Blood Clot Awareness Month

March is Blood Clot Awareness Month
Anyone can be affected by a blood clot regardless of age, gender, or race. This Blood Clot Awareness Month, learn the signs and symptoms of a blood clot and find free resources to share with friends, family, and colleagues to help raise awareness about blood clots.
Blood Clot blocking the red blood cells stream
What is a blood clot?
A deep vein thrombosis (DVT) is when a blood clot forms in one of the large veins, usually in the lower leg, thigh, pelvis, or arm. A blood clot can partially or completely block blood flow in the vein. When a DVT is left untreated, a part of the clot can break off and travel to the lungs, causing a blockage known as a pulmonary embolism (PE).
Why is it important to learn about blood clots?
In the United States, an estimated 900,000 people are affected by a blood clot every year, yet they are often underdiagnosed. Blood clots can cause serious medical conditions that can lead to illness, disability, and even death if not treated early. Blood clots can affect anyone, but certain risk factors such as pregnancy, cancer and its treatment, and hospitalization can increase a person’s risk for a blood clot. It’s important to know the signs and symptoms of a blood clot so that you know to seek medical treatment as early as possible.
Knowing the symptoms of a DVT or PE can help alert you to seek medical treatment as early as possible, although they sometimes occur with no symptoms.
Common signs and symptoms of a DVT include:
-Swelling of the affected area
-Pain
-Tenderness
-Redness of the skin
If you have these signs or symptoms, alert your doctor as soon as possible.
Common signs and symptoms of a PE include:
-Difficulty breathing
-Faster than normal or irregular heartbeat
-Coughing up blood
-Very low blood pressure, lightheadedness, or fainting
Seek medical attention immediately if you experience any of these signs or symptoms.

Brain Injury Awareness Month

Brain Injury Awareness Month is recognized during the month of March to bring awareness to traumatic brain injury (TBI) prevention and improve overall quality for those living with TBIs. About 166 Americans die every day from traumatic brain injuries (1). TBIs affect millions of people each year in the US. They are caused by impact or force to the head/body or by a penetrating injury to the head. Falls make up nearly half of TBI-related hospitalizations. Firearm-related suicide is the most common cause of TBI-related deaths in the US. Motor vehicle crashes and assaults are the most common cause of TBI (1).
TBIs are the leading cause of death and disability in children (2). These brain injury characteristics are generally recognized in accordance with age and are important to be aware of in children:
-Infants: accidental head injury, abusive head trauma
-Toddlers/school age children: accidental head injury (due to an increase in motor skills, child safety seats, pedestrian injury)
-Adolescents: bicycle and motorcycle-related accidents, sports-related head injuries.
One of the best things you can do to protect your child or teen form a TBI is to make sure they wear a helmet when partaking in high-risk activities such as bike riding or sports. While there is no concussion-proof helmet, it can help protect you from a TBI substantially.
Follow these helmet tips for best use:
-Helmet fits properly and is well maintained
-Age appropriate
-Worn consistently and correctly
-Appropriately certified for use
It is important both this month and every month to recognize the increasing prevalence of TBIs. Do your part to increase prevention awareness through education and taking preventative measures, and support those who endure such traumatic injuries.
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March is National Colorectal Cancer Awareness Month

March is National Colorectal Cancer Awareness Month
What is the Goal of Colorectal Cancer Awareness Month?
March was officially dedicated as Colorectal Cancer Awareness Month in February 2000 by President Bill Clinton. Involvement in this awareness month has only grown over the years, with those affected by this disease rallying together to spread awareness and information. The organization Fight Colorectal Cancer says that during March and throughout the year, they fight for more research, screening, treatment options, and lives saved. Similar organizations fight for the same goal because awareness is key to screening, which is key to detecting and even preventing colorectal cancer.
Who is Affected by Colorectal Cancer?
Although many people believe that colorectal cancer only affects older adults, the disease is on the rise in younger adults, and according to Fight Colorectal Cancer, it is expected to be the number 1 cancer killer for people 20 to 49 years old by 2030. With that being said, the disease is still more common in adults over 50 years old. The risk is greater for those with a first-degree relative with colorectal cancer compared to those with no family history of the disease. Other factors that can increase a person’s risk include a personal history of colorectal polyps or cancer, certain inherited syndromes, smoking and alcohol use, and a sedentary lifestyle. Those with Inflammatory Bowel Disease, such as ulcerative colitis or Crohn’s disease, are also at a higher risk for colorectal cancer and should be screened more often.
Why is Colorectal Cancer Screening So Important?
Cancer in the colon or rectum most often begins as a polyp on the inner lining that becomes cancerous over time, often over several years. The goal of colorectal cancer screening is to identify and remove polyps in their beginning stages so that they never have a chance to turn into cancer. According to the American Cancer Society, colorectal cancer has a 90% survival rate when found and treated early. Unfortunately, many colorectal cancers are detected after they have already spread. Regular screening, scheduled more often for those with certain risk factors, is crucial to detecting this disease early so the right treatment methods can be put in place. There are many screening options for colorectal cancer, with colonoscopy being the gold standard.
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National Endometriosis Awareness Month

