EDS facial features

Rare Form of EDS Marked by Distinct Facial Features, Short

CARDIAC-VALVULAR EDS involves severe cardiac-valvular disease that requires valve replacement surgery in conjunction with variable skin hyperextensibility, atrophic scarring, and joint hypermobility. CLASSICAL EDS affects skin, wound healing, and joints. Joints can stretch beyond normal, causing pain Prominent and characteristic facial features that includes bulging eyes, sunken cheeks, thin lips and nose and a small chin Problems of the heart valve like mitral valve prolapsed, etc. There are other types of Ehlers-Danlos syndrome as well, but are and ill-defined and tend to occur only in a few families. Ehlers Danlos syndrome Cause

Ehlers-Danlos syndrome facial features Learn More - FDNA

  1. Article updated August 1, 2019. Because Ehlers-Danlos syndrome (EDS) is still not as well-known as it should be, it often gets described in basic terms so others can more easily understand it: It's a condition that causes dysfunction in the connective tissue, resulting in joint hypermobility, fragile tissue and hyperflexible skin. However, EDS can cause many more symptoms than that
  2. Clinical diagnosis of vascular Ehlers-Danlos syndrome is based on four criteria: a characteristic facial aspect (acrogeria) in most patients, thin and translucent skin with highly visible subcutaneous vessels, ecchymoses and haematomas, and arterial, digestive and obstetrical complications
  3. or criteria. Minimal criteria suggestive of dEDS include the two major criteria of extreme skin fragility and characteristic craniofacial features, plus either: one other major criterion, or three
  4. Some people have characteristic facial features, thin skin, and tissue fragility. What other names do people use for Vascular Ehlers-Danlos Syndrome? Vascular Ehlers-Danlos Syndrome is also referred to as vEDS, Ehlers-Danlos syndrome type IV, Sack-Barabas syndrome, and the arterial form of Ehlers- Danlos syndrome

Vascular Ehlers-Danlos Syndrome Without the Characteristic

Infants with classical and hypermobile EDS have skin that feels soft and velvet-like, a feature that is lifelong. The skin texture has also been described as doughy. [ 1, 2, 7, 10] Note the.. These are the facial features I have that are common with EDS. (I forgot about the small chin and my super narrow palate - dentists have to use children's te.. Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients. Colombi M., Dordoni C. - Clinical Genetics, September 2017 Abstract: Classical Ehlers-Danlos syndrome (cEDS) is characterized by marked cutaneous involvement, according to the Villefranche nosology and its 2017 revision Vascular Ehlers-Danlos syndrome is typically caused by a change (mutation) in the COL3A1 gene.Rarely, it may be caused by a mutation in the COL1A1 gene. The COL3A1 gene provides instructions for making a component of type III collagen. Collagen is a protein that provides structure and strength to connective tissues throughout the body. Type III collagen, specifically, is found in tissues such.

Subtypes of Ehlers-Danlos syndrome. Under the 2017 International Classification for Ehlers-Danlos Syndromes, there are thirteen subtypes of EDS, classified according to the clinical features, inheritance pattern, and molecular genetic defects.. Each is a distinct disorder that 'runs true' in a family Characteristic facial appearance (thin lips and midline groove in the upper lip that runs fromthe top of the lip to the nose, small chin, thin nose, and large, dark, deep-set eyes) There are 13 types of Ehlers-Danlos syndromes (EDS), with a significant overlap in features:. Hypermobile EDS - characterized primarily by joint hypermobility affecting both large and small joints, which may lead to recurrent joint dislocations and subluxations (partial dislocation).In general, people with this type have soft, smooth and velvety skin with easy bruising and chronic pain of the. Children with vascular Ehlers-Danlos syndrome can have mild or severe signs and may have characteristic facial features such as a small chin, thin nose and lips, and deep-set, large eyes. Skin can appear translucent with veins easily visible. Signs of vascular Ehlers-Danlos syndrome

