Can anyone share their experience of the ... - Cure Parkinson's

Cure Parkinson's

26,582 members27,897 posts

Can anyone share their experience of the apomorphine pump? It's been recommended that I give it a try

Jinty8 profile image
11 Replies

I don't know quite how I feel about it - is it cumbersome and intrusive? Are there problems with skin sensitivity? I watched my Dad hooked up to a home dialysis machine for 6 hours 3 times a week and though I can rationally equate that the pump is a lot smaller - I think I might resent being 'battery operated' for 12 hours every single day.

Written by
Jinty8 profile image
Jinty8
To view profiles and participate in discussions please or .
Read more about...
11 Replies
Carrigan profile image
Carrigan

My husband tried the injections first to see if he was suitable for the pump. Initially it was great, but unforunately his Blood Pressure was affected and had to stop. , which is annoying as it really make him feel more active for longer. Hope this helps

Hikoi profile image
Hikoi

Jinty I know 2 people using it. You can private message me if you want to followup.

export profile image
export

I did at first I was happy. Very soon you run out of place's to put the needle .

If you get a year of happy days you will have done well.

I would go for it. JUST REMEMBER IT WILL NOT GOING TO LAST.

Good luck . yours EXPORT.

Jinty8 profile image
Jinty8

Thanks Export - I'm 14 years since diagnosis - I suppose 365 different needle sites takes it's toll. I'm not a fast healer either, but it might defer DBS am I being cynical in thinking that they are just putting off surgery and are budget switching?

lotl profile image
lotl

My experience with apomorphine pump has been generally good. Nearly three years on and still finding places to put needle. Mind you I have places I didnt have three years ago! This question has been asked before and I will try and bring it up for you. I will message you in the next day or two.

lotl profile image
lotl

If you search apomorphine at the top of this page it will bring up some answers which were given to this question in February.

Pxxx profile image
Pxxx

Hi I've been on the pump for 18 months now day and night . It's great but has some draw backs like anything some people it suits but not others .

I have 2 pumps day and night,so its 2 needle sites I have to find .

Yes your stomach does get sore but before that I was injecting myself 10 times a day . I hope you like the colour green because it stains every thing .

I would say try it ,takes a bit of time but worth it . If you have any questions I will gladly answer if I can .

saddle1 profile image
saddle1

My mom use the pump for about 1 year, she hated it, due to the green splashes on the carpet and the lumpy rash on her stomach, plus having nowhere to contain the pump she strapped it round her waist with a belt, not good really as it sometimes fell down and she found it so upsetting she finished the treatment and went back onto tablets, approx 1 year on, we are now looking at going back onto the pump simply because the tablets are not working well, mobility has gone and she is so upset again. So she now has to make the decision on what she would really like, mobility and uncomfortable pump or no mobility and tons of tablets. Watch this space!

Jinty8 profile image
Jinty8

Thanks to everyone for their responses - it's been very positive and supportive - I know I will give the pump a 'go' - I was just having collywobbles. I watched my Dad hooked up to a kidney dialysis machine for 7 hours 3 times a week for 6 years before he died and whilst completely the pump is vastly different I think I had a psychological 'thing' about being reliant on a machine. I've been on sinemet almost continuously for 14 years now - and the side effects are getting worse on a weeky basis. Dyskinesia alone is enough to encourage anyone to try something else.

rons profile image
rons

How did it go?

Ron

Sandmanliz profile image
Sandmanliz

i was in doc's office and his new assistant mentioned he was previously working with people in the "pump study". (CU Colorado). The study is going on its 3rd year. only 6 patients. He said everyone is still on except for 1 guy because he travels a lot and you have to keep the drug refrigerated and bring supplies and it was too inconvenient. Sounds like the pump is a little big and they put it in a fanny pak with a small hole in the back. The patients were happy. On a positive note: he said there is work going on for a patch and "lots of great stuff coming".

Not what you're looking for?

You may also like...

Bioness- Can anyone share their experience? I couldn't find any recent posts on here.

My hwp has gait problems, balance issues, sometimes freezing, and weakness in his left leg. I know...

Can we give CuATSM a try without waiting for the Australian trial completion (5 years from now)

Collaborative Medicinal Development LLC ("CMD"), a privately-held biopharmaceutical company...
Farooqji profile image

The best advice I can or may ever give to anyone who has Parkinson's especially the newly diagnosed .

The Davis Phinney Foundation for Parkinson's in partnership with Parkinson's Canada has published...
Gymsack profile image

Is it possible that the onset of Parkinsons can be triggered by shock?

I have been thinking back to the days when I was me and trying to figure out how long this thing...
Court profile image