Design Contest!

design contest

Today, Lacuna Loft has officially been a nonprofit organization for 1 year!  In the spirit of our one year nonprofit anniversary, we are looking for an awesome design from you!  We have learned over our two years in existence and our year as a nonprofit that you all, our wonderful readers, are creative, powerful, and courageous!  You have shared your stories with us, your energy, your wisdom, and we hope that we have so far served you well with our diverse and ever growing program base.  You are the most important part of Lacuna Loft.  You and your needs feed into our programs and our mission on a daily basis.  We want our next design to reflect you too!

Have some young adult cancer creative juices that you’d like to share with us?  Want your design to be featured by the next release of Lacuna Loft gear?

Submit your design by May 7 to info@lacunaloft.org and we’ll pick our favorite for our upcoming gear!  Just think of how cool your design would look on Lacuna Loft t-shirts, posters, hats, you name it!  I can’t wait to see what you all come up with!  We’ll share all of the designs (with links and credit given to each of the wonderful artists) on our website once the competition is over and we’ve chosen our winner.

Ready?  GO!

 

Some fine print:

By submitting artwork/design/logo (“the Work”) to Lacuna Loft (“the Organization”), you (“the Artist”) grant the Organization an exclusive, perpetual, royalty-free license to reproduce and distribute the Work including a license to all rights to the Work, which include, without limitation, the right to modify or create derivative works base on the Work.  The Artist agrees that all Work he or she submits to the Organization will be entirely his or her own and will not include any plagiarism or any work of third parties.  Notwithstanding the foregoing, nothing contained in this Agreement shall be construed to create a master/servant, employer/employee, or principal/agent relationship between the Organization and the Artist.

Have An Inviting Weekend

No April Fool’s jokes happening around here!  It has been a very busy and fabulous week here at Lacuna Loft!  Our writing group launched on Wednesday and we are super excited to unmask a new look for Lacuna Loft today!  What do you think about the new homepage?

And, have you filled out our easy-peasy ‘Happy Birthday Lacuna Loft’ survey ?  Your feedback is so very appreciated!  🙂  It will only take a few minutes of your time!

Here are some inviting weekend links from around the interwebs…

[list type=”like”]
[list_item]the right way and the wrong way to microwave food[/list_item]
[list_item]what kind of a vacationer are you?[/list_item]
[list_item]21 ways to leave a never ending conversation without being rude[/list_item]
[list_item]#ruleyourself[/list_item]
[list_item]morning pages[/list_item]
[list_item]35 random corners of the internet[/list_item]
[list_item]lifestyle support to the max[/list_item]
[/list]

Have an inviting weekend Lacuna Lofties!

P.S.  Lacuna Loft is pleased to partner with Cancer and Careers on the National Conference on Work & Cancer!  Check out the link for more details on this great event for cancer survivors.  Applications for travel scholarships are open now! The deadline to apply is April 15th. More information can be found here.   #CACconf

Book Club: Everything Changes, Chapter 7

cancer and mortality

Welcome to the comments and discussion of Chapter 7: Mortality Bites of the book, Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Catch up on Chapter 1: RamenonmicsChapter 2: When G-d Things Happen to Sick People, Chapter 3: Single, Chapter 4: Human Spectacles, Chapter 5: Malignant and Indignant, and Chapter 6: Something in the Air.

Let’s get started!  Chapter 7!

Mallory:

This chapter was hard for me.  The phrase mortality bites hits the nail right on the head.  Living is hard.  Living with a cancer diagnosis, manifesting itself into chronic symptoms that may or may not be taken seriously by a healthcare team bites.  Outliving a loved one bites.

“My brother’s death was an awakening for me.  For me, cancer was the C word at that point. I had to dispel a lot of fear around the C word.  I finally realized that cancer can be a vehicle for transformation, even if it means death.”

“Mourning someone I had met only once for four hours felt like an act of trespassing, as if I were sneaking into the backyard of those who were grieving the loss of Amilca as a wife, mother, a daughter, a sister, a friend.”

