FARE Kids Who Care: Callie Milner

Callie FARE BlogCallie Milner wants everyone to be able to enjoy dessert together, which is why she started Callie’s Nut-Free Treats, a home-based bakery business that has been churning out nut-free baked goods and delighting customers in the Chicago area. At just nine years old, Callie and her mother Dara are donating all proceeds from their sales to FARE so they can help raise funds for food allergy research, education, advocacy and awareness. We asked Callie to tell us more about her successful fundraiser:

What are your food allergies? What’s it like having food allergies?

I am allergic to peanuts. When I go to a restaurant and I am ordering food, I have to be really careful that the server understands that my food cannot touch anything with peanuts. Cross-contact is the biggest thing about having food allergies. Having a food allergy makes you have to think in every situation about what you are eating and what others are eating around you. It is usually ok, but sometimes people don’t listen or understand and that is when it gets tiring. It is also tiring when there are really good treats around you that you can’t eat, and that is why I made Callie’s Nut-Free Treats!

Tell us about how you have been fundraising for FARE.

I have been making Callies’ Nut-Free Treats to raise money for FARE. I dance at All About Dance in Chicago and Ms. Jessica and Ms. Shannon (the owners) have let me have bake sales there for 3 years.  All of my treats are peanut, tree-nut and shellfish free and many are gluten-free and egg-free. I also have a website that people can order off of as part of the bake sale. I have raised over $9,000 so far and I don’t plan to stop!

Why did you want to do it? Why was it was important to you?

Callie’s Nut-Free Treats was really important to me because when I would see a good treat, I would really want to eat it, but I couldn’t because of my food allergy. So that’s why I made Callie’s Nut-Free Treats. I know how it feels for kids with food allergies and I want to make treats that a lot of people with food allergies and also without food allergies can eat. Now I don’t feel bad when I see great treats. I also wanted to teach people about food allergies and why they have to be really careful.

Which of your baked goods is your favorite? Which is the most popular seller?

My favorites are chocolate-covered chocolate sandwich cookies, chocolate sandwich cookie and potato chip milk chocolate bark, chocolate covered graham crackers with sprinkles and marshmallows. Our best sellers are the chocolate-covered chocolate sandwich cookies and solid chocolate pops.

How can you be a good friend to someone with food allergies?

You can be a good friend by not eating something they are allergic to when you are near them. You can also help protect someone with food allergies by telling your mom, dad or nanny to not serve foods they are allergic to and not allow foods to touch what you are allergic to when they come to your house. Like if a knife was used on peanut butter and then put in the jelly jar, I can’t eat that jelly.

What advice would you give a kid or a friend who was just diagnosed with food allergies?

Some tips I would give a friend that was just diagnosed with food allergies would be:

  • Be very very very very very very careful when you go to a restaurant. You have to say my food can’t be touched to what I am allergic to. You can ask the server to ask the chef what is safe for you to eat.  Make sure they understand cross-contact.
  • If someone is eating something you are allergic to, you have to speak up for yourself and say can you please not eat that and go wash your hands.
  • There are still a lot of great things you can eat. You can eat out and you can make lots of good things at home. I have traveled lots of places and I get to eat many yummy things.
  •  I have made lots of great friends and done special things because of my food allergies so don’t worry.

Thank you, Callie, for supporting FARE and providing safe treats for individuals with food allergies in the Chicago area. Callie’s treats are available for pick up to those in the Chicago area and can be ordered online at calliesnutfreetreats.com.

Food Allergy Action Month Highlights

For the first time,FARE expanded Food Allergy Awareness Week in 2014 by declaring the entire month of May as Food Allergy Action Month. We would like to thank all of you who contributed by taking action – whether it was educating others about food allergies and life-threatening anaphylaxis, making a donation, signing up for a FARE Walk for Food Allergy, advocating on behalf of the 15 million Americans with food allergies, or wearing teal. We were thrilled to see many wonderful photos of people and pets rocking their teal for our #TealTakeover – be sure to check out our photo album on Storify!

