Jenna is a long-time member of Upopolis and a regular contributor to our blog post series. We appreciate and value everything she teaches us about being a young adult living with a chronic illness.
Today, she shares 5 things she wish others knew about living with a chronic illness. This is so insightful to those of us who don’t have a medical illness, as well as incredibly validating for those who do. Check out what she has to say:
1. The invisibility of an illness does not diminish its existence or impact. Invisible illnesses, often overlooked due to their lack of visible symptoms, can be just as debilitating as those with outward signs. Individuals including myself facing these conditions may struggle with daily challenges that go unnoticed, emphasizing the importance of empathy and understanding. Acknowledging the presence of invisible illnesses promotes a more compassionate and supportive approach to those dealing with such health issues.
2. The visibility or recognition of an illness does not determine its validity, and this holds true for individuals often referred to as “spoonies” who contend with chronic and invisible health conditions. Whether an illness is widely understood or remains unknown, the experiences and challenges faced by those dealing with chronic health issues are valid and significant. The term “spoonie” is often used to describe people managing conditions like fibromyalgia, lupus, or chronic fatigue syndrome, emphasizing the daily allocation of limited energy “spoons.” Recognizing and respecting the validity of these experiences promotes empathy and a more inclusive understanding of diverse health struggles.
3. When chronic illness warriors find themselves needing to cancel plans, it’s not an expression of dislike or a desire for isolation. Rather, it reflects the unpredictable nature of their health challenges. It’s crucial for friends and loved ones to continue extending invitations, engaging through FaceTime, and making efforts to foster a sense of inclusion. Chronic illness warriors appreciate gestures that make them feel loved and understood, such as learning their unique love languages. In doing so, relationships can thrive despite the challenges posed by chronic health conditions, reinforcing the importance of compassion and ongoing support.
4. Experiencing occasional colds or minor illnesses may provide insight into temporary discomfort, but it doesn’t equate to a full understanding of the complex and enduring challenges that come with chronic illnesses. Chronic conditions often involve persistent symptoms, fluctuating health, and long-term impacts on daily life. It’s essential to recognize the distinction between short-term ailments and the ongoing struggles faced by those with chronic health issues. Empathy and genuine understanding can only be cultivated through acknowledging the unique and sometimes invisible aspects of chronic illness experiences.
5. Choosing not to drink alcohol, whether due to health reasons or personal preferences, doesn’t diminish one’s coolness or ability to enjoy social gatherings. The decision to abstain from alcohol is a valid choice that deserves respect and understanding. Many still find joy in partying and dancing without the need for alcoholic beverages, embracing alternatives like delicious mocktails. Creating an inclusive environment where individuals feel validated in their sobriety fosters a more considerate and accepting social atmosphere, acknowledging the diversity of preferences and lifestyles.
Thank you to Jenna, and all our Upopolis members, who teach us something new every day!
Journaling is often suggested as a way to cope with challenging life events, such as illness or grief. It offers many benefits for our mental, emotional and even physical well-being.
Over the past few months, the Upopolis Instagram page (@upopolis) has been sharing journal prompts for youth who are experiencing challenging life events, including youth with a medical illness, and youth with a parent or caregiver with a medical illness.
Today, we are sharing these journal prompts all in one place for easy access and BONUS, we have added journal prompts for youth who are grieving, and youth who have a brother or sister with a medical illness.
Check out the full list below, and be sure to save this article!
Journal Prompts for Youth with a Medical Illness
Journal Prompts for Youth with a Parent/Caregiver with a Medical Illness
Journal Prompts for Youth who are Grieving
Journal Prompts for Youth who have a Brother/Sister with a Medical Illness
Be sure to follow @upopolis on Instagram to get more coping tips and strategies like these journal prompts!
We have an amazing virtual opportunity taking place July 8th – 12th for youth with cystic fibrosis!
Camp Maple Leaf and Upopolis are teaming up to provide youth living with cystic fibrosis from all across Canada the opportunity to participate in our virtual camp, “Camp Fromaway”! Last year was Camp Fromaway’s inaugural year, and it was a huge success. We can’t wait to do it again!
What is virtual camp?
It’s the experience of camp, but online!
Camp Fromaway provides youth aged 11-17 from across Canada who are living with cystic fibrosis, and their siblings, the opportunity to meet each other while participating in fun daily camp activities. Campers who register by April 30 will receive all activity supplies they need to participate.
The best part? Campers will meet others just like them! This will provide them with a sense of belonging, teach coping skills, and help reduce feelings of isolation often associated with chronic or medical illnesses.
How to register?
Applications for Camp Fromaway are will be accepted until April 30th, 2024 at the link:
https://forms.gle/SiciN6pnPg3fivz36
To receive a digital poster to print or e-mail to your patients/clients/students/families, e-mail support@upopolis.com – just ask for a Camp Fromaway poster.