Man oh man…I underlined more in this chapter than in all of the other chapters combined.  Over the weekend, while at CancerCon, I had the privilege of volunteering for the Chronic, Metastatic, and Advanced Cancer session.  I walked into the session, introduced myself to the two women running the hour and a half discussion, and figured out what my role would be in time keeping and tissue monitoring.  I made it very clear that I was not a metastatic patient, respected the safe-space needed by those who were, and insisted that I therefore not actually participate in any of the sharing/participatory pieces of the session.  I knew when I walked into the room that my role would be one of quiet support and love.

It was one of the hardest hour and 30 minutes of my life.

These brave and courageous souls shared of their fears of being forgotten, their acknowledgements that death could be close or far away, and the silent truths held by those who face death and mortality every.single.day.

I had trouble holding in my emotions during various points in the session.  I looked up at the ceiling a few times, willing the tears to stay in my eyeballs.  I wiggled my toes and started messaging the other members of the steering committee with about 20 minutes to go, hoping someone could grant me access to the locked room we stored our CancerCon-magic-making supplies.  I needed a place to let it out and I knew that I could not do that while in the session or out and about the rest of the conference.

Usually, when I am scared of something difficult and cancer related, like death, my healthy peers wait it out as I speak (or blather) while keeping their distance physically and emotionally.  When I finally was able to burst through the door into the steering committee office, tears flooded from my body and I spent the next 20 minutes repeating myself and shoving starbursts into my mouth.  My fellow steering committee member hugged me with tears filling her own eyes.  Slowly, other steering committee members started coming in.  Each one would hear what I needed to say and start to cry themselves, hugging me all the while.  They stepped up, came forward, and stood with me emotionally and physically as I melted into fear and anxiety.

In that moment, I knew that I needed to be a part of CancerCon and the steering committee for the 2017 conference.  Understanding the frightening reality running rampant in the Chronic, Metastatic, and Advanced Cancer session is not for the faint at heart.  And most of my healthy peers refuse to approach the issue with any authenticity.  I get it! I really do!  It is scary thinking about an illness manifesting itself into something that cannot yet be cured.  I live with that fear though, and my fellow young adult cancer survivors do too.

Thank you to all of the young adult cancer survivors who have shared their stories with me; who have given me pieces of their courage, their warmth, and their love.  I am forever grateful for the tears, fears, laughter, joy, and love that we have given.  Here is to sharing so much more quality of life together, even in cases where quantity of life is lacking.

And to all of those metastatic warriors out there…you are my heroes.

Thanks for joining us for our Chapter 7: Mortality Bites of Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Join in next Monday for Chapter 8: The Myth of Eternal Optimism.

If you’re just joining us, here are some logistics:

We will talk about a chapter each Monday until the book is done.  Then, we’ll use one more Monday to talk about general feelings from the book and anything else you’d like to discuss.  Join in, in the comments every week!  Also, there will probably be spoilers.  Read along with us!

How are you enjoying our young adult cancer book club?

Have A Fetching Weekend

Have you filled out our easy-peasy ‘Happy Birthday Lacuna Loft’ survey ?  Your feedback is so very appreciated!  🙂

Here are some fetching weekend links from around the interwebs…

[list type=”like”]
[list_item]50 snarky jokes[/list_item]
[list_item]that weird white string inside a raw egg[/list_item]
[list_item]the most popular porn searches by state[/list_item]
[list_item]15 things that are way bigger than you thought[/list_item]
[list_item]22 emojis and their real meanings[/list_item]
[list_item]FightPretty.org…a great nonprofit that helps women feel strong and beautiful during and after cancer treatment[/list_item]
[list_item]Treatmintbox.com…a very cool company that offers subscription gift packages for survivors, caregivers, and kids[/list_item]
[/list]

Have a fetching weekend Lacuna Lofties!