Highlights of our first Food Allergy Action Month included:

  1. Thirty-four states and the District of Columbia issued Food Allergy Awareness Week proclamations, and U.S. Rep. Steve Israel (D-NY) introduced a resolution into Congress.
  2. The incredible mom-daughter duo of “Fashion by Mayhem” raised awareness and funds for FARE with their first dress auction. The dress sold for $355 – a generous donation for a dress made from paper and packaging tape!
  3. FARE’s Twitter chat (#FAREChat) provided answers to questions submitted by the community about food allergies and anaphylaxis from Drs. Ruchi Gupta and Wayne Shreffler.
  4. Terminal Tower in downtown Cleveland was lit teal on May 12 and the Duke Energy Center in Charlotte, NC was lit teal on May 18.
  5. Food allergy musician Kyle Dine joined in our #TealTakeover and sang at the Food Allergy Education Network’s annual Dance-A-Thon in Connecticut; his performance was sponsored by FARE as part of our Community Outreach Grants Program.
  6. Recipe Rehab, a competition cooking show, featured a family managing food allergies in an episode sponsored by FARE.
  7. Students in schools across the country dressed in teal and helped educate their peers about food allergies through presentations and by reading facts over the school public address systems.
  8. Numerous media outlets featured stories about Food Allergy Action Month and Food Allergy Awareness Week, including The Huffington PostCharlotte ObserverSalt Lake Tribune, and About.com.
  9. A 100-ft-long soy nut butter and jelly sandwich was constructed in the Chicago area to bring the community together and highlight the issue of food allergies.
  10. FARE’s “Give $15 on the 15th” campaign received great support from the food allergy community in honor of the 15 million Americans with food allergies.

It truly has been a tremendous month, but in order to make a real and lasting difference, we need each member of the food allergy community to continue taking action on behalf of those with food allergies beyond just the month of May. Check out our Action Challenge List for suggested actions you can take throughout the year to make an impact!

Food Allergy Action Challenge – Make Your List!

walkvolunteer

We are grateful for and inspired by the food allergy community’s efforts during FARE’s first Food Allergy Action Month to take action and raise awareness of food allergies and anaphylaxis. Food Allergy Action Month was a huge success, and now it’s time to take it to the next level!

You can join us in making a real and lasting difference year-round by creating your own Food Allergy Action Challenge!  Here’s how you do it: make a list of ways that you want to make an impact and schedule them each month throughout the year. Check out our sample Food Allergy Action Challenge list below for ideas on how to get started! We’ve provided some ideas here to get you started – one for each month leading up to next year’s awareness week!

FARE Food Allergy Action Challenge 2014-2015
June 2014 Continue learning about food allergies by attending the FARE National Food Allergy Conference and our free educational webinars, or viewing an archived webinar.
July 2014 Sign up for a FARE Walk for Food Allergy, recruit others to join you, and set a fundraising goal. You can also find other events in your region by connecting with your FARE Regional Office.
August 2014 During Back to School season you can help spread the word about the Centers for Disease Control & Prevention’s, “Voluntary Guidelines for Managing Food Allergies in Schools and Early Care and Education Programs.” Find out how on our blog.
September 2014 Connect with others by joining a support group, and work with other local food allergy families or hosting a presentation at your school or office.
October 2014 Share our SafeFARE flyer with restaurants in your area to encourage them to get allergen-trained and added to our database.
November 2014 Learn about FARE’s strategic plan for research. If you or your child is interested in participating in a clinical trial, sign up for ResearchMatch.
December 2014 Join our Advocates Network to make your voice heard on federal and state legislation.
January 2015 Create your own fundraiser. From participating in athletic challenges to having a lemonade stand in your front yard, there are lots of ways to create a fundraising event to help raise funds for food allergy research, education, advocacy and awareness programs. Your event will not only support FARE’s mission, it will spark a conversation about food allergies, giving you an opportunity to educate others in your community.
February 2015 Spread the word on social media by sharing facts and resources like our infographic, Discovery Channel documentary, “An Emerging Epidemic: Food Allergies in America,”  and food allergy bullying “It’s Not a Joke” PSA.
March 2015 Become a FARE member. Every new member makes a difference and helps us turn up the volume on critical food allergy issues.
April 2015 Plan ahead for the next Food Allergy Awareness Week and Food Allergy Action Month. Putting up posters, making a presentation, or planning a awareness or fundraising event are just some of the ways you can help support the food allergy cause. Prep ahead by downloading our free resources.

Thank you again for your support of FARE and efforts to raise awareness and take action last month! We look forward to continuing to build momentum throughout the year to make the world a better place for all those with food allergies.

Exploring the Natural History of Egg Allergy

eggEgg allergy is among the most common food allergies in children. One of the most comprehensive examinations of the natural history of egg allergy to date was published in the February 2014 issue of the Journal of Allergy and Clinical Immunology. Researchers from the Consortium of Food Allergy Research (CoFAR) set out to describe the natural course of egg allergy and to identify early predictors of the disease. Over a period of 74 months, they tracked the allergy in 213 children who were between 15 months and 3 years old at the beginning of the study.

