The Chronically Hopeful Award

Brigid over at Watching the Daisies  was kind enough to nominate me for the Chronically Hopeful Award. There is no way I can express what Brigid means to me, I will let her own words tell you who she is and have to leave it at that.

Brigid P. Gallagher is a retired natural medicines therapist, passionate organic gardener, and author of “Watching the Daisies- Life lessons on the Importance of Slow,” a holistic memoir dedicated to the art of mindfulness and healing from a debilitating illness.

The Chronically Hopeful Award has been created by Pamela, “to recognize the incredible people who blog about chronic illness, mental health, and disability.”

The rules:

  • Thank your nominator
  • Recognize Pamela from There Is Always Hope as the creator of this award and link her URL –
  • Use the Chronically Hopeful Award logo somewhere in your post
  • Copy these rules onto your post
  • Answer your nominator’s questions
  • Write 5-10 of your own questions (they don’t need to be illness-related)
  • Nominate 5-10 other chronic illness, mental illness, or disability bloggers
  • Comment on each of your nominees’ latest posts to tell them they have been nominated.

Brigid’s Questions for Me:

  1. What advice would you give to a new blogger?

Just write. Be real. Write about your day, your ideas, what you hope to achieve, what your dog did! Don’t worry about perfection. Don’t worry about followers. I know its tough to look at other peoples blogs and see the number of followers and the number of comments. But believe me, you will end up reblogging many of your old posts, probably yourself. Once you get the hang of the style of blogger you hope to become, you will go back an re-do your first few posts. (I PROMISE you… it’s true!) For now, write and visit other blogs! Comment and don’t expect anything back. Reach out to one or two bloggers for advice. A little mentorship never hurt anyone. Blogging should be a way of expressing yourself, some use it as a ‘platform,’ and that is not my kind of blogging. I like to feel a sense of accomplishment when I get done with a post. Period. End of story. 

2. How has blogging changed your life?

Oh my! I don’t know if I can count the ways. I adore blogging, and I live for the communication that I receive from it. The blogging community welcomed me, and I now have a sense of belonging to something much better than I could have ever dreamt of. I love my tribe!

3.  What is the biggest lesson you have learned about your own health condition, that you wish you had learned sooner?


The reality is that no matter what I learn and how much I move forward, there are still people in my life who do not care to move forward with me. My Fibromyalgia Syndrome is chronic, it is here to stay! I was caught off guard at how much this certainty has turned some against me. (No, I am not going to “beat” this one.) It doesn’t matter how much I fight back, there is never a winner. I have to say that is the biggest lesson, about living with a chronic illness, I have learned and definitely needed to.

4.  What hobbies do you enjoy?

Well, I like hobbies that are tangible. I like to write, so I wrote a book! The Shadow Boxers, Fighting Fibromyalgia, Your Personal Journal. This is an interactive journal and the first, ever, published on Amazon about Fibromyalgia Syndrome. I am so proud of that! I believe my book is a useful resource for anyone with fibro no matter where in life you are with your illness. My co-writer and I wanted to offer options, not opinions. It is definitely not a ‘how-to’ book.

5. What dreams do you still want to fulfill?

Well! (Remember that tangible thing I have going on with me.) I have always wanted to travel. I love it, but I thought once I got sick, that part of my life was over. The hubby and I have been working towards becoming mobile so we could start traveling fulltime in an RV. It is now happening! Our house goes on the market on August 1, and upon that sale, we are ready to purchase our rig and start off on a new adventure! Crazy cool. We can finally see the goalie, and it looks like it’s all net!


Thank you, Brigid! I am truly honored to accept this award.

Now my nominees, and my five questions for them:

Caz at Invisibly Me

Wendi at Simply Chronically Ill

Mer at MerBear’s World

Wendy at Picnic With Ants

Karen at MS graceful…NOT!

  1. At what age were you were diagnosed?
  2. What were your first thoughts after you received this diagnosis?
  3. Do you think chronically ill people are expected to behave a certain way when they are in public?
  4. What is the biggest misconception about your illness?
  5. Have you seen any significant strides in the treatment for your illness? 

I’m looking forward to your answers. You have been given this award from me. I hope you have time to accept and answer the questions. Either way, you are phenomenal bloggers! I count myself lucky to have come across your site, more importantly, your friendship. All of you truly deserved to be recognized!





35 thoughts on “The Chronically Hopeful Award

Add yours

  1. Congrats on your award. Love your responses. Full timer travel in a RV -exciting and fabulous. Another silly question, then how will you medicines etc get to you, clearly i am clueless?


    1. I thank you again, Brigid. Realizing some people will never accept you, since your illness or because of your illness is a lack of common human courteously. When they are close to you, unwilling to learn and accept this “new” you, it tears you up. Then I finally realized an illness to someone who doesn’t have it, doesn’t need to understand it. If they try, I’m willing to help them learn. If they want to push me, to ‘get better,’ saying they want the old me back? I need to acknowledge their unwillingness or inability to move forward with me. As much as it tore me up, their privileges of being present in my daily life were revoked. They are better off, I am too. I knew you’d understand, Brigid. Now if I could just figure out how to stop missing them.🥀🌹☀️

      Liked by 1 person

        1. Tempting. I will be carrying your contact information at all times. Would be so fun to meet you and emaa, your son and husband. And Doris! OH my. I love that name, Doris! Mine is named Dora, probably why! Teehee.


          1. I believe in “never say never” because things work out exactly as they are meant to and I think we are meant to meet! I would love you to be able to meet my family & of course Doris! She is such a dote, just like Dora I’m sure! XX

            Liked by 1 person

  2. Congratulations Kim – definitely well-deserved! You picked some wonderful nominees as well. I love it that we can all come together, share our experiences, and really, become a sort of family here in the blogosphere. I’m so happy for all you’ve accomplished so far and I’m looking forward to seeing your ‘reports’ 😊 on fulfilling your dream of traveling. Blessings to you sweet friend!

    Liked by 1 person

    1. We have come together. I have gained so much strength from all the ladies, and men, who I am so thrilled to call ‘our’ tribe! Many times you have all come together to assist me. I will never forget. I will get those reports out Terri, promis! Thanks my friend. xo

      Liked by 1 person

  3. Congrats on the well-deserved award! You should definitely be humungously proud of the book. Wow, really not long to go before the house hits the market now! Your tribe love to you, Kim  ♥
    And thank you very much for the kind nomination!
    Caz xx

    Liked by 1 person

  4. Kim,
    You totally deserve this award and good for you! Great advice to new bloggers and I’m with you about how amazing blogging is in life. Who would have thunk it? Also, I’m so pleased that even though the fibro is such an integral part of your life now, you continue to work on those things that matter to you. It may interfere, but you’ve not let it stop you. You are, indeed, an inspiration to us all!

    Liked by 1 person

  5. What a lovely award.
    I’ve been meaning to thank you for the longest time. I haven’t done one of these in a long while, but I love this one and you, so I’d love to pass it on. I promise I will soon. A little over my head right now, between appointments and reasons for appointments.
    I’m so ho bored you thought of me Kym! Love to you my friend.

    Liked by 1 person

    1. Awe. Love right back! You accept when you are able. There are no deadlines, no expectations. You are deserving of this award. You have helped me so much on my journey and have helped others as well. You are my definition of a tough warrior lady battling a chronic illness! xoxo

      Liked by 1 person

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