P.S.  Lacuna Loft is pleased to partner with Cancer and Careers on the National Conference on Work & Cancer!  Check out the link for more details on this great event for cancer survivors.  Applications for travel scholarships are open now! The deadline to apply is April 15th. More information can be found here.   #CACconf

You Are Not Alone

young adult cancer support

Going through something tough? Feel alone? Well, you don’t have to be. In the Internet Age, if you have a computer and Internet access, you can connect with another human being twenty-four hours a day, seven days a week, 365 days a year.  Anytime you want, you can have access to tech-support for the soul, and chances are, there is someone going through the exact same thing you are right now. And if multiple people are going through the same thing as you, then there is a strong chance there exists a free, online support group for people trying to overcome your same set of challenges. If there’s not, then you can build one, and they will come.

But being open about your problems and personal weaknesses is much easier said than done. I didn’t even tell my own family about my cancer diagnosis until two months after my diagnosis. And I didn’t tell most of my friends about it until four months after my diagnosis. When I first found out about the cancer, I just thought I could power through it on my own. I didn’t want to tell my mom because she still had an exposed nerve about losing my dad to cancer, and I didn’t want her to have to worry about losing me the same way. And generally, I was just embarrassed about being sick and needing help.

Because of my own pride, I didn’t even join a support group until six months after my diagnosis because the ones I had found were through Facebook and I was afraid if I joined, everyone would know.

Finally, I reached my low point emotionally. The chemo was not really doing anything to shrink the cancer. I felt terrible all the time, and I needed the support of people who were going through what I was going through and who had been through what I had been through.

I was in a unique position because we were living as expats in England at the time, so I didn’t really have much of a community around me for support. I had a handful of solid friends spread across the UK, I had my amazing husband and adorable daughter, but at the time, for the most part I just felt like misery, party of one.

So I mustered my courage and joined two online support groups: Younger Breast Cancer Network and Berkshire Breast Cancer Support Group. Both of these groups were great for different reasons.

The Younger Breast Cancer Network was great because it was a large and active online community. You could post a question or comment and have twenty responses in five minutes. For the most part, everyone was very positive and encouraging, and it felt good to be part of a group of women who were so fun, young and alive, while going through the same things as me. I spent a lot of time interacting with this community while I finished my treatment.

The Berkshire Breast Cancer Support Group was smaller and less active online, but it was this group that showed me how powerful online support groups can truly be.

Because my husband and I did not have a lot of friends in our community, our daughter also did not have a lot of friends in the community. She went to a posh preschool three days a week, where she had some friends that she could play with, but we were generally snubbed by the parents there because my husband drove a white van and a falling-apart Fiat and wore dirty overalls to drop our daughter off with all the dads in suits.

Our only social interaction with the parents was at birthday parties to which her whole class was invited, and then people mainly just stuck to talking to the people they knew, and the hosts would hardly say ‘hi’ and ‘goodbye’.

10606498_10152571644341609_2978149737915864427_n

The Birthday Girl

When it came time for my daughter’s birthday, I wanted to throw her a nice party because in the back of my mind I wanted to make the celebration memorable because I didn’t know how many more birthdays I’d live to see. I rented the local sports hall and one of those inflatable play structures and I let her pick the theme of “Under the Sea”.

Then I sent out invitations to her class, and immediately I got a lot of ‘no’ responses. I was gutted. One of the moms informed me another child from the class was having a party on the same day to which my daughter had not been invited. She was one of four other kids from a class of twenty-six who had not been invited to the little boy’s party. I cried a lot about it. It was one thing for adults to choose not to spend time with other adults, but to do that to children? It seemed pretty heartless. Especially when we went to another child’s birthday party, and the little boy whose party she had not been invited to was wanting to play with our daughter the whole time.

After a couple of hours of wallowing in self-pity, I decided to invite my support groups to the party. It seemed like a waste to cancel it, and it seemed like a sad reminder of how friendless we were to have a party in a big sports hall with just five children. Because the YBCN was made up of members from all over the UK, none of them actually lived close enough to attend the party. However, the Berkshire group was made up of ladies who lived locally, and they really saved the day. Especially Lucy Price and Rosalind Ansell, who brought children and other mothers to the party.

