I have been given this product as part of a product review through the Chronic Illness Bloggers network. Although the product was a gift, all opinions in this review remain my own and I was in now way influenced by the company. I once heard EDS described as living the...
While May has ended, the need for EDS Awareness hasn’t. I’m teaming up with these awesome bloggers who also live with Ehlers-Danlos Syndrome (EDS) in order to sponsor a giveaway to promote continued awareness throughout the year! My co-hosts are Hannah...
and disability advocate extraordinaire (kind of) aspiring to find happiness with chronic illness and pain.