Hello Friends!
Thank you all for your kind comments on my last blog which was a bit of a Pity Party.
While I am trying my best not to wallow, it isn't easy not to. A sad fact compounded by the events of last Tuesday afternoon.
I had a long overdue consultation, if you can call it a consultation, via video link with the doctor who is overseeing my Parkinson's treatment and management. I say this because his title is Doctor for the Care of the Elderly. In other words, he looks after the over 60's and does not specllialise in any one field. I know he was seeing my dear friend for COPD, a far cry from Parkinson's. This in itself does not instill me with confidence. Anyhow, I digress. The Parkinson's nurse was also supposed to be linked in to the video call but she failed to show up.
I had to put up with the usual diatribe that I should consider moving house, leaving the area and uproot hundreds of miles away to be nearer to better care provision than is offered in my remote area. This would also offer me better socialising opportunities {do I want that?} with no thought for the few friends I have here, or the stress that would come with looking for somewhere else to live, buying, selling, moving and so on. Most of us have done that, would most of us want to do it when we were already not in the best of health? Uproot our entire world where our roots run deep in exchange for pastures new? Giving up what few friends you have and be dropped in some strange and alien community miles from home. No, not for me, thanks all the same.
Then came the discovery that for many, many months I have been near overdosing on a tablet that was prescribed to be taken five times a day and which should have been no more than twice a day. Heigh ho, just when you think your management can't take any more twists and turns. I take copious notes during such consultations, and during this one the Doctor made a minimum of three changes of mind as to what I should be taking and in what combination. This is par for the course, and I wonder if it doesn't lie behind me being given the incorrect dosage instructions.
So, effective immediately, I'm now on this new, lower dose and guess what? My tremors are now twice as bad today as they were at the start of the week.
No one knows who is to blame, everyone is blaming someone else, and I'm stuck in the middle. I have already started making enquiries. I don't want to get anyone into trouble, Lord knows the department could do without that, but my faith in the system is totally shattered now. First things first, I have been advised to request to be copied in to the results of the investigation. Now, I have not asked for this but have been told that when any mistake is made it must be investigated, So, Monday morning I will be in touch with them over this. Then, I will request a complete transcript of my medications since the beginning of my diagnosis. After that I will decide how to proceed, but right now I am stuck with a team of medical providers whom I can no longer trust to do the best they can for me.
Watch this space!
In the meantime, there have been no applicants to my advertisement for assistance at home. This is worrying indeed. I need help at home desperately now. My case worker on the Direct Payments team at the Council left and somehow my case file got misplaced. If I hadn't phoned to follow through, I would still be missing in the cracks that seem to be everywhere.
Sometimes I feel as if I am in freefall over no man's land. It is making an already stressful time even more difficult and more stressful.
At least I have a gardener! We've planted up some osteospermum Purple Sun, so hopefully they'll be providing some stunning colour soon.
Debbie xx
Golly. I hope this gets sorted promptly. Wishing you the best.
ReplyDeleteWell, doesn't sound as if you got the help needed from the consultation. Will you be able to speak to the Parkinsons nurse? How can a medication be so wrongly prescribed? It's frightening.
ReplyDeleteAnd as for telling you to move house - that's crazy.
I hope you get some positive answers next week.
I've no real advice, only sympathy for what sounds SO frustrating. I hope you will be the squeaky wheel, though that does sap one's energy and time.
ReplyDeleteI’m a retired nurse and would advise you to contact your hospitals PALS ( patients advisory liaison services) who are totally independent and can give you a lot of help and advice. Helen
ReplyDeleteoh gosh Debbie that is just awful re the nightmare over the medication. How on earth can this happen? It is also worrying that the consultant is not a specialist where Parkinson's is concerned. As for the suggestion you move house that is completely diabolical. Honestly I have no idea what is wrong with the nhs these days. I do hope you can get it all sorted out because none of this will be helping your condition. Your missing case file is worrying too. On a positive note the osteospermums are really lovely. Take care Debbie
ReplyDeleteI have no words...just sympathy for all you are needlessly going through. I am trying to think of something to say, but I am just so mind-boggled at this mess you are in. I will double my prayers for you, my dear friend.
ReplyDeleteThe flowers are stunning!
Oh, Deb! What a complication! Sending along encouragement to you as you make decisions! Take care! Hugs and love to you!
ReplyDeleteThank goodness you have the ability and confidence to challenge things. How many just go along with everything the medics say.
ReplyDeleteI feel for you, Debbie. On top of everything else, you should be able to, at least, have confidence in your treatment providers.
ReplyDeleteI hope you get some more positive news very soon. X
Wow -- having to be your own advocate is essential but it is exhausting. I'm grateful you take thorough and complete notes and can get transcrpts or whatever you might need to deal with this. At least you have the cognitive ability to wade through it all, which so many don't have. I so wish you could get the help you need and hope that now that you've found your way through the cracks, things can move forward. Hang in there. And enjoy that gorgeous garden.
ReplyDeleteOh my goodness! Who needs this? You certainly don't!
ReplyDeleteI am so sorry you are having this utter nightmare.
I find myself agreeing with Sue when she said "you have the ability and confidence to challenge things" ... certainly not a situation you would want but unfortunately it is what it is!
I'm thinking of you and sending many positive vibes hoping they may further help you sort things out.
On a positive note three cheers for your gardener, I do like the look of the osteospermum Purple Sun.
All the best Jan
PS Seeing a comment above from Helen regarding PALS ( patients advisory liaison services).
I know when my beloved Eddie was unwell they were quite helpful, so it may be worth making contact with them
Hello, I found your blog today and am following you. I am cheering for you and for you to get the best care and treatment. I think moving far away and the stress and work of selling, buying, etc. would be hard on most people. Nice you have a gardener, flowers bring cheer to me and likely to you too.
ReplyDelete