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

0 tháng 5 24, 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

0 tháng 5 24, 2022

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Ehlers-Danlos Syndrome Awareness Month 2022

<p>Tip: <a href="https://zonecouponcodes.com/15-off-uk-tights-coupons/">UK Tights discount codes</a>: 15% Off Miss O Styles. UK Tights Coupon Code: MO15. Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.#UKTightsCoupons#UKTightsPromoCodes</p><p><a href="https://www.retailmenot.com/view/uktights.com">UK Tights promo codes</a>: 15% Off UK Tights Coupons & Promo 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://zonecouponcodes.com/greeting-card-universe-coupons/">Greeting Card Universe coupon codes</a>: Cards For $2.09 Each With Purchase of 5+. Greeting Card Universe Coupon Code: MAY209. Cards For $2.09 Each With Purchase Of 5+ Cards: Your cards will ship the next business day and theres no extra charge for personalization. Also if you order 10 cards or more, standard shipping is Free!#GreetingCardUniverseCoupons#GreetingCardUniversePromoCodes</p><p><a href="https://capitaloneshopping.com/s/greetingcarduniverse.com/coupon">Greeting Card Universe coupon codes</a>: Greeting Card Universe May Coupons & Promo Codes 2022</p>

Ehlers-Danlos Syndrome Awareness Month 2022

0 tháng 5 19, 2022

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Ehlers-Danlos Syndrome Awareness Month 2022

<p>Tip: <a href="https://urbizdeals.com/hero-nutritionals-coupons/">Hero Nutritionals promo codes</a>: $5 Off Your Order when you Join. Discover our latest promotional deal for Hero Nutritionals. Click this link and save $5 straightaway. No coupon code is required for heronutritionals.com.#HeroNutritionalsCoupons#HeroNutritionalsPromoCodes</p><p><a href="https://www.retailmenot.com/view/heronutritionals.com">Hero Nutritionals coupon codes</a>: Hero Nutritionals Promo Codes & Coupons 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://urbizdeals.com/au-marksandspencer-com-coupons/">Marks & Spencer AU coupon codes</a>: Loungewear from AU$16.5. Try this Marks & Spencer online promo before wrapping up your shopping session on marksandspencer.com. Don't miss: Loungewear from AU$16.5!#Marks&SpencerAUCoupons#Marks&SpencerAUPromoCodes</p><p><a href="https://capitaloneshopping.com/s/au.marksandspencer.com/coupon">Marks & Spencer AU discount codes</a>: Marks & Spencer AU Promo Codes & Coupons May 2022</p>

Ehlers-Danlos Syndrome Awareness Month 2022

0 tháng 5 08, 2022

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International FND Awareness Day 2022

<p>Tip: <a href="https://urbizdeals.com/woods-supplements-coupons/">Woods Supplements discount codes</a>: £5 Off £35+ Orders. Enjoy and save money at Woods Supplements applying: £5 Off £35+ Orders. You can simply click this link to use "DW208" coupon code at the checkout on woodshealth.com.#WoodsSupplementsCoupons#WoodsSupplementsPromoCodes</p><p><a href="https://www.retailmenot.com/view/woodshealth.com">Woods Supplements discount codes</a>: Woods Supplements Promo Codes & Coupons Apr 2022</p><p>When it comes to disorders and diseases, one of the most common misconceptions is that people are in control of their symptoms. With disorders like FND, that’s not the case.</p><p>As a matter of fact, many disorders and diseases don’t have cures to them, so for disorders that don’t have much in the way of research, it can be hard for doctors and patients to find ways of treating symptoms and diagnosing the problem.</p><p>FND is just one of those disorders that leave many puzzled and wanting answers. Read more here to find out what FND is all about, what this holiday means for people everywhere, and what you can do to help this cause.</p><h2>History of International FND Awareness Day</h2><p>FND, or Functional Neurological Disorder, is a disorder that breaks down the communications between the brain and the body, even when both the brain and the body are functioning correctly. FND can mimic other conditions because varying patients can have symptoms ranging from chronic pain to immobility.</p><p>However, many patients that come into a doctor’s office get diagnosed with diseases that have routes in the organic body rather than that of the mind. With FND, the symptoms come from neither psychological or organic routes, but the pain still exists, hence why FND is not as widely heard of unlike diseases such as Parkinson’s Disease. Currently, the best treatment plans available are through physical therapy.</p><p>FNDHope.com hopes to help people who potentially have FND understand what it is and learn how they can find treatment. FND Hope is a non-profit patient advocacy organization that aims to help educate people about what FND is and how people can help towards the cause of funding research for the disorder and finding a potential cure for it.</p><p>FND Hope has locations throughout the US, UK, and Australia and their main goal is to help <g>other</g> connect globally through networking and encourages others to be advocates in hopes of finding a cure for FND. With multiple publications through various research magazines and thousands of people conversing in their public forums, the conversation about FND through their annual holiday, which they founded back in 2017.</p><h2>How to celebrate International FND Awareness Day</h2><p>If you want to help out with this holiday, then share their main holiday page on your favorite social media websites and use the hashtags #LetsTalkFND and #intenationalFNDawarenessday to let everyone know what day it is. If you want to help out more, share your personal experiences online about how FND affects you, donate to their organization and help educate people about what FND is and what others can do about it.</p><p>Note: <a href="https://urbizdeals.com/shipito-coupons/">Shipito coupon codes</a>: Free US Shipping on Orders when you Sign Up. Click this Shipito sale and you can enjoy Free US Shipping on Orders when you Sign Up. Take advantage of promotional prices and never pay full price again on shipito.com!#ShipitoCoupons#ShipitoPromoCodes</p><p><a href="https://capitaloneshopping.com/s/shipito.com/coupon">Shipito coupon codes</a>: Shipito Promo Codes & Coupons Apr 2022</p>

