those familiar with early simon and garfunkel will recognise the title :))
I was recently diagnosed with PSP after 2yrs as a Parkinson patient;
after retiring i was appointed to a professorship at the university of aberdeen (established 1495) where i work --by internet--on advanced quantum physics an
i get up about 4am each day to work on my latest book. It has the snappy title 'Modelling conflict an competition far from equilibrium.
2 years ago we went to venice --picture shows a medieval staircase carved in marble in a back alley - typical venice.
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jmoffat
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Lovely photo. I have been to Venice but never noticed that beautiful building. Or if I did I sadly just walked on. Maybe thinking next time? There never was a next time though! A lesson there for all of us?
Sorry you have been told now that you have PSP. However you have come to the right place as people here are so kind. We have all gone through it as carers and there are a few people who are sufferers from PSP or CBD. MSA patients find this a good site too because we are an active site.
I am glad you can still work from home. I am in awe that your area of expertise is quantum physics! Keep up the good work as long as you can.
My wife suffers from PSP. The first specific symptoms show up in March 2012: difficulty speaking as if she had a stone in her mouth and a slight tremor in the ring finger. The definitive diagnosis was done in June 2015 (after problems in eye movements were detected, which was the specific symptom that was added to the difficulty in speech and walking instability confirmed the PSP diagnosis).
I have a summary of our experiences, problems and solutions regarding PSP.
Hi there Luis - I must admit that I too am very keen on reading your paper on PSP - I received my diagnosis of PSP in August 2015 and I must admit I fulfil all the criteria... but I am always learning more things about it the more I read about it.........in fact my whole day and everyday seems to revolve around PSP!!!! Funny that HEY!!!!!!???????????cheers Bindi
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