Share Your Story Today

young adult cancer stories

Are you a young adult cancer survivor or caregiver?  Are you ready to tell your story to help someone else who is going through what you went through?

In the middle of the night, someone out there is wondering if they are the only one who has ever gone through young adult cancer.  They are feeling alone, isolated, and wanting to feel connected to someone who understands.  You can help someone, just like you, going through young adult cancer by sharing your story.  Our contributors are courageous story tellers, giving back to a community of young adult cancer fighters and thrivers.

Your story matters.

To add continually to the stories we share, we need *YOU*!  Sit down, have a coffee with us, and share your voice!

The Thing About Cancer + Kids Is…

young adult cancer and kids

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During the month of May, we’ll be bringing back some of your favorite posts in groups of 5!

Today, we’ve got 5 GREAT posts focused on getting to the nitty gritty of young adult cancer and kids.

[/spb_text_block] [spb_single_image image=”14097″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/tell-kids-cancer/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14094″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/three-lessons-learned-cancer-mom/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14095″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/book-review-a-monster-calls/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14099″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/waiting/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14096″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/doorways-to-arkomo-review/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first last”][/spb_single_image]

The Thing About Young Adult Caregiving Is…

young adult caregiving

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During the month of May, we’ll be bringing back some of your favorite posts in groups of 5!

Today, we’ve got 5 GREAT posts focused on getting to the nitty gritty of young adult caregiving.

[/spb_text_block] [spb_single_image image=”14141″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/steps-reduce-stress-caregiver/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14140″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/the-family-diagnosis/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14138″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/how-to-care-for-a-caregiver/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14139″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/living-with-the-dying-what-every-caregiver-ought-to-know-by-jcutlerlopez/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14137″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/caregiving-for-a-parent-as-a-young-adult/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first last”][/spb_single_image]

The Thing About Cancer + Tough Decisions Is…

young adult cancer and tough decisions

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During the month of May, we’ll be bringing back some of your favorite posts in groups of 5!

Today, we’ve got 5 GREAT posts focused on getting to the nitty gritty of young adult cancer and tough decisions that come with it.

[/spb_text_block] [spb_single_image image=”14029″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/stopping-cancer-treatments/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14027″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/letting-go-of-hope/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14030″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/death-with-dignity/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first”][/spb_single_image] [spb_single_image image=”14034″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/harsh-realities/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”last”][/spb_single_image] [spb_single_image image=”14035″ image_size=”full” frame=”noframe” lightbox=”yes” image_link=”https://cactuscancer.wpengine.com/young-adult-cancer-slow-down/” link_target=”_blank” fullwidth=”no” width=”1/2″ el_position=”first last”][/spb_single_image]

CancerCon 2016 In Photos

CancerCon 2016

CancerCon was an absolute blast.  I wasn’t sure what to expect…I’ll admit that I had my reservations.  While I have a strong LOVE (seriously…some of the best folks around) for the people I work with on the Steering Committee and many others I’ve met at the conference, the angry branding of Stupid Cancer is not one that I enjoy.  I knew that I would be busy and tired and maybe not have a ton of time to myself.  We all have different tastes, right?  With a year in between one CancerCon conference and the next, it is easy for me to forget the real strength that comes from the event.  It isn’t the branding of the organization that holds it (though I do enjoy the rock star like glam that they adhere to the entire weekend), or the local celebrities that come…

The power of CancerCon is found in each and every survivor and caregiver that shows up, speaks their truth through tears and laughter, and shows love to everyone around them.  It’s the late night banter, the fatigue induced laughter, the new definition of “normal” that appears in a place when everyone there has been through something as profound as cancer.  This is what will bring me back to CancerCon next year.

I’ll speak more in the next few weeks about various pieces of the wonderful event that is CancerCon, until then enjoy some photos and remember, you are never alone.  If you missed CancerCon or were there but aching for some more connection with your young-adult-cancer-having-peers, check out some of the great programs here at Lacuna Loft.  You still have time to sign up for the next Writing Group or the soon to come Drawing Workshop.  These programs happen from the comfort of your own home while still connecting you directly to 10 other young adult survivors or caregivers through video chat.

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Today I Am – Caregiving For Me

In the land of illness, cancer survivorship, and being a caregiver, some days are better than others.  How we care for ourselves is important.  My most recent article with the Cancer Knowledge Network focuses on all of the feelings that can come with survivorship and caregiving … and how through it all, the one constant is *you.*  You can make all the difference for you, whether you enjoy your current set of emotions or not.

There isn’t always a silver lining and there isn’t always a happy ending, but through it all, there is me.

You can read the whole article here!  Self-care isn’t always easy but it is always necessary.

