Books to Help Kids Living with Chronic Illness

These books reviewed by families dealing with periodic fever syndromes, aka autoinflammatory diseases, come highly recommended to share with your child. We’ve included books that will help kids who themselves are living with a chronic illness, or who have a sibling or parent who is chronically sick. These stories and journal will help kids and their families understand and become more comfortable with all the medical appointments, start conversations, and feel less alone in their struggles.

Buy Digging Deep here on Amazon.

Digging Deep, A Journal for Young People Facing Health Challenges

Reviewed by Jennifer Tousseau

This journal, written by Rose Offner and Sheri Brisson, is absolutely the best I have ever seen for a child living with an illness of any kind. Each page has a prompt for kids to answer with writing, words, drawings, photos, or however they want. They can make it their own. The art draws you in and perfectly reflect each page’s prompt. And the prompts creatively and with sensitivity and sincerity touch on all the emotions and challenges that kids with health challenges face, from spending a lot of time with doctors to how relationships with family and friends may change. With topics such as Pieces of Myself, Heart Songs, and My Boiling Point, they get to explore how they felt when they were diagnosed, fears, hopes, new friends, and future dreams. The journal also opens up communication with family about topics you may not have even realized your child was thinking about. Although this book is to help work through the life changes and challenges of an illness, it also helps remind kids that there is more to them than their illness with pages dedicated to what makes them unique and special.

In short, I think every child, whether young or teen, facing a health challenge could benefit from this book. You can buy it here on Amazon.

Book to Help Chronically Sick Kids and Their Families

Wonder is a must read for the entire family. You can buy it here on Amazon.


Reviewed by Jennifer Tousseau and Katie Baily

Wonder, written by R. J. Palacio, is a must read for the entire family. Told with humor (everyone will laugh) and respect, Wonder follows Auggie, his family, and friends through 5th grade, Auggis’s first year going to school after being homeschooled due to his medical condition. Readers aren’t told exactly what Auggie has until midway through the story, because the story is not about the diagnosis; the story is about living life with the diagnosis. (Although the Genetics 101 chapter will feel familiar and poignant to those with a genetic condition.)

Of course that doesn’t mean life is easy for any of them and the reader experiences that from the personal perspective of Auggie and each person close to Auggie, which sets this book apart. Hardly any of us can relate to being Auggie, though we want to better understand. But all of us can relate to the humanity and imperfections of the other characters, and how those characters can also show resilience, humility, and integrity. His friend Jack Will’s story is impactful because that’s how many kids with even the best hearts would be. His friend Summer is more of that “one of a kind” friend we all hope to have in our lives.

It’s hard to give a good review of this book without giving everything away, so we’ll just say it has it all: good friends and family, life’s high points and low points, and lots of laughter, cheers, and some tears.

To give you a peek into Wonder here are a couple of our favorite quotes from the book (It was hard to narrow this down to just two!):

“Don’t tell me the sky’s the limit when there’s footprints on the moon” – One of the many inspirational precepts from Auggie’s teacher that you’ll find in 365 Days of Wonder. Click here for more.

From the sister who struggles with watching her brother struggle and yet feels their parents put her second behind her brother’s needs. She’s also one of Auggie’s biggest supporters. –

I’ve seen August after his surgeries: his little face bandaged up and swollen, his tiny body full of IVs and tubes to keep him alive. After you’ve seen someone else going through that, it feels kind of crazy to complain over not getting the toy you had asked for, or your mom missing a school play. I knew this even when I was six years old.

From Auggie’s homework assignment –

This precept means that we should be remembered for the things we do….The things we do outlast our mortality….are like monuments that people build to honor heroes after they’ve died. They’re like the pyramids that the Egyptians built to honor the pharaohs. Only instead of being made out of stone, they’re made out of memories people have of you. That’s why your deeds are like your monuments. Built with memories instead of stone.

When reading Wonder we both thought for sure the author had personal experience dealing with chronic medical condition. She got so many things right; the fears and uncertainty that parents face making what to others would be mundane decisions, the child living life with their medical condition in tow, the sibling struggles, and even dealing with outsiders looking in who don’t care to try and understand.  But it turns out, R.J. Palacio developed this story after meeting a child with facial deformity and regretting how she reacted. That night after her encounter she started writing Wonder. –

wonder new book by palacio

We’re All Wonders, A picture book of Auggie’s world for younger readers. Order it here.

