yeah

SolveCFS, cool channel!

Hi Kim .

Have CFIDS ,SINCE 1070 ,LIVE IN A ASSISTED LIVING PLACE NOW FOR 10 YEARS .Ijust can mostly take care of my self .Wrote the best seller ,beyond the dark cloud ,helped a lot of syrvivors .I can never thank ypu and your staff ,how much you all mean to me .
1098 ,NOBODY KNEW WHERE TO GO FOR ANY INFORMATION ,YOU DID AND PRO HEALTH .
It trully is a crippling dease ,we have to put up with the wrong name ,an d still being rejected from medical proffession.
That is do to the wrong name.
kindest regards
thea s schlosser

Thank you for sharing this valuable information!

I had CF since October. I found out my acid in my body was at 4.5. I went on the raw food diet, and it went up to 6.6. I feel like I am 90% recovered. I think CF may be many things in different people but that's what my issue was.

I would find a way to return to my life as an aeronautical project engineer. I have many ideas for better and safer aircraft. but i'm just too tired to get as involved as I would like..Sudden-onset, full blown CFIDS, began for me in 1979. I can only watch the world from my computer and tv...

I started "crashing in 2004". I was under stress that couldn't be helped... I knew I was sick. I didn';t have insurance, so I tried our state insurance program which was a flop. I have been sick too long, but finally have a dr that helps. Expensive, but he is worth it. All my family and friends have made comments about the change they have seen in me. One described it as "Withering", and I thought that was appropriate. I will pray for each of you. May God allow me to live long enough, that I see a cure... a vaccine... an acceptance and acknowledgement of this horried life altering disease! Bless you all.

We get all kinds of reports ,regarding this or that findings ,in reallty it does not help us that much.
H .

ow about a proper name for cfids,that is number one ,since 99 " of Americans do not know ,cfids is a horreble desease ,
Americas unknown epedemic-thea s schlosser -author -speaker on cfids ,my book is beyond the dark cloud ,it is a selfhelp book ..

one day we will all be dancing again. we have to keep hope or this syndrome will eat us alive. i have lost so much to this but it can not take away my soul. the hardest part of this is the miunderstanding from friends, family and even dr's.we are limited to what we can do but if you find what makes your heart still sing it what gets me through the really bad days. to all of you cfs survivors i hope you are doing the best you can and you are in my prayers.

Thank you, so much!