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New JoyRide Show this week: Walking the Talk with Tiffanie Williams
Kerry here: I love looking for the synchronicities life throws our way. Please allow me to share with you how this week’s show came to be...
Picture this: Tiffanie and me sitting in The Meadow (really, that’s what it’s called) under a 200 year old tree. We’ve chosen this place as our unofficial, official meeting spot. The branches are weighted with age allowing gravity’s pull to create it’s own little room. It’s really cozy here, under our tree.
We were discussing the show, tossing around different ideas when it hit me, “I want to use our real life situations, both happy and difficult, and talk about how we utilize both the seen and unseen worlds and the metaphysical tools we’ve picked up along the way for everyday life. Or how we try applying the 30,000 foot view we always talk about. Daniel
AND I want to start with your sons' Daniel and Evan's story. (Tiffanie’s youngest son was diagnosed with a really rare disorder when he was around 6 years old
and her oldest is currently experiencing symptoms of a different rare disorder). I want to ask you questions surrounding the intuitive hits you’ve gotten along the way. I also want to tell them about the help you are receiving from Spirit and how you manage to keep calm and trudge along.” I got a tentative “Hmm, ok”…. (in a small voice) “but we don’t have a conclusion..." That was exactly the point!
I’ve never seen someone faced with such fear inducing scenarios, navigate rough waters with such hope and grace. I know my friend well enough to know when she’s frightened or upset. I know when she wants to just lay down and cry. But she never does. She catches herself, shaking off the dark feelings and gets busy finding a better way.
Tiffanie takes us on her journey that twists and turns through hospitals, messages from dreams, and help from heaven (literally). She shares her sure-fire “go to’s” for raising her vibration. (Emotional Freedom Technique
- EFT/tapping is her favorite stress busting tool, and studies the Law of Attraction
). This is a super important component to keeping yourself in that center point.
One more behind the scenes fun fact. While sitting under our tree, Tiff mentioned that the last day of February was “Rare Disease Day
” which also happened to be the day her show would air. We’d had a guest scheduled to record that day, for almost a month, and really cringe at the thought of rescheduling someone last minute. The VERY NEXT DAY, our sweet scheduled guest contacted me asking if she could move our interview. She too, hated asking, but later told me that she just knew it would somehow work out for the best. We were thrilled.
Welcome to the tender, sweet inner world of Tiffanie and how she navigates this world with her beautiful sons, Daniel and Evan.
It's the 10th anniversary of Rare Disease Day! A day created to raise awareness about rare diseases and their impact on patients’ lives. On this day the FOP community raises awareness of FOP and also raises funds to end this devastating disease.
More than 60% of the International FOP Association's annul budget funds research to find treatments and, one day, a cure for FOP. It takes $1,950 to provide one day of funding by the IFOPA at the Center for Research in FOP and Related Disorders at the University of Pennsylvania. In honor or Rare Disease Day, help the IFOPA fund one, or even two days, of research
Tiffanie wants to give a huge THANK YOU to her husband and sons, all her family, friends, the school and church, and the rare disease community for all their love and support!! This is journey we're all on together, and we couldn't do it without you!!