It was so touching, I cried again. I will always be grateful for that kindness.

If I hadn’t joined those groups, it would have been a lot more emotionally difficult to get through my treatment, but in the end, I left both groups. Partly because we moved back to the States and they were UK-specific groups, and partly because it was hard to continue to think about cancer when all I wanted to do was not have cancer anymore. Especially in the YBCN, around the time I finished treatment, several of the women who had been diagnosed around the same time as me died. That’s the nightmare, the one you never wake up from, and even though I wanted to stay in to be strong for people who were just starting their journey…I just couldn’t.

There are some of my fellow survivors from those sites who I stay connected with through Facebook and Twitter, and it does my heart good to see them living, really living, and moving forward from this awful disease.

And while I am no longer active in support groups, cancer remains an inexorable part of my life. Now I have Lacuna Loft as a platform through which to connect with other survivors, and I am in a better place physically and emotionally, and full of new-found wisdom like the fact you should never be afraid to share your fears or weaknesses with someone else, and you should always ask for help when you need it.

As long as you have Internet access and a computer, you never have to be alone.

You never have to be alone.

You can find Mahalia on twitter @30ishTweets

The Spring Session Of The Unspoken Ink Writing Group Is Full!

young adult cancer writing group

Wow!  I am so excited about the fabulous response this new program received!  The spring session of the Unspoken Ink: Young Adult Cancer + Chronic Illness Writing Group is full!  We have a group of 9 survivors in the spring session and I cannot wait to get started!  If you weren’t able to join the writing group this time around, have no fear!  We’ll run another session later this year with a slightly larger group.  In the mean time, check out the other great stuff happening here at Lacuna Loft!

In the next few months, we’ll be bringing more programs, workshops, and groups onto the site.  Want to make sure you’re keeping up to date with all the great happenings over here?  Sign up for our newsletter!

Have an idea for a workshop that you’d like to experience here at Lacuna Loft?  Email us at info@lacunaloft.org!

Interested in helping support the great programming that happens here at Lacuna Loft?  Make your tax-deductible donation today!

Book Club: Everything Changes, Chapter 6

young adult cancer book club

Welcome to the comments and discussion of Chapter 6: Something in the Air of the book, Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Catch up on Chapter 1: RamenonmicsChapter 2: When G-d Things Happen to Sick People, Chapter 3: Single, Chapter 4: Human Spectacles, and Chapter 5: Malignant and Indignant.

Let’s get started!  Chapter 6!

Mallory:

I wasn’t sure what to expect from the title of this chapter, “Something in the Air.”  Was it going to be about sex, air toxins, what?  While not what I expected, this chapter has been one of my favorites so far.  The first line, “…I uncovered a gigantic cancer taboo: admitting the fact that having cancer does not necessarily make someone a nice or interesting person.”  It made me laugh out loud.  Exactly as the author pointed out, this is a very taboo statement and yet so very very true.  I have met many cancer survivors in my role with Lacuna Loft, and you know what?  I don’t like all of them!  Some of them are mean, some are boring, some are self-obsessed…just like the variety you find in healthy, normal people!  This of course works in both ways.  Many of the cancer survivors that I have met have quickly become very close friends…the kind that you can text very late at night, the kind that you know you can count on.

The author also delves into dating a bit more in this chapter, unveiling personal moments of finding the right time to divulge about a history of cancer and the relief of having a loving side kick through it all.  She also gets into the contentious topic of “the good and the evil in cancer,” finding her own truths and quietly beseeching the reader to do the same.  She talks about a little bit of death and a little bit of environmental toxicity.  Such good things in this chapter.  Her resources include items about cancer and the environment and building support systems.

I’ll leave you with my favorite quote from chapter 6, “I’ve spent much of my life reading, studying, theorizing, and cancer made me want to go out and feel, touch, taste new things.  I’m more adventurous with food, more into getting hugs, I go to the petting zoo more often, but it’s not like I’m doing ecstasy or having sex in bathrooms.”

