Category Archives: Outreach

DHEC Observes National Alzheimer’s and Brain Awareness Month

June is Alzheimer’s and Brain Awareness Month, and DHEC recognizes the vital work that healthcare facilities, healthcare professionals, and caregivers do in providing treatment and improving the quality of life of those afflicted with brain trauma and disorders. There are currently over 95,000 people living with Alzheimer’s disease and other related dementias (ADRD) in South Carolina. According to the South Carolina Alzheimer’s Disease Registry, 25% of the ADRD population in the state resides in a long-term care facility (LTCF), including nursing homes and assisted living facilities, while the remaining 75% live independently or with loved ones in the community.

It comes as no surprise that COVID-19 has been an unexpected hurdle in providing special care to each resident or patient afflicted with these diseases. The risk for persons with Alzheimer’s disease and other dementias poses a unique challenge for caregivers, families, and facilities. Changes to routines, use of unfamiliar personal protective equipment (PPE), and disruption to daily schedules can lead to fear and anxiety resulting in increased depression and worsening behavioral changes, such as agitation, aggression, and wandering. While the Centers for Disease Control and Prevention (CDC) recommends specific guidance to facilities for infection control and prevention, it also recommends keeping environments and routines as consistent as possible for patients and residents suffering from ADRD and other brain disorders.

As facilities and caregivers continue to care for patients and residents, the following tips can help improve brain health for those afflicted with these diseases while preventing the spread of COVID-19:

  • Maintain the same environments and routines for the patients or residents while introducing frequent hand washing, social distancing, and use of cloth face coverings (if tolerated).
  • Introduce virtual games and activities for enrichment and memory care.
  • Use face coverings wisely. Face coverings should not be used for anyone with breathing issues or who is unconscious, incapacitated, or unable to remove the mask without assistance.
  • Keep staff consistent in memory care units at facilities.
  • Structured activities may need to occur in the resident’s or patient’s room, or be scheduled at staggered times throughout the day in order to maintain social distancing.
  • Provide safe ways to remain active, such as staff going on walks around the unit or outside with the patient or resident.
  • Limit the number of people in common areas while practicing social distancing.
  • Frequently clean often-touched surfaces, especially hallways and common areas.

Those suffering from ADRD may not be able to communicate that they are feeling ill. It is important to be informed and able to recognize symptoms in order to protect our most vulnerable from COVID-19. Early signs to recognize for a patient or resident who cannot communicate their symptoms are cough, shortness of breath, difficulty breathing, fatigue, or vomiting. Emergency warning signs are trouble breathing, new confusion, inability to wake or stay awake, and bluish lips or face.

Family and friends that would still like to visit loved ones in facilities are encouraged to use messaging systems such as emails, phone calls, cards and letters, recorded video messages, care packages, and even song and poem dedications through the facility intercom. The Centers for Medicare & Medicaid Services (CMS)’s Civil Monetary Penalty (CMP) Reinvestment Program is a great funding opportunity for facilities wishing to procure technical equipment for communication purposes. Nursing homes can also benefit from applying to CMS’ COVID-19 Communicative Technology grant that provides funding for residents to communicate with loved ones.

Lexington Medical Center (LMC) Extended Care recently took advantage of this COVID-19 grant opportunity and purchased two iPads and three iN2L tablets for the nursing home. Though the facility encourages families to make phone calls and chat with loved one outside of the facility’s windows, the technology procured through the grant allows more residents the opportunity to connect with loved ones and to do is in the most convenient, readily accessible, and intimate way. The facility already averages 700 calls per month, not including the calls made by residents with their personal devices. The use of the virtual technology for tele-videos, texts, calls, games, and a myriad of other activities connects loved ones together and helps augment the quality of life for these residents, especially those most vulnerable to brain dysfunction and memory loss.

“Without this COVID-19 communicative grant funding and the opportunity for communities to purchase needed devices, our residents might not have the opportunity to see their family nor would their family see them, which could be detrimental to everyone,” states Debbie Bouknight, Lexington’s Life Enrichment Director. “It is both heartwarming and sometimes heartwrenching, but so worth it to see the interactions happen. I feel we would see far more decline in our residents’ physical and emotional well-being if they did not have these video visit opportunities.

More ideas of how you can connect with loved ones during COVID-19 are available here.

