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...
Motivation & Life Dreams
Meghan has found competitive swimming to be her outlet. Her refuge. Her comfort. Her hope for being normal - as she won't share her...
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...
The Importance of Good Friends
The importance of support is critical to any difficult situation. It's hard when one feels isolated and alone - even in a crowd of...
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...
Misdiagnosis & Patient Advocates
This past year we have talked to many families with similar stories. Most have seen the same doctors - and share the same stories of...
Mast Cell Activation
I am continually learning about new things...and it certainly is an important time for discoveries in auto-immune disorders, the immune...
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...
504 Education Plans for Students
When Meghan and I started looking for ways to handle joint pain that can be caused by both EDS and POTS, our doctor suggested physical...