National Endometriosis Awareness Month was an initiation taken by The Endometriosis Association in 1993. This month is observed worldwide through various activities that involve educating people about the condition, fundraising, and marches. Yellow ribbons and brochures are distributed worldwide to honor National Endometriosis Awareness Month.
Endometriosis is a disorder where the endometrial tissue migrates to areas outside the uterus. The endometrial tissue (inner lining of the uterus) is the same tissue that thickens during the menstrual cycle. When the endometrial tissue sheds it is discharged along with blood causing menstruation. In Endometriosis this process occurs outside the uterus, where the blood has nowhere to go, causing pain in the pelvic region.
The symptoms include pelvic pain, heavy periods, bleeding between menstruation, and infertility. Endometriosis is often difficult to diagnose because there are many other conditions that can cause these symptoms. In a few cases, endometriosis remains undiagnosed because it is mistaken for other conditions or women do not experience any symptoms at all.
The causes of endometriosis are uncertain, but several factors such as genetics, retrograde period flow, (where blood flows back into the pelvis instead of out of the body,) immune system disorders, and hormones are possible influencers.
Treatment ranges from symptom management with pain medication and hormone therapy such as oral contraceptives to surgical treatment. Conservative surgery involves removing the misplaced endometrial tissue while preserving the uterus, though in severe cases a hysterectomy may be performed.
Endometriosis can have a devastating effect on the quality of life of individuals suffering from this disorder and can have a huge impact on their physical, mental, and social well-being.
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Multiple Sclerosis Awareness Month

