Overactive bladder (OAB) is a term that encompasses a group of urinary symptoms. It is not categorized as a disease, but it could make participating in everyday activities at home, work, or school a little more challenging. The condition may occur due to factors like age, health conditions, and other environmental influences. One needs to know about these eight early signs and symptoms of OAB, as it could help get the right treatment options. 1. Urinary urgency (dysuria) One of the first signs of an overactive bladder is abnormally frequent urination, termed urinary urgency. A stinging, burning, or itchy feeling usually accompanies the discomfort caused by the symptom. Urinary urgency makes an individual feel a strong urge to urinate and makes them feel like a leak may happen if they do not go to the bathroom immediately. 2. Urge incontinence Sometimes, when an individual has an overactive bladder, they might leak urine, which is known as urge incontinence. The sign makes them feel a sudden and urgent need to use the restroom. One may also leak urine when sneezing, doing physical activity, or laughing. This may also occur due to certain treatment options, changes in eating habits, and infections. Experts may recommend pelvic floor exercises and therapies like nerve stimulation to manage the symptoms.

Narcolepsy is a sleep disorder that can make one feel extremely drowsy during the day. Those affected also find it harder to stay awake for longer periods and consequently experience trouble carrying out daily tasks. Narcolepsy can be managed with prescriptions and other remedies, with early treatment helping control symptoms that affect daily routine. So, here are early warning signs of narcolepsy that should prompt one to seek medical intervention: 1. Excessive daytime sleepiness One of the most visible early warning signs of narcolepsy is feeling excessively sleepy during the day. Further, one may fall asleep without warning anytime and anywhere. For instance, one might be working or talking to their friends and fall asleep out of the blue. They may stay asleep for a few minutes or up to half an hour. While they might feel refreshed when they wake up, the symptoms might return soon after. 2. Automatic behavior Those with narcolepsy may continue to function even through their episodes of sleep, such as talking or putting away things. However, they may have no memory of performing these tasks once awake. These activities may also be routine activities that one typically carries out while awake. Studies show that about 40% of people with narcolepsy experience episodes of such automatic behavior.

Muscular dystrophy refers to more than 30 types of genetic disorders that may damage or weaken muscles over time. It generally occurs due to a deficiency of the protein “dystrophin,” which is crucial for muscle function. The signs and symptoms may vary depending on the type of MD, condition, and its severity in every affected individual. This article aims to identify six types of muscular dystrophy disorders and their early warning signs. Duchenne Muscular Dystrophy (DMD) DMD is one of the most common and chronic types of muscular dystrophy. Its onset typically occurs in early childhood, between the ages of 2 and 3. The condition typically affects boys, although there have been rare occurrences among girls as well. Due to its severity, people living with this health condition tend to have a shorter life expectancy. Common symptoms of DMD include: Trouble walking, running, or jumping Loss of reflexes Difficulty standing up Poor posture Waddling gait Bone thinning Abnormal curvature of the spine (scoliosis) Learning differences Delayed growth Breathing difficulties Difficulty swallowing Lung and heart weakness Becker Muscular Dystrophy (BMD) BMD is a rare genetic disorder that causes muscle weakness and degeneration over time. Symptoms generally begin to develop between the ages of 5 and 15.

Dental implants are a remarkable solution for those seeking to restore their smile and oral function. Their benefits include retaining bone structure, freedom from food restrictions, effective speech and communication, and a complete smile. However, like any medical procedure, complications can arise. A spectrum of signs might signal a potential issue with dental implants. Therefore, it’s essential to recognize the following early signs of possible problems to ensure the longevity and efficacy of dental implants. Persistent pain and discomfort Beyond post-operative discomfort, an intensifying pain can indicate an underlying issue. This pain may manifest as a lingering ache, sharp spasms, or even a throbbing sensation. If the pain persists or worsens over time, it is vital to seek a professional assessment. This could indicate early inflammation, nerve involvement, or implant instability. Swelling and inflammation It’s normal to experience some mild swelling and inflammation after a dental implant procedure. However, if these symptoms persist or worsen, it may indicate an underlying issue. When brushing, you may notice redness, swelling, or bleeding of the gums around the implant site. It’s important to keep a close eye on these symptoms. Prolonged inflammation could be a sign of healing, infection, or problems with implant integration.

Colorectal cancer is an umbrella term for cancers affecting the colon and rectum. The colon (large intestine) and rectum are vital parts of the digestive system, where the body processes food and eliminates waste matter. Colorectal cancer is generally called colon cancer and is more commonly seen in older adults. While the condition can be managed well, it must be diagnosed early. Here’s a closer look at colorectal cancer and its symptoms. What is colorectal cancer? When abnormal cells in the colon or rectum multiply and grow out of control, they can form a tumor. Over time, these cancer cells can also spread to other body parts if not treated, leading to complications. Colorectal cancer often begins as small growths called polyps on the inner lining of the colon or rectum. These polyps are not always cancerous and may not even trigger symptoms. However, if left untreated, the polyps may become a life-threatening tumor. Symptoms of colorectal cancer The following are a few symptoms of the condition that should not be ignored. Those who experience these should visit a healthcare professional for evaluation and guidance: Changes in bowel habits One of the most common early signs of colorectal cancer is a noticeable change in bowel habits.

