Say Hello/Contact


I am always interested in finding out who views my blog, follows my blog, what interests you in following my blog and what interests you in general!

Most of what I started writing about when I started this blog was about having a chronic illness but I am finding that writing has done something to me… it has some how heightened my senses. I listen more. I see more. I want to learn more.

And the best place to learn, I am finding is by hearing from other people about their interests and their journey through life.

So feel free to say hello and let me know a little about yourself if you’d like – like why you chose to view my blog, why you chose to follow my blog if you did that, where you’re from, what makes you happy and how you find joy.

Your thoughts are important to me so don’t be shy. Feel free to leave me a comment any time. Or you can reach me at my email address:

Many thanks for taking the time to stop by!



32 thoughts on “Say Hello/Contact”

  1. Hello! Thanks for visiting my blog; I thought I’d come by and visit yours as well 🙂 Your dogs are adorable, and I can already tell that I am going to be “Like”-ing some posts as I look around your page. Hope you’re having a good day! -Nic

    Liked by 1 person

    • Thanks. I like your blog too!


    • Thank you – You have such a gift with words and transforming the very real emotional/physical challenges that many of us face with this illness. I realized upon being off on medical leave and not having a lot of activities/work to occupy my mind re: fatigue/other symptoms – that I actually became more mindful of my situation and had to truly face my own mortality for the first time. Scary but actually hopeful for me because I realized I was not attending to me in the way I needed to – now that I am off the roller coaster I am rethinking my present and future – I was going to retire in 5 years, now I am trying to see if I can retire now or in the near future and focus more on my self-care. I am glad I found your blog!
      Susan (SKG1)

      Liked by 1 person

      • Hi Susan – Thank you for stopping by the blog. I am glad you are rethinking your choices and realizing that YOU are important. It’s such a difficult thing to start putting yourself first. It felt selfish to me at first but now I know I am actually better able to be present for my family and friends in my own life. Looking forward to getting to know you better here!


  2. I really love reading your posts so I nominated your blog for the One Lovely Blog Award. You can read it here, including how to participate if you want to pass it on.


  3. Hello Sarcoidosissoldier! You have been chosen as “The Winner” of my “Cutest Pet Contest.” Please message me with anything you would like the viewers to know about your pets and I will use that Bio as well as photos of your pets on my blog post for the day. I will also mention the name and link of your blog. I’d like to do this by tomorrow evening, Monday, November 24, 2014 so please send along the information ASAP. Thank you and Congratulations Lisa!


  4. I know I nominated you for the lovely blog award but I put you in my Liebster award post as well!

    This is an award for new bloggers with less than 200 followers.
    This a great way to do some networking. The Liebster award nominees are chosen by fellow bloggers. Each blogger that accepts chooses 11 other blogs to nominate, and so on, so it helps those of us with few followers get out there and be seen.

    If you choose to accept the nomination, there are a few things for you to complete and post on your site. Take a look at the requirements, you can see them at the link to my Liebster award post, then see what you think.

    After you select your nominees, feel free to cut and paste parts of this message in order to make your own version. That is what I did.

    You are not obligated to participate, but it would be very beneficial for you to do so.

    The details and questions are in my post at

    I was nominated by cjohera. You can find her post with her questions and answers at


  5. Dear Smaller Human Being…

    Today’s blog is beautiful.
    It’s reflective.
    It’s introspective.
    It’s healthy.
    It’s soothing, isn’t it?

    Now, I’m hungry.
    What do you have to eat?


    Liked by 1 person

  6. Hi Sarcoidosis Soldier,
    I am Seab, I have talked with you before on the Inspire Website.
    I have Pulmonary Sarcoidosis (Stage3), Fibromyalgia and some other stuff I won’t bore you with.
    I live in Surprise Arizona, and have lived in Arizona my whole life. I just love Surprise!

    I have a really hard time with the social isolation I have with this disease. I used to be really outgoing and had lots of friends. Now, I cannot make any plans as I don’t have the energy to go out many days. The friends have moved on.
    The new normal, right…

    I do look at life so differently now that I have this disease. I appreciate the little things in my life more, my family, taking a walk outside.. Arizona is just beautiful right now. (it is not hot yet!)

    I really enjoy your blog and your dogs are just adorable! Please give them a pet from me.
    Thanks for listening!
    Terri (a.k.a.Seab).

    Liked by 1 person

    • Hi Terri,

      Nice yo meet you outside of Inspire! I totally get going from being outgoing to feeling isolated…same for me. Not working anymore has been really hard for me as well and I am always trying to hopelessly figure out how to get back to where I was…a useless exercise.

      I’m glad you like the blog. It really helps me. It keeps my brain functioning, It gives me an outlet for all my thoughts and hopefully my experience and thoughts are of use to others sometimes…..who know! LOL!

      I’m here to listen any time…you also now have my email so we an keep in touch that way too if you want.

      Take care!

