| Posted: 08 August 2008 at 12:33pm | IP Logged
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Hi all I’m not sure posting this will help but I need to try and work out in my head whats going on and looking at letters isn’t helping, but writing it down does sometimes so I’m hoping it will.
I posted recently about my trip last Friday to have phototherapy. I also chatted about my medication as my doctor wasn’t sure what to do (even though she’s specialised in Gynaecological and obstetrics) she’d never heard of spd. None of the docs at my surgery has but she goes onto the net to research it etc and find out all she can from her contacts so she tries bless her.
At the hospital the doctor told me it’s a grey area…. With the amount of codeine I’m taking daily, taking morphine (slow release) wouldn’t do me any harm but probably be better for me constipation wise etc but I’d not be able to drive. Also she’s concerned and doesn’t know how it would affect my body long term. Her guidance was very hypothetical:- if your going to take it to lie in bed and take it then no it’s not a good reason to go onto it but if you need to take it to make you able to get up and about and run after your kids then that’s the right reason….
I also raised concerns about the initial meeting I had with her about the lack of sedation in future injections due to my needle phobia etc she told me due to the constrains, the fact that sedated patients should have one on one care till they have come round etc limits the amount they can admit etc and that if that was to be the plan I could be waiting up to 15mths for another course and where as if I can bite a wooden spoon then I can have it 6mths without.
I received my letter today that she has sent to my gp and I’m now confused scared and petrified to say the least.
Letter says:
I think is she is using that much codeine regularly. And that she feels the morphine would make a difference to her mobility then by all means she should go onto MST, which will probably give her much better pain relief with no increase in constipation and so on. However she understands that the reason to use morphine is for mobility rather than for being pain-free at rest. She can still continue to take paracetamol as required and on good days (when she does not feel she needs the mst) she can of course just take codeine.
( I thought that once on morphine you couldn’t chop and change the days you took it.)
I hope to get her back into clinic in about 3mths time again for a further injection of the pubic symphysis. I will ask one of my clinical nurse specialists to ring her in four weeks time, just to make sure things are still moving in the right direction. I suspect that this phototherapy will be without sedation.
Urm so does this mean at my clinic appointment (which I have though for a day I can’t do if it’s going to involve treatment as it has to take place on a Friday due to childcare and club commitments) it’s not fair it affects them too much and at the intial appointment she promised all treatment would be on a Friday.
I’m relieved I’ll get a phone call as I’m not convinced this set is working as I’m in as much pain as I was before the injections the only difference is the tenderness and bruising has gone from the injection sites…. At least by the time the nurse calls I’ll be able to say if they’re working and if it’s going to be done I thought it had to be under xray conditions! I’m going round in circles and I know I need to compile a list of questions but I can’t think straight at the moment I’m thinking is zany shaped hole…. Injections with no sedation! Silly thing is due to being sedated last time I can’t remember what the whole thing entails apart from a canula and argh cold fluding and some strange memory of biting a pillow screaming! Then the nice porter! Eek I hate not knowing.
Sorry it’s a long rant but I’m seeing my gp on Monday and my dp’s ignoring it all at the moment and has been very cold since I had them last week… he wasn’t even his usual supportive self when we where there.
Any suggestions on the questions I should ask?
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