I’ve reblogged posts from my neice, Linda before. She always has something to say, and it’s never based on vicarious experience. She’s generous, direct, and funny. So, from the bottom of my heart – via my funny bone – I share this post for your benefit and for the possible benefit of those in your circles just in case you sense any tangible or intangible applicability.
I spent the entire weekend documenting everything I’ve tried for my MS. Thank God for iCal, my Amazon order history and the “purchase” file I keep in my email app. I’m not surprised by the vast majority of medicines, therapies and equipment as much as I’m shocked at what I forgot. For example I literally had no memory of taking an expensive medication as well as many treatments until stumbling upon them in my digital calendar.
At this point I need to stop, post and hit publish. Over the next few weeks I’ll be describing what’s been working for me these last two years. In the meantime if you have a specific question about what I’ve tried at any point feel free to ask in the comment section or message me.
And no, I didn’t have the courage to tally up how much this has cost me out of pocket.
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