Jims continued use of Fumaderm

[jiml]

No worries, Jim. It's your loss.

Cheers

I'm not worried Bill and it's certainly not a loss to me ....my Fumaderm costs me nothing as at my age it's funded by our national health service (even when I had to pay it was just the cost of a prepayment certificate which can be used for all the medications I get prescribed for a year) as I say the cost to me is nothing but a couple of hospital car park charges to usually get my psoriasis checked .
I would rather have that with an approved treatment where I can get backup if needed rather than doing it myself and risking overdosing if I measure wrongly
If I lived somewhere that DMF wasn't available and insurance refusing a quality treatment and knowing what I know now after reading your experience ...I would probably give it a go ....providing I could get monitored

So as I say I love what you do, but perhaps now you can understand why I prefer to stick with the (free to me) treatment under the watchful eyes of healthcare professionals