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Chronic Fatigue Syndrome
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Posted 9/29/2005 5:25 AM (GMT -6)
Hi everyone, I am new here so finding my way around.  I was just so isolated and desperate to find other people with CFS to communicate with who know what I am talking about.  I have had CFS for 4 years and only diagnosed 2 years.  Terrible battle with doctor not to be labelled "depressed" or "menopausal"!!  In the end I paid for my own consultation to get a diagnosis, but have no specialist support locally. 
Posted 9/29/2005 8:50 AM (GMT -6)
Hi Macquelius,
Welcome to HW, we are so glad you found us, I too was going thru test after test after test not knowing what was wrong with me, the pain, the fatigue, memory loss, depression and so forth, I thought I was going insane, I thought everything was in my head because noone had answers for me until I found the right family Dr who actually stopped and listen to me and she referred me to the right Dr who on the spot dx me with Fibro, CFS, Anxiety/panic attacks, anyways enough about me, again welcome and please ask us anything we're here for each other.
Annie


Fibromyaligia, dx Oct 2004 but we are sure I have had this for about 4-5 yrs maybe longer.
Chronic fatigue Syndrome dx 1995
Anxiety/Panic attacks dx 1990
M.S. dx June 29th 2005
Anemia dx Jan 2005

Meds: Amitriptyline
Lorazepam
Celexa
Ferrous Glouconate
Ibuprofen 600mg
and soon to start on
Rebif or Avenox
Posted 9/29/2005 12:27 PM (GMT -6)
Thanks for the welcome guys.  I hope I can learn a bit how to share my life with this thing 'cos I seem to be going round in circles getting no-where.  confused Seems strange to see myself called Macquelius - it's my dog's name!!  Every user name I tried was already in use.  I knew that one wouldn't be 'cos my daughter made it up.  My real name is Alison
Posted 9/29/2005 7:16 PM (GMT -6)
Hi Macquelius!!!
Just wanted to welcome you aboard.
Like Jennifer has said you have found a great place full of caring people.
Hope to see you in chat someday
Mel
Posted 9/30/2005 10:12 AM (GMT -6)
Thanks. I've put some posts on some of the threads. First time I've ever talked about CFS with people who have it! Wow
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