For the rest of the day, I couldn’t stop thinking about how that scene had played out…What could I be teaching my children so they could understand how to respond better next time? Is “don’t stare” even the right thing to teach, or is there something deeper? All this stuff was flying through my head, and I realized that I was disappointed in myself because I had missed a good teaching moment for my kids. What I should have done, instead of trying to get my kids away and avoid the situation, was engage the girl and her mother in conversation. If my son cried, so be it: kids cry. But I should have set a better example for him…Instead I panicked. I simply didn’t have the wherewithall to know what to do in that situation. – R. J. Palacio

R.J. Palacio has turned her moment of regret into a positive story full of simple kindness, a teachable moment for us all, and sparked the Choose Kind Campaign which you can learn more about here.

It can’t be said enough that this book is well worth the read. Read it with your kids and keep the tissue box close by. You can buy Wonder here on Amazon.

book for kids who are sick

This book is perfect for toddlers, preschoolers, and beginning school-aged kids who have to spend a lot of time with doctors. Buy it here on Amazon.

A Day with the Animal Doctors

Reviewed by S.T.

My son, age 3, loves reading A Day with the Animal Doctors written by Sharon Rentta, a sweet book about a little boy named Terrence who joins his mom, a doctor, for a day at the hospital. Through Terrence’s antics, readers learn about different reasons people come to the hospital and some of the equipment doctors use, such as X-rays, etc. The pictures are cute and funny, with small details to engage older readers, such as the endless work of the cleaning mice, who constantly tidy up after Terrence and sweep up a leopard’s spots, or an elderly crocodile who loses his false teeth and must have “nil by mouth”. Overall, the book normalizes hospitals and doctors, making them seem friendlier and more welcoming.

arthritis kids book

Families dealing with autoimmune and autoinflammatory conditions will relate to this book.

Taking Arthritis to School

Reviewed by Katie Bailey

Taking Arthritis to School, written by Dee Dee L. Miller and illustrated by Tom Dineen, is a wonderfully illustrated, informative, and child-centered book about pediatric arthritis.  The story outlines several experiences that many families who are affected by autoimmune or systemic autoinflammatory diseases will find familiar.  The author manages to balance a sense of optimism while still explaining some of the challenges these children face in simple terms.  The reader is frequently reminded that although there are difficulties including labs, procedures, medications, and days where Eric is not feeling well, he is still an ordinary kid who loves exercising his imagination, going to school, and playing with friends.

book for kids who have a sick sibling

This book will help siblings of kids who are often in the hospital or doctor’s office.


Reviewed by Katie Bailey

Sometimes, by Rebecca Elliott, is a book written especially for siblings of children with chronic illnesses.  The story follows a brother and sister through the sister’s hospital visit, which you can tell is likely a recurring event. The author does a beautiful job of highlighting the special relationship between the sibling pair.  The brother’s love for his sister is evident throughout the story, and parents might also get an idea or two on how to incorporate the healthy siblings during difficult times such as hospital stays.  The author leaves several details open to interpretation, so families dealing with various chronic illnesses can use it to touch on their own children’s experiences.  This is a quick and meaningful read for any family that has toddler through elementary age siblings.

book for kids with a sick mom

This book is written by a mom with a chronic illness for her son.

Why Does Mommy Hurt?

Reviewed by Katie Bailey

Why Does Mommy Hurt?, by Elizabeth M. Christy, is an insightful and honest portrayal of life with a chronically ill parent told from the perspective of her young son.  The reader gains understanding of how the mom’s illness impacts both her and her family’s daily life, yet the young son is quick to point out her inherent irreplaceable value as his mom and all the important and special things they still enjoy doing together.  The boy expresses authentic feelings, but is also full of patience and a desire to help his mom feel better in this sweet, simple story.  This book is a great book for any chronically ill parent to read with their young children.

book to help sick kids

In this book, Little Tree weathers a dangerous storm with the help of those around her.

