Heading back to school with juvenile arthritis (JA) can be tricky on your joints. Follow this list from elementary to high school to make the most out of your school year!
1. Apply for a government disability code (IPP). This recognizes that you have a physical disability and allows you to use accommodations in the classroom.
2. Ask your physiotherapist to write a list of accommodations that you can distribute to teachers and gym instructor.
3. Ask for extra time on tests, computer use for in-class essays, and extensions on assignments when you are away for an appointment.
4. Ask for printed copies of notes or have power points emailed to you. Have your teachers prepare pre-packaged notes for infusion days! Don’t let your disease impact your grades.
5. Make sure to empty out your overflowing binder to reduce the weight you carry. Use two sets of textbooks (for at home and in your locker).
6. Use pencil grips!
7. Use a laptop, iPad and voice recognition software.
8. Back to school fashion doesn’t have to been a strain on your joints. Look for comfortable foot wear (Birkenstocks or Nike) and find a trendy backpack. Don’t hurt your joints by wearing flats or using a satchel.
Your first year of college is only a month away! Don’t let arthritis hold you back from the degree you deserve. Follow these 12 tips to finish your school year with straight A’s!
1. Register with your college’s accommodation center.Benefits include extra time and breaks during exams.
2. Apply for physical disability scholarships, loans and grants for scribes and arthritis-friendly equipment like a lightweight laptop, an iPad and voice recognition software to record lectures.
3. Apply for a scribe. Not only will they take your notes in fast-paced lectures, but they can also provide you with notes if you miss a lecture for an appointment.
4. Learn to type your notes. Color-coordinated notebooks look pretty, but they may put an unnecessary stress on your hands.
5. Apply for a handicap pass and parking pass. Ask for permission to park in multiple parking lots, so you can park close to each of your classes or so you can drive across campus instead of walking.
6. Meet with your professor to explain your disease. This will help them understand how they can further assist you.
7. Get online textbooks. Use an iPad to view textbooks instead of carrying heavy textbooks.
8. Download the PowerPoint presentations on your iPad instead of copying out notes you can fill in the blanks.
9. Leave enough time in your schedule to walk between classes.
10. Don’t book an 8 a.m. class if you experience fatigue and morning stiffness. Make sure you have flexibility set up in the schedule when you select classes. Start after 10 a.m., take evening classes and try to have a day off!
11. Don’t be afraid to take a reduced course load or spring courses. You can still graduate on time, and your body will thank you for it. Remember you will have to miss classes for appointments, and it’s better to take on an amount you can handle.
12. Keep your joints moving by using your campus gym and sign up for cheap fitness classes. Don’t forget that yoga, biking and swimming are all arthritis-friendly activities at a reduced student rate!
Eight years ago, my father passed away after a long battle with Alzheimer’s. As I sat by his bedside, my thoughts turned to all those moments in my life when he was my caregiver. More than just his role as the dutiful parent, he became my main caregiver when I developed juvenile rheumatoid arthritis at 13 years old.
My father was the one who drove me to and from doctors’ appointments, reminded me to take my medicines and even was my therapist. For two long years, my after-school activity consisted of sitting in a chair watching “General Hospital,” wearing a neck brace that was tied to a thick rope, and on the other side of the door was a bag filled with gallons of water. My father had to place me in “traction” every single day, although it was very difficult for him to see me in such pain. I remember begging him, “Not today, let me have a day off,” but he never gave in. He knew that although it hurt me, in the long run it would be beneficial for me.
As I sat there by his side those long days before he died, I thought of the important role of caregivers. Since arthritis is a disease of mobility, the role of the caregiver is essential. There are over 50 million Americans diagnosed with arthritis, and each has at least one caregiver. The role of the caregiver is important no matter what age we are diagnosed with arthritis. The role takes on various forms throughout the lifespan of a person with arthritis.
It is the parent of a child with arthritis who wakes up earlier than usual to prepare a warm bath, so their child can move his/her joints before heading off to school.
It is the parent who has to prepare a good breakfast because their child will need to take morning medicines. It is the strength of a parent who cries in the shower alone, but puts on a brave face in front of their child as they prepare their Enbrel injection.
It is the boyfriend/girlfriend of a person with arthritis who learns to hold their hands differently because crossing their fingers is way too painful.
It is the spouse of a person with arthritis who quietly helps his loved one dress, put on their shoes, and get ready to face the world every day, while no one else has any idea of what it may have taken to get them out the door.
It is the spouse who waits patiently after the surgical doors close, leaving them alone with their thoughts and prayers as their loved one undergoes yet another surgery.