      (AKA – Sarcoidosissoldier/ZoeyandAbbysMom)


  7. Hello my friend. The blog is lovely. I love it. I also love the pictures. The one of you and Abby on the beach is my favorite. We had a great thing going at that wonderful hospice. Taking care of patients, quality, each other. Miss you but am really at peace to know you are. Take care, Susan

    Liked by 2 people

  8. Hello Sarcoidosis Soldier,
    Hope this finds you having a good day. I ran across your lovely blog and appreciate your thoughts and feelings. my husband has pulmonary sarcoid and perhaps Nero sarc (not yet verified). He was diagnosed 2 years ago and you both have the same symptoms and very much the same feelings.
    Thank you for sharing your story and thoughts on living with a chronic illness.
    Peace to you on this journey,

    Liked by 1 person

    • Hi Chris, Thank you for taking the time to read my blog. I am so sorry about your husband’s situation. I know it is very hard for both of you as it is a difficult journey. Wishing you both only the very best.


  9. Lisa,
    I just wanted to say hi and congratulate you on your blog. I appreciate your reflectiveness and honesty. I am a fellow blogger/writer/storyteller and sarcoid patient. If you are ever interested in working on a collaborate piece let me know.
    Be well,

    Liked by 1 person

    • Hi Jay – Thank you so much for stopping by and sharing your blog with me. I just read it and “liked” it on FB. It might be fun to collaborate some time. I’ve never done that before and might be really fun to do with someone else who shares the same journey! Take care and be as well as you can be! – Lisa


  10. Samantha Liston said:

    Good morning!
    I came across your blog and am looking forward to following you and reading your writings. I myself was diagnosed with Neurosarcoidosis in 2004 after becoming ‘ill’ and lucky me, I seem to have the version of sarc, that is active, more than not. So, I wanted to say ‘Hello!’ and introduce myself.
    Have a GREAT day!
    Samantha Liston

    Liked by 1 person

    • Hi Samantha…so sorry to hear about your diagnosis…this is a difficult disease to be sure! Thanks for stopping by and reading my blog and thanks for introducing yourself and saying hello!


  11. Hi, I’m a one month-ish into my official diagnosis. But 6 months into being unwell. I’m so pleased to find this blog. In a very short space of time I have had an attitude to life change- don’t worry about the little things just get on a live life!


    • Hi – Thanks for contacting me! I’m glad you are enjoying the blog. The beginning of the sarcoid journey is tough…a lot of ups and downs but it sounds like you’ve got one of the hardest parts figured out already…enjoy life…it’s short for all of us! Hope you continue reading!


  12. I’ve just recently found your blog, and it is so helpful. Thank you so much. I’ve just been diagnosed with sarc, and am trying to learn all I can.

    Liked by 1 person

    • Hi Equestrian57 – I’m glad you found my blog and that it has been helpful. Being newly diagnosed is the hardest part of having this disease, I think. There are still so many unknowns and a lot to learn. Please feel free to use my contact email any time, if you have questions or need support! There are also a lot of good FB support groups for sarcoidosis, if you’re not part of them I highly suggest you look them up and join any that look like they might be of benefit to you. Connecting with others who share this disease is a HUGE part of learning to manage living with it. HUGS to you!


  13. linda minnix said:

    Zoey, I NEED you! It’s Imursnhin. Have been sicker than I ever thought possible and cant find my inspire peeps.


    • Hey there – So glad you found me…I’m so sorry that you are not feeling well. A lot of our Inspire peeps are in a FB support group called Sarcoidosis and Neurosarcoidosis SARC WARRIORS. You might want to join it if you are on FB.


  14. Hi there [wavey] from the UK. My names Dave.

    I live in Yorkshire. The shire of York! [Old York, jorvik, not New York!] Just in case that was not clear, which it was. Eh?!
    Babble babble tripe and wabble.

    Here I am sitting in my dressing gown, at 44 years old, in my parents house, after losing my house, business, life etc etc.

    You know how it is. Good days, bad days, but never normal days. I’ve forgotten what it feels like to feel normal again. Have you?

    Just thought I’d pop my head in and say howdy doody.

    7 years, 6 years pf pred and methotrexate, cant work, cant do anything……Limbo, thats the word isnt it?

    Im stage 3, depression kicked in a few years after diagnosis, lorazepam, citralopram….

    Dont you get sick of, ‘well you look ok’ [?]

    Big sigh, goodbye…..Dave


    • Hi Dave – Thanks for dropping by my blog and for taking the time to send a comment. I’m very sorry that you are having such a rough go of this stupid disease! Hang in there…one day at a time! Trying to find a little joy in each day is how I survive this disease. I used to get sick of the “you don’t look sick” comments but now I know that people are just ignorant about what they don’t understand and I try to educate them. Not a lot about this disease, or any other, I suppose, is easy!


  15. Hi, Sarcoidosis Soldier! My husband and I were just talking about you and wondering if you’re ok. We haven’t read anything from you in awhile. We certainly understand how hard it is to keep on producing, but we wanted to check in on you. You mean a lot to us both! ❤


    • Hi Mudfoot…Thank you for checking in on me. Yes, I am doing okay. I stopped writing as much because I felt I was becoming too repetitive and now only write when the mood strikes. But, you inspire me now to write again! I have also recently taken up learning to draw and paint and this is taking up much of my time. I probably do need to get back to my first love…writing…again soon! I hope you are both doing as well as you can in the face of this stupid disease! Thank you for checking on me…it means far more to me than I could put into words!


  16. Hi there, hope you getting along? I got diagnosed with pulmonary fibrosis last week. I watched this video, which helped me a bit.

    Just shows how hard life is. And doesnt neccesarily mean you’ve got it all wrong!


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