General Chat

fingers crossed then that there is a solution that lets you continue using them

morning all well its sunny here at moment how long for though ,im of to docs in a bit to see nurse to see if she will do a ecg on hubby he has a feeling its come out of rhythem again and he had some cheast pain as well saturday night so going to get her to cheak it out will catch up with you all later hugs to all elaine x

Good afternoon all.
It is very chilly and damp today, bad enough to make me consider putting the heating on.
Thanks once again for the scone recipe Caz.will have a go at making them soon, and hope they will be better tham earlier attempts. Am sorry to hear about your reaction to the morphine plasters, hope this can be resolved soon
Elaine, hope your hubby is feeling a bit better now.
Am useless at remembering names, musy write them down before posting next time, but I just want to wish you all a good day, and a pain-free one.
Eileen xx

Caz of course we remember you! It's lovely to see you here. Good luck with the patches.

Feel very tired so going to have a sit down xx

Hi Caz, I hope you can sort something with the patches, they can be such an effective way of dosing. There is more than one type and one brand so hopefully a change would fix your reaction. We use a lot of the patches in my job, very few react, but it does happen. Sometimes a change of location of the patch will help. If there is no choice available, taking antihistamine might be effective in the short term. Please don't let it go on too long before reporting it.
sending hugs,
Mary

Morning all, thanks for advice Mary, I rung my doctor and had a word, she said she wanted to see it for herself so booked me in last night. She said I have an intolerance to it and if anyone was going to it would be me, laughing, (remember chemo?)
I have got another type now that is slightly higher dose but changed every 72 hours instead of a week, also some cream as she was surprised at how bad it still was after nearly a week.
She also noticed I had slipped back out of going for a lie down with my feet up in the afternoon, my ankles and feet are very puffy again, she's not worried as it is because I can't walk very well so not using the muscles properly.
I have to go back next Friday to check on how the patches are working, only thing is, I checked the date when I got home and it the same afternoon I have my CT scan. Nothing's ever easy is it.
I am like Eileen and useless with names (ask Dutch lol) so I include everyone in hoping you have a good day.

Love and hugs to all
Caz xx

Morning everone

Caz my dad can't walk and his feet and ankles get very swollen. He has to have a very tight knee length stocking on.

I wanted to stay in bed this morning. But I have to go and earn my money. So I sit here thinking of you
all and am happy that I am fit enough to go and do this. Bless you all xxx

Goodmorning All
Caz .your not that bad by the way putting that up again today as pm Gwynn ,so it will stay on like it did yesterday and then deleted
Tinkerbell,hope your abot better this morning
Liz.hope you ok been thinking about talk to you soon
Eileen,hope your well nice chatting to you
Betty,hope you had anice break away its abit cold here at moment
Deanna,are you ok and is Allan any better such aworry for you
Gail,hope your having better days hang on in there
Gill,hope your ok to and feeling abit better also
for anyone i may have missed,all have better days ahead
Dutchxxx

Hope that has solved the problem then Caz and there will be no more itching.

we are not very active on here are we, just had to rescue the thread from page 5!!!!

Ann
Glos

Morning, Caz I'm glad you were able to see the Dr so quickly, we use Dilaudid a lot via patch (hydromorphone - synthetic morphine, usually well-tolerated). be sure you change the location of the patch each time you re-apply a new one.
One wonderful 'side effect' of Dilaudid is that it provides a bit of a feeling of well-being, which I'm sure you'd appreciate.
have a better day,
hugs
Mary

hello everyone--thinking of you all
love and (((((((((((((((hugs))))))))))))))))) all round

Paula xx

Hello all, Mary the patch I have now is Durogesic DTrans transdermal patch, it releases 12 mcg/hr.
They are tiny about an inch square and transparent, of course with my hands not doing as my brain wants them to do it was awkward to get on this morning. I only have one eye that sees anything properly, I opened the big packet and couldn't see anything, then saw this tiny little transparent thing against the foil insides. They could have at least put a coloured backing on lol. Then when my sister came and I wanted to show her I couldn't find the blooming thing.

