23 signs you grew up with ehlers danlos syndrome

Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls.

Connective tissues are made up of proteins and other substances that provide them with elasticity. In people with Ehler-Danlos syndrome, the strength of collagen is affected. Though people with Ehler-Danlos syndrome are born with the condition, it may take years before it gets diagnosed. Ehler-Danlos syndrome is a genetic condition. Over 20 genes have been found to be associated with EDS. Changes variants in these genes may disrupt the production or processing of collagen, resulting in weak bones, skin , or other parts of the body.

23 signs you grew up with ehlers danlos syndrome

Urgent Care. This connective tissue disorder affects individuals in various ways, impacting their joints, skin, and overall quality of life. If you suspect that you may have grown up with EDS, it's important to understand the signs and seek appropriate support. EDS is a group of genetic disorders that affect the body's connective tissues, which provide support and structure to various organs and systems. This condition is characterized by faulty collagen production, leading to symptoms such as hypermobility, joint instability, and fragile skin. If you resonate with several of the signs mentioned above, it's crucial to consult with a healthcare professional who specializes in EDS. They can provide an accurate diagnosis and develop a personalized treatment plan to manage your symptoms. At Statcare, we understand the challenges faced by individuals with EDS and offer comprehensive healthcare solutions. Our team of specialists is experienced in managing EDS-related symptoms and providing support throughout your healthcare journey. Living with EDS can feel isolating, but you're not alone. Join our community of individuals with EDS to connect with others who understand your experiences. Share your stories, ask questions, and find the support you need to navigate life with this condition. Growing up with Ehlers Danlos Syndrome can present a range of challenges, from chronic pain and joint instability to skin fragility and delayed wound healing. By recognizing the signs and seeking appropriate support, individuals with EDS can improve their quality of life and find the resources they need to thrive.

If you suspect that you may have grown up with EDS, it's important to understand the signs and seek appropriate support.

Back to Health A to Z. Ehlers-Danlos syndromes EDS are a group of rare inherited conditions that affect connective tissue. Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs and bones. EDS can affect people in different ways. For some, the condition is relatively mild, while for others their symptoms can be disabling.

For the Ehlers-Danlos syndrome EDS guide, we interviewed three medical experts, read numerous studies and surveyed more than people living with EDS. The guides are living documents and will be updated with new information as it becomes available. Ehlers-Danlos symdrome EDS affects your collagen, a connective tissue found everywhere in your body. While most types of EDS include joint hypermobility and dislocations, loose or stretchy skin, and easy bruising, your exact symptoms will depend on which of the 13 EDS subtypes you have. Other common EDS symptoms include eye trouble, digestive health issues and bone growth differences. Medically reviewed by David S.

23 signs you grew up with ehlers danlos syndrome

Ehlers-Danlos Syndrome EDS is a rare genetic disorder that affects the body's connective tissues, causing joint hypermobility, skin fragility, and other symptoms. While it can be diagnosed at any age, many people with EDS experience symptoms from a young age, making it a part of their childhood and adolescence. If you grew up with EDS, you may have experienced a range of symptoms that you didn't realize were related to the disorder. In this article, we'll explore 25 telltale signs that you grew up with Ehlers-Danlos Syndrome. Before we dive into the signs, let's first understand what Ehlers-Danlos Syndrome is. EDS is a group of genetic disorders that affect the body's connective tissues, which provide support and structure to the skin, bones, blood vessels, and other organs. There are 13 subtypes of EDS, each with its own set of symptoms and severity. The most common type is hypermobile EDS, which is characterized by joint hypermobility, skin fragility, and chronic pain. Due to the hypermobility of the joints, many children can do what many call "party tricks" with their hypermobile joints.

Ecovacs deebot n10 plus robotic vacuum review

I ordered one health report from Xcode and received results within an hour. Most people with Ehler-Danlos are unaware of their condition as they are unable to spot signs like easy skin bruising and joint dislocation. Pregnancy can increase the risk of a rupture in the uterus. Ehlers-Danlos National Foundation. Orthostatic Intolerance : Individuals with EDS may experience dizziness and lightheadedness upon standing. Most children with EDS have hypermobile joints that are prone to full or partial dislocation. Is Elhers-Danlos Syndrome Genetic? Accessed Aug. Join our community of individuals with Ehlers Danlos Syndrome and find the support you need to navigate life with this condition. What are the symptoms of Ehlers-Danlos syndrome?

Urgent Care. This connective tissue disorder affects individuals in various ways, impacting their joints, skin, and overall quality of life. If you suspect that you may have grown up with EDS, it's important to understand the signs and seek appropriate support.

Coronary Artery Program Program The Coronary Artery Program specializes in the assessment, diagnosis, and treatment of coronary artery anomalies. While for some, it may be related to an underlying medical condition, these may be signs of Ehler-Danlos syndrome for a few people. An educator's guide: Meeting the needs of the Ehlers-Danlos child. Learn more about Complex Cervical Spine Program. Your gift holds great power — donate today! But it's also important not to be overprotective and avoid living an otherwise normal life. When you engage with these links and decide to make a purchase, we may receive a percentage of the sale. Ferri FF. This has been really helpful for me. If there's a possibility you may have 1 of the rare types of EDS, the GP can refer you to your local genetics service for an assessment. If you are unsure of which package to buy - do the biggest - it is so worth it! I finally have some answers I always wanted from my original dna company ancestry. The following websites provide more information, advice and support for people with EDS and their families:. Overview of management of Ehlers-Danlos syndromes.