Speaking Up For Young Adult Caregivers

young adult caregivers

This post is brought to us by Feylyn!

As the United Kingdom celebrated its Young Carer Awareness Day on January 28, 2016, I celebrated in solidarity with much excitement. The UK has an estimated 700,000 children (“young carers”) and 300,000 young adults who provide care for their family members with disabilities or health conditions. These young people‒some as young as three years old‒ are responsible for daily living activities for their family members in need, such as administering medicines, cooking, cleaning, and personal care, e.g., bathing and dressing. On Young Carer Awareness Day, I was ecstatic that the young carers in the UK received a national day reserved to spread awareness about their lives. My excitement waned to disappointment when I discovered that American news outlets were silent about the 1.4 million child caregivers and 5.5 million young adult caregivers in the United States. I knew we didn’t have a Young Caregiver Awareness Day on the calendar. I knew that most Americans hadn’t even heard of the terms “young caregiver” or “young adult caregiver”. I knew most could not identify a young adult caregiver if asked. I have been told that young adults are too selfish to be caregivers; accordingly, our advocacy work should be focused on Baby Boomers who were caregiving for their elderly parents.

I spent the majority of my childhood watching my older brother care for me and our mother who has a physical disability. All of his young adulthood years were spent helping our mother walk, working to pay our household bills, and driving me back and forth to school. When people repeatedly told me that young adult caregivers couldn’t possibly exist, I felt like our story was overlooked. I felt like my brother and I were invisible. Knowing that there are millions of other young adults who provide care without support and recognition, I decided that I wanted to do my part to increase awareness about our hidden lives as caregivers—I decided to speak up.

If you are a young adult caregiver, I encourage you to speak out whenever and wherever you can. You deserve recognition for the vital role you play in your family. I often felt that my friends wouldn’t understand my life or the things going on with my family. I know first-hand the difficulty of sharing the uncomfortable and painful moments that occur when you provide care for someone you love. I was emotionally overwhelmed, fearful about my mother’s health, our finances, and the guilt I felt about my brother’s many sacrifices. I didn’t expect my friends, as well intentioned and kind-hearted as they all were, to handle the problems in my life or be able to relate.

Many of the young adult caregivers I’ve interviewed in the UK and US report feeling the same way: the fear of how they may be perceived by their peers held them back from telling others about their caregiving role. Others told me that they were afraid of burdening their friends and extended family members with the ugly side of caregiving. The daily act of looking after someone with a physical disability, mental illness, or drug addiction isn’t pretty. It is emotionally draining, frustrating, and awkward. You feel tired. You feel angry. It can be hard to navigate the complexity of feeling resentment and love towards your family simultaneously. Those caring for family members with substance abuse issues or a mental illness or HIV-AIDS diagnosis are particularly vulnerable to experiencing associative stigma and may not want to reveal whom they care for out of fear of exposing the cared-for individual. Internalized stigma, embarrassment, and shame can serve as a barrier to speaking out and perpetuate social isolation. Because of these realities, young adult caregivers may understandably stay quiet about their role as caregiver or chose to share with only very close friends.

If you’re a young adult caregiver, I implore you to share your story. Make yourself known. This may mean opening up to a friend, forming an online peer support group, or meeting with your state representative. Whatever you do, however seemingly big or small, is incredibly important in ensuring that the world knows that you serve an invaluable role as a young adult caregiver. Your acts of sacrifice are courageous and inspiring, particularly in a society that increasingly argues that today’s millennials are selfish and narcissistic. You are irreplaceable. You matter.

For those who don’t call themselves “caregivers”, I also present a challenge. Listen and fight. Listen to our stories, our voices, and our feelings. Practice empathy when we choose to share and respect our space when we choose to stay silent. You must also take up the fight. Partner with us in advocating our right to remain employed and take time off as needed while caregiving. Create work and school environments that communicate understanding and demonstrate flexibility. Tell our stories on Capitol Hill when we’re too exhausted or busy with our caregiving responsibilities to share our stories ourselves. Advocate with us and for us because you know that we are utterly irreplaceable. Show us that you believe young adult caregivers matter.

We can’t afford to be silent any longer.