By age six, approximately half of these children were able to tolerate egg. Compared to children who were not able to tolerate egg, these children had lower levels of egg-specific IgE, the antibody associated with food allergy. Based on these and other observations, the authors of this study—many of whom serve as advisors to FARE—have developed a calculator that may predict the history of egg allergy in individual patients. Further studies are needed to validate the accuracy of this calculator. The study authors estimate that approximately 50 percent of children with egg allergy will become tolerant to egg by the age of 6. The National Institutes of Health (NIH) was the principal funder of this study.

This article was originally published in the Spring 2014 issue of FARE’s Food Allergy News. Read more of the newsletter here.

Meet Pete Wright: Attorney and Workshop Leader at FARE’s National Food Allergy Conference

The FARE National Food Allergy Conference is quickly approaching, and we are excited this year to have Pete Wright, nationally known attorney and co-founder of Wrightslaw.com, joining us on Sunday, June 22, to lead “From Emotions to Advocacy: An Expert’s Guide to Safety and Inclusion for You Child At School.” During this 5-hour, hands-on workshop, parents of children with food allergies will learn practical strategies and tips for working with school personnel to ensure their child’s safety and inclusion at school.

Pete was featured in a special “Ask the Expert” web series in fall 2012, answering questions from FARE members about Section 504 plans. Section 504 of the Rehabilitation Act of 1973 is a federal law designed to protect the rights of individuals with disabilities in programs and activities that receive federal financial assistance from the U.S. Department of Education. We’ve reprinted excerpts from this feature below.

The 2014 FARE National Food Allergy Conference will be held June 21-22 at the Hyatt Regency O’Hare in Rosemont, Ill. and will feature dozens of world-class experts and panelists providing practical tips and resources for living well with food allergies. Don’t miss this chance to learn from leading food allergy experts – register and reserve your place in the “From Emotions to Advocacy” workshop today.


 

Pete WrightI recently read about the Office of Civil Rights April 23, 2012 resolution of a case involving an Individualized Health Care Plan (IHCP) in the Memphis, TN schools. Their press release stated that:  “If a student currently has an IHCP, the district will provide parents or guardians with information regarding the student’s possible rights to evaluation, placement, and procedural safeguards. An IHCP for a student who has a qualifying disability is insufficient if it does not incorporate these rights.” Does this mean that if a student is considered disabled and needs aides, services, or accommodations, that a 504 plan is the way to document what is needed to allow a food allergic child access to a FAPE (Free Appropriate Public Education)?

If a child has a disability as defined by either the Individuals with Disabilities Education Act (IDEA 2004), Section 504 of the Rehabilitation Act or the Americans with Disabilities Act, Amended Act of 2008 (ADA AA), and needs “aides, services, or accommodations,” the child should have either an Individualized Education Plan (IEP) or a Section 504 Plan, dependent upon the nature of the disability. Per the question, if the disability is solely limited to a food allergy, then an IEP would not be appropriate, but a Section 504 is appropriate.

It is important for parents to understand that an IHCP is not an agreement that provides specific rights and procedural safeguards, but instead is more akin to a nursing care plan.

The concept of an IHCP is not recognized in or created by the Individuals with Disabilities Education Act (IDEA 2004), Section 504 of the Rehabilitation Act or the Americans with Disabilities Act, Amended Act of 2008 (ADA AA). Each of the three statutes do provide procedural safeguards for the student. An IHCP does not provide any procedural safeguards for the student. If an IHCP is created, to obtain the rights and protections of the preceding statutes, it should be attached to and incorporated by reference into either an IEP or a Section 504 Plan and considered as a part of the IEP or Section 504 Plan.

The ADA was revised in 2008 as the result of two U. S. Supreme Court cases that had narrowed the definition of those eligible for protections under the ADA. The 2008 “Amendments Act” has substantially broadened eligibility, thus gutting the impact of those two prior cases. That expansion applies to Section 504 of the Rehabilitation Act. Thus a child found ineligible for either an IEP or a Section 504 plan in 2007 may today, because of the change in the law, be eligible.

The Office of Civil Rights issued a FAQ monograph that addresses the ADA AA, Section 504 and IHCPs. It is titled “Questions and Answers on the ADA Amendments Act of 2008 for Students with Disabilities Attending Public Elementary and Secondary Schools.”

The critical questions are 4, 5, 11, 12 and 13.

