• Mid-Year Reflections In A Year Of Pandemic: June Linkup—A look at how quarantine has affected people with chronic illness, as well as thoughts on looking ahead with hope to the rest of the year. This month’s themes: Searching, Hoping, Honoring, Traumatizing, and Responding. | cassiecreley.com
    Blog,  Health

    Mid-Year Reflections In A Year Of Pandemic: June Linkup

    I can’t believe it’s been over a year since I joined A Chronic Voice’s linkup for the first time! I’ve been meaning to join this way for chronic illness bloggers to connect since, but life intervened (aka symptoms have severely limited my writing time). This month, I was thrilled that not only did I have the mental bandwidth to participate, but also that the prompts aligned with several things bouncing around in my head. Chronic illness in a pandemic presents its own unique challenges. (PS here’s my last linkup post.)

     I hope you all are doing as well as you can be. Those of you who love the sunshine, I hope that you are also enjoying the warmer days. I love that the weather will be warmer (in upper 60s or 70s) for about three days, and then rainy for two days—this gives me a good dose of vitamin D when I can sit and walk a little outside.

    The rain gives me a break from feeling like I *have* to get outside; we call that pressure to soak up as much warmth as we can “sun guilt” in the Pacific Northwest. The cottonwood trees had the air filled with tufts of white that looked like slow-drifting snow up until recently. Everything is blooming early, including my beauty bush, which is covered in bees and hummingbirds. (Ok, I’ve seen THREE hummers at once, so not exactly “covered!”)

    In the world beyond my yard, things are moving ahead as Washington counties move into Phase 2 of coming out of quarantine/social distancing. (My county was added to the list June 5.) High risk populations are to “Stay Home, Stay Healthy” through Phase 3. I’ll talk more about this below.

    Let’s dive in. The themes for this month are Searching, Hoping, Honoring, Traumatizing, and Responding.

  • Pinterest: Q&A with blogger Hailey Hudson: “Suffering and joy really can and do coexist. You can have pain and peace at the same time.” Chronic illness blogger interview on advocacy, not losing heart, and living with conditions including POTS, neuropathy, carpal tunnel, and restless leg syndrome. (Invisible Illness Visible Worth Interview Project) | cassiecreley.com
    Invisible Illness / Visible Worth Interviews

    Q&A with blogger Hailey Hudson: “Suffering and joy really can and do coexist.”

    I love that the Internet provides us with so many opportunities to connect with and be encouraged by fellow writers, and I’m excited to introduce you to Hailey Hudson, whose interests include blogging, freelancing, and fiction writing. She lives with health conditions including POTS (postural orthostatic tachycardia syndrome), carpal tunnel, and undiagnosed conditions causing chronic fatigue, seizures, and GI issues. (Raising awareness about POTS is of personal importance to me, as I also have a form of dysautonomia, an umbrella term for neurological conditions like POTS.)

    Hailey is a full-time freelance writer and content marketer who runs the blog The Hardworking Creative. You can also find her on her personal blog, Now All I Know is Grace. I love that she shares monthly wrap-ups highlighting what she’s reading, listening to, watching, grateful for, and more

    Earlier this year, Hailey spoke at the 2020 Diamonds Conference, which is an online conference for chronically ill Christians. (I didn’t get to go this year, but it’s something I learned about recently and hope to attend in the future. More info about it below!)

     I hope you’re encouraged by this conversation with Hailey on chronic illness, faith, and perseverance.

  • The Story Behind The Blog Name Starlight Through The Storm
    Blog,  Etc,  Write

    The Story Behind My New Blog Name: Starlight through the Storm

    Ta-da! You may have noticed that my blog has a new logo as well as a new name! I thought I’d share a behind-the-scenes look at the inspiration behind both. I hope this will give you more insight into what you’ll find on my blog, as well as help you know a little more about the person who runs it.

    I’ve literally been trying to pick a name before I even started blogging—over two years ago! (Yep, my blog had its anniversary in March and I kinda let it slip by. Oops!) I’m sure glad I didn’t wait until I had the “perfect” name picked before I started my blogging journey. (I think you should dive into blogging even if you don’t feel 100% ready.)

    From poems to PR pieces, the titles have always been a challenge for me. So I’ve been brainstorming (for, ahem, years)…how to choose a blog name that sums up living with chronic illness, and not just surviving but thriving? I wanted to choose a name that sounded specific enough but was also broad enough that it would allow me to talk about all the things that bring me joy when my health turns life upside down—such as my faith, my love of words (and books!) and creativity.

    Here’s the story behind coming up with a name for this blog, and why it’s special to me.

  • Q&A with blogger Jenna Ziegler “I thought I was letting go of my dream job. Turns out, this decision led me to this new career that brings me joy I didn’t know possible.” Interview on ulcerative colitis, autoimmune conditions, self care & adapting your writing dreams. (Invisible Illness Visible Worth Interview Project) | cassiecreley.com
    Invisible Illness / Visible Worth Interviews

    Q&A with Jenna Ziegler “I thought I was letting go of my dream job. Turns out, this decision led me to this new career that brings me joy I didn’t know possible.”