Feylyn is a PhD student in Social Work at the Institute of Applied Social Studies at the University of Birmingham in England. A native of Hendersonville, Tennessee and graduate of Vanderbilt University, she is a nationally certified mental health counselor. Her doctoral research focuses on the identity development of young adult caregivers living in the United Kingdom and United States. During Feylyn’s childhood, her older brother was a caregiver for her and their mother who has a physical disability. This experience motivated Feylyn to pursue research and advocacy work for young adult caregivers; thus, she came to England from the United States in 2013 to further study under the expertise of Professor Saul Becker, world-renowned researcher on young people with caring responsibilities. Feylyn’s research with young adult caregivers in the United States is currently ongoing, and she invites 18-25 year old caregivers to contact her if they are interested in participating in her research study. You may learn more about her research by watching her video.

references

Contact Feylyn:

Email: FML402@bham.ac.uk
Twitter: @FeylynLewis

A Young Adult Cancer & Chronic Illness Writing Group!

writing group

Lacuna Loft is incredibly excited to introduce you to a new program that is starting here in mid-March called Unspoken Ink! Unspoken Ink is a creative writing group, designed to help address issues that transport us from initial diagnosis into the new normal and survivorship. The group will consist of 8-10 people, and will meet over 10 weeks for 2 hours each week over google hangout video chat.

If you’re interested in joining us, read more below and fill out the form!  Our Spring Session is forming now!

For the Spring Session of Unspoken Ink, we will be forming a group of 8-10 survivors. Caregiver groups will start slightly later in the year. If you are not able to attend the Spring Session for any reason (you’re a caregiver, the group was full already, the time didn’t work for your availability, etc.) please fill out the form anyway and we’ll put you on the list for future writing groups!


Welcome to the Unspoken Ink writing group! Jen and Mallory are so excited that you are considering joining us!

This group is designed to take you on a journey through your cancer or chronic illness diagnosis and into your survivorship with a small group of your young adult cancer/illness survivor peers. Each 10-week program consists of a weekly writing session attended via google video hangout. We will get to know one another in an intimate, 8-10 person setting and address issues that transport us from initial diagnosis into the new normal and survivorship.

The Unspoken Ink writing group uses a creative writing method (Amherst Writing and Artists (AWA) Method) wherein the facilitator provides a writing prompt and you can use that prompt in any way you’d like to create a story over a set amount of time. Once we’ve finished our writing (yes, the facilitator writes too!), everyone is given the opportunity to read their writing out loud. Hearing your own story and hearing someone else’s teaches us all so much about our experiences and our stories. Once the piece is read, we reflect on the writing – what did we like, what stood out, what do we remember. Everything is considered fiction so we do not respond to the writer as a support group may, but keep the focus on the writing.

Sometimes the prompts are about cancer/illness, sometimes indirectly related to cancer/illness, and sometimes not about cancer/illness at all. Above all, the writing program emphasizes that we are more than a diagnosis.

Our Spring writing group is forming soon!

Some logistics:
– The writing group meets for 2 hours each week, for a period of 10 weeks. A commitment to attend each week is important to group continuity and in creating a safe space. Please be on time. The group will begin in mid-March with a TBD meeting time.
– Each participant will receive a name@LacunaLoft-writinggroup.org email address to use when attending each writing group session. At this email address, you will receive a weekly invitation to a google video hangout where the writing group session will take place. These email addresses will help preserve individual privacy if desired and will make meeting as a group via video hangout easier.
– Following each weekly session, you may decide to submit your writing to Mallory (mallory@lacunaloft.org) for publication on LacunaLoft.org in their Young Adult Voices program section. This is not mandatory!

Looking To Speak With Young Caregivers!

young adult caregivers

Today we are helping spread the word for a PhD student looking to speak with young adult caregivers. Check out her announcement!

Are you aged 18-25? Do you provide unpaid care, support, or assistance to someone with a health condition or disability? If so, I want to hear your story!

My PhD research at the University of Birmingham is focusing on identity development in young adult caregivers in the United States and United Kingdom. This research seeks to understand the ways a young adult’s identity may have been shaped through caregiving, and to learn more about how to better support young adult caregivers as they transition into adulthood. Participating in this research is a great way for young adult caregivers to share their story to a warm and friendly listening ear whilst also providing information on what support they need. To learn more about my research and my own caregiving story, please watch the video link.

Are you:
–  18-25 years old
–  Providing unpaid care, support, and assistance to a family member (s) with a health condition such as a physical or learning disability, mental illness, and/or other conditions that require support (e.g. substance misuse, HIV/AIDS, dementia and Alzheimer’s, and injuries sustained through military service).

If so, please get in touch!

Feylyn M. Lewis, M.A.
Email: FML402@bham.ac.uk
Twitter: @FeylynLewis
Telephone: 615-638-8281

Our Stories Make Caregivers Of Us All

young adult caregiving

I recently wrote an article with the Cancer Knowledge Network about running Lacuna Loft and about telling our stories.  Feeling safe enough to share our experiences and slowing down enough to hold someone else’s story in our hearts takes practice.  These stories are delicate and special.

We have an impact on each other and the price of sharing our stories makes caregivers of us all.

You can read the whole article here!  The post even includes a short intro video by me!