Could this be misdiagnosed as multi infart dementia which late mother had severely after/with polymyalgia rheumatica [ GCA?} I too have similar symptons ignored by NHS to point of MI ie: heart failure symptons .Even when had full blown MI dying 3x revived with angioplasty they still ignore the dysponea affecting mobility & function calling apnea .Yet CPAP machine ineffective.
My independent reseach finds a vascular connection but noone to diagnose. When this involves negligent social care if acquire later no wonder social care is witheld & assesment are incompetent as done on remits.It also involves test results being questionable.
The IFO Commissioner employs the same set up with same types who do not question or investigate just follow blindly what directed to do & say on remits.
Why wouldn't they record the health & safety issues regarding the restorative & their rules on sedation .Where anaethetists don't want the risk not even in Europe for implants yet the NHS makes rules yet cannot provide for the care .So discriminates via access & delay .That is why the Dentist said did not want to treat anymore as was questioning why said too complex yet it was routine.Does that mean students & gas & air to which I am allergic. Why are imnplants regarded as cosmetic when restorative & can be a problem with congenital cellulitus.Mother with multi infart dementia had the same problems.
And what about the confidential Records you can't see change discuss sign it is a true record .Do they want to know .I suspect not as went 6 yrs ago & since they were set up inappropriately .
Are we guinea pigs neglect [ Watchful Waiting] then get the records on death as that what Alzheimers charity says.You can donate your brain.Too late then.
EYE SPECIALIST FOR DIAGNOSIS?
No diagnosis yet. Possible PSP
Delayed psp diagnosis 
Yay! Finally...a PSP diagnosis.
Recent diagnosis for PSP