International FND Awareness Day 2022

0 tháng 4 14, 2022

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International FND Awareness Day 2022

<p>Tip: <a href="https://savingspromocodes.com/sony-promo-codes/">Sony coupon codes</a>: Headband Headphones from $19.99. Save money when you shop on sony.com. Use this Sony sale to enjoy Headband Headphones from $19.99!#SonyCoupons#SonyPromoCodes</p><p><a href="https://www.retailmenot.com/view/store.sony.com">Sony promo codes</a>: Sony Promo Codes & Coupons Apr 2022</p><p>When it comes to disorders and diseases, one of the most common misconceptions is that people are in control of their symptoms. With disorders like FND, that’s not the case.</p><p>As a matter of fact, many disorders and diseases don’t have cures to them, so for disorders that don’t have much in the way of research, it can be hard for doctors and patients to find ways of treating symptoms and diagnosing the problem.</p><p>FND is just one of those disorders that leave many puzzled and wanting answers. Read more here to find out what FND is all about, what this holiday means for people everywhere, and what you can do to help this cause.</p><h2>History of International FND Awareness Day</h2><p>FND, or Functional Neurological Disorder, is a disorder that breaks down the communications between the brain and the body, even when both the brain and the body are functioning correctly. FND can mimic other conditions because varying patients can have symptoms ranging from chronic pain to immobility.</p><p>However, many patients that come into a doctor’s office get diagnosed with diseases that have routes in the organic body rather than that of the mind. With FND, the symptoms come from neither psychological or organic routes, but the pain still exists, hence why FND is not as widely heard of unlike diseases such as Parkinson’s Disease. Currently, the best treatment plans available are through physical therapy.</p><p>FNDHope.com hopes to help people who potentially have FND understand what it is and learn how they can find treatment. FND Hope is a non-profit patient advocacy organization that aims to help educate people about what FND is and how people can help towards the cause of funding research for the disorder and finding a potential cure for it.</p><p>FND Hope has locations throughout the US, UK, and Australia and their main goal is to help <g>other</g> connect globally through networking and encourages others to be advocates in hopes of finding a cure for FND. With multiple publications through various research magazines and thousands of people conversing in their public forums, the conversation about FND through their annual holiday, which they founded back in 2017.</p><h2>How to celebrate International FND Awareness Day</h2><p>If you want to help out with this holiday, then share their main holiday page on your favorite social media websites and use the hashtags #LetsTalkFND and #intenationalFNDawarenessday to let everyone know what day it is. If you want to help out more, share your personal experiences online about how FND affects you, donate to their organization and help educate people about what FND is and what others can do about it.</p><p>Note: <a href="https://savingspromocodes.com/major-lens-promo-codes/">Major Lens promo codes</a>: Toric Lens from $25. Try this Major Lens online deal before wrapping up your shopping session on majorlens.com. Don't miss: Toric Lens from $25!#MajorLensCoupons#MajorLensPromoCodes</p><p><a href="https://capitaloneshopping.com/s/majorlens.com/coupon">Major Lens coupon codes</a>: Major Lens Promo Codes & Coupons Apr 2022</p>