MAC is a group of pathogens known as Mycobacterium Avium Complex or nontuberculous mycobacteria (NTM) found in the environment. They infect the lungs and lead to MAC lung disease, which is of two types: one type causes the development of nodules in the lungs and is called nodular disease, and the second type affects the cavities in the upper parts of the lung and is called upper lobe cavitary disease. Here are some of the common signs of MAC lung disease and how to manage them: Common signs of MAC lung disease The signs of MAC lung disease differ on a case-to-case basis. In most cases, the symptoms are generally nonspecific. Also, some may experience mild symptoms, or the signs may be nonexistent. As a result, there is often a delay in diagnosis and treatment. Some people have mild or unnoticeable symptoms. When the symptoms do occur, one may experience the following: Disruption in lung function When the NTM pathogens accumulate in the lungs’ cavities, they can create a hole in the lung tissue. This can cause pain in the chest. In addition, a person may experience persistent wheezing and coughing. In some cases, the coughing is accompanied by bouts of breathlessness.

Leukemia is a type of cancer in which the body’s blood-forming tissues grow out of control. It has several subtypes, such as acute myeloid leukemia, lymphoblastic leukemia, and chronic lymphocytic leukemia. Like many cancers, leukemia is relatively treatable in its initial stages. Hence, individuals must diagnose it early. One way to detect this condition quickly is to look for its early signs and symptoms. Here are a few common signs of leukemia: Fever Leukemia tends to affect nearly every organ, including the immune system. When one’s immunity is compromised, it results in frequent bouts of fever and raised body temperature. Consequently, a person with this condition may experience night sweats on a daily basis. Sometimes, fever is a side effect of treatments used for managing leukemia. Muscle and joint pain Besides fever, individuals with early-stage leukemia may experience persistent pain in their muscles and joints. If the pain increases and leads to tenderness in the affected areas, it is a clear indicator of this cancer. Such symptoms tend to be felt more than seen. If untreated, the progressive pain can cause rapid organ damage. All these factors bring about noticeable muscle loss. Fatigue Since leukemia is directly associated with the blood cells, it causes circulation issues.

Maintaining eye health is crucial for ensuring healthy vision throughout life. However, individuals often fail to notice how their lifestyle and several environmental factors negatively affect their eye health. Whether it is long exposure to harsh sunlight or hours spent in front of the screen, everything affects the eyes. So, prioritizing eyes and taking proper care of them becomes important. Here are a few simple ways to maintain eye health to ensure healthy vision. 1. Following the 20-20-20 rule Facing the screen constantly for a long time can lead to the drying of the eyes and put a strain on them. Dry eyes further cause irritation and itchiness, leading to discomfort and disruptions throughout the day. So, whether facing their phone screen or working in front of their laptop, it is important to take breaks in between by following the 20-20-20 rule. The rule suggests that after every 20 minutes of facing the screen, one must take a break for 20 seconds, look away, and focus on something at least 20 feet away. It is a simple but effective way to reduce eye strain and maintain visual comfort. 2. Wearing sunglasses Sunglasses might be a fashion accessory, but they are not just that.

Itchy skin or pruritus is a sensation most people experience at some point. It is generally harmless and often annoying. However, if itchy skin persists continuously over a long period, it may indicate an underlying health condition. Also, if the itching occurs over the same body area and does not go away with simple remedies, one must consult their primary care doctor for a proper diagnosis. Here are some common signs of itchy skin that may require attention. Dry skin Dry skin is one of the most common causes of itching. When the skin cells lose hydration, the top layer becomes dry and flaky, which leads to irritation and repeated itching to get relief. Dryness can occur due to cold weather or low humidity. Excessive bathing, frequent showering with hot water, and using harsh soaps may also cause the skin to lose its natural hydration, leading to itchiness. Rash or redness Another common sign of itchy skin is when rashes develop over the affected areas. There can be redness as well, which results from inflammation. These rashes and red patches will vary in shape and size. These are usually areas of intense itching that worsen unless treated properly. Such rashes may develop due to allergic reactions, contact dermatitis, insect bites, or infection.

Sickle cell anemia is a genetic blood disorder characterized by abnormal, crescent-shaped red blood cells. It is caused by a specific genetic mutation that alters the structure of hemoglobin, the protein responsible for carrying oxygen in red blood cells. According to the World Health Organization, approximately 300,000 infants worldwide are born with sickle cell anemia yearly. These misshapen cells have difficulty passing through small blood vessels, leading to reduced oxygen delivery to tissues and organs. Causes of sickle cell anemia Sickle cell anemia, a genetic blood disorder, has its origins in specific genetic mutations. Understanding these mutations is essential for comprehending the condition’s causes. Genetic inheritance Sickle cell anemia is primarily a hereditary condition rooted in the inheritance of specific genetic mutations. A unique genetic combination occurs when both parents carry an abnormal hemoglobin S (HbS) gene. In this scenario, there’s a 25% chance that their child will inherit two copies of the HbS gene, leading to sickle cell anemia. The sickle cell trait The sickle cell trait comes into play when an individual inherits one HbS gene and one normal hemoglobin gene. Carriers of this trait typically do not experience severe symptoms associated with full-blown sickle cell anemia. However, they can pass this trait on to their children, making it a crucial consideration for family planning and genetic counseling.