jann1033
<font color=darkcoral>Right now I'm an inch of nat
- Joined
- Aug 16, 2003
- Messages
- 11,553
I have CFS - official diagnosis in 2001 after years of testing, surgeries, etc. I am at WDW right now!
I got here yesterday but did not try to go to the parks today. I did go to Downtown Disney.
I rented an ECV last September when I was at WDW and that helped SO MUCH. What has helped me more than anything the past few years is to not over extend myself. If I overdo I get into a deficit that literally will take months to overcome.
I know first hand about being unable to have the energy to take a shower. It becomes an ordeal just to brush your teeth. You take care of basic hygiene just because you have to, but can be very difficult.
Someone that I have known for about 6 years was shocked the other day to hear that I have CFS. She said "You are on the go more than anyone I know." She does not know about the days and weeks where it takes every ounce of energy just to get dressed as I don't talk about those days.
you know i think that is the worst thing about cfs( well not the worst but up there among the top 25 worst things about cfs)
since they only see you on your best days they assume you are like that all the time...i can not count on both hands how many tell me they have a knowledge of CFS then in the next breath ask me what i "do" all day...uh i lay on the couch for most of it, what do they think