At least the cream she gave me has stopped the itching on my now two red patches.
Going to get ready for bed, I am shattered after a long day family hunting. We fell lucky and found my sisters husbands family back to 1690, and he was a Yeoman. Thank the Lord for parish records.

Love and hugs to all
Caz xx

Hey Caz the Durogesic is excellent, hard to find the patches so I always write the date on them to make it easier to find and keep the days straight. The adhesive on the clear ones seems much less irritating than the others.
Good luck
Mary

Hope your new patches help Caz.At least the itching has stopped.

As I said to Joyce, when she phoned me some days ago, I sometimes feel so out of sorts that I can't bring myself to even post here.When reading through everyone's messages, it makes me feel guilty for mentioning my tales of woe.

One of my daughter's phoned this morning to say that her eldest step daughter gave birth to a boy at 6.15 this morning.They are calling him Storm!! She warned me not to make any jokes about this name when we go to see mum& dad & Storm.Hope his character turns out to be sunny, not stormy....

The return journey from Amsterdam last week was the wierdest I have ever experienced, it still makes me giggle though.If I had been alone,Í don't think I would have found it funny, especially after dark.

Wishing you all well, and a sunny afternoon.

Eileen x

Love and hugs to you all

Kathy xxxx

the coward who wouldn't allow the doctor to put a metal tube down her throat today !!!

apparently I am one in a thousand who refuses to have the prosedure done .!! Made me feel better and I don't think !!

Why can they not realise that we with anxiety problems can't cope easily with this sort of invasive treatments ?

Hi Kathy, poor you, that can't have been nice, what does he suggest now you don't want a tube in your throat?

I had a dreadful time once with a metal thing put up one nostril to wash out my sinuses (in the late 1970s). It was awful and what was worse was that I had to walk back past the waiting room with it still in my nose! I should think I scared everyone else away.
Then they said, make an appointment to come back and have the other side done! I don't think so, still haven't been back 30 years later lol

Am struggling to keep up with everything at the mo so my apologies to all I owe calls or replies to and hope I will get round to you sometime soon.

Next week will be awful, o.h. has four days off work, it's bad enough with him on nights so around most of the day, next week 4 x 24 Help lol

Take care everyone and hope life is good to you

Lizxx

Sorry, have been very quite past few days. Had to go to funeral then to sort some things at my dads. Needed some legal papers for solicitor and could not find them as brother has every thing to his house, thought we may get lucky. Brother had changed the locks to dads house, when I finally got hold of the keys I had a set cut for all of us and not just him. Brother is away on holidays overseas for the next few weeks so everything just stops.

Was not at all happy being in the house, it feels soooo empty now. The grass is a foot high and so much needs doing to keep the house going and I feel so useless not being able to do anything. Plus I have instructions (brother again) not to touch anything, I just want to scream.

Liz, Had the same thing with my sinus, also had it operated on twice, (through the mouth) very nasty, and do not blame you for not going back.

be back later

Love and hugs

Gail

Hi Gail, sorry you are having so much on your plate - must be awful with your brother trying to be so controlling.

Will catch up with you soon, have to get to bed now so I can get some sleep before o.h. gets home from night shift!
take care, love. thinking about you and all my pals on here.

Lizxx

morning everyone first id like to say i hope everyone has a good day and hugs to all that need them ,well just at the moment i dont no weather im coming or going ,went to hospital with hubby yesterday for his mri scan well after wating was told they couldnt do it they needed the make model no and seriaial number of his heart valve well thats not somthing i thought of asking for when he had it done ,thaen whaen i got home i rang stoke hospital for the information that mri needed and to my surprise the surgion dealing with hubby was there and was just dealing with hubbys case and wanted to speak to me (alarm bells rang then )he looked at ecg hubby had done on friday after cardioversion treatment and was not happy with the results he wants to see him next week to decuss him going in for a pacemaker now ,as soon as posible .just as i thought everything was getting better here we go again ive been up since 5 carnt sleep sorry for going on an on without you lot on here i dont no how id cope hugs to all and i mean that xxx elaine xx

Bless you both Elaine. I'm so sorry you are both having to go through all this. xxx