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Post by mrsphilc55 on Jun 2, 2014 19:54:47 GMT
Hi,
I'm doing some research for Honeybones and I'd like to hear your experiences of your treatment to date.
I'm also interested in hearing about : Diagnosis, pre op/ post op and any time you had medical team involvement.
Which hospitals are delivering really well against your needs and which areas needs some guidance.
If you could ask the medical team to do one thing better for the next person in your situation - what would that be?
If you've had a joint replacement, how long was the waiting list in your area? Were you a prior approval candidate or did you need to prove your exceptionality in order to gain funding ?
If you opted out of the NHS and paid for your treatment how has that experience been for you and why did you chose that route?
Thanks for reading and I will share back with you my findings.
Lisa x
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