I stumbled upon your blog while looking up vegan ice cream. I found it very interesting, while I have never had lyme (though tested for it numerous times) I was diagnosed with CFS in 2002. I don't really know what caused it, but reading some of your entries made me remember everything i went through. I was in college at the time, so people didn't understand why i never went out for two years or dated anyone, but i could barely do my homework and almost failed out a semester.
Anyway, It took me about 5 years to feel better, at a time when i was supposed to be young and having fun! Sometimes, i still get tired and am always afraid of going back to that place when i never felt good, i would get lost driving places i had been to before and sleeping my free time away. I suppose the residual effects of my illness are being easily run down if i don't take care of myself and mentally not knowing if what is wrong is in my head or real now that i am 'better.'
I remember being bounced from doctor to doctor, and being asked if i was depressed all the time. Now, i live in fear that overexertion will bring me back to those days.
I am always saddened by the years i lost being sick, but i can only focus now i the years ahead where i will get to do all the things i wanted to do back then (run again, bike long bike rides, pilates, yoga, get better at surfing, long hikes in the mountains). Im 27 now and sometimes it feels like i am behind everyone in doing all these things, but i am thankful that now i can go for a 45 minute walk instead of a 10 minute walk, and do a whole pilates workout instead of just half.
I mostly wish that people knew how debilitating it was to have CFS, and that I could just say, I had CFS, instead of having to explain in detail exactly what happened to me and how it affected me, because it was my life for so long.
Anyways, i hope your road to recovery begins to shorten.
In November 2007, I got sick and didn't get better. Many doctors later, I was finally diagnosed with chronic fatigue syndrome and, later, Lyme disease. This blog is my way of keeping family and friends updated on my journey towards wellness.
Hello,
ReplyDeleteI stumbled upon your blog while looking up vegan ice cream. I found it very interesting, while I have never had lyme (though tested for it numerous times) I was diagnosed with CFS in 2002. I don't really know what caused it, but reading some of your entries made me remember everything i went through. I was in college at the time, so people didn't understand why i never went out for two years or dated anyone, but i could barely do my homework and almost failed out a semester.
Anyway, It took me about 5 years to feel better, at a time when i was supposed to be young and having fun! Sometimes, i still get tired and am always afraid of going back to that place when i never felt good, i would get lost driving places i had been to before and sleeping my free time away. I suppose the residual effects of my illness are being easily run down if i don't take care of myself and mentally not knowing if what is wrong is in my head or real now that i am 'better.'
I remember being bounced from doctor to doctor, and being asked if i was depressed all the time. Now, i live in fear that overexertion will bring me back to those days.
I am always saddened by the years i lost being sick, but i can only focus now i the years ahead where i will get to do all the things i wanted to do back then (run again, bike long bike rides, pilates, yoga, get better at surfing, long hikes in the mountains). Im 27 now and sometimes it feels like i am behind everyone in doing all these things, but i am thankful that now i can go for a 45 minute walk instead of a 10 minute walk, and do a whole pilates workout instead of just half.
I mostly wish that people knew how debilitating it was to have CFS, and that I could just say, I had CFS, instead of having to explain in detail exactly what happened to me and how it affected me, because it was my life for so long.
Anyways, i hope your road to recovery begins to shorten.
- C