International FND Awareness Day 2022

0 tháng 4 13, 2022

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Kidney Month 2022

<p>Tip: <a href="https://bestpromotionalcodes.com/photowhoa-promo-codes/">PhotoWhoa discount codes</a>: No coupon code needed. Prices as marked. Tap to shop the sale now.</p><p><a href="https://www.retailmenot.com/view/photowhoa.com">PhotoWhoa coupon codes</a>: PhotoWhoa 20% Off Sitewide</p><p>Deep within our torso lay two little bean shaped (or are the beans them shaped?) organs that do a big job, and are in fact vital to our continued health. Introducing, the Kidney!</p><p>It filters 53 gallons of blood a day, keeps your blood pressure in check, and even assists with the production of red blood cells. While these useful little organs spend their day happily performing their function, as many as 26 million Americans may already be suffering from kidney disease and may not even know it.</p><p>Kidney Month reminds you that you need to take care of these amazing little filters, your life may very well depend on it!</p><h2>History of Kidney Month</h2><p>Kidney Month was established by the National Kidney Foundation to help spread awareness of Kidney disease and ways it could be tested for and prevented. With so many Americans in danger of contracting kidney disease from high blood pressure, diabetes, or a family history of the same. Kidney disease is so prevalent that it’s the 9th leading cause of death in the United States, and over 95,000 people are waiting every day to get kidney transplant, surviving each day on dialysis.</p><p>Kidneys are most commonly associated with the creation of urine, but they do so much more than that. While yes they help to break down and excrete waste into the bladder, they also are vital in reabsorption of certain nutrients, include the ever important amino acids. They also serve a vital role in making sure that your bodies pH balance is maintained to help prevent ketosis, and produce hormones that are important in several functions of the body. Blood cell production, absorption of calcium, and regulating aldosterone levels are all important roles the kidney plays. These bean shaped organs do much much more than they’re given credit for, and Kidney Month is your chance to give them the care they deserve.</p><h2>How to celebrate Kidney Month<br></h2><p>Kidney Month is recognized as an opportunity to get people interested in the health of their kidneys. As such, it’s the perfect time to participate in one of the free screenings that show up all over the country. The National Kidney Foundation has a listing of locations and information on their website. You can also pop on over to www.kidney.org and participate in one of their ‘are you at risk’ quizzes to help find out if you NEED, or just <em>should</em> get to a clinic to be tested. These are just a few of the things that pop up each Kidney Month that can help you extend your life and the health of your kidneys.</p><p>Note: <a href="https://bestpromotionalcodes.com/cover-fx-promo-codes/">Cover FX coupon codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Cover FX Promo Code: FALLFAM (-1 People Used Today)</p><p><a href="https://capitaloneshopping.com/s/coverfx.com/coupon">Cover FX coupon codes</a>: Cover FX Friends And Family Event! 25% Off Sitewide + Free Shipping</p>

Kidney Month 2022

0 tháng 3 27, 2022

Tip: PhotoWhoa discount codes: No coupon code needed. Prices as marked. Tap to shop the sale now.PhotoWhoa coupon codes: PhotoWhoa 20% Off SitewideDeep within our torso lay two little bean shaped (or are the beans them shaped?) organs that do a big j… Đọc thêm »