It is the child of a person with arthritis who grows up all too soon by taking care of their parent, reversing the traditional caretaker roles. These children, who mature before their time, learn to take on a myriad of adult-type responsibilities.
I intimately know each of these caregiver roles because my husband and daughter have continued the legacy my father began. Throughout the years, my arthritis has destroyed both my hips, my right shoulder, and both jaws. Thus, I have had to undergo seven joint replacements. To have a part of your body removed and replaced by metal makes you feel less human and more robotic only if you allow it to do so. For though it is quite painful, it quickly puts life into perceptive.
After each surgery I felt as though I had been robbed of my abilities as a human being. I could not move without aid. When I began to walk, I could not simply get up and move. I remember giving my legs the command to move, but they stood as still as Roman pillars on an archaic building. With time, as my muscles came back to me, I began to move my legs, and soon I was walking ever so slowly again. Through the weeks of therapy, I progressed from a walker a cane to walking on my own. I felt as autonomous as a toddler taking her first steps.
With this newfound independence also came a great deal of inner wisdom. The little everyday movements became small victories as I acquired them. I began to realize what truly matters in life are the people around you, the support system that stays behind when the surgical doors close. Once they are reunited with you, they search for ways of helping you deal with your pain and inability to move. This support system, the caregivers, whether it is comprised of one or many, is the essence of recovery. I got up and walked across the room because my husband or daughter was on the other side, waiting to surround my body with their arms.
It was that one hug that made all the pain worth it. It was their mere presence day after day that made me realize that although I have one more piece of metal inside my body, I am still the same person with the same hopes and aspirations.
Although my father is gone, he left me with wonderful memories and a legacy to help others in need. This example of service to others is what lies at the core of the Arthritis Foundation’s mission statement. Let us never lose hope that one day arthritis will be conquered, but in the meantime, let us continue to fight the good fight and care for everyone around us.
To ensure that I am living my life as “normal” as possible, I simply need to make modifications to my lifestyle that best suits me and my disease.
2. Your health advice is (respectfully) BS.
Unless you are a healthcare professional with accurate information regarding my illness, or you are powerful healing shaman that can take away my disease with a simple touch (please email me if you can do this), you have no business offering any health advice.
I appreciate your eagerness to help, but respectfully, stop.
Any mainstream supplement, diet, treatment, prayer, affirmation or drug, I have already tried or considered.
A note to multi-level marketing (MLM) sales peeps: Most products you’re selling consist of fake nutrition laced with soy, sugar, and chemical bi-product. Just because you bought a “welcome kit” and watched some info videos doesn’t mean you know how to ease inflammation. In fact, I’m personally offended you think my struggle is a business opportunity.
I have very specific drug, diet, and lifestyle protocols implemented that are tailored to my genetics and disease, so that pill you saw at GNC with “joint support” doesn’t apply.
An autoimmune disease is when your immune system can’t tell the difference between foreign invaders and it’s tissues. As a result, those that have autoimmune issues present different symptoms depending on their diagnosis.
In my case, I have arthritis in my joints. Arthritis is often labeled an “old people” disease; however, anyone at any time can get it.
4. Stop calling me out.
For the last 12 years, I have been battling pain and inflammation in my entire body. My knees are the biggest problem area. Over time, my knee joints developed deformities and as a result left me with a sickkkkkpimp walk (I kid…but I have a little limp even with knee replacements).
I can’t for the life of me understand how “normal” strangers over the course of 12 years, at least once a day, have come right up to me and asked, “Why do you walk that way?”
Thousands of times (not exaggerating), I have been approached with the question, “What’s the matter with you?” or “What happened?”
Seriously?I appreciate the concern, but it’s none of your f*ing business.
According to the Arthritis National Research Foundation, arthritis is the leading cause of disability in America. That means an estimated 50 million Americans, including about 300,000 children, deal with the pain of arthritis on a daily basis. It’s by no means an “old person’s disease.”
