I’m hoping some of you are willing to share what symptoms led to your diagnosis with MS. I’m trying to read blogs but many are so well established that it’s difficult to find those early posts. I’d really like to hear more about those oddish type symptoms that changed enough or increased in intensity to finally lead you to pursue a diagnosis. I am finally at that place after decades of symptoms and I’m really interested in others experiences.
Join Alex Hunter as she blogs her way through her eventual diagnosis of Multiple Sclerosis. Her heart warming descriptions of her experiences and her playful commentary make for an insightful and powerful read. Alex is in her mid-forties and has lived with this condition since her early 20's. She shares her experiences to provide support and hope for those walking a similar path.
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