Little Tree

Reviewed by Katie Bailey

Little Tree, by Joyce C. Mills, is an empowering tale of a tree who is forever changed after weathering a dangerous storm.  The book is colorfully illustrated and its wording is simple enough for young children to relate to.  However, the pages are filled throughout the story with deeper meaning from which older kids and adults may appreciate even more fully. It follows Little Tree’s journey, highlighting many common struggles and emotions felt by those who suffer from chronic illness.  Acceptance is not immediate, but with the help of a loyal friend and two kind caretakers, Little Tree reminds the reader that having “strong roots and a brave heart” is even more powerful than she imagined.

The Fantastic Interleukins

Part of  becoming accepting and comfortable with all that comes with an autoinflammatory illness is learning about your illness. It’s good for even young kids to learn what they can so they are able to participate in conversations with the doctor and just understand what is happening inside their body. The Fantastic Interleukins, written by an immunologist, gives an explanation to what each cytokine’s role is in the body. You can download it free here, or buy a paperback book or Kindle version here on Amazon.

Cryopyrin-associated Periodic Syndrome (CAPS) Treatment Guidelines – Studies and Other Resources

There are three forms of CAPS, familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MES), and neonatal-onset multisystem inflammatory disease (NOMID). FCAS is the mild form of CAPS, MWS is moderate, and NOMID is the most severe form of CAPS.

Common symptoms for all forms of CAPS include (but are not limited to):

  • Rash
  • Headaches
  • Recurrent fevers
  • Joint pain
  • Conjunctivitis

To learn more about CAPS, here is the Autoinflammatory Alliance information on CAPS and here is the autoinflammatory database.

Studies below include what complications to monitor for, updated research-based effective treatment options, recommended dosing of medications, and other important information for managing and treating CAPS in both children and adults. Only some highlights from each study are included below. For the full study and more comprehensive information, follow the links directly to the study.

In this video, expert Dr. Lachmann of The Royal Free in London discusses CAPS treatment:

Diagnostic criteria for cryopyrin-associated periodic syndrome (CAPS)

“The best diagnosis model included: Raised inflammatory markers (C-reactive protein/serum amyloid A) plus ≥two of six CAPS-typical symptoms: urticaria-like rash, cold-triggered episodes, sensorineural hearing loss, musculoskeletal symptoms, chronic aseptic meningitis and skeletal abnormalities.”

Read more here.

Canakinumab in patients with cryopyrin-associated periodic syndrome: an update for clinicians

“Early and aggressive treatment for CAPS patients is crucial to avoid end-organ damage. Most CAPS specific symptoms are reversible if treatment is given early…Growth retardation, CNS inflammation and hearing loss have been reported to improve with anakinra in some patients.”

“CAPS disease activity is monitored by the patient’s assessment of disease activity, by a physician’s examination and assessment of judged disease activity, and by examination of inflammatory parameters at defined intervals. As CAPS disease activity may fluctuate, it is important for patients to take notes of their symptoms in a designated diary.”

“Laboratory parameters such as CRP, ESR, and SAA should be monitored.”

“If the skeletal bones are affected, lesions should be monitored on an annual basis. If the CNS is involved, MRI with fluid-attenuated inversion recovery (FLAIR) imaging is recommended and children under five should be monitored by spinal tap and analysis.”

“CAPS patients should be followed by medical centers specialized in the care of patients with auto-inflammatory diseases.”

“Some NLRP3 mutations are present in the general population without essential association to CAPS symptoms, e.g. the V198M or Q703K sequence variants However, when patients carrying these polymorphisms display clinical symptoms, their response to IL-1β inhibition is less favorable, meaning that dosage and frequency of application have to be increased.”

“…use of canakinumab is associated with a persistent satisfactory control of disease activity but needs progressive dose adjustments in more severely affected patients. The clinical phenotype, rather than age, represented the main variable by which the need for more frequent administrations of the drug at a higher dosage was determined.”

“In one study with six NOMID/CINCA patients (aged 11–34 years), patients received 150 mg (2 mg/kg) or 300 mg (4 mg/kg) every 4–8 weeks. A dose increase up to 600 mg (8 mg/kg) was allowed if needed. In 5 out of 6 patients remission was experienced according to patient’s disease activity diaries. However, CRP remained elevated in 1/6 patients and CNS leukocytosis persisted in 5/6 patients…In all patients the canakinumab dose had to be increased to the maximum of 600 mg (8 mg/kg), which however was well tolerated by adults and children alike.”

Read more here.