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Social Work Month 2022

<p>Tip: <a href="https://urbizdeals.com/yaasa-coupons/">Yaasa promo codes</a>: 10% Off Your Purchase when you Sign Up. Offer Applies Sitewide. No Code Required#YaasaCoupons#YaasaPromoCodes</p><p><a href="https://www.retailmenot.com/view/yaasa.com">Yaasa coupon codes</a>: Yaasa Promo Codes & Coupons Mar 2022</p><p>When things are at their most challenging it is typically a Social Worker who can step in and bring order to the chaos. It is their super power! You will find them all around the community just waiting and willing to help. Having such an amazing super power makes it easy to see why we need Social Work Month!</p><h2>History of Social Work Month</h2><p>In 1984, the White House officially recognized Social Work Month. Since then each year has had its own theme and goal to bring more understanding to what social workers do. Some past themes have focused on issues within society like AIDS/HIV, hate crimes, violence prevention, children in poverty and homelessness just to name a few. In the late 1990’s and early 2000’s, the themes for this month were geared more towards awareness on how social workers can help their communities.</p><p>The National Association of Social Workers sponsors this event each year with the goal of acknowledging those who are practicing and to help children understand the profession so that they might choose to make social work their profession. Statistics from the Department of Labor stated in 2008 that the need for social workers has been expected to more than double in size. This was expected in the areas of substance abuse, home health care, school social work and social service agencies.</p><h2>How to Celebrate Social Work Month</h2><p>If you are still thinking about what you want to do in life, celebrate Social Work Month by learning more about this essential profession. There are wonderful resources that will tell you all about the education needed, expected salaries, and more about what they do on the internet, at the Department of Labor and in most career counseling centers.</p><p>Do you have a social worker in your life? You are lucky if you do! Help them celebrate the month by letting them know how important they are to you. A hand-written note or a card will let them have something to look at and let them know they are doing great things when a hard day comes around! They often come into our lives when we are not at our best, and that must take a toll on them at times. It is nice to give them the positive feedback.</p><p>Some social workers spend most of their time in their car going from client to client. You can help them celebrate this month with gift certificates for their favorite coffee, or even where they might try to get a bite to eat during the day! Better yet, a gift certificate for something that would be a treat is a way to go as well. A favorite candy shop or a relaxing message could go a long way to making their day!</p><p>No matter how you choose to do it, just make sure to recognize the people around you who have picked social work as their life’s work. They use their super power every day to make a difference in other people’s lives. How cool is that?</p><p>Note: <a href="https://urbizdeals.com/fsa-store-coupons/">FSA Store coupon codes</a>: Save 10% Off with Code. FSA Store Coupon Code: 25SAVE22. Score up to 10% off with discount code#FSAStoreCoupons#FSAStorePromoCodes</p><p><a href="https://capitaloneshopping.com/s/fsastore.com/coupon">FSA Store promo codes</a>: FSA Store Promo Codes & Coupons Mar 2022</p>

Social Work Month 2022

0 tháng 3 18, 2022

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Multiple Sclerosis Month 2022

<p>Tip: <a href="https://stcouponcodes.com/mac-cosmetics-coupon-codes/">MAC Cosmetics promo codes</a>: Get 25% Off When You Join the M·A·C Lovers Rewards Program + Free Lipglass or Lipstick with $60+ AND a Free 3-Piece Kit when You Spend $75+.</p><p><a href="https://www.retailmenot.com/view/maccosmetics.com">MAC Cosmetics coupon codes</a>: MAC Cosmetics 25% Off With M·a·C Lovers Rewards Program + Free Gifts With Minimum Spend</p><p>Most of us never think twice about how lucky we are to be able to take a walk to the store, dance it up at a party or just have a conversation with a friend or loved one over coffee—these are just things we take for granted.</p><p>Sadly, there are many people who would give anything to be able to do any of those things independently and without pain. Many of these people have Multiple Sclerosis. March is Multiple Sclerosis Awareness Month, so let’s help those suffering from it and raise some awareness!</p><h2>The History of Multiple Sclerosis Month</h2><p>Multiple Sclerosis, also known simply as MS, is an autoimmune disease of the central nervous system. This disorder damages and eventually destroys the myelin, or protective covering, surrounding the nerves, causing reduced communication between the brain and nerve pathways. This in turn leads to various parts of the body—and MS can affect practically anything—not being able to work properly.</p><p>Common symptoms include overwhelming fatigue, problems with vision and/or speech, difficulty with balance and coordination, and various levels of impaired mobility. Some people also experience debilitating acute pain, go completely blind, or become paralyzed.</p><p>Multiple Sclerosis can also be the cause of chronic depression that often results in suicide. In 2010, the number of people with MS was estimated to be 2-2.5 million worldwide, but no treatment has yet been discovered that would be able to change the course of progressive MS.</p><p>March was proclaimed Multiple Sclerosis Awareness month in 2015 by New Jersey Governor Chris Christie, who encouraged both public officials and residents to organize and take part in activities and programs meant to raise awareness about the struggles of people who have this disease.</p><h2>How to Celebrate Multiple Sclerosis Awareness Month</h2><p>There are a few great ways to celebrate this month. Do you know someone who has Multiple Sclerosis? If so, this month is the perfect time to show you care about them, so give them a call, make them a pot of stew or just drop by their place to see if there is anything they need help with. Being disabled often makes people feel helpless, useless, and like they don’t matter anymore. But nothing makes a person feeling lonely, scared or just plain miserable feel better than knowing they haven’t been forgotten.</p><p>Last but not least, since Multiple Sclerosis Awareness Month is all about raising awareness, take some time this month to educate yourself! The National Multiple Sclerosis Society in the United States, for example, organizes different events all over the country, such as Walk MS, that you can take part in to show your support for the cause. The Multiple Sclerosis Society in Great Britain offers the opportunity to help out by doing little jobs like driving a minibus or managing a website.</p><p>If you don’t know anyone with MS, maybe you could consider donating to someone with MS who needs your help? This brave woman, for example, has been fighting the disease for over 20 years and needs help paying for the care home she will have to finally move to: <a>https://www.gofundme.com/jbrvcn6c</a> Remember, every dollar and every share counts!</p><p>So what are you waiting for? March is only 31 days long, and there’s so much work to be done!</p><p>Note: <a href="https://stcouponcodes.com/cool-lcd-coupon-codes/">Cool LCD discount codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Cool LCD Coupon Code: LOVE10010011 (-1 People Used)</p><p><a href="https://capitaloneshopping.com/s/coollcd.com/coupon">Cool LCD discount codes</a>: Cool LCD 10% Off SmallRig Universal Smartphone Holder BSP2415</p>

