What is wrong with us having Aricept?

Sigurd Fordham

Registered User
Oct 8, 2008
3
0
North West London
My Wife has recently being diagnosed with Posterior Cortical Atrophy. Now I know and can look back at letters she wrote several years ago the illness has clearly started some time ago. Like Terry Pratchett we can see that there is a process that we can address, and we do want to take whatever hope may be on offer. The anticholinesterase treatments are explained by a causal hypothesis. The benefits may be so small that the crude mental tests which are available to statisticians do not show much improvement. The improvement that has been quantified does not balance the cost in the judgement who do not have to experience the disease. However any perceived comfort like the pleasure derived from coffee, tea, icecream, travel, or even aricept is worth exchanging for some money. If the benefits from the treatments on offer are very small and the side affects are also negligible why do we have to wait for a prescription to buy the relief that we can get from trying some form of treatment. I believe even acupuncture can be offered by the NHS. The Bureaucracy of the NHS surrounds treatments that are perceived as not worth the cost. We are not able even to know what it might cost. We are certainly not allowed to make the choice as to whether we would like to buy this comfort. We cannot obtain it without declaring that our NHS health insurance was a confidence trick of the worst kind and will not disgorge £1000 per year to 1% of the population.
I have found out that a 5 mg tablet of Aricept costs about £00.80 to me and that 2 x 5 mg are needed per day. Say £500 pa. It is absolutely disgracefull that the cost is given as a reason to avoid the comfort of this possibly innefective treatment. Oh by the way some improvements have been detected by the crudest tests. What is wrong/ Is this a line of reasoning that is being applied accross awide variety of NHS treatments?

Max Fordham
 

EllieS

Registered User
Aug 23, 2005
170
0
SOMERSET
I don't know what to say to you Max but....

The NHS is supposed to be there at our point of need - which, I guess it has been for the "normal" needs we've had in our family.
But this Alzheimers thing - it can't really be a disease, or it would be a primary health need and the financial aspect of it wouldn't be an issue in any way would it?
I believe everyone who's touched by it are too quiet - I think maybe the Government do know the extent of it but I heard it said recently (from someone who's seeking legal aid to assist through the maze of continuing care) that as the percentage of people affected is relatively small (can't remember the figures) it can't be considered. The fight I think is going on.........but meanwhile, there's you, your wife, me, my Mum and all of the other wonderful people who are members of this forum - all left with their lives in tatters.

I do wish you well - please let me know if you find the wishing well that works!!

Ellie