Vascular Ehlers-Danlos syndrome without the characteristic

  1. a risk of organ problems, such as the bowel tearing, the womb tearing (in late pregnancy) and partial collapse of the lung hypermobile fingers and toes, unusual facial features (such as a thin nose and lips, large eyes and small earlobes), varicose veins and delayed wound healin
  2. The series of pictures of David Daniel Bowen III, who has vascular-type EDS, provide a very real face to a rare syndrome. The features of EDS may not be immediately recognizable in infants at.
  3. Ehlers-Danlos Syndrome (EDS) Ehlers-Danlos syndrome (EDS) is a group of disorders involving connective tissue. Connective tissue is what provides the body support, structure, stability and normal scar formation. Most people with EDS have loose joints, sometimes called double-jointedness.. This is due to abnormal connective tissue
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  5. imal subcutaneous facial fat and a triangular shaped face. Picture B: A young female with.
  6. Ectodermal dysplasia (EDS) is a term including several conditions. All these conditions show differences in the formation of parts of the body derived from the ectoderm. The ectoderm is one of three tissue layers found in very early embryonic development. It is involved in the formation of several parts of the body including the skin, hair.
  7. The Ehlers-Danlos Society has a EDS Medical Professionals Directory and an EDS Center for Research & Clinical Care. To find a medical professional who specializes in genetics, you can ask your doctor for a referral or you can search for one yourself

Oral and dental implications of the Ehlers-Danlos

PhotoDiva is a breeze to master, even with no portrait photo editor experience. Transform your photography with intuitive sliders and free one-click effects. The face editing software detects facial features like lips, eyes, and cheeks. Now you can sculpt, beautify, and add color without making tedious selections in Photoshop Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels [pediatricfocus.wordpress.com Some people with vascular EDS are diagnosed on the basis of subtle signs in their physical appearance, together with their medical history. Many people who do not have vascular EDS can have similar features as many are common in the general population. Also, not everyone with a confirmed diagnosis of vascular EDS has all of the typical features

Video: 25 Pictures of Real People With Ehlers-Danlos Syndrome

Ehlers-Danlos Syndrome is a group of genetic disorders that affects the body's connective tissue. Its key characteristics are stretchy skin and flexible joints. Many people with EDS experience other symptoms, such as chronic pain, fatigue, easy bruising, poor wound healing and abnormal scarring Ehlers-Danlos syndrome (EDS) is the name given to a group of related genetic diseases characterized by weakness in the connective tissue that makes up joints and holds tissues together. The symptoms of the different types of EDS overlap. Vascular EDS (vEDS) is characterized by thin, translucent skin that is easily bruised, and fragile arteries, muscles, and internal organs

Ehlers-Danlos syndrome - Symptoms and causes - Mayo Clini

Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth (prenatal and postnatal growth retardation), short stature, a varying degree of mental deficiency, and distinctive facial features that typically become more pronounced with age Ehlers-Danlos syndrome (EDS) is a hereditary disorder of the connective tissue. The pathological features described are those of a visceral myopathy and are consistent with EDS although similar findings can be found in visceral myopathies associated with other connective tissue disorders (e.g. systemic sclerosis). including facial. Ehlers-Danlos syndrome is a group of genetic disorders that affect the connective tissues and cause several symptoms, including stretchy skin and loose joints. Learn more here

My Face Has Ehlers-Danlos! - YouTube

Stickler syndrome was first described in the medical literature in 1965 by Gunnar Stickler et al., who called the disorder hereditary progressive arthro-ophthalmopathy. Stickler syndrome refers to a group of disorders of connective tissue. Connective tissue, which is the material between cells of the body that gives the tissue form and strength. Giunta C et al. Ehlers-Danlos syndrome type VII: clinical features and molecular defects. J Bone Joint Surg Am. 1999 Feb;81(2):225-38. Review. Byers PH et al. Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen Ehlers Danlos syndromes, of which there are 13 sub-types, are barely beginning to become known by doctors, if at all. 95% of patients don't even know they have it, according to EDS experts. And most doctors have a vague memory of it mentioned in med school

Abnormalities in type III collagen are characteristic of EDS IV (130050); no features of that disorder, such as thin skin, typical facial features, or vascular fragility, were found in affected members of the family 3 of 5 Facial Features. 1. One point can be assigned based upon facial characteristics if the patient shows at least three of these five typical facial characteristics: Dolichocephaly - disproportionately long and narrow head; Downward slanting palpebral fissures - down-slanting of the space between the eyelids Characteristic facial features in a child with fetal alcohol spectrum disorders. Findings may include a smooth philtrum, thin upper lip, upturned nose, flat nasal bridge and midface, epicanthal. Loeys-Dietz syndrome was first described in 2005. Its features are similar to Marfan's syndrome and Ehlers-Danlos syndrome, but Loeys-Dietz syndrome is caused by different genetic mutations.

