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Showing posts from August, 2026

Understanding Creutzfeldt-Jakob Disease (CJD) By: Nichole Michael-Avabore

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Introduction Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, and always fatal neurodegenerative disorder. It belongs to a family of diseases known as prion diseases, also called Transmissible Spongiform Encephalopathies (TSEs). Spongiform refers to the way affected brains look. With prion diseases, the brain is filled with holes and looks like a sponge when the tissue is examined under a microscope. Like other prion diseases, CJD causes problems with muscle coordination, thinking, and memory. There are about 350 cases per year in the United States, and about 70% of people with CJD die within one year of getting the disease. Why Is It Important? It is vital to understand CJD because it is rare, and although it isn’t very well known, it is universally fatal. Many people struggle with dementia, problems with thinking, balance problems, etc. As of now, there is no known cure; thus, research is vital for developing early diagnostic tests and effective treatments. Who It Affe...

Ehlers–Danlos Syndrome: Understanding a Complex Connective Tissue Disorder. By: Ayomide Makinde

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Introduction. Ehlers-Danlos syndromes (EDS) are a group of 13 inherited connective tissue disorders caused by genetic changes that affect the body's connective tissues, which provide support and strength to the skin, joints, blood vessels, and internal organs. Each type of EDS has its own distinct set of characteristics and diagnostic criteria. However, many people with EDS experience common features such as joint hypermobility (unusually flexible joints), skin hyperextensibility (skin that stretches more than usual), and tissue fragility. EDS is estimated to affect approximately one in every 5,000 people worldwide and can occur in individuals of any sex, race, or ethnic background. Main Body EDS is caused by genetic changes that affect connective tissue - It is especially caused by a faulty gene that causes your body to produce not enough collagen. Since the function of collagen is to maintain support across the connective tissues in your body, having the condition can result in o...

Premature Ovarian Insufficiency: More Than Early Menopause By: Mariam Mubarak Saeed Sayyah Al Dhaheri

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 Premature Ovarian Insufficiency: More Than Early Menopause Introduction: Premature ovarian insufficiency (POI), also known as primary ovarian insufficiency, occurs when ovarian function declines before age 40. As a result, the ovaries produce lower amounts of estrogen and releaseeggs less frequently, leading to irregular or absent menstrual periods andreduced fertility. Although POI affects reproductive health, it can also influencebone health, heart health, and emotional well-being. Because it is often mistakenfor early menopause, increasing awareness of POI is important to ensure thatindividuals receive an accurate diagnosis and appropriate medical care.   Causes:  Premature ovarian insufficiency can result from a variety of causes, although in  many cases the exact cause remains unknown. Some cases are linked to genetic conditions such as Turner syndrome or Fragile X premutation, while others may develop because of autoimmune diseases, chemotherapy, radiation the...

Underdstanding Lipedema: Causes, Sympotoms, Diagnosis, and Current Research By: Mariam Mubarak Saeed Sayyah Al Dhaheri

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 Understanding Lipedema: Causes, Symptoms, Diagnosis, and Current Research Introduction: Lipedema is a chronic connective tissue and fat disorder that primarily affects women. It is characterized by an abnormal buildup of fat, usually in the legs, hips, buttocks, and sometimes the arms. Unlike ordinary body fat, lipedema fat is often painful, bruises easily, and does not respond well to diet or exercise. Despite affecting millions of women worldwide, lipedema remains widely underdiagnosed and is frequently mistaken for obesity or lymphedema. Raising awareness of this condition is essential to help patients receive earlier diagnoses, appropriate treatment, and better support. Causes: The exact cause of lipedema is still unknown, but researchers believe it results from a combination of genetic and hormonal factors. The condition often runs in families, suggesting that inherited genes play an important role in its development. Lipedema commonly begins or worsens during periods of horm...

Chronic Fatigue Syndrome (ME/CFS) By: Maya Chahbi

  Chronic Fatigue Syndrome (ME/CFS) Introduction: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex, long-term illness that causes severe fatigue that does not improve with rest. Symptoms can significantly affect a person’s ability to carry out physical and mental activities. ME/CFS is important to understand because it can affect people’s daily lives, education, work, healthcare, and overall well-being. Causes: Researchers have not yet identified one exact cause of ME/CFS. However, a combination of factors may play a role, including: ● Genetics: Genetics may contribute to a person’s likelihood of developing ME/CFS. ● Infections: Some people develop ME/CFS symptoms after recovering from an infection. ● Energy Use: Research suggests that some people with ME/CFS may have differences in how their bodies produce and use energy. Symptoms: Symptoms of ME/CFS can vary from person to person, and their severity can change from day to day. In addition to fatigue, sy...