Showing posts with label Food Allergies. Show all posts
Showing posts with label Food Allergies. Show all posts

Wednesday, April 23, 2014

UPDATE on Call to Action: Food Allergy Children’s Literature

The #FoodAllergy Awareness and Resources Campaign to donate "The No Biggie Bunch" series to 500 Libraries throughout 50 States was a resounding success. They raised the money to send the series of  four children's books to over 500 libraries and schools.  These four books help kids with and without food allergies to realize that their situation is just another aspect of what makes them uniquely special. The characters are kids who look just like any child in the classroom with their own styles and interests. 

Each state in the US is at a different level of food allergy awareness, education and advocacy, however, every state has public libraries where all can access resources for free. The vital piece is ensuring that resources are available. That’s how we can made a difference! 

The No Biggie Bunch 50 States – 500 Libraries campaign offset the shipping and postage costs to deliver a bundle of 4 No Biggie Bunch books to each of 500 libraries across the 50 United States, timed to coincide with the American Library Association’s 2014 National Library Week. This year, the ALA is recognizing that “Lives Change @ your Library.” Lives of kids with food allergies and their friends can change at their libraries. Having this food allergy resource accessible to the little hands that might need them most is in your hands! 


Here is the link to learn more: No Biggie Bunch Website
 #makeadifference:

Monday, April 21, 2014

STOCKING EPINEPHRINE IN SCHOOLS 2014

With all the recent news of students who have passed tragically away due to an anaphylactic reaction to their food allergy, it is more important than ever to make certain that our schools have access to epinephrine and the training to inject it.  The Asthma and Allergy Foundation of America supports school policies that promote access to life-saving medications to treat students and staff who experience severe allergic reactions. Huge progress was made in  2013 when President Obama signed The School Access to Emergency Epinephrine Act into law.


The School Access to Emergency Epinephrine Act creates a preference for states that require schools to maintain a supply of the epinephrine to allow trained school personnel to administer it in an apparent emergency, and offer limited protection from civil liability to those who act. Thus, states that require schools to meet these requirements will have an advantage in obtaining federal asthma program funding.  States should implement policies that promote access, including: supplying schools with epinephrine auto-injectors to be used in emergencies, appropriately training school personnel, and addressing liability concerns for those who use this medication in good-faith.
Thus far there are 27 states which have passed laws which either require or authorize schools to stock epinephrine auto-injectors.

If all schools have access to undesignated epinephrine auto injectors and staff trained to administer the medication, children will not die at school when a snack lands in the wrong hands or has unfortunately been contaminated through cross-contamination. As of September, 2014 only 8 proactive states have laws/guidelines which require stocking epinephrine while 34 states have laws/guidelines which allow schools to stock it.  Shockingly, there are 8 states which have nothing in place or have bills languishing in their state congress. 
If each of us, contact our legislators and senators, we can make an impact and help to prevent another unnecessary death due to ananphylaxis. Will you advocate for epinephrine stocking laws in your state? You can make a difference by emailing advocacy@aafa.org to get started. 

Or you can use this link to their template for a letter to your state legislators: http://www.aafa.org/pdfs/Advocate%20Letter%20Final.pdf
To read their statements of support:  www.aafa.org/epinephrine

Data source: http://www.foodallergy.org/advocacy/epinephrine/map

Friday, April 11, 2014

Children's Food Allergy Author wins Mom's Choice Award 2013



Stephanie Sorkin has a degree in English Literature and lives in New York. As a mom of a child with multiple food allergies, she wrote Nutley, about an adorable squirrel who doesn't let his nut allergy slow him down. He inspires children with food allergies to live their lives to the fullest.  She is proud to donate 100% of the book proceeds to +Food Allergy Research & Education (FARE) because she wants to give back to the food allergy community so we will be closer to answers and solutions!
While allergies have become so common in so many classrooms, this book is a great tool to inform students and parents.  I love the writing and illustrations which are so easy to identify with. The fact that the author and her daughter collaborated to write the book is so special. I highly recommend it as a resource for discussion about food allergies in any home or elementary classroom setting.
So join Nutley on his journey to stay healthy and safe with the help of his friends while supporting advocacy & research about food allergies.

You can find it on amazon: http://www.amazon.com/Nutley-Nut-Free-Squirrel-Stephanie-Sorkin/dp/1620861585

Thursday, February 20, 2014

Peanut Butter Alternatives - There are Choices!