1ehlersdanlos - YouTube

Indeed, researchers have found that modifying one facial feature can alter the spatial arrangements among all features, which may in turn impact impressions (Keating & Doyle, 2002). Thus, in exploring impressions created by babyfaces, it is important to consider not only combinations of facial features but also unique spatial configurations Does this patient have a hypermobility syndrome such as Marfan syndrome, Ehlers-Danlos syndrome, or joint hypermobility syndrome? Marfan syndrome (MFS) and Ehlers-Danlos syndrome (EDS) are connective tissue disorders with multisystem manifestations. Joint hypermobility syndrome (JHS) is a connective tissue disorder that primarily affects the musculoskeletal system. All of these disorders may. The signs and symptoms of Stickler syndrome — and the severity of those signs and symptoms — can vary widely from person to person, even within the same family. Eye problems. In addition to having severe nearsightedness, children who have Stickler syndrome often experience cataracts, glaucoma and retinal detachments. Hearing difficulties

Facial Features. ABSTRACT. It has traditionally been assumed that Children's ability to label individuals as older precedes their tendency to associate particular behavioral competenciii with individuals who vary-in age. To test this assumption, 64 preschool * children were-presented with 9 pairs of stimulus faces reflecting different ages A patient with Ehlers-Danlos syndrome may have one or more dysmorphic facial features Occasionally there may be other features present including: - Hypermobility of small joints. (i.e. fingers and toes). - Premature ageing of the skin on hands and feet. - Facial features, including a thin nose and lips, large eyes, small earlobes and fine hair. - Joint contractures caused by shortening of the ligaments Ranked as one of the #Top10 Youth Media worldwide* (for the second year in a row), awarded the BEST BLOG at India Digital Summit Awards 2019 by IAMAI & Times Now, ED Times is a youth media publication; the No. 1 Source For In-depth News Stories That Matter To Millennials

More Than Hypermobile: Ehlers-danlos and Its Rarer Forms

Abstract. The human face communicates an impressive number of visual signals. Although adults' ratings of facial attractiveness are consistent across studies, even cross-culturally, there has been considerable controversy surrounding attempts to identify the facial features that cause faces to be judged attractive or unattractive The adverse effects of prenatal alcohol exposure constitute a continuum of disabilities (fetal alcohol spectrum disorders [FASD]). In 1996, the Institute of Medicine established diagnostic categories delineating the spectrum but not specifying clinical criteria by which diagnoses could be assigned. In 2005, the authors published practical guidelines operationalizing the Institute of Medicine. facial features in this regard, particularly internal ones such as the eyes and mouth. Surprisingly, however, one rather prominent facial feature has received little attention in this domain: the eyebrows. Past work has examined the role of eyebrows in emotional expression and nonverba #Models #ModelingAgenciesI RESPOND TO ALL COMMENTS When modeling agencies look for new models to sign, they first check for a very specific set of physical c..

The study notes 8% of the population has diseases with key genetic components, and many have recognizable facial features. The technology could identify, for example, Angelman syndrome, a disorder. In children and adolescents: GH stimulates growth in all body tissues prior to fusion of the growth plate. In adults: GH causes continued growth of soft tissues and small bones of the hands/feet & the membranous bones of the skull and face. Signs and symptoms of: Child 7ft tall. Changes in facial features