DHEC would like to express its gratitude to all facility staff and loved ones keeping our Alzheimer’s and other dementias population healthy during COVID-19. Residents and patients suffering from these diseases are not just physically vulnerable during this pandemic, but they are also highly susceptible to mental anguish and confusion due to the necessary changes being made at facilities for infection control and prevention. We recognize the extraordinary cooperation between facility staff and families in ensuring excellent care for the quality of life of those afflicted with ADRD, as well as adapting to new forms of communication that keep loved ones both connected and safe.

Links

CDC – Considerations for Memory Care Units in Long-term Care Facilities

CDC – Supporting Your Loved One in a Long-Term Care Facility

USC, Arnold School of Public Health – Alzheimer’s Disease Registry

South Carolina Alzheimer’s Disease Report 2019: Annual Report

Alzheimer’s Association Facts Video

June 19th is #WorldSickleCellDay

Today (June 19th) is World Sickle Cell Day!  Every year, the international health community recognizes Sickle Cell Disease (SCD) as a debilitating genetic disease that impacts families across the globe. Keeping individuals and communities informed about the struggles that come with daily management of SCD, can help raise awareness as well as debunk stereotypes and stigmas associated with persons who have SCD.   

SCD affects millions of people worldwide and is particularly common among people originating from sub-Saharan Africa, Saudi Arabia, India, South America and Central America, and Mediterranean countries, such as Turkey, Greece and Italy.

SCD affects approximately 100,000 Americans and occurs in about 1 out of every 365 African-American births. Individuals living with SCD suffer from both acute and chronic complications that require frequent contact with the medical system. These complications include acute sickle cell pain, fever, and acute chest syndrome (ACS), which is the term used for a number of different findings that includes chest pain, cough, fever, hypoxia and new lung infiltrates.

Here are some quick facts about SCD:

  • Sickle Cell Disease is a group of inherited red blood cell disorders. The red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle” and the cells die early, which causes a constant storage of red blood cells. Healthy red blood cells are round and move through small blood vessels to carry oxygen to all parts of the body.
  • To get SCD, the trait must be inherited from both parents who already have the SCD trait. People with the trait usually do not have any of the signs of the disease and live a normal life, but they can pass the trait to their children.
  • SCD is diagnosed with a simple blood test.  It is most often found at birth during routine newborn screening tests. Early diagnosis and treatment are important.
  • There are several treatment options available for individuals living with different complications of SCD, but the only cure for SCD is a bone marrow or stem cell transplant.  Transplants are very risky, and can have serious side effects, including death.  For the transplant to work, the bone marrow must be a close match (usually a brother or sister). 

SCD and COVID-19

Amid the COVID-19 pandemic, there is significant concern that the overlap of lung disease from COVID-19 with ACS may result in increased complications and amplification of healthcare utilization among individuals with SCD. Patients with SCD often have underlying cardiopulmonary co-morbidities that may predispose them to poor outcomes if they become infected with COVID-19. Source: hematology.org. 

Below are recommendations from the Sickle Cell Disease Association of America (SCDAA) for patients with SCD regarding COVID-19:

  • Patients and parents should be educated about COVID-19 signs and symptoms and the importance of physical distancing to limit chances of exposure and infection.
  • Patients and parents should receive counseling to continue to monitor for fever or other signs of infection. Call  hospital, doctor, or nurse first for advice on where to go for an evaluation.
  • Be sure that patients have an ample supply of all prescribed medication at home (including analgesics) to manage both acute and chronic pain.
  • Patients should adhere closely to the correct use of medications.

SCD Partnerships

DHEC is committed to educating the community and public about the availability of resources and services for individuals and families living with sickle cell disease.  DHEC’s Division of Children and Youth with Special Health Care Needs (CYSHCN), provides assistance to persons with sickle cell disease by covering services, such as, medical expenses, physician visits, durable medical equipment, medical supplies, and prescription drugs.  Assistance is offered to both children and adults who meet eligibility requirements. 

Additionally, CYSHCN engages with the four Sickle Community Based Organizations in the state — the James R. Clark Memorial Sickle Cell Foundation, – Louvenia D. Barksdale Sickle Cell Anemia Foundation, – Orangeburg Area Sickle Cell Foundation and – COBRA Human Services Agency Sickle Cell Program – to ensure persons living with SCD have access to community resources and support services. 

Help Camp Burnt Gin Win “Best of Sumter” Title

Camp Burnt Gin, DHEC’s residential camp for young people with physical disabilities and chronic illnesses, has been nominated for the Best of Sumter awards. Voting for this recognition event sponsored by The Sumter Item is open until February 29, 2020.

