Hello!
I was diagnosed with fibro/CFS in 1992 after I contracted chicken pox at age 28 and then a couple years later mononucleosis. In 1997, one month after I got married, I relapsed with mono and had a rather severe case. Fibro has steadily worsened ever since.
I am interested in connecting with others who have this condition; particularly as it relates to central sensitivity. It's frustrating trying to find out information about things like more comfortable clothing, how central sensitivity affects others, what works and what doesn't, etc.
I was diagnosed with fibro/CFS in 1992 after I contracted chicken pox at age 28 and then a couple years later mononucleosis. In 1997, one month after I got married, I relapsed with mono and had a rather severe case. Fibro has steadily worsened ever since.
I am interested in connecting with others who have this condition; particularly as it relates to central sensitivity. It's frustrating trying to find out information about things like more comfortable clothing, how central sensitivity affects others, what works and what doesn't, etc.