Hi Dave and all you carers, relatives or friends of Alzheimer's sufferers, this is my first post on TP and naturally happy/sad at some of the posts on here.
I have just returned home to Barnsley from Denmark to help my Mum with Dad, they are both 74 and my Mum just doesn't have the patience or strength to cope any more.
I have basically being assessing the situation for the first couple of weeks to see Mum's ways of coping and to be honest it is quite upsetting seeing and hearing her frustrations aimed at my Dad.
She is always very distraught after the temper subsides because she knows she has done wrong, but we are seeing a little light at the end of the tunnel in regards to my Mum getting time to herself and even getting out with friends for a couple of hours on an evening.
I have just about got my Dads trust to help him with certain things and my Mum is also giving me more responsibilities too.
Dave if you need anyone to talk to, let me know and anyone with tips and advice please let me know......I am going the whole hog on this if it is just to give my Mum her life back.
Hi SoundsNorthern and welcome to TP and my "Tonight I actually snapped" topic
How long has you Dad has the symptoms or diagnosis of AD (if that is what he has)?
I have read so many times where family members are shocked when they visit a sufferer and see the difference from what they remember that person to be some time ago
/AD creeps on up on you very slowly so if you are not around 24/7/365 it can be a shock to the system, however, if you are living with person 24/7/365 it creeps up on you so slowly over the years that it is impossible to really detect until you get to snapping point.
I started this topic as I got to snapping point after maybe 5 or 6 years of my wife's behaviour and reasoning and thought I was the one that had the problem as my wife kept telling me that there was nothing wrong with her so I started believing that I was the one going crazy.
So I did some research and found Talking Point (this forum) and read and read hundreds if not thousand of posts and every post I read rang alarm bells for me, this is what I am experiencing, this is what my wife is doing
Then it suddenly clicked, OMG, My wife is ill, she has a brain disease and there is no cure, no pills and no reversing this problem, she is going to die because of this disease in 2 years or 20 years but she is going to die from this disease
I have received so much support from members of Talking Point even though some are trying to cope as I am and others have the early onset of this terrible disease also offering advice and requesting help
So as you can see, there are a few groups of folk here, those wanting to know more information as they have just found out that a loved one has this disease, those of us (as I am) who are living and trying to cope with a loved one 24/7 with this disease and those that have the disease trying to help those that have it and those that are coping looking after a loved on with this disease
Yes, I have lost it on a few occasions, normally due to frustration, tiredness, anger, being confused, feeling helpless and above all not understanding
Sorry for the long post, I am only saying how my feeling have been and are at this time
If there is anything you need to know I am sure that if you pose your question here on Talking Point you will get a swift reply as there is always someone that has the answer, solution or advice to your question
I wish you all the best and I am sorry that you Dad is suffering as well as your Mum and yourself alike
Thinking of you