Health & ME/CFS, This Crazy Life

Guest Post: Rhiannon Tells It Like It Is – to the SSDI Appeals Council

Today I want to share something very special with you - a letter my daughter, Rhiannon, wrote to the Social Security Disability Appeals Council, about growing up with a sick mom, and the changes over the last couple of years. She has quite the voice, my daughter. by Rhiannon To whom it may concern: I… Continue reading Guest Post: Rhiannon Tells It Like It Is – to the SSDI Appeals Council

Health & ME/CFS, Migraines

Shock and Dismay: Re-visting Tick-Borne Diseases

Last week, I saw my LLMD (Lyme Literate MD) again, and left after spending an hour with her, in shock & dismay. Where neither my PCP or neurologist have any ideas really where else to go with my deteriorating health, other than the "band-aid" approach - treating the symptoms as best we can - my… Continue reading Shock and Dismay: Re-visting Tick-Borne Diseases

Health & ME/CFS, Migraines

Migraines: A Radical New Look At An Evolutionary Advantage

Laying curled up in bed tonight, I suffered through yet another severe migraine. This time, I asked myself exactly what my body was trying to tell me, and, more importantly, why??? I think I found the answer... Imagine: It is sometime during what is commonly called the Stone Age. Small groups of people, hunter-gatherers, spread… Continue reading Migraines: A Radical New Look At An Evolutionary Advantage

Health & ME/CFS, Migraines

Notes to Myself on Migraine Hell

Remember! It will end. Four days and four very long nights I have spent in the deepest, darkest, most silent, depths of migraine hell. Hormonal migraine hell - the "hormonal" part is important, because that's always the worst, most impossible to live through, of the migraine hells. Four days & nights of wearing a blindfold,… Continue reading Notes to Myself on Migraine Hell

Health & ME/CFS

We Know the Enemy, or ME/CFS/FMS Explained Again.

Wee little note - this is out of date. I started this blog in 2010, for my family for the most part. To help them understand my illness, and help me work out my thoughts on it and also other matters. Since 2010 I've learned a lot of things about the nature of my illness,… Continue reading We Know the Enemy, or ME/CFS/FMS Explained Again.