Below I have copied and pasted those questions and portions of their answers. I provided the complete answers to Questions 12 and 13. The bold emphasis was added by me.

Q4. How does the Amendments Act alter coverage under Section 504 and Title II?

A: The Amendments Act emphasizes that the definition of “disability” in Section 504 and the ADA should be interpreted to allow for broad coverage. Students who, in the past, may not have been determined to have a disability under Section 504 and Title II may now in fact be found to have a disability under those laws. A student whom a school district did not believe had a disability, and therefore did not receive, as described in the Section 504 regulation, special education or related services before passage of the Amendments Act, must now be considered under these new legal standards . . .

Q5: Should a school district revise its policies and procedures regarding the determination of coverage and provision of services under Section 504 and Title II?

A: Yes, if those policies and procedures do not implement the Amendments Act’s new legal standards. As noted above, the definition of disability is to be interpreted broadly, so determining whether one has a disability should not demand extensive analysis, and the determination shall be made without regard to the ameliorative effects of mitigating measures . . .

Q11: What must a school district do for a student who has a disability but does not need any special education or related services?

A: As described in the Section 504 regulation, a school district must conduct an evaluation of any individual who, because of a disability, needs or is believed to need special education or related services, and must do so before taking any action with respect to the initial placement of the person in regular or special education or any significant change in placement. 34 C.F.R. § 104.35(a). If, as a result of a properly conducted evaluation, the school district determines that the student does not need special education or related services, the district is not required to provide aids or services. Neither the Amendments Act nor Section 504 obligates a school district to provide aids or services that the student does not need. But the school district must still conduct an evaluation before making a determination. Further, the student is still a person with a disability, and so is protected by Section 504’s general nondiscrimination prohibitions and Title II’s statutory and regulatory requirements. See 28 C.F.R. § 35.130(b); 34 C.F.R. §§ 104.4(b), 104.21-23, 104.37, 104.61 (incorporating 34 C.F.R. § 100.7(e)).

For example, suppose a student is diagnosed with severe asthma that is a disability because it substantially limits the major life activity of breathing and the function of the respiratory system. However, based on the evaluation, the student does not need any special education or related service as a result of the disability. This student fully participates in her school’s regular physical education program and in extracurricular sports; she does not need help administering her medicine; and she does not require any modifications to the school’s policies, practices, or procedures. The school district is not obligated to provide the student with any additional services. The student is still a person with a disability, however, and therefore remains protected by the general nondiscrimination provisions of Section 504 and Title II.

Q12: Should school districts conduct FAPE evaluations as described in the Section 504 regulation for students who, prior to the Amendments Act, had health problems but might not have been considered persons with a disability?

A: The answer depends upon whether, because of the health problem, that student has a disability and, because of that disability, needs, or is believed to need, special education or related services. A medical diagnosis alone does not necessarily trigger a school district’s obligation to conduct an evaluation to determine the need for special education or related services or the proper educational placement of a student who does have such need. As explained in Q11, a student with a disability may not need any special education or related service as a result of the disability.

Q13: Are the provision and implementation of a health plan developed prior to the Amendments Act sufficient to comply with the FAPE requirements as described in the Section 504 regulation?

A: Not necessarily. Continuing with a health plan may not be sufficient if the student needs or is believed to need special education or related services because of his or her disability. The critical question is whether the school district’s actions meet the evaluation, placement, and procedural safeguard requirements of the FAPE provisions described in the Section 504 regulation. For example, before the Amendments Act, a student with a peanut allergy may not have been considered a person with a disability because of the student’s use of mitigating measures (e.g., frequent hand washing and bringing a homemade lunch) to minimize the risk of exposure. The student’s school may have created and implemented what is often called an “individual health plan” or “individualized health care plan” to address such issues as hand and desk washing procedures and epipen use without necessarily providing an evaluation, placement, or due process procedures. Now, after the Amendments Act, the effect of the epipen or other mitigating measures cannot be considered when the school district assesses whether the student has a disability. Therefore, when determining whether a student with a peanut allergy has a disability, the school district must evaluate whether the peanut allergy would be substantially limiting without considering amelioration by medication or other measures. For many children with peanut allergies, the allergy is likely to substantially limit the major life activities of breathing and respiratory function, and therefore, the child would be considered to have a disability. If, because of the peanut allergy the student has a disability and needs or is believed to need special education or related services, she has a right to an evaluation, placement, and procedural safeguards. In this situation, the individual health plan described above would be insufficient if it did not incorporate these requirements as described in the Section 504 regulation.