Check out 11 reasons why you should use an eye massager! 1. Eye Massager is Super Comfortable. One of the biggest eye massager benefits is that it is extremely comfortable to wear. While this may not seem like such a huge deal at first, it's incredibly important to choose a comfy eye massager, especially since the skin around your eyes is so. In physical attractiveness studies, averageness describes the physical beauty that results from averaging the facial features of people of the same gender and approximately the same age. The majority of averageness studies have focused on photographic overlay studies of human faces, in which images are morphed together. The term average is used strictly to denote the technical definition of. The Crossword Solver found 20 answers to the Facial feature (2 eds.) crossword clue. The Crossword Solver finds answers to American-style crosswords, British-style crosswords, general knowledge crosswords and cryptic crossword puzzles. Enter the answer length or the answer pattern to get better results. Click the answer to find similar crossword clues D. Forsyth, P. Torr, and A. Zisserman (Eds.): ECCV 2008, Part IV, LNCS 5305, pp. 504-513, 2008. c Springer-Verlag Berlin Heidelberg 2008. Locating Facial Features with an Extended Active Shape Model 505 Fig.1. A face with correctly positioned landmarks. This image is from the BioID set [15] Can hEDS cause the same facial features as Vascular EDS? Questions. I have a friend (UK) who was recently diagnosed with hEDS since they meet the hEDS criteria, they're scheduled for genetic testing but because of COVID it's going to take a while

12. Dermatosparaxis EDS (dEDS) Another extremely rare variation among Ehlers-Danlos Syndrome types, Dermatosparaxis EDS's main features include severe bruising, fragility, and sagging of the skin. In the very few reported cases (only about 10), patients are diagnosed by the age of 2. Additional symptoms: Umbilical hernia; Very wrinkled palm A new classification system for EDS was released in 2017 (1). It's called the 2017 International Classfication for the Ehlers-Danlos Syndromes. This new system names 13 different subtypes of EDS. It relies primarily on descriptive terms for different types of EDS (e.g. vascular EDS, meaning that it affects blood vessels prominently).Two other systems existed before this one Ehlers-Danlos Syndrome is a group of inherited connective tissue disorders, caused by faulty collagen (a protein in connective tissue). Connective tissue helps support the skin, muscles, ligaments, and organs of the body. People who have the defect in their connective tissue associated with Ehlers-Danlos Syndrome may have symptoms which include joint hypermobility, skin which is easily. Ehlers-Danlos Syndrome, Arthrochalasia Type, is an extremely rare, inherited disorder caused by abnormalities in collagen formation. Collagen is the most abundant protein in the human body. It plays an important role in connective tissue function. Connective tissue is made up of structural proteins known as collagens and fibroblast cells, which.

Ehlers Danlos Syndrome Picture

In order to find out the characteristic differences between attractive and unattractive faces, we presented pairs of one sexy and one unsexy image for both sexes to test subjects. The task was to report which facial features were perceived to be different between the two faces. For the results see the list below. Female faces Many systemic and neurological conditions may involve the facial musculature. From tetanus to blepharospasm, the majority of them are characterized by muscular spasms. 1 While some of them are easily recognizable, anecdotal reports have recently focused attention on atypical presentations. 2-5 Although most of these cases have been reported as representing rare phenotypes of organic focal. VCFS includes many common features: cleft palate, heart defects and a characteristic facial appearance. Other common findings include minor learning problems and speech and feeding problems. Velocardiofacial syndrome is the most common syndrome associated with a cleft palate. It is estimated that one in 2,000 to 5,000 children per year are born. The script is run like so: ./faceswap.py <face image> If successful, a file `output.jpg` will be produced with the facial features from ` ` replaced with the facial features from `<face image>`. - Rossichan/FaceSwa