FROM WWW.ALLERGYFREETABLE.COM
Thanks to +DaniellaKnell,Smart Allergy Friendly Education, for creating a list of Peanut Butter Alternatives with SO Many Delicious Choices! 
If you're new to peanut allergies, and worried about how you are going to live peanut-free or tree-nut free, RELAX!  There are a variety of choices available at budget-friendly prices in your local supermarkets.  The list that Smart Allergy Friendly Education has put together is a helpful guide to 6 different alternative brands with links to each of those products:

1) No-Nut Butter, Nut-free, Gluten-free, Soy-free and 100% Nut-free facility from the Sneaky Chef - No Nut Butter S.A.F.E.Review

2) I.M. Healthy, Nut-free, egg-free, dairy-free, gluten-free Soybutter

3) SunButter, Nut-free Sunflower Butter and 100% Nut-free facility - SunButter S.A.F.E.Review

4) Don'tGoNuts, Nut-free, Gluten-free, Vegan and 'Field to Fingers' Nut-free Processing from Nut Free Foods - Don't Go Nuts S.A.F.E. Review

5) Biscoff Spread, Vegan and Nut-free from Lotus - Biscoff Spread Review

6) WowButter, Nut-free Soybutter - WowButter S.A.F.E. Review


There are actually a couple more options out there that are also safe for those with peanut & tree nut allergies that my family enjoys and buys on a weekly basis:

7) Trader Joe's Sunflower Seed Butter (a family favorite) 


                                   and

8) Swanson Organic Sunbutter: http://bit.ly/1oNJ7F8.


Lastly, I would recommend one other product, but would make the distinction with this IMPORTANT NOTE Blue Mountain Organics Sunflower Seed Butter: http://bit.ly/1jD06Gg IS MADE IN A PEANUT-FREE FACILITY BUT they do PROCESS TREE NUTS in THEIR facility SO there is a chance for cross contamination. THEY do THEIR best to control any possibility of cross-contamination in THEIR factory - THEY are extremely sensitive to this issue and very, very careful. Completely different machines are used in separate parts of the factory for grinding the nut butters and milling the grains, and THEIR machinery is broken down and thoroughly cleaned between production runs.

Sunday, November 3, 2013

NEW STUDY SHOWS NEARLY 1-IN-50 AT-RISK FOR SEVERE ALLERGIC REACTIONS

Anaphylaxis is More Common than Many Thought, Most Patients are Not Prepared

October 21, 2013, WASHINGTON, DC – A novel study by the Asthma and Allergy Foundation of America (AAFA) published today in the Journal of Allergy and Clinical Immunology (JACI), finds that severe life-threatening allergic reactions – anaphylaxis – are common in the U.S.  According to the peer-reviewed study, anaphylaxis very likely occurs in nearly 1-in-50 Americans (1.6%), and the rate is probably higher, close to 1-in-20 (5.1%).
The article, Anaphylaxis in America: The Prevalence and Characteristics of Anaphylaxis in the United States, based on AAFA’s study of the same name, provides one of the most reliable estimates to-date of the prevalence of severe, life-threatening allergies in the general population.  It is also helping experts understand how the public, patients and caregivers think, feel and behave regarding anaphylaxis.  For the full text of the article, visit www.aafa.org/AnaphylaxisInAmerica.
Dr. Robert Wood is the lead author of the article, chair of the AAFA research panel that conducted the study, and Director of Allergy & Immunology at Johns Hopkins Children’s Center.  “This study provides the first estimate of anaphylaxis prevalence in the United States using a large unbiased survey,” according to the article.  But the authors also pointed out that patients do not appear adequately equipped to deal with future episodes, indicating the need for public health initiatives to improve anaphylaxis recognition and treatment.
“One of the most alarming things we found is that, despite the common occurrence of anaphylaxis, most people are not prepared to do the right thing when emergency reactions occur,” says Mike Tringale, Senior Vice President at AAFA and one of the authors of the article.  “We need to re-double our efforts to make sure that people are informed and have access to the right medication.”

