• Blog

    A Playlist of Calm Songs

    I have some ideas to share that will help you create a calm playlist when you need some quiet, relaxing music. 

    A few years ago, I started creating a calm playlist to listen to while I do my physical therapy stretches and when I’m trying to unwind at night.

    Because of my POTS (postural orthostatic tachycardia syndrome), a form of Dysautonomia, my autonomic nervous system doesn’t function correctly, One of the symptoms I deal with is rapid heartbeat, which can make it especially hard to relax. Music isn’t a cure by any means, but its one of the tools in my toolbox (including medicine) that I can turn to.

  • My Experience Fundraising for Medical Expenses—Here’s how organizations like Help Hope Live can help people in financial need due to chronic illness or catastrophic injury. Fundraise for medical bills including doctors’ co-pays, prescription costs, home modification, in-home care, physical therapy, travel expenses and more. | cassiecreley.com
    Blog,  Health

    My Experience Fundraising for Medical Expenses

    Today I want to share about an organization that can help chronic illness patients fundraise for medical expenses. Chronic illness is expensive, and I am so thankful to have recently found out about Help Hope Live, which can help with co-pays, prescriptions costs, insurance premiums, and more.

    In this post, I’ll share about my experience fundraising with this organization, so you can see if it would be a good fit to help you or a loved one living with chronic health conditions or a serious injury.

  • How to Find Financial Assistance for Chronic Illness Expenses—Connect with organizations that can provide help with copays, prescription costs, insurance premiums, and other medical bills. | cassiecreley.com
    Blog,  Health

    How to Find Financial Assistance for Chronic Illness Expenses

    Did you know that patients with chronic illness can apply for grants to help with medical expenses? Me neither! I’m going to share about several organizations that provide medical grants and financial assistance.

    I can’t believe I’ve been seriously ill for over six years and am just now hearing something like this exists! I thought medical grants were something only doctors or researchers could apply for.

    These programs may be able to help with costs like copays, insurance premiums, prescription costs, and more.

  • Q&A with Katerina of Beauty in the Pain “Even if you feel alone, God will always be by your side.” Interview on chronic illness, life with CMT (neuromuscular disease), the gift of compassion, and seeing God’s faithfulness. (Invisible Illness Visible Worth Interview Project) | cassiecreley.com
    Invisible Illness / Visible Worth Interviews

    Q&A with Katerina: “Even if you feel alone, God will always be by your side.”

    Today I get to introduce you to Katerina, who is a dancer and teacher, as well as a college student working towards a bachelors degree in psychology.

    Last year she started a blog called Beauty in the Pain to share her journey with the neuromuscular disease CMT and encourage those who struggle with chronic pain.

    I’m so glad she reached out for an interview because I’ve been so blessed to read how she is adapting her passion for dance and seeing God’s faithfulness in the midst of chronic illness.

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

  • Q&A with Lauren Watt: “I've had to learn to find contentment in my difficult circumstances, and I've realized that true contentment only comes from knowing God and delighting in Him.” On contentment in chronic illness: POTS, MCAS, adrenal insufficiency and Babesia and Bartonella infections. (Invisible Illness Visible Worth Interview Project) | cassiecreley.com
    Invisible Illness / Visible Worth Interviews

    Q&A with Lauren Watt: “I’ve had to learn to find contentment in my difficult circumstances.”

    I’m thrilled I get to introduce you to Lauren Watt, an artist and blogger who is going to share some of her story and how she finds contentment in chronic illness.

    Lauren is the youngest interviewee I’ve featured on the blog so far, and she writes with wisdom and clarity about her chronic illness journey, which began when she was just 14.

    I’ve really enjoyed reading her blog after we connected online, and I hope you’ll check out her artwork and blog on her website, Lauren’s Easel.

  • Throw A Cyberpunk Virtual Escape Room—Fun and easy ideas for hosting an escape room online or in person. Tips for sci-fi inspired costumes, party planning tips, and other ways to bring your cyberpunk party to life. | cassiecreley.com
    Blog,  Create

    Throw A Cyberpunk Virtual Escape Room + Giveaway!

    Want to throw a cyberpunk virtual escape room? This is my second escape room party I’ve hosted, and I’m excited to share tips that will help you bring this theme to life! It’s surprisingly easy, and adding some fun details will really make your party memorable, whether it’s in person or over Zoom!

    Plus, I’m so excited to be offering a giveaway! One winner will get a free escape room from Lock, Paper, Scissors! Keep reading for details.

  • Q&A with Leah: “It’s okay to feel different and talk about it.” Interview on life with On Hyperthyroidism, Early Onset Osteoporosis and Primary Ovarian Insufficiency. (Invisible Illness Visible Worth Interview Project) | cassiecreley.com
    Invisible Illness / Visible Worth Interviews

    Q&A with Leah: “It’s okay to feel different and talk about it.”

    I’m excited to introduce you all to my friend Leah in this invisible illness Q&A. We’ve been friends as well as pen pals for over half my life.

    Leah and I quickly bonded over our love for animals and books as kids, and we’ve encouraged each other in our faith, especially when we’ve both faced health challenges. Leah is one of the most kind-hearted people you will ever meet, and my hope is that you will take encouragement from her story.

    I love getting to do this interview project—it’s wonderful to connect with other bloggers and it’s also such a privilege to provide a platform for people like Leah who do not have a blog. I’m passionate about helping people with chronic illness share their insights and hard-earned wisdom, both so they feel heard and also so they can make a difference by sharing what they know. You can find out more about being interviewed here.