skullgirl -
Why on earth would you spend all that money and drive all that way to see a doctor who doesn't believe in CFS and doesn't know about Lyme? Your chances of having anything productive coming from that meeting is nil to zilch!
SS
Quote:
Originally Posted by skullgirlboo  Hey im 23 and from England.
self diagnosed Morgellons- however i have a docs app today, but i have little faith in him as he disregards CFS as an illness and i had to explain what 'Lymes' disease was over the phone.......
Basically this nightmare reached a peak about 3 1/2 weeks ago for me-thats when i woke up and actually realised *I* was making the fluff not cheap socks. 
I am not really getting anywhere, i have found a private doctor but it will be £100. ($156) for a 30 min phone call, then an 45min appointment would be £125. ($195) and that means travelling from London to Bolton which would take 6 hrs and cost another 100 quid plus there is the follow up app 6 weeks later at another 125 quid so overall for 30 mins on the phone and 1hr 30 mins with Dr Wright we are looking at around £600 0r $940.
I am more mad then sick right now.
i must say tho soluble vitamen c tabs all the way! if you are going to take meds crush them and take them in a drink as u loose around 50% of pills through digestion- sorry if you already know this.....
Anyway hello, here i am all mouldy and furry  |