The nature of the regular or special education and related services provided under Section 504 must be based on the student’s individual needs. As noted in Q2 above, the student would also be protected from discrimination under Title II’s statutory and regulatory requirements, as well as Section 504’s general nondiscrimination provisions.

Parents should download and read the Memphis, TN press release and the above FAQ monograph from OCR. Afterwards, to get a better handle on this, parents should go to our wrightslaw.com and read the following:

www.wrightslaw.com/blog/?p=58

www.wrightslaw.com/blog/?p=2831

www.wrightslaw.com/law/504/OCR.va.peanut.pdf

www.wrightslaw.com/info/adaaa.elig.bruce.htm

www.wrightslaw.com/info/sec504.index.htm

www.wrightslaw.com/info/sec504.adaaa.htm

My son’s school principal told me that they handle food allergies with an IHCP. They said any accommodations could be written into the IHCP. My son has life-threatening food allergies and will need accommodations in the classroom, and a trained adult and EpiPens® with him on field trips, etc. In your experience, is it better to have a 504 plan or will an IHCP suffice?

Presumably you have now read the Memphis, TN press release, the  FAQ monograph from OCR and the above articles on our website. Bottom line, you know that there are no protections under an IHCP and it will not suffice. On another note, you write that the principal “told me . . .” Remember, if he did not put it in writing, it was not said. There must be a paper trail. More about this shortly.

If school administrators are going to sit down and write an IHCP, why are they so reluctant to write a 504 plan? Our school says they are “the same.” What is the difference between an IHCP and a 504? What do you recommend for life-threatening food allergies?

A Section 504 plan provides the student with rights and remedies, i.e., it has procedural safeguards, if the school breaches the 504 plan. There are no such procedural safeguards in an IHCP. It is not a legal concept recognized in any of the statutes discussed in the opening answer. Dependent upon the child and other possible issues, I recommend either an IEP or a Section 504 Plan. The IHCP can be incorporated into a Section 504 Plan.

How would you proceed if you were told by a district that, “We don’t do 504 plans for food allergies”?

Again, repeating the answer to the second question, if you were told something and it is not in writing, you are mistaken, it was never said! So, what do you do? The first step is to become educated about IDEA 2004, Section 504, and the 2008 Amendments to ADA that impact the Section 504 eligibility. Read the OCR articles and websites listed above. IDEA 2004 and Section 504 are on our website and also included in our book, Wrightslaw: Special Education Law, 2nd Ed.

Second, once you have a handle on the law and the eligibility issues, then you have to take the same steps any parent has to take to obtain eligibility for their child for either a Section 504 plan or an IEP. You must have an organized file. (See Chapter 9 in our book, Wrightslaw: From Emotions to Advocacy, 2nd Ed.) You must understand all of your child’s test data. (See Chapters 10 and 11.) Then you must understand how to create and maintain a paper trail (Chapter 22) and learn to write good evidence letters (Chapter 23) that do not blame or finger point, but instead create empathy and a desire to fix the issue. This is done using the “Letter to the Stranger” principles (Chapter 24).

When that is accomplished, the parent is able to write a nice letter to the administrators in which they describe their child, the medical/allergy issues, provide the documentation, express some confusion about the law and the OCR documents, provide those documents, and ask the school to help you understand why your child does not fit and why an IHCP is not a Section 504 document and what can be done.

As a part of the self-study, the parent will also need to learn effective negotiation skills that

are in the subsequent chapters of that book. Many of the other questions submitted for this feature were related to “How can I get the school to . . .” The answer is to motivate them, not by a threat of litigation or letter complaint to OCR, but instead by a letter seeking their help to educate you about the law (actually you already know it, but you have created your newly merged personality of Ms. Manners and Columbo) and to provide help regarding your child.

Copy and paste the following links into your browser for more about developing an organized file, understanding the test data, creating the paper trail, and writing persuasive evidence letters using the “Letter to the Stranger” approach.

www.wrightslaw.com/info/organize.file.htm

www.wrightslaw.com/blog/?p=877

www.wrightslaw.com/nltr/12/ss.organize.file.htm

www.wrightslaw.com/advoc/articles/tests_measurements.html

www.wrightslaw.com/advoc/articles/advo.create.trails.htm

www.wrightslaw.com/advoc/articles/12rules_letters.htm

www.wrightslaw.com/nltr/11/ss.short.course.htm

www.wrightslaw.com/nltr/08/nl.0226.htm

www.wrightslaw.com/blog/?tag=paper-trails

www.wrightslaw.com/info/ltrs.index.htm

www.wrightslaw.com/advoc/articles/Letter_to_Stranger.html

www.wrightslaw.com/advoc/stranger/brody.html

www.wrightslaw.com/advoc/ltrs/strngr.joejames.htm

www.wrightslaw.com/advoc/articles/ltr.to.stranger.miata.pdf


 

Pete Wright, an attorney who represents children with special education needs, is the co-author of From Emotions to Advocacy: The Special Education Survival Guide, and co-founder of Wrightslaw, a website specializing in education law and special education advocacy founded by Pamela Darr Wright. 

