Genetic Multi-infart dementia & Dyspraxia

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I have just realised todayas well as underlying conditions it is Dyspraxia found on MA at the University in 2004 , aged in 50's.I had just received a BA & was taking my own MA re Conceptual How one doesn't access the system especially if the genetic & history ignored ie Visual Arts re Identity & how one is dissolving into the ether as far as the system & Govenment concerned .

I have realised the dyspraxia may lead to the MID via Patient.Co uk .What did National Neurological UCH who also gave Test eventially do gave same Test as the Ed,Psych. of University had The outcome was the University recognised what National didn't give the results like Tilt test too.

The Neurologist via Cardioogist saw 3x instead of yearly appt Cardiologist put Watchful Waiting on appt I have still to go to London for to yet another Dr yearly but was arranged stay there as what was happening here no provision worse re my Records suspect will try & obtain after my Death even though would have allowed if get patient orientated treatment by Specialists within my lifetime as the surgeries are unsafe via policy & procedures. & confidentiality.This was also happening to my elderly parent on otherside of London .Father a pharmacist??!!!My Employment teaching with Post had just targeted me via Function when antibiotics witheld so disabling further with flare ups pylonephritus as movement & breathing becoming a severe problem .There was also classic heart symptons whilst the new GPs told me was only for 6 mths meanwhile was costing too much money & not going to refer or give medication antibiotics /pyuria/sepsis provided by hospitals.

Even though re findings of research 1969 where a spina bifida seen plus Yet the GP Surgery when home [ single/solo] when neurogenic bladder one ureter too many with continence control a problem since a child with immunity & cellulitus too ,had referred me to many hospitals as not taught about

The surgeries here Gloucestershire6 yrs ago have later recorded in online record of no consequence seen.Meanwhile the Government had changed the Medical & Art Schools control to University Remits & Contracts as the more ethical Drs could not have worked in such an unethical system.

They had taken the monitoring & Fund holding by Specialist Depts where the f/t to were in control fund holding .. So the Surgeries via LAs joining u eg Camden & Islington allowed their cash strapped employer to balance the books as Funding inappropriate so the easy targets the Vulnerable get not even the most basic of social care was provided now medical it appears re Integarated Care .

As a result my mobility nearly non existent due to inability to PRIMARY CARE unable to see patterns & research appropriately as directed by the LA/CCG s so appear to be on autopilot not thinking or researching the core of a Drs practice & who gets blamed & cause our safety to be at risk us & every mental patient .They have allowed some Boroughs to discriminate as divided up unresonably with MPs not intervening on our behalf the Pa ignores using unconfidential closed groups involving GPs when you have not agreed to

And guess what because Alzheimers sits on cusp say re mental v neurological & progressive so can hoodwink us [ endemic fraud '

I believe as downright discrimination & no fair hearing is taking place with bullying harrassment & illegak practice .This can be seen with the management of Europe fiasco? T hey have allowed infiltration by moderation in closed groups [ facebook] And suspect as no fair hearing know civil liberties abuse.

PS Will only take one group I wonder why?When relevent to many .Divide & rule by IT ? & admin systems with no management except PAs on autopilot.

0 likes, 4 replies

4 Replies

  • Posted

    This is under the wrong topic,NOBODY knows what you are talking about.

    Bye Felicia

  • Posted

    It's a shame we have little power to change things , neglect from the medical system due to lack of funding is shocking!! My dad Didnt fit the category for further testing altho there were evident physical signs and positive tests to say he had something serious going , at 68 healthy and sporty, he rapidly lost weight over 2 months and all energy , doctors sent away with pills to see how things go for a month, week later we had to call ambulance, he was rushed in and was later diagnosed with aggressive non Hodgkins lymphoma. Why couldnt the doctors suspect this ? Or did they ? Either way the system is foul

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