Life after secondary Symphis Pubis Dysfunction.

For those of you that follow my blog you’ll know that for the last 7 months I’ve been using crutches and a mobility scooter because for the second time in my lifetime I developed Symphis Pubis Dysfunction during pregnancy, rendering me unable to walk unaided. Symphysis pubis dysfunction (SPD) is a condition that causes excessiveContinue reading “Life after secondary Symphis Pubis Dysfunction.”

To my friends (and family) who don’t have fibromyalgia.

Hey, Thanks for being you, for listening, watching, reading and learning about my condition whilst riding this wave with me. I know it’s been years now. I know it ‘gets old’ boring even, to hear me talk about it ALL. THE. TIME. Part of me is sorry, though I’m not sure I’ll ever stop, becauseContinue reading “To my friends (and family) who don’t have fibromyalgia.”