IT happened yesterday at my local Lido . I went for a dip I say dip because of my coordination problems I have not been able to swim for six yeas in fact that is why I first went the doctor. I was not far from the rail in the shallow end ( water depth about 1 metre) when I tried to to do few strokes of course it was not successful but when I tried to stand up i could not but was stuck in a strange position with my face firmly in the water my feet on the floor and my back arched all i could do was push at the water with my hands to try get my face out. Well after about two minutes of this I next found myself at the pool side being revived. Apparently I had stopped breathing and was blue when they pulled me out the life guard then slapped my back and I started to breath again. the strange thing was I found that the time between me losing consciousness and coming around
was not unpleasant but a really weird dream which I could not try to explain. has anyone else had similar experiences ?
Written by
steph02
To view profiles and participate in discussions please or .
how terrifying - i too cannot swim anymore which makes me very sad as i used to swim each summer in the sea at SELSEY where we lived for a long time- also since moving to france we have had a beautiful pool built which i hardly ever use due to my fear of doing exactly what you did -- i dont know what the answer is but if you dare to go back again just be aware of the condition which tips you up!!!
love from sharon
ps i did try using a snorkel at one time which did help - good luck ...
##
I have not experienced near death other than in a truck crash and my own drowning experience as a child.
As I write this reply I begin to realize other near death opportunities in my life. When I do finally have the true "near death experience" maybe I will get back to you.
Phew, I'm glad somebody spotted you and that it wasn't absolutely terrifying when you look back on it.
I was told that for many people their buoyancy changes as their Parkinson's develops. I think it was supposed to be due to changes in muscle: fat: bone proportions but I'm not sure if it is true.
yes sometimes I think That I Have a form of PSP instead of atypical parkinson's I am not on any pakinsons medications as they do not have any effect on me , I also do not experience any tremor. my co-ordination is bad and I tend to fall quite often about 3-4 times /day if I am active, and my speech and handwriting is bad. I did however have a positive DATScan about 2-3 yrs ago which showed signs of dopamine depletion. and my parkinsons nurse and neurologist bot say no mainly because I have a normal upward and downward glaze which I am happy with because PSP is much worse.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.