    A few years ago, I was planning to start a writers’ group, but due to my health changing unexpectedly, I was never able to get one up and running. So I was pleasantly surprised when blogging made that happen in a way I didn’t expect. Blogging allows me to connect with other writers, and I get especially excited when those writers love the creative side of writing, like fiction and poetry. That’s one of the reasons I’m thrilled to be able to introduce you to Jenna Ziegler, a chronic illness blogger and aspiring novelist.

    Jenna runs the blog The Comical Colon, where she shares her medical journey in a comical light to encourage others to share their unique health journeys. When I found her blog, I immediately sent a link to a friend who was recently diagnosed with colitis because I knew she could benefit from Jenna’s informative and upbeat writing.

    When chronic illness threatened her opportunities to have the schooling and career she desired, Jenna found that her health also brought new options for pursuing her love of writing. She’s been blogging since March 2018 and she’s also an aspiring author. Jenna shares about her writing journey (including participating in NaNoWriMo) plus numerous helpful chronic illness resources in this interview.

    I hope you’re encouraged by this conversation with Jenna on chronic illness, faith, and perseverance.

  • May 2019 Musings - Regrouping, Investigating, Boosting, Setting & Reviving. Here’s what has been going on with me lately with my health, pacing, expectations, writing, and creating. | cassiecreley.com
    Health

    May 2019 Musings – Regrouping, Investigating, Boosting, Setting & Reviving

    I’m excited to participate in A Chronic Voice’s link up for the first time! Link up parties are a fun way for bloggers to connect and write about similar themes, and this one is geared towards those of us in the chronic illness community. I’ve never had a chance to participate in one before, so I’ve been eager to give it a try. Let me know what you think of this style of post in the comments.

    The themes for this month are Regrouping, Investigating, Boosting, Setting and Reviving.

    It was a nice change to have guidelines “assigned” for writing a blog post. (I think Andy Warhol was onto something about having a “boss on retainer.” Having the framework for a post given to me felt a little more structured—like having a boss vs. winging it on my own.)

    So, using A Chronic Voice’s five writing prompts for this month as a jumping off point, here’s what has been going on with me lately.

  • My One-Year Blogiversary—Highlights From The Year. A look back at my most popular posts and other blogging milestones as well as thoughts on how blogging creates valuable community. | cassiecreley.com
    Blog,  Etc,  Write

    My One-Year Blogiversary—Highlights From The Year

    Wow, it’s already been one year since I could start calling myself a blogger! Today is my blogiversary.

    I think it’s important to celebrate blogging “firsts” and milestones. I had some trepidation starting this journey due to my chronic illnesses, and I wasn’t sure how much blogging I would be able to do.

    I’m not gonna lie—it’s been quite a challenge to keep up, but I’ve enjoyed it so much. I’ve especially loved the connections I’ve made blogging. It’s wonderful when someone lets me know—in a comment, or in person—that they struggle with the same health problem and didn’t realize anyone else understood, that they love that book too, or that they were encouraged by something I wrote.

    Blogging, for me, has been a beautiful reminder of how we can use our words to positively impact others, in spite of any challenges or limitations we may be facing.

    I’ll be sharing tips in an upcoming post about what I learned over the last year. If you have questions you’d like me to answer in the post, leave them in the comments! I’ll try to answer them all.

    My One-Year Blogiversary—Highlights From The Year. A look back at my most popular posts and other blogging milestones as well as thoughts on how blogging creates valuable community. | cassiecreley.com

  • Brain fog broke my internal editor - "Fibromyalgia has impacted my ability as a writer, and I’m just starting to understand all the ways it has. Brain fog has made it extremely hard for me to objectively edit my work. It’s like the editing part of my brain is broken." | cassiecreley.com
    Health

    Brain Fog Broke My Internal Editor

    Fibromyalgia has impacted my ability as a writer, and I’m just starting to understand all the ways it has. I’ve been trying to express it for awhile, with the irony being that it takes way more effort now for me to express anything. Brain fog has made it extremely hard for me to objectively edit my work. It’s like the editing part of my brain is broken.

    Blogging has been much harder than I thought it would be, for reasons I didn’t expect. I knew energy to write was going to be a challenge, in addition to fighting through brain fog to express myself. But I wasn’t expecting to have so much trouble evaluating the quality of my work.

    I was given a great piece of advice

  • Listen to the Winning Song from Our Contest! + Behind the Scenes Creating the Song. Learn about the inspiration behind the winning song, “This Love For Swing.” | cassiecreley.com
    Blog,  Etc

    Listen To The Winning Song From Our Contest! + Behind The Scenes Creating The Song

     

    A little while ago, fellow blogger Melissa Miles and I held a contest for a chance to win a custom song if you subscribed to both our blogs. I am so excited to announce that the song is done and you can listen to it here!

    I’ll also share the story that inspired the song and my thoughts on the collaborative process working with a musician as a lyricist for the first time. (Hint: It was awesome!)

    Without further ado, here’s the song, This Love For Swing. I wrote the lyrics, and Melissa wrote the music and recorded the instruments and vocals.