Multiple Sclerosis Month 2022

0 tháng 3 13, 2022

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Multiple Sclerosis Month 2022

<p>Tip: <a href="https://stcouponcodes.com/hoover-coupon-codes/">Hoover coupon codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Hoover Coupon Code: FLASH25 (5 People Used)</p><p><a href="https://www.retailmenot.com/view/hoover.com">Hoover promo codes</a>: Hoover 25% Off Sitewide</p><p>Most of us never think twice about how lucky we are to be able to take a walk to the store, dance it up at a party or just have a conversation with a friend or loved one over coffee—these are just things we take for granted.</p><p>Sadly, there are many people who would give anything to be able to do any of those things independently and without pain. Many of these people have Multiple Sclerosis. March is Multiple Sclerosis Awareness Month, so let’s help those suffering from it and raise some awareness!</p><h2>The History of Multiple Sclerosis Month</h2><p>Multiple Sclerosis, also known simply as MS, is an autoimmune disease of the central nervous system. This disorder damages and eventually destroys the myelin, or protective covering, surrounding the nerves, causing reduced communication between the brain and nerve pathways. This in turn leads to various parts of the body—and MS can affect practically anything—not being able to work properly.</p><p>Common symptoms include overwhelming fatigue, problems with vision and/or speech, difficulty with balance and coordination, and various levels of impaired mobility. Some people also experience debilitating acute pain, go completely blind, or become paralyzed.</p><p>Multiple Sclerosis can also be the cause of chronic depression that often results in suicide. In 2010, the number of people with MS was estimated to be 2-2.5 million worldwide, but no treatment has yet been discovered that would be able to change the course of progressive MS.</p><p>March was proclaimed Multiple Sclerosis Awareness month in 2015 by New Jersey Governor Chris Christie, who encouraged both public officials and residents to organize and take part in activities and programs meant to raise awareness about the struggles of people who have this disease.</p><h2>How to Celebrate Multiple Sclerosis Awareness Month</h2><p>There are a few great ways to celebrate this month. Do you know someone who has Multiple Sclerosis? If so, this month is the perfect time to show you care about them, so give them a call, make them a pot of stew or just drop by their place to see if there is anything they need help with. Being disabled often makes people feel helpless, useless, and like they don’t matter anymore. But nothing makes a person feeling lonely, scared or just plain miserable feel better than knowing they haven’t been forgotten.</p><p>Last but not least, since Multiple Sclerosis Awareness Month is all about raising awareness, take some time this month to educate yourself! The National Multiple Sclerosis Society in the United States, for example, organizes different events all over the country, such as Walk MS, that you can take part in to show your support for the cause. The Multiple Sclerosis Society in Great Britain offers the opportunity to help out by doing little jobs like driving a minibus or managing a website.</p><p>If you don’t know anyone with MS, maybe you could consider donating to someone with MS who needs your help? This brave woman, for example, has been fighting the disease for over 20 years and needs help paying for the care home she will have to finally move to: <a>https://www.gofundme.com/jbrvcn6c</a> Remember, every dollar and every share counts!</p><p>So what are you waiting for? March is only 31 days long, and there’s so much work to be done!</p><p>Note: <a href="https://stcouponcodes.com/improvements-coupon-codes/">Improvements coupon codes</a>: Summer Solstice Sale! Get 15% off Everything + Free standard shipping on your order. Improvements Coupon Code: MM8W499 (-1 People Used)</p><p><a href="https://capitaloneshopping.com/s/improvementscatalog.com/coupon">Improvements promo codes</a>: Improvements 15% Off Sitewide + Free Shipping on Your Order</p>

