As I was scouring the BBC for ideas about my blog topic this week, and I came across an interesting article, which is quite close to my heart.
http://news.bbc.co.uk/today/hi/today/newsid_9703000/9703651.stm
Basically, a study was conducted by Howard et al. to find whether the drug, Aricept, had any effect on the effects of Alzheimer’s disease. Alzheimer’s is a degenerative disease that is the most common cause of dementia. Alzheimer’s is a disease, which affects the brain, to put it in simple terms many of the brain cells die due to protein plaques on the brain.
If you want to read more about Alzheimer’s go here
http://alzheimers.org.uk/site/scripts/documents_info.php?documentID=100
The study was conducted on 272 Alzheimer’s patients and they found that the drug decreased the time taken for the symptoms to take effect. This means that it would give families more time with patients diagnosed with Alzheimer’s and it would give them a bearable quality of life. Alzheimer’s is a terrible disease for both the sufferer and also the family, it is difficult to watch a family member go through such a traumatic time.
Taking in to account these things it could be argued that the drug gives the patients and their families a better quality of life, certainly in my point of view I think this is a great thing to have been found because there was nothing worse than watching somebody lose their precious memories
However despite the advantages of giving sufferers the drug, in my opinion I would rather my family not have years and years of suffering and heartache through having to look after me and the onset being even slower than it already is.
Obviously some ethical issues are raised, such as at what point should they stop giving the drug to patients? and at what point would they not be able to give informed consent to take the drug? I believe that even though they may be in the very early stages of Alzheimer’s you may not be able to make correct decisions for yourself. On a contrasting point, people may argue that your family would be able to make the right decisions for you. I somewhat agree with this, however they may not know the long-term advantages and disadvantages of taking the drug. To overcome this I think people making this decision need to be educated and shown what life would be like with the drug or without the drug.
Overall, even though this topic is close to my heart and I may be a bit biased because there was a horrible time when a family member had Alzheimer’s disease. I believe that we should think sensibly about decisions, which can be made in haste and eventually turn out badly, as seen in the example given by the BBC, where a woman, who’s husband was diagnosed with Alzheimer’s who was taken off the drug, which then made his symptoms rapidly deteriorate faster than usual, which can be devastating for the family to go through. I don’t think many people would want their family to go through that and personally I wouldn’t want my family to go through that either.
I believe that more evidence is needed for the drug to be prescribed to every patient because it is not a cure and should not be used or thought of as a cure for the disease. And when that evidence is found then they should think about making the drug publically available.
Here is the original study
http://www.nejm.org/doi/full/10.1056/NEJMoa066583#t=articleDiscussion
Thanks for reading!