Between trick-or-treating and Halloween parties, there are plenty of opportunities to eat sweet treats. Here are just a few examples of how some yummy foods can be made with allergies and dietary restrictions in mind. Plus, there are always non-food treats. The Teal Pumpkin Project from Food Allergy Research and Education is a campaign to get houses food allergy friendly by handing out non-food items instead of candy.
But, if you can’t help your sweet tooth, take a look at these recipes:
Always check the packaging, as product change, but these are generally allergy-friendly.
In fact, in 2002, the American Medical Association declared that bullying was a “complex and abusive behavior with potentially serious social and mental health consequences for children and adolescents.”
According to the Boston Children’s Hospital, both victims and perpetrators of bullying may struggle with mental health issues such as depression and anxiety.
What is bullying?
It’s much more than simple cases of kids being mean to each other. It consists of aggression over time that produces an imbalance of power. Simply put, calling someone a name once may be mean, but it’s not necessarily bullying. Call someone a name every day relentlessly over a series of days, weeks, months so that the person feels less about himself is definitely bullying.
The three types of bullying involve using words, reputations or physical contact to hurt someone emotionally or physically.
Who is Bullied?
Since bullying is as much about the bully as it is the person receiving the bullying, there’s no way to predict who will be affected. However, since it is also about power, victims are usually perceived as being different or weaker than their peers. They may have low self-esteem and be less popular than other, or perhaps they do not get along well with classmates. Victims may have some physical difference that sets them apart such as weight or race, glasses or different clothing.
Children who have chronic medical conditions that warrant the use of a medical ID may also stand out as potential victims of bullying, both because of their medical conditions and because they wear an ID. Don’t let the potential for bullying become a deterrent for wearing and ID. The U.S. government’s anti-bullying website Stop Bullying.gov states “even if a child has these risk factors, it doesn’t mean they will be bullied.”
The nonprofit Food Allergy Research and Education cites that about 30 percent of kids with food allergies report they have been bullied specifically because of their allergies. The organization has coordinated an anti-bullying campaign, “It’s Not a Joke,” to highlight the seriousness of food allergies, and the harm that is caused by being bullied.
Bullying Prevention Month
Established in 2006 by the PACER’s National Center for Bullying Prevention, National Bullying Prevention Month occurs each October to raise awareness about the impact of bullying on our children. The organization coordinates community efforts nationwide.
By Leslie Vandever
The flu virus is around throughout the year, but when temperatures are warm it’s sluggish and slow, unable to replicate quickly or easily. As the seasons turn to autumn and winter, the air becomes colder and the humidity levels lower. Cooler air energizes and activates the flu virus. By early to mid-winter—the height of the flu season—it’s thriving.
When the weather is cold, most people stay indoors. They don’t get lot of fresh air and exercise during the winter, which increases their vulnerability to wayward cold and flu viruses. And, since people spend more time in close proximity to others, the virus spreads easily from one person to the next.
In the U.S., flu season generally runs from December to February, but it can start as early as October and last as late as May. Distribution of the 2014-2015 Flu Vaccine began in August and will continue through October.
According to the Centers for Disease Control and Prevention, everyone, from the age of six months old, should get an annual flu shot. Here’s why: influenza is a serious illness that can lead to hospitalization or even death. Anyone can catch it—even the healthiest people among us can—and can become very sick. The more people who are vaccinated, the fewer people there are who can get it and spread the disease. About 90 percent of the deaths from influenza occur in people who are 65 years old or older.
Flu complications, such as pneumonia, bronchitis, and sinus and ear infections, account for most of the serious flu-related illness each season. And the flu can make chronic health problems worse, too. Someone with asthma or congestive heart failure may have more attacks or worse symptoms triggered by the flu.
Some people are at greater risk from the flu than others. These include:
It takes the body two weeks to gain protection from the viruses in the flu vaccine. During those two weeks you’re still vulnerable to the particular viruses in the vaccine. Also, your annual flu shot can’t protect you from all types of flu virus, just the specific ones that are in it.
You can’t get the flu from a flu shot. Most flu vaccines have “inactivated” viruses in them that are not infective; some don’t have flu viruses in them at all. After receiving the vaccine, some people experience soreness at the injection site that can last a couple of days.
Flu symptoms include fever, cough, sore throat, a runny or stuffy nose, muscle or body aches, headaches, fatigue, and perhaps vomiting and diarrhea, though those symptoms are more common in children than adults.
Talk to your health care provider about getting a flu vaccine or check with your local county health department for reduced-price vaccination schedules. Better safe than sorry. For more information about this or other health subjects, visit Healthline.