25 Pictures of Real People With Ehlers-Danlos Syndrome

10 Photos of Little-Known Symptoms of Ehlers-Danlos

Fig. 2 summarizes the importance of features representing the eyes and facial micro-movements (listed in Table 1). Firstly, there is a clear difference in the importance measure between most of the eyes related features (e.g. rshift, rright, rleft, rhclosed, lshift, rshift, rhright) and facial features (e.g. fbm, fdm, fhs, flm, fvm, etc.) Ehlers-Danlos syndrome, hypermobile type is a connective tissue disorder that affects approximately 1 in 5.000 people. This is a video explaining the most important characteristics of this condition. Ehlers-Danlos Symptoms and Risk Factors. Chronic pain is the most prominent symptom of Ehlers Danlos syndrome Ehlers-Danlos syndromes are a group of disorders which share common features including easy bruising, joint hypermobility (loose joints), skin that stretches easily (skin hyperelasticity or laxity), and weakness of tissues.; Ehlers-Danlos syndromes are inherited in the genes that are passed from parents to offspring.; Ehlers-Danlos syndromes symptoms and signs are joints that are more flexible. Knowing the signs of Marfan syndrome can save livesPeople are born with Marfan syndrome and related conditions, but they may not notice any features until later in life. However, features of Marfan syndrome and related disorders can appear at any age. Some people have many features at birth or as young children. Other people develop features, including aortic enlargement, as teens or even as. The majority of facial cosmetic operations performed on Asians are considered Westernizing procedures. Two of the most popular, nose jobs (rhinoplasty) and eyelid lifts (blepharoplasty), are.

Ehlers-Danlos Syndrome Movements - YouTube

The facial muscles are said to act as ligatures on veins and arteries, and they thereby are able to divert blood from, or direct blood to, the brain. An implication of the vascular theory of emotional efference is that habitual use of facial musculature may permanently affect the physical features of the face Facial hemorrhages can appear severe and quite difficult to manage, but generally the best treatment is direct pressure and bulky dressings. Following these, frequent reassessment is a must 3D facial reconstruction and visualization of ancient Egyptian mummies using spiral CT data , E y, E z ed E t are partial derivatives. We say that x is a reliable Los Alamitos, CA, 1990; S.D. Michael and M. Chen, The 3D Reconstruction of Facial Features Using Volume Distortion, Proceedings of Eurographics (UK Chapter) (eds. H. Jones, R. Ehlers-Danlos syndrome (EDS) is a group of inherited disorders marked by extremely loose joints, very stretchy (hyperelastic) skin that bruises easily, and easily damaged blood vessels. Causes. There are six major types and at least five minor types of EDS

Ehlers-Danlos syndrome type IV Orphanet Journal of Rare

Minding Kaling has larger facial features. She is petite, but has larger bone structure and a full-figured body, so she can wear medium to large prints. If you have a mix (say you're tall but small boned with medium sized facial features), go with medium sized prints. Qualit A human face reveals a lot about a person. In creative writing, describing a character's face can uncover information about who they are and how they feel. Writers can zoom in on individual features, like the eyes or mouth, or describe a face in its entirety to paint a picture of a character. Learn how to develop a character through their most telling attribute—their face

22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.22q11.2 deletion syndrome has many possible signs and symptoms that can affect almost any part of the body Editors: Li, Stan Z., Jain, Anil K. (Eds.) Free Preview. Fully updated, revised and expanded, covering the entire spectrum of concepts, methods, and algorithms for automated face detection and recognition systems; Provides comprehensive coverage of face detection, tracking, alignment, feature extraction, and recognition technologies, and issues. Reggio: Examining Self Portraits. Malaguzzi and Musatti (1996), Pelo (2007) believe that self-portraiture is deeply connected to children's identity perceptions stories children tell in their portraits. A self-portrait is an intimate, bold declaration of identity. In her self-portrait, a child offers herself as both subject and artist


EDS Types The Ehlers Danlos Society : The Ehlers Danlos

Effects of Region Features on the Accuracy of Cross-database Facial Expression Recognition. DOI: 10.5220/0008966306100617 In Proceedings of the 12th International Conference on Agents and Articial Intelligence (ICAART 2020) , pages 610-61 The science behind anti-redhead prejudice Studies show that people are less likely to make a move on a redheaded girl or accept the advances of a redheaded guy Ehlers-Danlos syndrome (EDS) dermatosparaxis type (type VIIC) and the related disease of cattle dermatosparaxis, are recessively inherited connective tissue disorders, caused by a deficient activity of procollagen I N-proteinase, the enzyme tha Micro-momentary facial expressions as indicators of ego mechanisms in psychotherapy. In L. A. Gottschalk & A. H. Auerbach (Eds.), Methods of research in psychotherapy (pp. 154-165). New York: Appleton-Century-Crofts. Hwang, H. S., & Matsumoto, D. (2010). Training improves the ability to recognize subtle facial expressions of emotion. Paper. Patients with Bell's palsy usually appear normal. Physical examination of patients with Bell's palsy is usually remarkable for: unintended eye closure with an effort to smile, incomplete closure and the of the eye when patient attempts to close the eyes, inability to puff the cheek in affected side and impaired or absent taste in affected side.

