Has anyone seen Dr Pauline Ho in manchester?

[tjperfick]

I am due to see her in a couple of weeks and would be interested if anyone else has seen her. I think that she works with Dr Bruce at MRI.

[Sjink]

I have not seen Dr Ho but every doc I see at the MRI is excellent. I have been attending their lupus clinic for over ten years. I have great confidence in Dr Bruce and his Lupus team. Hope it goes well for you x

[tjperfick]

Thanks for this. I am actually seeing here on a private appointment as Dr Bruce doesn't do private appointments, but am desperate to get some answers!

[roobarb in reply to tjperfick]

Hello, I just came across your post my accident & was wondering how you got on with Dr Ho? I am thinking about asking for referral to a lupus specialist as I have lost faith in my local rheumy & MRI seems like the best bet in the NW,

[mirren]

Could you tell me how you got on with Dr Ho please? I think I am developing psoriatic or seronegative Arthritis, I am likely to lose my job and home if I don't get answers soon and I don't have time to waste, so against all my principles am considering paying to be seen privately.

[tjperfick]

I have got on quite well with her. There is also an advice line and you can log a call for the nurses if you have a query etc and they will get back to you. I did have one incident with a registrar a few weeks, but saw my consultant the next week and was pretty happy with the outcome. It is very busy unit and I go on a Wednesday and clinic is always runnig late. I always allow myself to be seen an hour later than my appt time. She does have private consultations at The spire hospital as well. Hope you get sorted.xx