We will donate 20 percent of retail sales generated by AFA to the foundation to support its efforts to provide care for individuals with dementia and their families. The ID bracelets and necklaces can be purchased via AFA’s e-store (www.alzfdn.org) or American Medical ID’s website.
A medical ID engraved with the person’s name, an emergency contact, and medical conditions provides valuable information to emergency responders. In the case of Alzheimer’s disease and related illnesses, such a tool can be a vital means of identification since research shows that 60 percent of people with dementia become lost at some point during the progression of the disease. Symptoms such as memory loss and confusion put them in harm’s way if not found quickly and returned to safety.
“Our vision is to see an emergency ID on every person who needs one, which means we often educate about the importance of wearing an ID,” said Rick Russell, our president and CEO. “For people with Alzheimer’s disease and other forms of dementia who may not be able to communicate during an emergency, a medical ID is critical.”
Charles J. Fuschillo, Jr., AFA’s president and CEO, called wandering and becoming lost “a real risk” among people with Alzheimer’s disease and related dementias.
“Families need to be proactive and take steps to safeguard their loved ones so they are not exposed to potentially life-threatening situations,” Fuschillo said. “Should a person become lost, identification jewelry is essential in helping to ensure he or she realizes a happy and safe homecoming.”
Among the product selection are IDs with clasps that require two hands to remove, making it more difficult for people to remove; and jewelry with charms in teal—the international color of Alzheimer’s disease.
An estimated 5.1 million Americans have Alzheimer’s disease, and between one and four family members provide care for the individual with the disease.
“We recognize that with the rising incidence of this brain disorder, social services and advocacy programs like those offered by the Alzheimer’s Foundation of America are vital,” Russell said.
About Alzheimer’s Foundation of America
The Alzheimer’s Foundation of America, based in New York, is a national nonprofit organization that unites more than 1,700 member organizations nationwide with the goal of providing optimal care and services to individuals confronting dementia, and to their caregivers and families. Its services include a toll-free hot line, staffed by licensed clinical social workers; educational materials; a free quarterly magazine for caregivers; and professional training, along with teen- and college student-specific divisions. For more information about AFA, call toll-free 866-232-8484, visit www.alzfdn.org, follow us on Twitter, Facebook or LinkedIn.
Almost 30 years later, it has grown into an international awareness program that spans the entire month of October, and joins together hundreds of organizations dedicated to fighting breast cancer.
As the leading cancer among women globally, one in eight American women will develop breast cancer. There are almost 3 million women in the U.S. who have or had breast cancer. But it’s not just a woman’s disease. Each year, about 2,190 men are diagnosed with the disease.
During Breast Cancer Awareness Month, nonprofit organizations host a variety of events to garner financial and volunteer support. Much of the emphasis is on early detection, because diagnosing early can lead to a five-year survival rate of 98 percent.
Most organizations recommend regular self-checks as well as preventative doctor screenings including mammograms.
Women who have or have had breast cancer may be at risk for arm or leg swelling caused by lymphedema. Wearing a medical ID engraved with Lymphedema Alert – No BP/No Needle Sticks informs emergency medical personnel of the risk and can help provide safer, more accurate treatment.
The National Breast Cancer Foundation (NBCF) is one Texas-based nonprofit organization dedicated to promoting awareness about the disease. Founded in 1991 by breast cancer survivor Janelle Hail, the organization spends more than 80 percent of revenue on mission-related programs. With early detection so critical for breast cancer, one of the NBCF’s programs is to offer free mammograms to women in all 50 states through a hospital network.
NBCF also recognizes the value of having a community of support for those diagnosed with the disease. Their website Beyond the Shock features breast cancer facts, personal stories of survivors, and a question and answer forum.
By Leslie Vandever
Participants in the ALS Association’s Ice Bucket Challenge have included children, adults from all walks of life, Hollywood stars, and prominent politicians.
ALS is a progressive neurodegenerative disease. It affects nerve cells in the brain and the spinal cord that affect voluntary movement by disrupting and eventually destroying the motor neurons that send signals to muscles throughout the body. As the motor neurons die, the brain’s ability to initiate and control voluntary movement is lost.
More than 12,000 people in the United States have ALS; it’s one of the most common neuromuscular diseases worldwide and affects people of all races and ethnic backgrounds. It’s more common among non-Hispanics, white males, and people between the ages of 60 and 70, but people who are older or younger than that can get it too. Men seems to get ALS more frequently than women. Most cases of ALS—90-95 percent—occur apparently at random with no clearly associated risk factors. Five to 10 percent of cases to seem to be hereditary.