Although the number of young people with arthritis is so high, the condition is littered with misconceptions. So we partnered with the Arthritis National Research Foundation to raise awareness about JA. We asked our communities what they wish the rest of the world understood about JA. Here’s what they had to say:
1. “It’s a battle that comes with its own set of dragons and other obstacles, and sometimes you will be down and out for a while. But that doesn’t mean you have to give up on your dreams.” – Victoria Steed
2. “I was 18 months old when I was diagnosed. It was a hard childhood, however, it made me the resilient determined powerfully positive well rounded person that I am today. JA is a horrible thing, but life doesn’t end, and don’t ever let anyone tell you that you cannot do something!” – Danielle Lindoff
3. “You don’t have to put limitations on us. We are aware of our physical limitations. We are just like you, so please don’t treat us differently.” — Carrie Folkerts
4. It’s not just achy joints; it’s doctor visits, missed school days and missed special events. Our kids still have to put up with bullying at times for having what is known as an ‘old person’s disease.’” – Gaby Baldenegro
5. “I am not my disease. I am not the medication, the canceled plans, or the wheelchair. I’m not the swollen joints or even the pain. I’m a survivor. What you don’t see is my fight to appear normal every single day. So please stop looking at my arthritis to define me.” – Katherine Herrmann
6. “I think the hardest part as a parent is hearing him wish for ‘one day without pain.’” – Andrea Thompson
7. “Children are stronger than you think, and sometimes they are hiding some of the pain. It’s easier to hide and ignore the pain than to address it.” – Becca Duane
9. “Watching your child’s body turn on itself, and then watching them have to go through such grown up things like monthly blood draws, injections, pills and more pills, is completely heart wrenching.” – Jessica Ferguson Garcie
10. “Even though you look normal on the outside and try to keep up and do things with everyone else, you may be dying in pain on the inside.” — Linda Syrko-Shapach
11. “I was diagnosed at 18 months and I am 30 years old now. Kids, keep your head up, it gets better. Plus, your friends will love you for who you are, your disease doesn’t control you.” — Megan Vanellope Mueller
12. “I was diagnosed at 8 years old and I turned 40 this year. I want everyone to understand how amazing these kids are and how much daily life can be a struggle. These kids are some of the toughest and most resilient kids. People should take the time to get to know them and learn about their journey.” — Cat Hicks
What are some things you wish others understood about living with juvenile arthritis? Let us know in the comments.
Despite that number, a lot of misconceptions exist around arthritis, even among friends and loved ones of people living with it. We partnered with The Arthritis National Research Foundation to raise awareness surrounding this complex disease. We asked readers: What are some things you wish others understood about living with arthritis?
This is what they had to say:
1. “The pain can cause depression. At night it hurts so bad, I don’t want to wake up the next morning.” — Marielle White
4. “It affects many children. Often I hear how young I am to have rheumatoid arthritis (I’m 34). When I tell people I was diagnosed at age 2, they can’t believe it. I wish people understood it’s not arthritis that comes with old age. RA is a disease that mistakes my joints as invaders and sends my immune system into attack mode.” — Jennifer Brennan Leach
5. “RA /autoimmune patients are the best actors out there. We push through every day despite how we feel.” — Sonya Enslow Caudie
7. “Some of us get sick easily. The medications we take to keep our disease in check lowers our immune system. That means the slight cold you have will probably turn into bronchitis or pneumonia if I catch it. We can’t fight off infections like healthy people.” Stacey Howe
8. “I feel sad and lonely about missing out.” — Julie Max
9. “We might look ‘normal.’ But the pain is sometimes so unbearable all over our bodies that it feels like broken bones, muscles and ligaments.” — Melanie Mulliken
11. “My illness is serious, but it doesn’t mean I’m checked out on life. I still want a dream career, to travel the world and do the impossible.” — Valerie Webster
12. “I don’t want to be ‘the sick girl,’ but it’s impossible not to have RA permeate every aspect of my life because it’s always there in the pain and fatigue.” — Rene Baloge
13. “I’m not super woman just because I don’t look sick on the outside!” — Mandy Dawkins
14. “It is not the same pain everyone is always using for comparison. Before my diagnosis I’d never experienced pain like the pain from this disease. It is pain that nobody can possibly fathom until they feel it personally.” — Jeanie Parker
15. “I can feel OK one day and be sick/fatigued/in pain the next. Living with this illness that has no schedule and a mind of its own isn’t easy to plan my life around.” — Candi Wilson
16. “Even after 10 hours of sleep, my body may feel as though I have just ran 5 miles, have the flu and have just been in a car wreck, all at once!” — Lynn Harrison
17. “I do not fake my disease. Some days I am fine… some days I kick my own ass.” — Brandy Abernethy
18. “It’s unpredictable. I’m constantly making plans and then having to cancel because my body is not cooperating. Constantly living with pain and/or extreme fatigue can break your spirit and make you want to disconnect from the world.” — Julier Ober Stebbens
19. “My disease is not the same thing as osteoarthritis. No, your ‘grandma’s knee problems’ are not the same thing as my systemic, debilitating, lifelong disease.” — Katie Jo Ramsey