Thursday, May 31, 2012

How Sundowning affects me

By Barry Pankhurst Thursday, September 09, 2010

How Sundowning affects me

 

Some time ago I was asked the same question in the (I have dementia section... of Alzheimer's Talking Point) about ‘Sundowning'... this was my reply.    


(Barry could you explain how you feel whilst Sundowning, does anything trigger it or does it happen just like clock work, hope you do not mind me asking)

The easy answer would be just to say yes (It happens like clockwork) but I think the subject is far more complex than that as it seems that Sundowning as it's called can affect people with our illness at different times of the day although the latter part of the day when the sun is setting seems to be the most significant time.

One thing I should explain is that here in Indonesia and some other parts of Asia Sun rise and Sunset occurs at about the same time everyday of the year, by 6am its broad daylight and by 6pm it's getting dark unlike European countries when during the summer you have extended hours of sunlight from 4am-9pm which in itself could have some significance as to when a person starts to feel the affects of Sundowning?

But how does it make me feel:

I think the best way I could describe it is to say that it causes a similar feeling that I can still remember after having had a nervous break down some years ago that at the time resulted in deep depression.

Normally at around 4 - 4-30pm I start to fell very lethargic and just seem to be wandering around the house totally lost in my own world mumbling to myself or sitting in a chair drifting into daydreams (in fact my wife says she can now tell what time of day it is without looking at the clock) I fell as though the day is trying to drain every last bit of energy out of my body, all my limbs become extremely weak and I find it very difficult even to go for our walk but still go in a effort to ward off the Sundowning effect, I can become very short tempered and loose all sense of rationality and sometimes become verbally aggressive and argumentative you feel as though the whole world is against you and that whatever you say or do is wrong so I don't like to be posed any questions at this time of day not even (what do you want for dinner) and I certainly don't like to have any visitors at this time not unless they want there heads bitten off as my mind is at a total lose of comprehension, all I want is to have my dear wife by my side but she now realizes its best to talk to me very gently and I'm sure that she now just agrees to everything I say in an effort to keep me calm and makes sure the house is kept peaceful without any excessive noise to further confuse my mind (Bless her as she has so much patients) as I start to feel as though I have the whole weight of the worlds problems upon my shoulders and everything becomes a effort so much so that my wife now has to help me bathe and get dressed as I'm so agitated and shaky.

So there is nothing that actually triggers the Sundowning as it just seems to automatically start by itself but if it's not handled with sensitivity then there could be untoward repercussions, also I should add that not everyday is the same as some can be worse than others and sometimes I can go for a few days without feeling any effects of Sundowning and the other strange thing is that even the weather conditions at the end of day can have some influence if its overcast I feel much better and responsive but if it's a strong bright sunset then the draining affect starts much quicker in fact I get much the same affect when I go into a shop that has to brighter lighting.

9/ 9/10 11:55pm

Barry,

 

I want to thank you so much for explaining what it is like as a person suffering with Alzheimer's. My father-in-law who is 89 has late stage of Alzheimer's and sundowning is indeed part of his everyday life. It is important for me to see in your own eyes what it is and how you feel. Often we really need to understand how you and others suffer with sundowning and other symptoms.

Bless your wife for taking good care of you. You are lucky she understands you.

I am pleased that you are able to write and tell us the experiences. I hope you will have many more years to educate other people in your writings.

Please take care of yourself.

 

Regards,
Nina

9/10/10 3:59am

Many thanks for your comments as I think Sundowning is a part of our illness that so many people have a problem to completely understand, so I'm pleased it was of help... don't worry I will be posting more on this site... as I've no intention of going anywhere YET

God bless you

Barry  

Carol Bradley Bursack, Health Guide
9/10/10 11:18am

Barry, no one can help people understand as much as someone with the disease. You, like Leah, are a teacher and we appreciate you so.

Carol

9/10/10 2:55pm

Thank you for sharing this with us.  My father had vascular dementia prior to his death in 1993, and he suffered with sundown syndrome for awhile.  There was so little information at that time about the situation that we, his family, really didn't know what to make of his situation or how to help.  I'm grateful for your insights on this, as I am now the primary caregiver for my mother, who has Alzheimer's.  She remembers well my father's situation at the end, and lately she has begun trying to make a joke about her occasional restlessness and imperiousness as evening settles in.

 

Please keep posting about your experiences, if you are inclined.  We will benefit a lot from hearing from you, as we benefit from Leah's thoughtful posts, as well.

 

Thanks again.

 

CJ

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By Barry Pankhurst— Last Modified: 10/20/10, First Published: 09/09/10