Real-life effectiveness of canakinumab in cryopyrin-associated periodic syndrome

Overall, complete response (CR) was seen in 72% of CAPS patients, significantly less often in severe (14%) than in mild CAPS phenotypes (79%). Only 53% attained CR on standard dose canakinumab. Dose increase was more commonly required in children (56%) than in adults (22%). Centres with a treat-to-target approach had significantly higher CR rates (94 vs 50%).”

“Conclusion: Real-life effectiveness of canakinumab in CAPS was significantly lower than in controlled trials. Treat-to-target strategies may improve the outcome of children and adults living with CAPS.”

Read more here.

Dose Adjustment of Anakinra (Kineret®) Based on Clinical Response in Patients with Severe Cryopyrin-Associated Periodic Syndromes

“For patients with inadequate clinical response or a disease flare, the dose could be increased by 0.5-1 mg/kg for up to a maximum of 10 mg/kg/day.”

“The actual dose range during the study was 0.9-7.6 mg/kg/day, with the highest dose maintained for 15 months followed by a decrease thereafter. The doses were not only increased for preventing disease flares e.g. rash, fever and elevated CRP but also to preserve organ function, e.g. hearing and vision.”

“Anakinra doses were adjusted based on clinical response in order to achieve systemic inflammatory remission and absence of organ inflammation. In one patient doses up to 7.6 mg/kg/day were needed to control CNS inflammation. Dose adjustments were well tolerated with adverse event reporting rates similar in patients on doses <3.5 and ≥3.5mg/kg/day.”

Read more here.

Recommendations for the management of autoinflammatory diseases

This includes the current recommendations for the treatment and management of cryopyrin-associated periodic syndromes (CAPS), tumour necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) and mevalonate kinase deficiency (MKD). These recommendations were developed by the European project Single Hub and Access point for paediatric Rheumatology in Europe (SHARE).

Read more here.

Long-term safety profile of anakinra in patients with severe cryopyrin-associated periodic syndromes

“In this study of severe CAPS, anakinra was continued during the course of infections in 272 out of a total of 273 events. In one case anakinra was temporarily stopped during an infection, after which the patient developed a severe CAPS flare and was re-started on anakinra after 8 days, without complications and with resolution of the infection. In two serious infections and two non-serious infections, the dose of anakinra was increased due to disease flares that occurred in connection with the infections. All infections during anakinra treatment were carefully monitored. Anakinra was maintained with the same dose. In patients who experienced a concomitant CAPS flare with their infection, anakinra was temporarily increased without impact on the resolution of the infection. Although the clinical threshold for starting an antibiotic was low, the organisms isolated and the treatments used did not suggest opportunistic infections and the resolution of the infections on anakinra was as expected and not associated with complications. Observations that patients with CAPS can develop disease flares in the context of triggering infections, and that abrupt drug withdrawal results in disease flares that can be severe [4], illustrate that withholding anakinra during an infection can increase the risk of severe disease flares, suggesting that in CAPS patients continued anakinra treatment should be considered during infections, with careful monitoring of the resolution of the infections.”

Read more here.

Severe Inflammation Following Vaccination Against Streptococcus Pneumoniae in Patients with Cryopyrin-Associated Periodic Syndromes

“Pneumococcal vaccines can trigger a severe local and systemic inflammatory reaction in patients with CAPS.”

All patients diagnosed with any form of CAPS should discuss this study with their doctors before being vaccinated a pneumococcal vaccine.

Read more here.

Safety of vaccinations in patients with cryopyrin-associated periodic syndromes: a prospective registry based study.

“Pneumococcal vaccines, unlike other vaccines, frequently trigger severe local and systemic inflammation in CAPS patients. Clinicians must balance potential benefits of pneumococcal immunization against safety concerns. The 13-valent pneumococcal conjugate vaccine might be favourable over the polysaccharide vaccine in CAPS patients.”

Read more here.

2016 Autoinflammatory Alliance Year in Review

One of the Autoinflammatory Alliance slogans

2016 Highlights for the Autoinflammatory Alliance

A special thanks to all our supporters and volunteers that have helped make this year a great one for advocacy, support, and awareness for autoinflammatory diseases.  Here is a short list of some of impact this year.  A donation now will help us be able to do more for 2017 and beyond!  We help thousands of patients every year individually, in our patient groups, and with special projects. We also help hundreds of doctors and medical professionals that use our resources or request materials for their patients, and have collaborated on some groundbreaking research projects.