Access to Health Care and Food in Children with Food Allergy

Access to health care and food are serious concerns for families managing food allergies. A new study, funded in part by FARE, set out to research whether patients with food allergies experience impaired access to these basic needs—a topic which had not previously been evaluated.

The study, led by Christina B. Johns and Jessica H. Savage and published online by the Journal of Allergy and Clinical Immunology: In Practice in February 2014, found that families managing food allergies are more likely to face food insecurity and reduced access to health care. Based on data reported by more than 26,000 parents, the researchers’ analysis found that among families managing food
allergies:

  • 21 percent of children had low food security
  • 34 percent reported having problems paying medical bills
  • 4 percent reported not being able to afford needed prescriptions
  • 3 percent reported not being able to afford needed follow-up care
  • 2 percent reported having trouble finding a doctor to see the child

These values were all significantly higher for children with food allergies than for those without. Additionally, there were significant disparities associated with race/ethnicity. The researchers concluded that “parents of nonwhite children with food allergy were significantly more likely to report difficulty with access to care and food.” This study is noteworthy in that it demonstrated disparities in access among families managing food allergies and opens the door to further studies that can help determine whether improvements in access can improve disease outcome.

The authors are affiliated with Brigham and Women’s Hospital in Boston. Dr. Savage is the recipient of the 2012 AAAAI/Food Allergy Research & Education Howard Gittis Memorial 3rd/4th Year Fellowship/Junior Faculty Research Award. FARE funds this grant, which is awarded annually to a promising young investigator who is selected by an American Academy of Allergy, Asthma & Immunology
committee. This award was created in 2008 to attract gifted researchers to the field of food allergy.

This article was originally published in the Spring 2014 issue of FARE’s Food Allergy News. Read more of the newsletter here.

Resources for Anaphylaxis Awareness Day

Today is Anaphylaxis Awareness Day on our Food Allergy Action Calendar! We encourage everyone to learn about anaphylaxis and how to use an epinephrine auto-injector, or train someone else if you are already knowledgeable.

To help you educate yourself and others, we’ve provided a list of anaphylaxis resources below. From posters to emergency care plans, these materials and information can help you learn and spread the word about how to recognize and treat this life-threatening reaction:

Information about anapyhlaxis:

About Anaphylaxis: Symptoms, Treatment, and Coping
Treating & Managing Reactions
Webinar recording: “All About Anaphylaxis: Understanding the Risks, Symptoms & Treatment” with Dr. Robert A. Wood
Your Questions Answered: Anaphylaxis

Epinephrine resources:

Epinephrine Auto-injectors
2014 Patient Assistance Resources for Epinephrine Auto-injectors

FAAEPthumbMaterials:

Food Allergy & Anaphylaxis Emergency Care Plan (English and Spanish versions available)
Common Symptoms of Anaphylaxis Poster
Common Symptoms of Anaphylaxis Poster (premium version for purchase)
Common Symptoms of Anaphylaxis Magnet

Fast Facts About Anaphylaxis:

  • Food allergy is the most common cause of anaphylaxis, although several other allergens – insect stings, medications, or latex – are other potential triggers.
  • Anaphylaxis often begins within minutes after a person eats a problem food. Less commonly, symptoms may begin hours later.
  • Teenagers and young adults with food allergies are at the highest risk of fatal food-induced anaphylaxis.
  • It is possible to have anaphylaxis without any skin symptoms (no rash, hives).
  • People who have both asthma and a food allergy are at greater risk for anaphylaxis.
  • Epinephrine (adrenaline) is a medication that can reverse the severe symptoms of anaphylaxis. It is given as a “shot” and is available as a self-injector, also known as an epinephrine auto-injector, that can be carried and used if needed.
  • Epinephrine expires after a certain period (usually around one year), so be sure to check the expiration date and renew your prescription in time.
  • About 1 in every 4 patients have a second wave of symptoms one to several hours after their initial symptoms have subsided. This is called biphasic anaphylaxis.