What is Camp Maple Leaf?
Camp Maple Leaf is a not-for-profit sleepover camp for children of Canadian Military families and children living with unique challenges. Their sleepover camp provides children and families who share similar life experiences with a special place to call their own.
Upopolis and Camp Maple Leaf are on a mission to support youth going through challenging life events by connecting them with others through the camp experience. For more information, visit www.campmapleleaf.ca or e-mail support@upopolis.com.
Camp takes place July 8th – 12th from 12:00pm – 2:00pm EST. Can’t wait to see you there!
When someone you know dies, it can affect you and the people you know in many different ways. These changes can be very hard, so it can be helpful to find healthy ways to cope with strong emotions.
Here are 10 ways you can cope with all the strong emotions that come with grief:
Children’s Grief Awareness Day is on November 16 and was designed to help bring awareness to the needs of children and youth who are grieving. Click here to learn more: https://www.childrensgriefawarenessday.org/cgad2/index.shtml
I’m Jenna – a former pediatric patient, current adult patient, chronic illness advocate, veteran Upal, current Upopolis member, and a 19-year-old disabled queen. I want to share some valuable insights for healthcare providers on how to better support and communicate with teenagers.
It’s crucial to bridge the gap between treating teens like children and acknowledging that they are not quite adults yet, all while avoiding stigmatization and promoting a comfortable environment for their care. Here are a few tips for every professional who works with teenage patients who have a chronic or critical illness:
1. Respect Their Maturity: Teenagers, regardless of their medical condition, appreciate being treated with respect. It’s essential for healthcare providers to acknowledge their maturity and individuality. Try not to speak down to them or dismiss their feelings and concerns. Teens may not be adults, but they are capable of understanding their health conditions and making informed decisions.
2. Avoid Stigmatization: Teens are pretty cool, and they don’t want to be judged or stigmatized based on their age or appearance. Avoid making assumptions about their behavior or lifestyle choices. Be open-minded and supportive, recognizing that everyone’s journey is unique. Stigmatization only creates barriers to effective healthcare.
3. Offer Distraction and Support: For teenagers, undergoing medical procedures or facing chronic illnesses, distraction items, or offering support from a professional like a child life specialist, can be incredibly helpful. These professionals are skilled at providing emotional support and creative distractions that make the medical experience less intimidating. Whenever possible, involving them can ease the stress and anxiety teenagers may feel during their healthcare journey.
4. Address Body Image Issues: Body shaming has no place in healthcare. Teenagers, just like adults, can experience body image insecurities. When providing care, be mindful of your language and actions. Promote positive body image and self-acceptance. Encourage open conversations about body-related concerns, but always do so with empathy and sensitivity.
5. Be Kind and Empathetic: Kindness goes a long way, especially when working with teenagers facing health challenges. Showing empathy and compassion can make a significant difference in how teenagers perceive their healthcare experiences. Listen actively, validate their feelings, and offer emotional support. A little kindness can alleviate anxiety and foster trust.
6. Encourage Independence: While it’s important to provide guidance and support, empowering teenagers to take charge of their health is equally vital. Encourage them to ask questions, express their concerns, and actively participate in their treatment plans. By promoting independence, healthcare providers can help teens develop essential life skills for managing their health in the future.
7. Foster Communication: Effective communication is the cornerstone of quality healthcare. Ensure that teenagers have the opportunity to voice their opinions, ask questions, and participate in shared decision-making. Create a safe and non-judgmental environment for open dialogue, which can lead to better treatment adherence and overall well-being.
As a former pediatric patient, current adult patient, and chronic illness advocate, I can attest to the importance of healthcare providers following these guidelines when working with teenagers. It’s crucial to strike a balance between recognizing their maturity and providing age-appropriate care, avoiding stigmatization, and fostering a respectful, supportive environment. Distraction items, kindness, and empowerment are essential components of ensuring a positive healthcare experience for teenagers, regardless of their health challenges. By implementing these tips, healthcare providers can make a profound impact on the lives of their young patients, promoting their overall well-being and encouraging them to take an active role in their healthcare journey.
When any child faces illness or hospitalization, the entire family is impacted, including the siblings. During this time, the focus for parents is typically on the sick child; unfortunately, this means that the challenges and needs of siblings often go unrecognized and as a result, siblings do not receive the attention or support they need. It’s very common for siblings of every age to face numerous challenges, feelings, and reactions in response to their brother or sister’s illness.
When a child becomes ill, youth siblings may be confronted with changes to their typical routines, are often separated from family members, may receive less attention from caregivers, have difficulty relating to their peers, and may have fears or misconceptions in relation to their sibling’s condition. These challenges can lead to siblings experiencing feelings of anger, jealousy, worry, anxiety, and guilt. In response, siblings may become more withdrawn and engage less with others, have increased outbursts, and face challenges at school.