Multiple Sclerosis Month 2022

0 tháng 3 10, 2022

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Social Work Month 2022

<p>Tip: <a href="https://stcouponcodes.com/shark-clean-coupon-codes/">Shark Clean discount codes</a>: Tap offer to copy the coupon code. Remember to paste code when you check out. Online only.. Shark Clean Coupon Code: MOM30 (3 People Used)</p><p><a href="https://www.retailmenot.com/view/sharkclean.com">Shark Clean promo codes</a>: Shark Clean $30 Off Select Models</p><p>When things are at their most challenging it is typically a Social Worker who can step in and bring order to the chaos. It is their super power! You will find them all around the community just waiting and willing to help. Having such an amazing super power makes it easy to see why we need Social Work Month!</p><h2>History of Social Work Month</h2><p>In 1984, the White House officially recognized Social Work Month. Since then each year has had its own theme and goal to bring more understanding to what social workers do. Some past themes have focused on issues within society like AIDS/HIV, hate crimes, violence prevention, children in poverty and homelessness just to name a few. In the late 1990’s and early 2000’s, the themes for this month were geared more towards awareness on how social workers can help their communities.</p><p>The National Association of Social Workers sponsors this event each year with the goal of acknowledging those who are practicing and to help children understand the profession so that they might choose to make social work their profession. Statistics from the Department of Labor stated in 2008 that the need for social workers has been expected to more than double in size. This was expected in the areas of substance abuse, home health care, school social work and social service agencies.</p><h2>How to Celebrate Social Work Month</h2><p>If you are still thinking about what you want to do in life, celebrate Social Work Month by learning more about this essential profession. There are wonderful resources that will tell you all about the education needed, expected salaries, and more about what they do on the internet, at the Department of Labor and in most career counseling centers.</p><p>Do you have a social worker in your life? You are lucky if you do! Help them celebrate the month by letting them know how important they are to you. A hand-written note or a card will let them have something to look at and let them know they are doing great things when a hard day comes around! They often come into our lives when we are not at our best, and that must take a toll on them at times. It is nice to give them the positive feedback.</p><p>Some social workers spend most of their time in their car going from client to client. You can help them celebrate this month with gift certificates for their favorite coffee, or even where they might try to get a bite to eat during the day! Better yet, a gift certificate for something that would be a treat is a way to go as well. A favorite candy shop or a relaxing message could go a long way to making their day!</p><p>No matter how you choose to do it, just make sure to recognize the people around you who have picked social work as their life’s work. They use their super power every day to make a difference in other people’s lives. How cool is that?</p><p>Note: <a href="https://stcouponcodes.com/bloomingdale-s-canada-2-coupon-codes/">Bloomingdale's Canada discount codes</a>: Deal Reveal! Get an extra 20%,25%, 30%, or 40% off almost all sale and clearance items when you sign up for email. Total savings of 40-65%.</p><p><a href="https://capitaloneshopping.com/s/canada.bloomingdales.com/coupon">Bloomingdale's Canada discount codes</a>: Bloomingdale's Canada Up to an Extra 40% Off Almost All Sale & Clearance Items With Email Sign Up</p>

Social Work Month 2022

0 tháng 3 02, 2022

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