the rst recognised 2D facial feature and maps it into 3D, then a further CNN is applied to track the head orientation. These models allow real time tracking of eye gaze independently from orientation of the head. Due to the facial features and applied facial symme-tries, the eye gaze recognition is robust towards face and image-based occlusions Frequency not reported: Hirsutism, hypertrichosis, coarsening of the facial features, enlargement of the lips, Peyronie's disease. Dupuytren's contracture and drug rash with eosinophilia and systemic symptoms (DRESS), erythema multiforme, SJS/TEN risk in patients of Asian ancestry who have HLA-B 1502 . Endocrin Permanent rounding of facial features or squaring of the jawline. Bodily and facial hair that never goes away. To Read the Full Story Subscribe Sign In Continue reading your article with. Classical Ehlers‐Danlos syndrome (cEDS) is characterized by marked cutaneous involvement, according to the Villefranche nosology and its 2017 revision. However, the diagnostic flow‐chart that promp..

What is Vascular Ehlers-Danlos Syndrome? - The VEDS Movemen

Ed and several Easton police officers supposedly caught the ghost on film. Related: The Conjuring Universe: The 10 Scariest Moments, Ranked. When Ed described his encounter with the ghost, he claimed that several ghost lights came together to form a woman without any facial features, dark hair, and a white dress Op-Ed: Bias in the justice system is real, and the death penalty reveals it so-called black features. In research I led in 2006, looking more black more than doubled the chances that a.

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Pictures of vascular Ehlers-Danlos Syndrome (vEDS) Fight ED

5 Different facial expressions during teaching help the students to understand the lesson in a more effective way. 20 19 1 --- --- 40 100 6 Teacher's facial expressions positively affect the teaching learning process in classroom. 21 18 1 --- --- 40 100 7 I mostly use my facial expressions to appreciate the performance o Predict Baby's Facial Features. This is one of the sillier baby shower games. You and your friends and family will be in stitches over the collaged faces they end up with after combining cut and pasted features of the mom- and dad-to-be. Bun in the Oven & Burgers on the Grill Co-ed Baby Shower by Whitney Irene Approximately 24% of polio infections in children consist of a minor, nonspecific illness without clinical or laboratory evidence of central nervous system invasion. This clinical presentation is known as abortive poliomyelitis, and is characterized by a low fever, sore throat, and complete recovery in less than a week For years, HireVue's fully autonomous software, which uses AI to analyze facial features and movements during job interviews, has raised concerns and criticisms for both its grandiose claims and.

Signs And Symptoms Of Ehlers-Danlos Syndrome - HealthPrep

The Windows 10 Hello Facial Recognition feature requires an Intel RealSense or 3D Camera to support facial unlock features. Resolution. NOTE: On many systems, IR or 3D capable cameras are an OPTIONAL item. If this option is not selected during the order process, then the system will not be Windows Hello compliant. Many system configurations. Jun 10, 2021 at 2:08 PM. Baltimore Cityy Councilman Kristerfer Burnett introduced legislation that would temporarily ban the use of facial recognition technology at city departments until an audit. Amazon.com Books has the world's largest selection of new and used titles to suit any reader's tastes. Find best-selling books, new releases, and classics in every category, from Harper Lee's To Kill a Mockingbird to the latest by Stephen King or the next installment in the Diary of a Wimpy Kid children's book series. Whatever you are looking for: popular fiction, cookbooks, mystery. Studies on first impressions from facial appearance have rapidly proliferated in the past decade. Almost all of these studies have relied on a single face image per target individual, and differences in impressions have been interpreted as originating in stable physiognomic differences between individuals In March, the University of Wisconsin-Madison disabled facial recognition features offered through Honorlock, an online exam proctoring service, after three students with darker skin tones said.

Genes That Don&#39;t Fit!: If You Have Ehlers Danlos Syndrome