Reaction and Inaction

Anaphylaxis is a severe, sudden allergic reaction that typically involves two or more organs, such as the skin, airways, lungs, stomach, heart or blood pressure.  Reactions can be deadly.  Anaphylaxis is most commonly triggered by allergies to foods, medications, insect bites/stings and latex.  For others, exercise can be a trigger.  Symptoms may include: difficulty breathing; rashes, hives or swelling of the lips, tongue or skin; vomiting; loss of blood pressure; or, even loss of consciousness.  In the public survey portion of the study, the most common symptoms among those reporting anaphylaxis were respiratory symptoms (73%), followed by skin (61%), cardiovascular (24%), neurological (15%), and gastrointestinal (7%).  The patient survey portion of the study had similar findings.  More than 1-in-6 respondents (17%) who reported anaphylaxis also had a history of asthma, potentially putting them at higher risk for complications.
There is no cure or preventative treatment for most causes of anaphylaxis, so immediate use of a prescription epinephrine auto-injector at the first sign of a severe allergic reaction is the standard-of-care for adults and children.  Patients at-risk for anaphylaxis should be prescribed epinephrine auto-injectors to keep on-hand at all times and ready to use if an emergency occurs.  But AAFA’s study showed alarming patterns of inaction:  most patients are not getting these prescriptions, not keeping their auto-injectors nearby or not using them during allergic reactions when they should.  Researchers found that only 11% of survey respondents who experienced anaphylaxis had used epinephrine, and only 10% called 911.  Within this group 6.4% received no treatment at all, and 52% had never even received a prescription for an epinephrine auto-injector.  In fact, 60% of respondents did not have an epinephrine auto-injector available to them at the time of the telephone survey.
Since anaphylaxis is not a one-time event – a majority of respondents reported 2 or more anaphylactic reactions in their lifetime with 19% reporting 5 or more – researchers were even more alarmed about the lack of preparation among patients in the event of future reactions. 

Counting on the Public

Anaphylaxis can occur anywhere, and parents, teachers and neighbors can unexpectedly find themselves at the front-line dealing with this increasingly common condition.  Even though the study found a majority of reactions occurred at home (54%), the overall lack of preparedness among patients in the study indicates that most won’t have emergency medication when needed, even in their own homes.  Researchers also found that anaphylaxis occurred at the hospital or clinic (13%), at a relative or friend’s home (6.4%), in the workplace (6.1%), at a restaurant (6.1%) or at school (2.6%).    
“Everyone plays an important role in recognizing and responding to anaphylaxis,” says Lynn Hanessian, Chair of AAFA’s National Board of Directors.  “ Knowing the signs and symptoms, and when and how to take action, such as helping someone get emergency treatment with an epinephrine auto-injector and calling 911, is critical to helping someone having an anaphylactic reaction.”
Lynda Mitchell, the mother of a son with a severe allergy to milk, learned about anaphylaxis the hard way.  “My son was only a toddler when he had his first emergency reaction to milk at home after biting into a piece of wrapped candy.  Almost immediately he broke out into hives, his face became swollen, he vomited and started having breathing problems,” says Mitchell.  “I was terrified.”
Today, her son carries an epinephrine auto-injector everywhere he goes to be prepared.  Mitchell became the founder and director of Kids With Food Allergies (KFA), the largest online social network in the world for families dealing with food allergies and anaphylaxis, now a division of AAFA.  “Education and peer support are key to avoiding triggers and being prepared, so I created this online community to help keep children safe and healthy.”

About the Study

Anaphylaxis in America is an independent research project of AAFA sponsored by Sanofi US. The study was designed by AAFA along with a leading group of health, medical and research experts to assess prevalence, as well as to better understand patient, public and caregiver attitudes and behaviors regarding anaphylaxis.  Two independent nationwide, cross-sectional random-digit-dial (RDD) landline telephone surveys were conducted by the survey research firm Abt SRBI – a public survey and a patient survey.  The study began in 2011 and was completed in 2012, resulting in over 500 pages of data, and researchers hope to publish additional findings in the coming year.
For the public survey, 1,000 interviews were completed.  For the patient survey, 1,059 interviews were completed. Household screening for the patient study was conducted to identify all persons with an eligible history of an allergic reaction and if more than one person was eligible, the respondent with a history of anaphylaxis or any reaction requiring immediate medical attention was chosen; otherwise he or she was chosen at random.  If the person with a history of an allergic reaction was under 18 years, the parent or most knowledgeable adult completed the interview about the child.  Data for the public survey was weighted by age and gender to be representative of the U.S. population.

About AAFA

The Asthma and Allergy Foundation of America (AAFA) is a not-for-profit organization founded in 1953 and celebrates its 60th anniversary this year.  AAFA is the leading patient organization for people with asthma, allergies and related conditions, and provides practical information, community based services and support through a national network of chapters and support groups.  AAFA develops health education, organizes state and national advocacy efforts and funds research to find better treatments and cures.  Learn more about AAFA and the study at www.aafa.org/AnaphylaxisInAmerica.

CONTACT:  Sanaz Eftekhari, AAFA External Affairs, sanaz@aafa.org, 202-466-7643, x238.