  • Fund more research-the more we raise, the more we can accelerate new discoveries and help for patients
  • Increase awareness in the United States and internationally about autoinflammatory diseases
  • Produce more educational materials in print and digitally for patients and medical professionals
  • Translate educational materials into more languages
  • Keep the Autoinflammatory Database updated
  • Maintain and update our blog and the website

February: Phase II of the Autoinflammatory Disease Damage Index (ADDI) evaluation process was started. In 2015, we started working on the development of the Autoinflammatory Disease Damage Index (ADDI) tool with a collaboration with a global team of researchers, and a survey of a sample of patient volunteers from our Autoinflammatory Alliance patient community.

The initial tool was presented in a poster and abstract at the Autoinflammation 2015 Congress.  In late September, 2015 all the researchers and Karen Durrant, president of the Autoinflammatory Alliance, met for two days to review the preliminary ADDI tool, that was developed based on the patient input in Phase I with the surveys.

In February 2016, we again reached out to our patient community in a larger sample to evaluate the tool, using the 1000minds program, and feedback from the patients led to the final ADDI tool that was presented at the Pediatric Rheumatology European Society (PReS) Congress in September, 2016, and was published in November 2016 in the Annals of Rheumatic Diseases.

Quinn Paduani obtained the Rare Disease Day Proclamation for South Carolina in honor of autoinflammatory diseases.

February 28: Rare Disease Day 2016 involved a month of advocacy and outreach at a local, state, and national levels by the Autoinflammatory Alliance and their supporters. So many members of our patient community got involved this year at their schools to state rare disease day events and many fundraisers! We are so thankful for their dedication and efforts!

Heather Briganti, one of our board members and advocates did a segment on the news in Albuquerque, NM about Rare Disease Day that you can watch here. Dorelia Rivera, our vice-president represented our organization and our patients at the national Rare Disease Day events in Washington DC.

Julie Cunningham, board member and advocate worked with the Global Genes Project for Rare Disease Month awareness, and launched this nice creative project for children to download and use in their classrooms for Rare Disease Day.

March 12: Our first Par2 Prodigy Disc Golf Tournament was held in Golden Gate Park, San Francisco, CA and we had the support of many sponsors, including Prodigy Discs, Infinite Discs, Sports Basement, Crossroads Health & Hospice Care, PrAna, and many others.  Everyone that came had a great time, got a great disc golf set, stickers and knit hats from Prodigy, and nice golf towels and gift certificates from Infinite Discs. We raised a lot of money and awareness for autoinflammatory diseases! Thanks to all that came, even in the rain to support the cause!

March 24: Colleen Paduani, board member and advocate, and her family appeared on “The Balancing Act” national morning television show to raise awareness for NOMID, a rare autoinflammatory disease, treatment with anakinra and the Autoinflammatory Alliance. Watch it here.

Celebrating 10 years of advocacy and awareness for autoinflammatory diseases!

May 1: Our official 10 year anniversary of our organization!  When we started our organization in January 2006, and were officially recognized by the State of California on May 1, 2006 (formerly as the NOMID Alliance), we were the first organization dedicated to autoinflammatory diseases in the United States, and one of only a few in the world (that also started around the same time as us) for these rare diseases. In 2014, we changed our name officially to the Autoinflammatory Alliance.  We decided to celebrate our 10 year anniversary during our second annual Autoinflammatory Awareness Month in August!

Rare Bears were granted to patients, based on their individual interests. Each one is unique!

July: Leading up to our awareness month, we partnered with Rare Science’s RARE Bear Project to have children autoinflammatory diseases get a one of a kind handmade bear mailed to them, that was picked out based on their interests on our sign up form. We had hundreds of children receive their RARE Bears in August for our Autoinflammatory Awareness month, and we donated funds to cover the shipping costs for hundreds of these bears to be delivered to our patients globally.  Many of these children submitted thank yous and photos, that are a part of the RARE Bear Kids photo gallery. If you are interested in a RARE Bear for a child with a rare disease, please submit this form to Rare Science directly.

