pills to pump

[blazyb]

My latest blog - big changes coming as o move from pills to pump hopefully very soon

fightingparkinsonss.com/202...

[Jess123dog]

Very intetested in your results

[BPW1]

My neurologist recommended the pump to me yesterday but no one in his practice has used it yet since it is so new so I decided to wait. Has anyone had any experience with it yet?

[JeanieBeanie]

It really upsets me that my HWP diagnosed 31 years ago hasn't been offered this and we live in the UK where it was developed.

[blazyb in reply to JeanieBeanie]

I am sorry to hear this.

[MARC1]

Ive been put on the list for a Produodopa pump. My Neurologist estimated they would be starting this towards the end of year but as they haven't started recruiting as yet, which is very frustrating!!but now the roll out may not start until the summer 2025 with no guarantees. I take Madopar 100/25 +50/12.5 @ 8 times a day and CR at night. I'm finding eating meals between medication can effect my on/off times all evening.

[blazyb in reply to MARC1]

Wishing you the best of success

[pearlette]

Offered but I want to put it off until there is more cumulative experience. I remember insulin pump launches and they had far more experience on dosing alogarithms.