Join An Origami Workshop

Join Lacuna Loft for our next Creative Art Workshop: Origami and #LetsMakeStuff together!  Brandie will go through everything you’ll need to know to craft several different kinds of this paper folding art form.  Enjoy time making them all while hanging out with other young adult cancer patients, survivors, and caregivers.  We’ll send you what you need!

Who: 20 young adult cancer patients, survivors, and caregivers.

When: Friday, February 12th @ 4:30-6:30 pm PT / 6:30-8:30 pm CT / 7:30-9:30 pm ET via video chat.* (*US time zones…please confirm what time this means for where you live).

How does it work? We’ll send you all of the materials you need to participate! Lacuna Loft will send you an email about a week before the workshop with information on how to join the video chat. ***You’ll need the link that we’ll provide you, a headset with a microphone, and a webcam.***

Please note: Due to the global pandemic and ever-increasing customs and delivery times, we have stopped shipping outside of the United States. If you are interested in joining, please fill out the form and we will send you a list of supplies needed to participate, so you can still join us! Thank you for your understanding! If you have any questions, you can contact aerial@lacunaloft.org.

Sign up here!

Join A Focus Group + Be Heard!

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Are you between the ages of 26-35 and have been diagnosed with ALL or AML? We’d love to chat with you!

Join a focus group, hosted by Lacuna Loft, Elephants and Tea, and Servier Pharmaceuticals. Servier is looking to speak with 15 young adults facing cancer, ages 26-35, about your survivorship. The good, the bad, and everything in between. Better understanding your survivorship challenges will help Servier better innovate in their creation and delivery of cancer tools and resources.

The group will be focused around ALL and AML survivors but young adults facing other diagnoses may also attend. The focus group will take place on Feb. 10th or Feb 11th. 5-6:30 pm PT / 7-8:30 pm CT / 8-9:30 pm ET.

Each focus group will bring together 5-10 young adults facing cancer for a moderated discussion over 2 hours. The discussion will happen over Zoom so you can be comfy and cozy at home for the whole thing. You will be compensated for your time and energy because your voice and perspective are so important in the delivery of cancer survivorship resources.

Sign up below to join the discussion today and offer your voice!

Have questions?  Email mallory@lacunaloft.org.

Join The Survivorship Series

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Welcome to the Survivorship Series!

Together, 25 young adults facing cancer (patients, survivors, or caregivers) will go through a 6-week, online program experience where you’ll hit the highlights of our workshops!  You’ll form a tight-knit community and every other week, you’ll take part in a different 2-hour program with the same group of young adults moving together through the series.

In week 1 you’ll join a Creative Art Workshop, in week 3 a Young Adult Cancer Hangout + Game Night, and in week 5 a Creative Writing/Journaling Workshop.  In between workshops, you’ll have access to a private Facebook group for your cohort of 25 young adults where you can connect and communicate.  You may only take part in the series once, and when you sign up you are committing to taking part in all 6 weeks.

The first round of the Survivorship Series has been scheduled and starts on Wednesday, Feb. 17th! 

Week 1:  Wednesday, February 17 @ 4 pm PT / 6 pm CT / 7 pm ET – Creative Art Workshop (a very cool, cactus paper mosaic)
Week 3:  Wednesday, March 3 @ 4 pm PT / 6 pm CT / 7 pm ET – YAC Hangout / Game Night
Week 5:  Wednesday, March 17 @ 4 pm PT / 6 pm CT / 7 pm ET – Journaling/Creative Writing Workshop

The Bridge – A Journaling Workshop for Grief, Loss, + Healing

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Jean Rowe, Certified Journal Therapist, is launching another program with Lacuna Loft!  You can connect with Jean here.

Lacuna Loft is pleased to offer The Bridge: When Before and After Meet – A Journal workshop for Grief, Loss, and Healing.  This will be a 6-week workshop using journal techniques to recognize, embrace, and cultivate acceptance around the themes of grief, loss, and healing.  Of particular focus is the “before” and “after” of a cancer diagnosis and the multilayered impact it brings.

Who: Young adult cancer patients, survivors, and caregivers.

Where: Online video chat. We’ll send you more information about joining after you register. Please have a microphone headset and a webcam.

When: Starting February 7th and going for 6 weeks on Sundays, 3-5 pm PT / 5-7 pm CT / 6-8 pm ET.  A commitment to attend every date is important to group continuity and in creating a safe space.  Please be on time 🙂

Create A Vision Board For 2021

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Kick off 2021 by creating your own Vision Board alongside other young adult cancer patients, survivors, and caregivers.  Join us in this online creative workshop to put your hopes, dreams, and goals together into a beautiful collage that you can use for inspiration and a positive focus throughout the year ahead.

This workshop will occur over 2 sessions.  During the first session, on January 26, 2021, you’ll learn about vision boards and begin to create your own vision board.  On February 2, 2021,  you’ll have the opportunity to share your vision for the year ahead with other young adult cancer patients, survivors, and caregivers. Please commit to both sessions!  Come together with other young adults facing cancer and #LetsMakeStuff!

Who: young adult cancer patients, survivors, and caregivers.

When: January 26th and February 2nd @ 4-6 pm PT / 6-8 pm CT / 7-9 pm ET via video chat.

How does it work? There will not be a supply box sent for this workshop and there will be no limit to how many can join.   Make sure you’re signed up on our Program List using the link below and turn on notifications for either (or both) creative art workshops and young adult cancer hangouts.  Those segments of the list will receive an email from Lacuna Loft a few days before the workshop with information on how to join the video chat.  ***You’ll need the link that we’ll provide you, a headset with a microphone, and a webcam.***

Click here to sign up to be notified when this program is announced by choosing it under ‘Programs you’re interested in.’ (Feel free to choose to be notified when other programs are announced too!)

