Dr. Mark Edwards (U.K.)

[sgaetna2013]

Has anyone been treated for FMD in the U.K. by Dr. Mark Edwards? If yes, was it inpatient or outpatient? Did you find the treatment effective? How long were you in treatment?

Thanks!

[Jofisher]

Hi I am under prof Edwards he’s lovely very knowledgeable and empathetic and non judgmental but I’ve not been an inpatient

[sykgirl]

Hi,I've been a patient of Prof Edwards for about 8 years. He is the most knowledgeable, empathetic and thoughtful doctor I have ever seen (and I have seen many!). Sadly inpatient treatment is contraindicated for me because I have multiple issues. We have tried many things over the years, but my body has never responded positively. Despite this, he has never given up on me. I trust him, and know that he is constantly on top of the latest research etc so as soon as there is anything new to try he will know and make it happen for me.

I hope he is able to help you 🤞

[Hidden in reply to sykgirl]

where is he based?

[sykgirl in reply to Hidden]

Atkisons Morley at St George's in Tooting, London

[giltnane]

I was diagnosed by prof mark Edward in 2015. it was his last day at UCLH I STILL SEE HIM AT TOOTING .Prof EDWARDS having DIAGNOSED ME WITHIN MINUTES WITH FND & DYSTONIA IN HANDS I HAD ALREADY DIAGNOSIED IN 2012 WITH PAN GI DISMOYTILLITY . PROF EDWARDS IS A BRILLIANT SO KIND and understanding.

any one who is lucky enough to have prof Edwards as their consultant he is EXTREAMNLY HELPFUL AS GPS LOOK UP TO HIM AND SUPPORT ANY REQUESTED MADE BY HIM.