Life isn’t always straightforward. It's a bit of a cliche, I know, but it’s so true!Eight years ago, I sat in pain with two broken legs, recovering from two major surgeries eight weeks apart. I was facing a future filled with so many “unknown” elements.At that moment, “Life isn’t straight forward”, is exactly what came … Continue reading Finding Ways To Survive “Living in Limbo” with Chronic Illness
This is your last opportunity to enter my Birthday Book Giveaway Competition. In this blog post, I'm sharing Chapter 38 of my book.... "We are so much more than our diseases. It’s OK to show others our strength of character, our funny side, our happy side, our lighter side, our talents. It’s OK to share our hopes and our dreams for the future."
Thank you to those of you who have supported my Podcast and your encouraging feedback over the past 4 years. I am so sorry to disappoint you.
In this blog post, I want to give you a bit of a sneak peek from portions of my book’s Preface and Introduction. As my blog followers, you have supported me for over 7 years, and it’s my little birthday gift to say “thank you”.
July is my birthday month, and I’m very excited to announce I’m running a competition on my podcast and the blog to give away a copy of my book: “My Medical Musings, A Story of Love Laughter Faith and Hope, Living With A Rare Disease “. All you need to do is listen to a … Continue reading Podcast/Blog Party Month Part Two- A Book Giveaway Competition (Chapter 2…A Full and Fulfilled Chronic Illness Life)
July is my birthday month, and I’m very excited to announce I’ll be running a competition on both my podcast and blog to give away a copy of my book: “My Medical Musings, A Story of Love Laughter Faith and Hope, Living With A Rare Disease “. All you need to do is listen to … Continue reading It’s Party Month… Announcing My Podcast/Blog Party Month Book Competition
I don’t want sympathy. I don’t want people to feel sad. I just need to express the exhaustion I feel living with an unrelenting, cruel and downright disgusting disease.
Feeling overwhelmed? Me too. I think that’s perfectly normal. They may be months away, but they are indelibly printed on our mind. It’s like we have a “post it note” stuck to our forehead, which, of course, only we can see!
I am not the only one who is stoic, I am part of an amazing community of others with chronic illnesses who are stoic too……yes that’s you!
I'm going to have to think outside of the box to replace this loss with a new love.
My Medical Musings 