What is Multiple Sclerosis (MS)?
Multiple Sclerosis (MS) is an unpredictable, often disabling disease of the central nervous system that disrupts the flow of information within the brain and between the brain and body.
While MS is not hereditary, having a first-degree relative such as a parent or sibling with MS does significantly increase an individual’s risk of developing the disease. Studies have shown that there is a higher prevalence of certain genes in populations with higher rates of MS. Common genetic factors have also been found in some families where there is more than one person with MS. Some researchers theorize that MS develops because a person is born with a genetic predisposition to react to some environmental agent that, upon exposure, triggers an immune-mediated response. Sophisticated new techniques for identifying genes are helping to answer questions about the role of genes in the development of MS. Understanding what causes MS will speed the process of finding more effective ways to treat it and, ultimately, cure it, or even prevent it from occurring in the first place.
The evidence is also growing that smoking plays an important role in MS. Studies have shown that smoking increases a person’s risk of developing MS and is associated with more severe disease and more rapid disease progression. Fortunately, the evidence also suggests that stopping smoking, whether before or after the onset of MS is associated with a slower progression of disability.
No single test can diagnose MS. The medical history, neurologic exam and lab tests help physicians rule out other diseases and confirm the MS diagnosis. Strategies to diagnosis MS include a careful medical history, neurological exam and various tests to include magnetic resonance imaging (MRI), evoked potentials (EP) and spinal fluid analysis.
Managing MS is an ongoing process beginning with the very first symptoms and continuing throughout the disease course. Knowing what to look for, where to find it, and how to work effectively with your doctor and other health professionals is essential to your health, wellness and quality of life.
Types of Multiple Sclerosis (MS)
~Relapsing-remitting MS (RRMS) RRMS is the most common disease course characterized by clearly defined attacks of worsening neurologic function. These attacks, also called relapses, flare-ups or exacerbations are followed by partial or complete recovery periods (remissions) during which symptoms improve partially or completely and there is no apparent progression of disease. Approximately 85% of people with MS are initially diagnoses with relapsing-remitting MS.
~Primary-progressive multiple sclerosis (PPMS) is characterized by steady worsening of neurologic functioning, without any distinct relapses (also called attacks or exacerbations) or periods of remission. A person’s rate of progression may vary over time — with occasional plateaus or temporary improvement — but the progression is continuous.
~The name for secondary-progressive multiple sclerosis (SPMS) comes from the fact that it follows after the relapsing-remitting disease course (RRMS). Of the 85 percent of people who are initially diagnosed with RRMS, most will eventually transition to SPMS, which means that after a period of time in which they experience relapses and remissions, the disease will begin to progress more steadily (although not necessarily more quickly), with or without any relapses (also called attacks or exacerbations).
~Progressive-relapsing multiple sclerosis (PRMS) is the least common of the four disease courses, occurring in approximately five percent of people with MS. Like those with primary-progressive MS (PPMS), people with PRMS experience steadily worsening neurologic function disease progression from the very beginning, in addition to occasional relapses like those experienced by people with relapsing-remitting MS.
Because PRMS is progressive from onset, it may be initially diagnosed as PPMS, and then subsequently changed to PRMS when a relapse occurs. Although this disease course is progressive from the outset, each person’s symptoms and rate of progression will be different.
Exercise and Diet:
Exercise is also helpful in managing many MS symptoms. A study published by researchers at the University of Utah in 1996 was the first to demonstrate the benefits of exercise for people with MS. Those patients who participated in an aerobic exercise program benefited from:
*better cardiovascular fitness
*improved strength
*better bladder and bowel function
*less fatigue and depression
*a more positive attitude
*increased participation in social activities
Additional studies have confirmed the benefits of exercise, including improvement in cognitive function and mood enhancement.
Inactivity in people with or without MS can result in numerous risk factors associated with coronary heart disease. In addition, it can lead to weakness of muscles, decreased bone density with an increased risk of fracture, and shallow, inefficient breathing.
Exercise doesn’t have to be a rigorous cardiovascular workout to provide benefits. Physical activity in general is beneficial and can include a variety of things most people can do in the comfort of their home or community. Physical activity includes but is not limited to:
-gardening
-household chores
cooking
Yoga
Water Exercise
An exercise program needs to fit the capabilities and limitations of the individual. It may need to be adjusted as changes occur in MS symptoms. Any person with MS who is initiating a new exercise program should also consult with a physician before starting.
Diet and Healthy Tips
While additional research is being conducted on diets in MS, the following recommendations are based on what is known today:
1. Maintain a balanced diet: A well-balanced diet helps maintain overall health and may prevent a wide range of diseases. In addition, diet may have an effect on the MS disease process, including direct effects on the immune system, indirect effects through modulation of the gut flora, and effects on components of the central nervous system.
2. Achieve a healthy weight: Research findings point to obesity as a possible risk factor for developing MS. The incidence of MS appears to be increasing worldwide at the same time that caloric intake and being overweight or obese are increasing. In recent studies, obesity and body size at age 18–20 were associated with an increased risk of MS, as was higher Body Mass Index (BMI) at age 7–13. It has also been shown that obesity can affect disability progression and health-related quality of life.
3. Reduce sodium intake: Some recent evidence points to sodium, which is a primary component of salt, as potential factor in MS disease activity. In an observational study, people who consumed a moderate or high amount of sodium had a higher rate of relapses and a greater risk of developing a new lesion on MRI than people who consumed a low amount of sodium.
4. Monitor vitamin D levels: Several studies have suggested that low intake and low blood levels of vitamin D play a role in the risk of MS and of disease progression. Vitamin D supplementation is currently being evaluated in randomized, controlled clinical trials in order to determine whether there is a causal relationship between vitamin D and MS disease activity — or some other non-influential association — and whether the potential benefits of vitamin D supplementation outweigh any risks for people with MS. In the meantime, vitamin D can be obtained from oily fish (including salmon, mackerel, sardines, herring and trout), egg yolks and cod liver oil, as well as dairy products, cereals and orange juice that have been fortified with vitamin D. Determining whether a person is a candidate for vitamin D supplementation depends on his or her blood level of vitamin D, which can be obtained with a simple blood test. The normal range of 25-hydroxyvitamin D is 30–100 ng/mL (75–250 nmol/L); a vitamin D level in the 20–30 ng/ML range is considered low; a vitamin D level below 20 ng/mL is considered deficient.
5. Consider polyunsaturated fatty acids (PUFAs): The potential role of PUFAs in slowing disease activity has been studied with mixed results. As with vitamin D supplementation, carefully controlled trials are necessary to identify potential benefits and risks.
6. Use caution with probiotics: Probiotics (bacteria and other microorganisms that may provide health benefits) may eventually prove to be a potential treatment for MS. However, studies of the safety and effectiveness of probiotics in MS are very limited. Since some probiotics may stimulate the immune system, both the potential benefits and risks must be studied.
Other Diet Tips:
• Limit sugar and processed foods
• Increase fruits and vegetables
• Choose lean sources of protein (including chicken, turkey, soy products, fish, beans)
• Choose healthy fats (polyunsaturated fats from nuts, seeds, vegetable oils and oily fish)
• Consume adequate fiber and fluids
The National Multiple Sclerosis Society provides access to accurate, current, and comprehensive information to people with MS and those who care about them.
For more information about Multiple Sclerosis (MS) click on links below:

March is Red Cross Month

American Red Cross recognizes our country’s everyday heroes who give their time to help people in need. In addition to supplying about 40 percent of our nation’s blood, the Red Cross relies on the heroic efforts of its workers and volunteers to provide shelter, food, and emotional support during emergencies and disasters.
Here’s five ways you can become a hero for the Red Cross:
-Become a Red Cross volunteer. Lend a hand in your community.
-Give blood. Help a patient going through a hard time.
-Take a class. Gain information and skills to help out in an emergency.
-Make a plan. Get your family involved and develop a preparedness plan for emergencies.
-Make a financial donation. Your generosity will help people in need.
For more information, visit www.RedCross.org

LUCAS is coming to Doddridge County Park

The WVU Cancer Institute’s mobile lung cancer screening unit, LUCAS, travels to 42 of West Virginia’s most rural counties to provide lung cancer screening.
The 48-foot unit is equipped with state-of-the-art lung cancer screening technology and provides lung cancer screening in a comfortable, convenient environment for women, men, and transgender and gender-diverse people with private insurance, Medicaid, or Medicare.
Uninsured patients living in West Virginia, who are age 50 and older and meet lung cancer screening eligibility requirements, may receive lung cancer screening on LUCAS through the generosity of grant funding and donations. With regular lung cancer screenings, cancer may be detected earlier, when it is easier to treat and cure.
More West Virginians die from lung cancer than colorectal, prostate, and breast cancer combined. Approximately 120,000 West Virginians are eligible for lung cancer screening, but only about two to four percent of those eligible for low-dose computed tomography (LDCT) are currently being screened. Most West Virginia counties do not currently have access to LDCT in their area.
LUCAS provides lung cancer screening and then refers patients in need of follow-up to facilities close to their home. Building upon the successful operations and infrastructure of our mobile mammography unit, Bonnie’s Bus, LUCAS is part of the WVU Cancer Institute Mobile Cancer Screening Program, which is focused on bringing cancer prevention services to underserved communities throughout the state.
The WVU Cancer Institute Mobile Cancer Screening Program is coordinated by Cancer Prevention and Control, and is a partnership between the WVU Cancer Institute and WVU Medicine-WVU Hospitals.
~Who can get a lung cancer screening on LUCAS?
The mobile unit provides screenings to individuals who fall within screening guidelines, including women, men, transgender, and gender-diverse people who:
*Are age 50 to 80
*Currently smoke or quit within the past 15 years
*Have a >20 pack/year smoking history
*Have no symptoms of lung cancer
Insurance coverage varies; check with your insurance carrier to determine coverage.
~What type of payment is accepted by LUCAS?
LUCAS will bill Medicaid, Medicare, and private insurance for screening.
Medicare and Medicaid will cover the cost for those who meet the above guidelines and go to a registered facility. Private insurance covers the scan; however, guidelines vary and may require additional risk factors or differ in covered age range.
No eligible West Virginian will be turned away due to lack of insurance or inability to pay. Grant funds and donations are available to pay for lung cancer screening for those without insurance coverage.
~What do I need to bring to the appointment?
Patients should bring their insurance information, driver’s license or picture ID, and a healthcare provider’s orders for the scan.
Please arrive 10 minutes prior to the appointment to check-in with staff and complete the appropriate paperwork. Patients should not wear any metal to their appointment.
~How often should I get a scan?
An annual lung cancer screening for eligible patients is recommended by the U.S Preventive Services Task Forces.
~How soon will I get my results?
Results and recommendations will be sent to each patient and their referring provider within 30 days.
~If I need follow-up care, who do I contact?
Patients with findings that indicate a need for further diagnosis and treatment will be referred to their local provider and healthcare facilities for evaluation. Our LUCAS program manager is available to help find care if needed.

Enfamil Prosobee Infant Baby Formula Recall

Reckitt Recalls Two Batches of Enfamil Prosobee 12.9 oz Simply Plant Based Infant Formula Because of Possible Health Risk for more information go to https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckitt-recalls-two-batches-prosobee-129-oz-simply-plant-based-infant-formula-because-possible

“Fans Don’t Let Fans Drive Drunk”

On Super Bowl Sunday, February 12, 2023, millions of fans will gather with family and friends to watch one of the nation’s most popular sporting events. There will also be lots of socializing that may include drinking.
If you’re hosting a Super Bowl party or out watching the game with friends, remember that fans don’t let fans drive drunk. Always have a plan to get home safely.
“Fans Don’t Let Fans Drive Drunk.”