Early symptoms of ALS can be subtle. They frequently show up first in the hands, feet, arms, or legs, then spread to other parts of the body. Symptoms may include:
As the disease progresses, the body’s muscles become weaker and weaker. In time, ALS affects speaking, chewing, swallowing, and even breathing. In the later stages of the disease, ALS may cause total paralysis.
Although ALS is always fatal at this point, there is hope. Scientific medical research has produced treatments that can slow the progression of the disease and improve some symptoms. Riluzole is the first drug approved by the FDA for use in treating ALS. It can’t reverse damage already done to motor neurons by the disease, but it does reduce new damage. Studies have shown that it can prolong survival for several months, and some patients survived longer without needing ventilation support.
Non-drug therapy is also an important way to treat ALS. It includes:
Caring for an ALS patient can be difficult and challenging. But there are many ways to soothe and relieve some of the disease’s symptoms and help improve the patient’s quality of life. They include (among many others) encouraging the patient to eat, giving medications on schedule, massaging cramped and painful muscles, ensuring regular doctor visits, controlling the stress levels in the home, and providing pleasant distraction from symptoms.
For more information about ALS and other health-related subjects, click here.
The round pendant crafted in scratch-resistant tungsten carbide is brilliantly beveled to reflect light, illuminating the contours of its unique design.
The rotating bail allows the pendant to spin a full 360° atop a decorative bead detail. The highly-polished jewelry finish comes in three distinct colors Silver Tungsten, Onyx, and Rose Gold. A strong, but lightweight titanium cable chain is available in 20” and 24” lengths.
The medical emblem is laser engraved providing a subtle, yet easy to recognize medical alert symbol. The back of the pendant offers a full six lines for personalized engraving of medical conditions, allergies, emergency contacts or more.
What is Gaucher disease?
Named after French doctor Philippe Gaucher, who first described the symptoms in 1882, Gaucher disease is a lysosomal storage disorder. That means the body is deficient in a certain type of enzyme. It is an inherited disease that is carried by as many as 1 in 200 of the general population.
Diagnosis and Treatment:
Symptoms of the disease include bleeding and bone problems such as anemia, bruising easily, nosebleeds, osteoporosis, easily broken bones, and swollen belly due to enlarged liver and spleen.
How can I help?
Although Gaucher is a rare disease, the foundation recognizes that many more people may be carriers of the gene than affected by the illness. Because it is passed down to children, it’s important that potential carriers are informed about the disease.
Since much of the education about the disease involves the community, the National Gaucher Foundation has set up a month long virtual event on their website. Visitors to the site can play games, watch videos, view photos, read the new Gaucher comic book, and more.
New to their website is the first patient-centered national registry of Gaucher disease. Families can submit their personal experiences for a more realistic record of how different people are affected by the disease.
If you’re looking to get involved, consider speaking to your community about the disease, sharing your story of how you or your family were affected, or making a donation to the foundation, There is also a list of other ideas for promoting awareness of Gaucher during October.
People who wear medical IDs rely on EMS to confirm their medical condition and medical information before providing aid. We know that 75 percent of EMS look for medical IDs and we thank them. Here are some stats on EMS in the United States.
While the general mood associated with football is one of excitement, the sport can also present some dangers, especially if the players have asthma or allergies.
According to WebMD, some kids can have an anaphylactic reaction before or during exercise. Symptoms include a rash or itching, trouble breathing or a choking sensation, wheezing, nausea or a headache.
Anaphylaxis is a serious medical emergency in which you should call 9-1-1.
But it shouldn’t always come to that for student athletes with allergies and asthma. Most often, serious situations can be prevented with a little planning and diligence.
First is proper diagnosis. Consult an allergy specialist who can inform you about triggers in diet and environment to avoid. The doctor can also give guidelines for activity levels. Along with your child’s doctor, you can develop an allergy action plan. This is a written procedure of how to act in an emergency situation. That way there is no confusion if an emergency does happen.
Part of an action plan will be what medicines your child should carry with him/her at all times. These can be over the counter antihistamines or epinephrine shots. Another important part of the plan is to wear identification that informs teammates, coaches, and others about your child’s asthma or allergies.
Medical IDs come in bracelet and necklace styles in materials durable enough to wear during sports. If your child is playing a contact sport, check with the coach to find out what style would be least intrusive. The last thing you want is a medical ID that could cause an injury during a game. One idea is to purchase an ID that stays with the gym bag to be worn during practice and games.
Asthma and allergies are serious conditions, but they don’t have to prevent your child from participating in school sports. With a plan in place, you can rest assured while your child reaps the physical and mental benefits of participating in sports.