten days in May of 1979 as ‘Asian/Pacific American Heritage Week.’”</p><p>This joint resolution was passed by the House and then the Senate and was signed by President Jimmy Carter on October 5, 1978 to become Public Law 95-419 (PDF, 158kb). This law amended the original language of the bill and directed the President to issue a proclamation for the “7 day period beginning on May 4, 1979 as ‘Asian/Pacific American Heritage Week.’”</p><p>During the next decade, presidents passed annual proclamations for Asian/Pacific American Heritage Week until 1990 when Congress passed Public Law 101-283 (PDF, 166kb) which expanded the observance to a month for 1990. Then in 1992, Congress passed Public Law 102-450 (PDF, 285kb) which annually designated May as Asian/Pacific American Heritage Month</p><p>The month of May was chosen to commemorate the immigration of the first Japanese to the United States on May 7, 1843, and to mark the anniversary of the completion of the transcontinental railroad on May 10, 1869. The majority of the workers who laid the tracks were Chinese immigrants.</p><p>This site presents only a sample of the digital and physical holdings related to Asian/Pacific heritage available from the Library of Congress and other participating agencies.</p><p>Executive and Legislative Documents<br>The Law Library of Congress has compiled guides to commemorative observations, including a comprehensive inventory of the Public Laws, Presidential Proclamations and congressional resolutions related to Asian Pacific Heritage Month.</p><p>Note: <a href="https://zonecouponcodes.com/25-off-eform2290-coupons/">eform2290 coupon codes</a>: 25% Off Form 2290 HVUT. eform2290 Coupon Code: 25TY2021. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#eform2290Coupons#eform2290PromoCodes</p><p><a href="https://capitaloneshopping.com/s/eform2290.com/coupon">eform2290 promo codes</a>: 25% Off eform2290 Coupons & Promo Codes May 2022</p>

Asian Pacific Heritage Month 2022

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Lyme Disease Awareness Month 2022

<p>Tip: <a href="https://www.weontech.com/looking4parking-promo-codes/">Looking4Parking coupon codes</a>: Exclusive! Up to 15% Off Your Order. Looking4Parking Promo Code: AWUSRMN15. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#Looking4ParkingCoupons#Looking4ParkingPromoCodes. » Looking4Parking Promo Codes</p><p><a href="https://www.retailmenot.com/view/looking4.com">Looking4Parking coupon codes</a>: Looking4Parking Promo Codes, Coupons May 2022</p><p>The natural world is a beautiful place, and not always the friendliest place around. Could be why we spent thousands of years making it so we didn’t have to go outside. One such danger is Lyme Disease, and for those who spend time out in the wild (especially campers and hunters) it’s a danger they face every time they get an unwanted passenger in the form of a tick. Lyme Disease Awareness Month reminds us to be vigilant, and to spread awareness to help save lives.</p><h2>History of Lyme Disease Awareness Month</h2><p>Lyme disease is a potentially life-altering illness that is caused by bacteria transmitted from the bite of a tick. Unfortunately, the incidence of Lyme Disease is on the rise throughout the Western Hemisphere, as tick populations are expanding due to climate change. To combat this spread, many people participate in <strong>Lyme Disease Awareness Month</strong>, and help educate the public about the symptoms and cause of Lyme Disease. Many regions and municipalities organize events and fundraisers to raise funds for research, and people wear green ribbons or replace their porch lights with green bulbs.</p><p>It is important to educate people about Lyme Disease, because it is often misdiagnosed. Early symptoms can include a rash, fever, headaches and fatigue. If the disease is left untreated, it can result in joint and heart problems, chronic pain, and cognitive problems such as difficulties concentrating or remembering things. As with many diseases, treatment is more effective if Lyme Disease is diagnosed early. Needless to say it’s absolutely vital that awareness is spread and people learn how to protect themselves, their families, and their pets from this potentially dangerous disease.</p><h2>How To Celebrate Lyme Disease Awareness Month</h2><p>If you have nature lovers in your family, make sure that they’re aware of the dangers involved with being bitten by ticks. Educate yourself and those you love about how to dress to minimize tick bites, as well as what to do when one is received, and what to watch out for that may indicate early signs of Lyme Disease.</p><p>The natural world is a wonderful place and we all want to be able to get out and spend more time in it, make sure you educate your friends and family on how to do it safely. Lyme Disease Awareness Month is the perfect time to organize flier campaigns, and remind everyone to be just a little more alert for ticks.</p><p>Note: <a href="https://www.weontech.com/nature-s-sleep-promo-codes/">Nature's Sleep discount codes</a>: 5% Off Your Order. Nature's Sleep Promo Code: ST8271NS82B. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#Nature'sSleepCoupons#Nature'sSleepPromoCodes. » Furniture » Bedroom Furniture » Mattress » Memory Foam Mattress » Nature's Sleep Promo Codes</p><p><a href="https://capitaloneshopping.com/s/naturessleep.com/coupon">Nature's Sleep promo codes</a>: Nature's Sleep Promo Codes, Coupons May 2022</p>

Lyme Disease Awareness Month 2022

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Ehlers-Danlos Syndrome Awareness Month 2022