Some of the attendees at the SF Autoinflammatory Awareness Month picnic

Attendees at the Texas Autoinflammatory Awareness Month gathering

Oceanside, CA Beach Party Our medical advisors, Dr Hoffman and Dr Broderick (lower left) were there too!

August was our Second Autoinflammatory Awareness Month!  We had many of our patients supporting various awareness and fundraising efforts throughout the month, and some of our board members and advocates attended the in-district lobby days to address the needs of autoinflammatory patients directly with their Senators and Representatives when they were back in their hometown in August.

In addition, we had Autoinflammatory Awareness Month patient gatherings and picnics across the US, and even in the Netherlands!  It was nice to have everyone come together, and many patients had not ever met someone with these diseases in person, until they came to one of these events.

2016 Autoinflammatory Symposium

1st Autoinflammation and Immune-Dysregulation Symposium

September 19th was the 1st Symposium of Autoinflammation and Immune-dysregulation at Walter Reed National Military Medical Center (WRNMMC) that launched the collaboration between the National Institutes of Health (NIH) and WRNMMC for a joint clinic for autoinflammatory diseases and research.  We helped to organize, promote, manage tickets and admission to the conference, presented as speakers, and supported the food and additional costs for this conference that were not covered by WRNMMC.  Leading experts on autoinflammatory diseases and research from the NIH and WRNMMC spoke, along with Karen Durrant, RN and Erin Wilson from the Autoinflammatory Alliance. Learn more about this conference here.

Your donations have helped this conference to happen! We want to raise more research funds in 2017 to support more collaborative research to help more patients, and train more doctors on these diseases. This is just the beginning of this joint collaboration with the NIH and WRNMMC, and we are so thankful to be a part of it!

September 27-October 1st: Karen Durrant RN, president of the Autoinflammatory Alliance, and Saskya Appelman, Autoinflammatory Alliance Dutch patient representative, and member of KAISZ represented patients at the Pediatric Rheumatology European Society (PReS) meeting and concurrent meeting of the European Network for Children with Arthritis (ENCA) in Genoa, Italy.

September 30: Karen Durrant, RN, BSN presented a poster and abstract in the poster walk on a collaborative research project that highlighted the impact and challenges of living with an autoinflammatory disease, specifically for patients with Familial Mediterranean Fever (FMF), Mevalonate Kinase Deficiencies (MKD/HIDS), and TNF Receptor-associated Periodic Fever Syndrome (TRAPS).  Here is our blog post with details of this poster and research project.

November 29th: For Giving Tuesday, we got involved with the #Unselfie movement, and also had a very successful fundraiser! Thanks to all that donated, and shared their Unselfies to raise awareness for autoinflammatory diseases, and support the Autoinflammatory Alliance! Take a look at our community Unselfie gallery!  Learn more here.


December 7th: 21st Century Cures Act becomes a law! Some of our board members have been leading advocates for this much needed law, and the Autoinflammatory Alliance, along with many other rare disease organizations. This law will help rare diseases greatly, and was an effort by many in the rare disease community, and Dorelia Rivera, Vice President had an active role in advocating for this as well.

In December, Colleen Paduani, board member and advocate led a fun “Caroling for Cures” fundraiser in South Carolina.  Some other families have been a part of this fundraising effort in the past, and it is a fun way to raise awareness too! Here is a blog post about Caroling for Cures.

Caroling for Cures in South Carolina!

We really appreciate all your support, and your donation makes a difference to many, all year round!  We help almost 4,000 patients in our private, moderated patient support groups online, and many others through direct contact with us via email, phone or from their doctors. Hundreds of doctors rely on our resources to help them educate their patients on these diseases, and also train fellows or learn more on their own about these rare and complex conditions.  Our blog reaches nearly 50,000 visitors a month, in addition to our website and We also mail out printed educational materials to patients and medical professionals, and do not charge for any of our resources. We work hard to raise the funds to make all materials, support, and information open access for all.

But we really need your support, and that of many more to help us to reach our goals. Learn more here, and make a donation today!


  • Fund more research-the more we raise, the more we can accelerate new discoveries and help for patients
  • Increase awareness in the United States and globally about autoinflammatory diseases
  • Produce more educational materials in print and digitally for patients and medical professionals
  • Translate educational materials into more languages
  • Keep the Autoinflammatory Database updated
  • Maintain and update our blog and the website

Thank you!