Opening The Conversation: Join A Research Study!

Young adult survivors of breast and gynecologic cancer face a number of challenges, including interrupted life plans.  As many as two-thirds of these young survivors experience negative effects of cancer and cancer treatment on their reproductive health, including sexual function and ability to have children.  These are among the most distressing aspects of life after cancer for young survivors and their partners, and when left unaddressed, lead to poorer mental health and quality of life.  Effective communication and coping are important for couples struggling with reproductive distress after cancer.  Through their research, scientists at Oregon State University learned that many couples encounter significant challenges when faced with the reproductive and sexual health consequences of cancer.  Yet, surprisingly, evidence-based programs are not available to help young couples manage this aspect of life after cancer.

These researchers are looking to adapt an existing program so that it specifically fills this gap. To do this, they will incorporate advice from young survivors, survivors’ partners, clinicians, and researchers.  The new program will focus on fertility/family building and sexual health concerns after cancer, be tailored to meet the needs of young adult breast and gynecologic cancer survivors and their partners, include information about strategies shown to be effective to cope with reproductive health concerns after cancer, and be delivered by videoconference to reach couples living in rural and urban areas.  They will enroll 100 couples in this study to compare this newly adapted program to the original program, which focuses on managing the impact of cancer more generally. Fifty couples will be randomly assigned to receive the new program and 50 couples will receive the original program.

They evaluate whether the new program leads to greater improvements in reproductive and sexual distress than the original program. They also expect to see improvements in other aspects of relationships, sexual functioning, and well-being.  Additionally, they are interested in gaining knowledge about how the program works.  They will study possible mechanisms, including improved coping and communication between couples, using data from both survey questions and interviews.  Researchers expect this study to yield a feasible and effective program to reduce reproductive distress, which will lay the groundwork for making this program available to a wider audience in real-world settings.  In the long term, this is expected to improve equity of access to information and supportive care for young survivors and their partners.

Help create a program for young couples dealing with reproductive and sexual health concerns after cancer! Get $20 for sharing your opinions during an interview. Find out more at health.oregonstate.edu/oc

GABFEST IS NEXT WEEK

Did you know…that GABFEST IS NEXT WEEK!  We’ve teamed up with Elephants and Tea, taken the greatest pieces of an in-person survivorship conference, brought it online, and spread it out over the next week.

Throughout the week of December 7th, we invite you to share, explore, and learn as we interact together.  You are the expert in your own care, so along with experts in the fields, Gabfest will combine and elevate the individual voices of the young adult cancer community.

We have a great agenda lined up, fabulous opportunities for learning and connecting, a raffle each night (more on that at our opening welcome), and more!

Learn more and sign up here!

Stupid Cancer’s Pushing Past Cancer: Stronger Together

Interested in a one-day survivorship conference, offered online and *this* weekend?  Stupid Cancer, UC Davis Health, and UCLA Health have you covered!  They’ve partnered on a free, one-day virtual event for the AYA cancer community.  Join in on Saturday, December 5, 2020 for important information and plenty of opportunities to chat and connect with your peers.

After a long and difficult year, it’s more important than ever to gather our adolescent and young adult cancer community together.

Learn more and register here!

Hodgkin Hub: Empowering the Hodgkin Lymphoma Community from Diagnosis Through Treatment

In the patient community, personal stories from people who have faced a similar cancer diagnosis have the power to offer invaluable insights, support and connection to others who may be starting on this life-changing journey.

Over the last several years, Seagen heard from many people living with Hodgkin lymphoma who shared that they wanted to know more about what to expect after their diagnosis, including how to navigate making difficult treatment decisions and getting through their treatment. To meet that need, in 2018, Seagen created Hodgkin Hub – a dedicated online resource for people impacted by Hodgkin lymphoma seeking information and support before, during and following treatment.

Visitors to Hodgkin Hub can find information and resources about Hodgkin lymphoma, and also watch real patient videos, providing a chance to hear directly from others who have been diagnosed and learn how they navigated their own journeys.

Two highlighted video series includes:

“Day in the Life” Stories

The “Day in the Life” videos highlight individual perspectives from Hodgkin lymphoma survivors on their day-to-day experiences through diagnosis, treatment, and life after. Visitors can hear from:

Kyle: A member of the U.S. military, Kyle was diagnosed with Hodgkin lymphoma after returning from his deployment in Afghanistan. Watch here.
Piper: Diagnosed during her sophomore year of college, Piper learned the importance of self-advocacy and asking her doctor questions about her treatment to get the answers she needed. Watch here.
Liz: As a young adult, Liz was diagnosed just as she was starting college and leaned on her support system of her parents and brother to help her through her treatment experience. Watch here.

“What the HL?!” Survivor Stories

The What the HL?! videos feature Hodgkin lymphoma survivors who talk about the questions they asked (or wish they had asked) after diagnosis. Each provides their perspectives on navigating diagnosis, overcoming treatment challenges and finding support during life with Hodgkin lymphoma. Visitors can hear from:

Sarah: Diagnosed while still in high school, Sarah found it challenging to continue her education while going through treatment but kept a positive outlook. Watch here.
Bryan: Bryan was first diagnosed when he was in graduate school and working full time. His support system was there for him as he faced mental struggles and needed help as he prepared for treatment. Watch here.
Philomina: After being diagnosed with Hodgkin lymphoma, Philomina became an advocate for herself, researching her diagnosis and treatment options. She maintained a strong relationship with her oncologist by asking questions and requesting more information when she needed it. Watch here.

Visit HodgkinHub.com for more information and resources for the Hodgkin lymphoma community.

This post was presented by Seagen.