Hi, would appreciate different views from recent suffers
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Hi I am a secondary teacher and I have just been diagnosed with cfs last summer. Although I suspect I probably had it for at least 2 years with my reoccurring flu like symptoms. I am lucky that there is a referral unit in the local hospital and both my gp and the clinic are supportive, including the Occupational Health dr. I get the impression that this illness is quite common with teachers but when I asked my union for contacts they said they do not keep records! My docs have all recommended that I paced myself and work my hours gradually which has worked for me now, I learned to ignore some of the earlier aches and pain in the last 6 months, rest in the weekend. I have gradually build up the hours from 2/3 to 4hrs each day after initially can't even wake/get up in the mornings last year. I have just got on the broadband to find a forum like this and I have read some of the postings. What I was hoping for is others who are in similar situations in teaching or is at least trying to get back to working full time who have recently been diagnosed for advice. What are your employers like? Is there light at the end of the tunnel? Thanks. :?
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sharon49
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I am not a teacher but I hate to think of the help available and you not being able to get to it.
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