Located in Wedgefield, SC, Camp Burnt Gin is a service of DHEC’s Maternal and Child Health Bureau/Division of Children with Special Health Care Needs and has operated since 1945. Staff members, in a ratio of one for every two campers, reside with the campers and assist them throughout a six-day session of activities. 

“The learning opportunities and experiences provided by the camp are invaluable,” said Camp Burnt Gin Director Marie Aimone.. “Camp Burnt Gin helps children to improve their social skills, self-esteem and independence. The camp’s activities are not only fun but help develop skills for a healthy, active lifestyle.”  

This summer’s sessions operate from June to August, and programming focuses on three age groups: 7-15, 16-20 and 21-25. Activities include swimming, arts and crafts, sports, and nature learning, and skits, carnivals, dances, and treasure hunts are part of special evening events. 

Click here to help Camp Burnt Gin claim this title!

How Can Campers Apply?

The camp is also accepting applications for the 2020 season.

“Camp Burnt Gin offers a variety of activities for children, teens and young adults who might not otherwise have a camping experience because of their health care needs,” Aimone said. “Some of the campers we serve live with physical disabilities like orthopedic conditions, hearing loss, epilepsy, sickle cell anemia, heart disease, cerebral palsy and craniofacial conditions.”

Camp Burnt Gin is seeking staff for the 2020 season, too, including counselors, activity specialists, waterfront assistants and nurses. 

“Working at Camp Burnt Gin is an excellent opportunity for someone planning a career in education, health-related professions or social services to gain experience,” said Thomas Carr, a seven-year staff member at the camp. “You come to Burnt Gin with the desire to make a difference in the life of a young person, but what you don’t realize is how much you can learn from the campers on a professional and personal level.”

The deadline for campers to apply for Camp Burnt Gin’s 2020 season is March 1. To apply as a camper or staff member, contact Marie at 803-898-0784 or campburntgin@dhec.sc.gov.

For more information, visit www.scdhec.gov/campburntgin.

Go Red For Women and Heart Health

As the number one killer of women nationally, heart disease claims the lives of nearly 500,000 women annually in the United States. This Friday, Feb. 7, DHEC is encouraging everyone to wear red to help raise awareness for women and heart disease.

In 2003, the American Heart Association introduced a new initiative known as “National Wear Red Day” to inform women of the dangers of ignoring their heart health and to teach them how to improve their heart and overall health. “Go Red Day” is held on the first Friday in February and encourages both women and men to dress in red clothing to show their support for heart disease awareness.

Since the inaugural “National Wear Red Day,” there have been significant accomplishments achieved to reduce the number of women dying from heart disease, including:

  • Nearly 90 percent of women have made at least one healthy behavior change.
  • More than one-third of women have lost weight.
  • More than 50 percent of women have increased their exercise.
  • 6 out of 10 women have changed their diets.
  • More than 40 percent of women have checked their cholesterol levels.
  • One-third of women have talked with their doctors about developing heart health plans.
  • Today, nearly 300 fewer women die from heart disease and stroke each day.
  • Death in women from heart disease has decreased by more than 30 percent over the past 10 years.

Join us, this Friday as we Go Red for women and heart health.

From Other Blogs: New Nutrient Content Information Now Available Online, How to Stop Spreading Germs, Addressing Antibiotic Resistance

A collection of health and environmental posts from other governmental blogs.

New Nutrient Content Information Now Online

Have you ever wanted to view food sources of vitamins, minerals, and other nutrients in your diet? The National Agricultural Library’s Food and Nutrition Information Center now houses 36 tables of foods according to their nutrient content. The tables are available for vitamins, minerals, phytonutrients, and macronutrients and are listed in household measure from the highest to lowest in nutrient content. – From U.S. Department of Agriculture’s blog

 

Stop Spreading Germs: Tips for Parents and Kids

It’s something all parents dread – a call from the school nurse telling you that your child is sick. We usually wonder how they got it and how to prevent everyone else in the family from catching it too. Katie Schill, nurse practitioner with Prisma Health Telehealth, offers some tips to share with your children on how to prevent the spread of illnesses. And if you do find yourself with an ill child, when to keep them home from school. – From Flourish, Prisma Health’s blog

 

Urgent Care Collaborating to Address Antibiotic Resistance

Laurel Stoimenoff, PT CHC Chief Executive Officer of the Urgent Care Association (UCA) and its member are concerned about the looming antibiotic resistance crisis. In collaboration with the College of Urgent Care Medicine (CUCM), we have decided to be part of the solution. From Safe Healthcare, Centers for Disease Control and Prevention (CDC) blog