School-aged siblings (6-13 years old) commonly worry about their sick sibling and losing them, they may become resentful because of the changes in their routines and life, and jealous of the attention their sibling is receiving. The sibling may feel embarrassed, confused, and guilty; they may also become withdrawn, clingy and uncooperative.
Here are 5 tips to help you support your school-aged child(ren):
Adolescent siblings (13-18 years old) are typically aware and concerned about the additional stress on their family and are impacted by the separation from family members and peers. Youth in this age range may fear the loss or change to their identity as they begin taking on more responsibility and their role within their family changes. They may also become insecure as they’re feeling different from their peers. Adolescents’ reactions may vary between wanting to be protective and caring, to being uncooperative, withdrawn, anxious, depressed, angry, frustrated and even resentful.
Here are 5 tips to help you support your adolescent child(ren):
Remember that it is normal for siblings to react, withdraw or act out, and even regress in response to their brother or sister’s illness. While there are many components of the illness and resulting impacts that are out of your control, there are ways you can help support your children through the challenges and journey your family is facing.
Finding strength in a community and support from others navigating similar experiences can also be extremely helpful for youth who have a brother or sister with an illness. Read about our new Sibling Island and how your child might benefit, here.
September’s around the corner and that means it’s back-to-school. Navigating this traditional yet unfamiliar life event can come with additional uncertainties and emotional responses for youth grieving the death of someone in their life.
If you are a grieving youth, remember that it’s normal to experience a range of emotions such as sadness, anger, confusion, and even happiness. It’s normal to worry about how you will concentrate in class or what you will say to your classmates when you see them again. These emotions and thoughts might feel really big right now as you are in a period of change and transition, but know that these are normal.
If you’re a parent or guardian who is supporting a grieving child or youth who is heading back to school, it’s also important for you to understand the wide range of emotions that the griever will feel. You should also recognize that children and youth may be yearning for a return to normalcy, which is completely normal; they may still grieve while demonstrating excitement, happiness or joy about returning to school, their classmates, and their regular activities. Acknowledge everything your child may be feeling and know, it’s all OK.
As we prepare to go back-to-school, there are some tips and tricks to help make the transition a little easier and more manageable. Encourage grieving children and youth to:
Remember, transitions can be hard and they can come with a variety of thoughts, feelings, and emotional responses. This is normal! As youth head back-to-school, look for the helpers, connect with trustworthy people, feel all the feelings, and take it one day at a time.
When a child or youth is hospitalized or diagnosed with illness, each and every member of the family is affected. An illness in the family can have adverse developmental, psychosocial, behavioural and emotional outcomes for siblings, yet support is rarely provided to this population and challenges are not typically addressed. The focus of pediatric health care settings is on the child with the illness, and unfortunately siblings’ needs and the impact the illness has on them goes unnoticed and unaddressed. Due to COVID-19 restrictions over the past few years, siblings and family members have been further removed as they have not been able to be present in hospitals, and so the impacts on them may be far greater.
Upopolis Sibling Island is a private online group specifically created for youth aged 10 – 18 who have a brother or sister with a chronic or critical illness, medical condition, or disability. The Island is monitored led by a Certified Child Life Specialist who monitors it daily, and provides ongoing psychosocial support, education, and engagement opportunities to the healthy siblings. Siblings of youth often experience feelings of loneliness and guilt, are at increased risk for mental health issues and may have trouble relating to or talking with peers at school who do not understand what they are experiencing. The Sibling Island provides a space for youth to openly express themselves, as well as meet and connect with a community of other siblings who are facing similar life situations.
Why siblings should join the Island?
To receive information and ask questions about their sibling’s diagnosis/condition.
To access tips, resources and activities to help cope with the feelings and experiences associated with being a sibling of someone with an illness.
To have the opportunity to socially connect with other youth and create a peer support network.
To join monthly programming and group sessions – including fun games nights!
Overall benefits of Sibling Island:
The Sibling Island provides an opportunity for youth to talk about their experiences, which helps them process what they’re thinking and feeling and in turn, helps them develop strategies to manage the challenges and difficulties they are facing.
Being part of a community helps minimize the sense of isolation that siblings often face when their brother or sister is ill, and helps normalize and validate all feelings youth are having about their sibling’s illness.
Youth can access completely trusted and vetted resources that are specific to their experience; child life specialists are present online to answer questions, concerns or worries.
What you can do?
If you are a professional who knows someone who you think would benefit from joining the Sibling Island, visit this link.
If you are a youth who would like to join the Island and connect with other siblings (or a parent of the youth), please email: support@upopolis.com