I found this forum while looking to see if anything was available for my hubby to attend because he has been diagnosed as having short term memory.
He has tried the tablets but unfortunately they gave him severe headaches so he was taken off them straight away.
Like others here it is hard work to cope with at times but I consider myself extremely lucky because this year will be our 65th wedding anniversary if we both get to September.
There are times when I feel like screaming and just wanting to have a bit of time on my own and I get very depressed at times but this is a natural re-action and I find it better to walk away from hubby when he gets a nasty mood on him and I finish up on my computer probably answering students because I have a big W.W.2 website that has had folk to it from around the world.
My son and I taught hubby how to use a computer although he is not brilliant at it BUT he can play Solitaire on it and send an e-mail to my son and granddaughter and I encourage him to do this because I want to keep his brain going as long as he can without giving in to this rotten illness.
Yesterday hubby and I went to the very first Dementia and Carers club BUT I wont be going any more because I thought there would be some sort of activity for those who have Dementia to join in.
I was amazed that they had a speaker instead who came to talk about Osteoporosis. I felt SO sorry for the Dementia sufferers because the look of confusion and being SO subdued on their faces spelt out that they had NO idea what was going off. To be honest I think I was the only one who did because I have had this complaint for 30 years and personally I did not think it a wonderful subject for those who needed stimulation.
I would have thought perhaps showing slides or photos of the area they lived would touch a chord in their memories or even some music.
I say this because when I went with hubby last week to see the consultant and I mentioned to him that I had found many U-tubes of my hubby's favourite big band sounds and he sat there absorbed in watching Glen Miller and other well known bands of his era AND could tell me exactly what part of the music had been cut out of a video. The consultant thought it was a briliant idea and said it certainly would help him.
I only wish we had somewhere near where I live to do something like this for others afflicted by this terrible illness.
I hope I have not bored anyone who reads this because I was only trying to show that although your loved one is NOT the same as he/she was years ago there is hope if one finds a way to get through the memory barrier. NOT in all cases I hasten to add but such as my hubby's case there could be glimmer of hope.
As I said I try to relax off with my website and answering folk from around the world who are fascinated with the fact that they are in touch with a W.W.2 evacuee who was bombed out twice and machine gunned twice. It helps me to know that I am still of some use to those who wants information of those years.
God Bless All.
He has tried the tablets but unfortunately they gave him severe headaches so he was taken off them straight away.
Like others here it is hard work to cope with at times but I consider myself extremely lucky because this year will be our 65th wedding anniversary if we both get to September.
There are times when I feel like screaming and just wanting to have a bit of time on my own and I get very depressed at times but this is a natural re-action and I find it better to walk away from hubby when he gets a nasty mood on him and I finish up on my computer probably answering students because I have a big W.W.2 website that has had folk to it from around the world.
My son and I taught hubby how to use a computer although he is not brilliant at it BUT he can play Solitaire on it and send an e-mail to my son and granddaughter and I encourage him to do this because I want to keep his brain going as long as he can without giving in to this rotten illness.
Yesterday hubby and I went to the very first Dementia and Carers club BUT I wont be going any more because I thought there would be some sort of activity for those who have Dementia to join in.
I was amazed that they had a speaker instead who came to talk about Osteoporosis. I felt SO sorry for the Dementia sufferers because the look of confusion and being SO subdued on their faces spelt out that they had NO idea what was going off. To be honest I think I was the only one who did because I have had this complaint for 30 years and personally I did not think it a wonderful subject for those who needed stimulation.
I would have thought perhaps showing slides or photos of the area they lived would touch a chord in their memories or even some music.
I say this because when I went with hubby last week to see the consultant and I mentioned to him that I had found many U-tubes of my hubby's favourite big band sounds and he sat there absorbed in watching Glen Miller and other well known bands of his era AND could tell me exactly what part of the music had been cut out of a video. The consultant thought it was a briliant idea and said it certainly would help him.
I only wish we had somewhere near where I live to do something like this for others afflicted by this terrible illness.
I hope I have not bored anyone who reads this because I was only trying to show that although your loved one is NOT the same as he/she was years ago there is hope if one finds a way to get through the memory barrier. NOT in all cases I hasten to add but such as my hubby's case there could be glimmer of hope.
As I said I try to relax off with my website and answering folk from around the world who are fascinated with the fact that they are in touch with a W.W.2 evacuee who was bombed out twice and machine gunned twice. It helps me to know that I am still of some use to those who wants information of those years.
God Bless All.
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