Ehlers Dalos Syndrome Research Paper

AMPs is an umbrella term for several pain disorders such as chronic regional pain syndrome (CRPs), fibromyalgia, myofascial pain syndrome, reflex neurovascular dystrophy (RND), and reflex sympathetic dystrophy (RSD). AMPs can cause pain all over your body while CRPs causes pain in just one part of your body. AMPS can change the way your body looks or even your entire personality. With AMPS my legs would turn blue and so would my hands. I also would become very upset and, extremely anxious all the time. My life was affected with Amplified Musculoskeletal Pain Syndrome, or AMPs, in a big way mentally and physically. There are three major causes for people who have AMPs, injury, illness, and psychological stress. When people have AMPs and are being treated for it, they have to do psychology sessions, physical therapy sessions, and occupational therapy sessions. For normal people, pain is felt like this: You get hurt, the damage sends a signal through the pain nerve to the spinal cord, the signal is then transferred up to the brain, and the brain recognizes this as pain. Consequently, for people with AMPs something different happens, the pain does not only go up to the brain it also goes to the neurovascular nerves, which control blood flow through the blood vessels. This causes the blood vessels to constrict which causes, even more, pain. The reason for this is because of

There is a low number of people that seek treatment specifically for ASPD. This is mostly due to the fact that people with ASPD usually deny their symptoms and may reject the diagnosis. Individuals with this disorder that do seek help

Ehlers-Danlos syndrome (EDS) is a clinical diagnosis and is a connective tissue disorder characterized by a variety of degrees of joint hypermobility, skin extensibility and tissue fragility. If you have the vascular variety of EDS there is a likely 50% chance it could be passed down from parent to child. When trying to clinically define the pain in EDS, the findings are poor. There are nine different types of EDS and each type is distinguished from others but that depends on the system involved. “Most types of EDS are inherited as autosomal dominant trait, although x-linked and autosomal recessive types have been described” (Beighton). EDS type III is the most common disorder with presenting with generalized joint hypermobility

The first issue I will address to Mrs. Thomas is how to manage the pain, because the problem really worsens her quality of life, it made her self care difficult to carry out, caused her feeling hopeless, dependent, distressed, fatigue, and losing appetite. Taking pain medications on time will keep the pain

Emery-Dreifuss muscular dystrophy (EDMD) is a rare form of muscular dystrophy. It is another one that only affects boys that appears from childhood to the early teen years and sometimes as late as the age of twenty five. It causes muscles weakness and wasting in the shoulders, upper arms, shins, and often causes problems with the joints becoming tighter. Life threatening heart problems are common and can also affect those who do not have this disease, but simply carry the genes for it. This is a slow progressing disease and often has slow progressing muscle weakness compared to other forms of muscular dystrophy.

It is available when both members of a couple are carriers. These tests can also be used to screen if you are a carrier of the disorder. Although there is no cure for Sandhoff, there is treatment. These are used to manage symptoms and pro-long life expectancy.” Supportive treatment includes proper nutrition and hydration and keeping the airway open. Anticonvulsants may initially control seizures (NINDS)”. As a result of research there are more experimental treatments. For example, children can receive transplants of stem cells from an umbilical chord. Another way is through gene therapy; which is done by “restoring the missing enzyme by introducing the correct genetic code so proper enzyme production can occur (NTSAD). “ Due to further research attempts, after diagnosis, there are ways to treat and manage symptoms to provide comfort.

Imagine a world where you have been diagnosed with a disease that has no cure and left your world upside down because your body has turned against you. Multiple Sclerosis is a potentially debilitating disease that is caused by the body’s immune system attacking the Myelin sheath of nerve fibers throughout the body (Multiple Sclerosis, 2017). This, in turn, creates miscommunication or lack of communication in the body, which can eventually lead to permanent disability. For those who are diagnosed, there are various symptoms to watch for and while not curable, it is treatable.

Noticeably high arches are common, and lead to issues when walking such as tripping and sprained ankles from running. Furthermore, cramps in the legs or cold legs are seen in almost every patient as a result of exercise. The hands and fingers can be influenced by CMT, making small tasks, like zipping a zipper, difficult (Krajewski 234)

Diagnoses include failed back surgery, lumbar; degenerative disc disease, lumbar spine; back pain; lumbar radiculopathy; spondylosis without myelopathy or radiculopathy, lumbar region; impingement syndrome of bilateral shoulders; myalgia; xerostomia; erectile dysfunction; testicular hypofunction; chronic anxiety; chronic depression; and chronic insomnia.

They may develop alone or in combination, but as the disease progresses, all are usually present. There is no true paralysis. The symptoms are always bilateral but usually involve one side early in the illness. Because the onset is insidious, the beginning of symptoms is difficult to document. Early in the disease, reflex status, sensory status, and mental status usually are normal. Postural abnormalities (flexed, forward leaning), difficulty walking, and weakness develop. Speech may be slurred. Autonomic-neuroendocrine symptoms include inappropriate diaphoresis, orthostatic hypotension, drooling, gastric retention, constipation, and urinary retention. Depression is also prevalent.

have been trying to find the exact cause of this disease and how it can be treated so

Symptoms of the disease vary; however, the two main occurrences consist of dizziness and blackouts, or arrhythmias. The first being common due to strenuous activities like working out, while arrhythmias are when electrical

Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain. When GJH is accompanied by pain in $4 joints over a period $3 months in the absence of other conditions that cause chronic pain, the hypermobility syndrome (HMS) may be diagnosed. In addition, GJH is also a clinical sign that is frequently present in hereditary diseases of the connective tissue, such as the Marfan syndrome, osteogenesis imperfecta, and the Ehlers–Danlos syndrome. However, within the Ehlers–Danlos spectrum, a similar subcategory of patients having similar clinical features as HMS but lacking a specific genetic profile was identified: Ehlers–Danlos syndrome hypermobility type (EDS-HT). Researchers and clinicians have struggled

 Typically, people who have this syndrome require a sizeable about of assistance throughout their lives because the combination of their symptoms can be a

Ehlers-Danlos Syndrome (Hypermobility Type) is a genetic connective tissue disorder characterized by joint laxity, velvety skin, joint pain, and other widespread complications of the body. It can be inherited from a parent with the same faulty gene, or it can be a newly developed mutation. Connective tissue is infused with collagen protein that provides strength and elasticity. It is spread abundantly throughout the human body in skin, muscles, tendons, ligaments, blood vessels, and surrounding the internal organs. In the individual with EDS-HT, abnormal collagen formation in the connective tissue causes the tissue to stretch beyond what is normal, resulting in damage and other multi-systemic problems.