Thanks for joining us for our Chapter 6: Something in the Air of Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Join in next Monday for Chapter 7: Mortality Bites.

If you’re just joining us, here are some logistics:

We will talk about a chapter each Monday until the book is done.  Then, we’ll use one more Monday to talk about general feelings from the book and anything else you’d like to discuss.  Join in, in the comments every week!  Also, there will probably be spoilers.  Read along with us!

How are you enjoying our young adult cancer book club?

P.S.  Apologies for having some of these posts come a little late or out of order!

Have An Enticing Weekend

It’s Mid-March already?!  Have you heard yet that Lacuna Loft has some great new programs?  Or that we have an easy-peasy ‘Happy Birthday Lacuna Loft’ survey you can help us with?  🙂

Here are some enticing weekend links from around the interwebs…

[list type=”like”]
[list_item]on 40 hour work weeks[/list_item]
[list_item]one of Neptune’s moons orbits backwards![/list_item]
[list_item]easy lemon pound cake[/list_item]
[list_item]the best cupcakes around[/list_item]
[list_item]10 reasons he probably hates you on linkedin[/list_item]
[list_item]stereotypes…great video![/list_item]
[list_item]how American parenting is killing the American marriage[/list_item]
[/list]

Have an enticing weekend Lacuna Lofties!

P.S.  Lacuna Loft is pleased to partner with Cancer and Careers on the National Conference on Work & Cancer!  Check out the link for more details on this great event for cancer survivors.  Applications for travel scholarships are open now! The deadline to apply is April 15th. More information can be found here.   #CACconf

An Interactive Self-Care Guide

Ever struggled with self-care or even deciding what you needed in a given moment?  Well now there is a website, just for that.  This interactive self-care guide asks you a series of questions, even offering you time to work through suggestions based on your responses, helping you to take steps towards greater self-awareness and self-care.

self care guideThe prompts invite you to take steps to assess your own state of being and to make any necessary adjustments to improve it.

Try the self-care guide out!  Let us know what you think!

 

Book Club: Everything Changes, Chapter 5

Welcome to the comments and discussion of Chapter 5: Malignant and Indignant of the book, Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Catch up on Chapter 1: RamenonmicsChapter 2: When G-d Things Happen to Sick People, Chapter 3: Single, and Chapter 4: Human Spectacles.

Let’s get started!  Chapter 5!

Carly:

I really appreciate those who are open and honest about what cancer really looks like. With my experiences, it is rarely a thumbs up and smile for a photo. It’s raw, painful, terrible, hard, and expensive. I have to admit…while I’m involved in Relay for Life and work with the American Cancer Society, their images (usually with the word SURVIVOR in bold) are a pretty upbeat representation of a cancer patient. When I think of cancer, I think of images like these.

To be completely honest, this chapter was a difficult read for me. I found myself feeling angry with Geoff for his lack of care and respect for his own body when first diagnosed and through most of his first year.

“So what do I do now? I felt like I had post-traumatic stress disorder or something.”

I hear this a lot. I’ve even been told that post-cancer world is even more difficult than fighting it. Having a set schedule (chemo, tests, doctor, chemo, tests…) was comforting (in a weird way) because you knew what to expect, what’s next. A clean bill of health is everything you want and spend time fighting for. But as soon as you get it, you don’t just go back to “normal”. How could you? How do you adjust? This is a topic that we need more research on and we should talk about more openly. I believe that insurance should cover therapy during your fight and after your clean bill of health, if you are that lucky.

Thanks for joining us for our Chapter 5: Malignant and Indignant of Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s!  Join in next Monday for Chapter 6: Something in the Air.

If you’re just joining us, here are some logistics:

We will talk about a chapter each Monday until the book is done.  Then, we’ll use one more Monday to talk about general feelings from the book and anything else you’d like to discuss.  We’ll also have a great “meet the author” post coming up!  Join in, in the comments every week!  Also, there will probably be spoilers.  Read along with us!

How are you enjoying our young adult cancer book club?