<p>Tip: <a href="https://bestpromotionalcodes.com/online-outdoor-closeouts-promo-codes/">Online Outdoor Closeouts promo codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Online Outdoor Closeouts Promo Code: CAMP10 (27 People Used Today)</p><p><a href="https://www.retailmenot.com/view/onlineoutdoorcloseouts.com">Online Outdoor Closeouts coupon codes</a>: Online Outdoor Closeouts $10 Off Orders of $100 Or More</p><p>Are you living with Ehlers-Danlos syndrome? Do you know someone who is? If so, then it’s time to get ready for the eponymous month, raising awareness for people across the globe with this rare and difficult-to-diagnose condition.</p><p>For years, the medical community has struggled to identify patients with this set of syndromes correctly. There’s a drive to highlight the symptoms of the condition, raise money, educate the public, and fundraise for those affected. </p><p>Ehlers-Danlos syndromes are a collection of more than thirteen hereditary disorders that affect the connective tissue throughout the body. People with the condition have mutations of specific genes that affect the ability of cells to create proteins to construct joints in the usual way. These syndromes, therefore, result in symptoms such as chronic pain, fragile skin, the ability to flex joints beyond the normal range, and rupturing of internal organs. While many of the effects of the disorder are mild, some can be life-threatening and require immediate hospitalization. </p><p>People with Ehlers-Danlos syndrome historically struggled to obtain accurate diagnoses. Many of the symptoms closely resemble those of other more common diseases, causing doctors to make incorrect diagnoses. At root, Ehlers-Danlos syndromes are genetically heritable. So in an era marked by a lack of DNA testing, an accurate diagnosis was difficult. </p><p>Recently, however, there has been substantial progress towards classifying and identifying the conditions. In 2017, researchers published more than eighteen papers in the Journal of Medical Genetics, clarifying the different varieties of the disease and better characterizing their properties. The Ehlers-Danlos Society added to the body of research and publicly-available information by releasing a review of the research materials, backed by more than ninety experts. It was the first significant update for more than twenty years. </p><p>The result of this effort is a considerably improved understanding of the syndrome at the scientific level. The challenge is to filter the information out to medics, schools, and the public at large. </p><h2>History of Ehlers-Danlos Syndrome Awareness Month </h2><p>Before 1997, researchers classified Ehlers-Danlos Syndrome into ten specific types, based on specific genetic mutations associated with symptoms (such as connective tissue issues). As genetic testing improved, however, the number of Ehlers-Danlos-type syndromes began to expand, with more than thirteen currently classified. </p><p>The rationale for Ehlers-Danlos Syndrome Awareness Month, however, isn’t as straightforward as calling for more accurate DNA tests. Many researchers believe that medical science is only just scratching the surface of syndromes related to the original set. Genetic testing, therefore, may not detect all instances of the disease. Some mutations may be so rare that there are just a handful of people affected by them throughout the world. In some cases, a person presenting with Ehlers-Danlos-like symptoms may be the only example. </p><p>There is a need, therefore, to pay close attention to the clinical manifestations of the condition, not just testing. Individual patients may present with all the hallmarks of the syndrome, but DNA procedures for the most common varieties of Ehlers-Danlos may not provide confirmation. </p><p>The Ehlers-Danlos Society ran the first Ehlers-Danlos awareness month in 2006. Since then, the organization has worked tirelessly to improve the public consciousness of the condition by supporting people around the world with the syndrome. In 2017, the society attempted some branding and social media outreach under the “Dazzle Together” hashtag. </p><p>The story behind the name for the campaign is interesting. Traditionally, medics called patients presenting with Ehlers-Danlos syndromes “zebras,” a reference to the medical school mantra “when the hoofbeats, think horses, not zebras.” The original saying inculcated trainee doctors in the idea that they should proceed with the most obvious diagnosis first – the horse – and only investigate less clear-cut symptoms afterwards – the zebra.</p><p>The problem for Ehlers-Danlos patients is that <em>they are zebras</em> – they have a rare disease. So applying the standard medical school wisdom doesn’t help them. In fact, it is counterproductive. </p><p>The “dazzle” part of the hashtag comes from the traditional way of referring to a group of zebras as a dazzle. Thus, the “Dazzle Together” campaign was born. And now, the community works together to improve awareness of the condition, raise funds for research, and reach out to the public over social media. </p><p>There are a lot of different people involved in Ehlers-Danlos Syndrome Month. Patients, health professionals, charities, donors, and caregivers all work to get the critical message discussed here out to the public. The Ehlers-Danlos Society provides brochures, posters, digital presentations, and instructions for members for how to best make use of their time. </p><h2>How to celebrate Ehlers-Danlos Syndrome Awareness Month </h2><p>So how do you get involved and show your support for the people who must currently live with Ehlers-Danlos Syndrome? It turns out that there are loads of things that you can do. </p><p>The first thing that you can do is join forces with the Ehlers-Danlos Society. Most years, the organization runs so-called “challenges” where people engage in various community events to raise money. Many of these events are fun and designed to suit individual interests. Some of the official events organized by the charity include things like dressing up as zebras, lectures, and coffee mornings. </p><p>Of course, you don’t need to join in with the official events to celebrate the month. There are plenty of things that you can do as an individual to do your bit for the EDS community. </p><p>Perhaps the best way to show your support is to donate money. Currently, there is a massive research effort underway to understand the condition better and find treatments. With further research, it may be possible to undo the genetic mutations that cause the syndrome and help people take back control of their health. We will have to wait and see.</p><p>There’s also a need for further education of the general public, people who work in schools, and the medical community. Rare genetic diseases tend not to get the same level of attention or support as more common conditions, so they require outreach. </p><p>Failing that, you can always dress up as a zebra!</p><p>Note: <a href="https://bestpromotionalcodes.com/naadam-promo-codes/">Naadam coupon codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Naadam Promo Code: katy15 (1 People Used Today)</p><p><a href="https://capitaloneshopping.com/s/naadam.co/coupon">Naadam promo codes</a>: Naadam 15% Off You Order</p>

Ehlers-Danlos Syndrome Awareness Month 2022

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