Back to Reality and the Importance of Meg's IVIG Study...
Sometimes I forget that Meghan goes through this once a month. She has made such huge improvements. Neuropathy in her hands and feet is...
Working out an IEP With Your School
Sometimes in life you need a Plan B... Meghan's freshman year of high school ended with the final two months completed at home - mainly...
Our Latest Speed Bump: Folate for Your Brain & Chronic Illness
We are finally looking in the rear view mirror at some of the toughest weeks we have had in over a year. Folate (or lack there of)...
Meg's Magazine
I am always looking for articles to read and there are so many out there! I tend to look for science and evidence based articles and...
One of My Favorite Quotes on POTS...
This pretty much sums it up...seems crazy, doesn't it? But it's not. Not one bit. Check out Dysautonomia International to learn more...
Compression Socks...
It's been nearly 3 years since Meghan's symptoms started. She has been less than cooperative with the many things we have tried to help...
The Chair by the Window
Sometimes when it's been a particularly hard week and I'm laying in bed, I imagine myself picking up the chair by the window and throwing...
What Swimming Did for Us...
Without a reason or a purpose, we might still be searching for Meghan's diagnosis. Most patients go a ridiculous 3 to 6 years average...
