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Lynne “Lynnie” Heal
Worked at DISABLED
Attended University of Cambridge
Lives in LEICESTER
276 followers|218,929 views
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Lynne “Lynnie” Heal

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Sensibilizzare l'opinione pubblica, i media e le istituzioni sulla 'Insufficienza venosa cronico cerebrospinale' (Ccsvi) per ottenere il riconoscimento della
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Lynne “Lynnie” Heal

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E' l'obiettivo con cui la Onlus bolognese 'Ccsvi nella Sclerosi multipla' ha organizzato la 'Settimana della consapevolezza sulla Ccsvi', celebrata in tutta Italia dal 3 al 10 maggio. A Bologna farà tappa il 5, in occasione 'Giornata mondiale della Ccsvi' (ANSA)
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Lynne “Lynnie” Heal

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E' stato pubblicato sul numero di maggio della rivista scientifica Phlebology della prestigiosa Royal Society of Medicine uno studio intitolato "Venous
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Lynne “Lynnie” Heal

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Disabled people are being left stranded in their own homes due to a “culture of law- breaking” within local government over obligations to adapt homes and make them more accessible.
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Lynne “Lynnie” Heal

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Sensibilizzare l'opinione pubblica e le istituzioni sulla 'Insufficienza venosa cronico cerebrospinale' (Ccsvi) per ottenere il riconoscimento della patologia da parte del ministero della Salute. © ANSA
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Lynne “Lynnie” Heal

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It's a chilling reality -- one often overlooked in annual mortality statistics: Preventable medical errors persist as the No. 3 killer in the U.S. -- third only to heart disease and cancer -- claiming the lives of some 400,000 people each year. At a Congressional hearing July 17, patient safety officials put their best ideas forward on how to solve the crisis, with IT often at the center of discussions.
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Lynne “Lynnie” Heal

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THIS  IS CRUELTY   TO ANIMALS 
Researchers at Cambridge University have been turning rats into junkies, animal welfare campaigners claim. Some rats were deliberately hooked on heroin, and others addicted to cocaine, in...
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Lynne “Lynnie” Heal

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WATCH: Whistleblowers reveal criminal practices of pharmaceutical industry in stunning interviews
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People
Have her in circles
276 people
Türkay Türkal's profile photo
Julia Turner's profile photo
De Beverly's profile photo
Chandima Dilrukshi's profile photo
Yaseen Ahmed's profile photo
balogun sikiru's profile photo
Alan Ranta's profile photo
Michael Arata's profile photo
Timothy “Arian Paigo Lokki” McDonough's profile photo
Communities
19 communities
Education
  • University of Cambridge
    1978 - 2014
    Have studied Geneaology for many years with help from many in Canada .Research on all this has helped me to research MS also .Have uncovered lots with MS and the real TRUTHS
Basic Information
Gender
Female
Story
Tagline
NO MS DRUG WILL EVER CURE MS EVER BECAUSE TOO MANY MAKE PROFITS, SHARES AND COMMISSIONS FROM ALONGSIDE VERY HIGH SALARYS AND THATS ALSO WHY A CURE WILL NEVER BE FOUND ALSO .Fed up of UK not moving forward with MS its wrong, Even MS charitys and BArts and London MS Research also . Millions given to them all and very highly paid to do nothing for us in UK with CCSVI
Introduction
Diagnosed with secondary progressive MS had to sell my home. keep a mortgage for 18 months because when I moved into disabled bungalow was told if I died within a year my family would be made homeless. Flew to Poland for CCSVI for my MS as the NHS wont do it! saying clinical trials needed, yet did bladder botox thats not been clinically trialled yet still given daily for MS.Doesnt make sense if am honest.  Nearly died 2 weeks after botox in 2010 and had to move home 2 weeks after too , full of internal bleedings and infections. MS society UK have banned me on facebook for speaking out.Many worldwide have banned the MS societys for not helping us properly . Had CCSVI in Poland a new way forward NOT a cure a better quality of life however ove 40,000 worldwide have had . Done lots in a parliament site they have deleted. The only one to stand up for CCSVI to David Cameron have printed off as proof before it was deleted.MS society wont help us. NHS wont and nor will any MP or Parliament and knows why its all about the phramaceuticals making billions out of drugs that kill us off faster and the neuros who want everyone dosed up on crap drugs . MS is hidden from the world diliberate and never ever shown anywhere its the hidden away disease that eats the brains, muscles nerves, bowels and bladder untill you are bedridden and left to die on morphene. NO  MS  DRUG  WILL EVER CURE MS  MANY MAKE PROFITS, SHARES  AND  COMMSSIONS  FROM THATS  WHY A CURE  WONT EVER BE  FOUND  ALSO  owndoc.com/lyme/multiple-sclerosis-is-lyme-disease-anatomy-of-a-cover-up/  MS has lots of cover ups going on #MS #MSAwarenessMonth #NHS #Health   DANGEROUS  MS  DRUGS https://plus.google.com/u/0/111592036218828730838/posts/2yRZc1K5Gqq?pid=6133987279417626610&oid=111592036218828730838&authkey=CNvCjNuk-JH91QE
Bragging rights
Done some pieces in They work for you Parliament to David Cameron about MS and CCSVI have kept copies of before they deleted did 4 to David Cameron for UK all ignored Our Queen sent me an e.mail to say Thankyou for supporting her on The Queens Jubillee with a loverly picture and words to me . Kept safe.Prince Augustus d'Este in the Royal lineage also had MS 1794–1848 he never ever had any MS drugs ever and lived to be 54 years old . More proof that the drugs again for MS are NOT good
Work
Occupation
Research on MS now am home all day and can no longer work
Skills
Geneaology and MS research
Employment
  • DISABLED
    MS SECONDARY PROGRESSIVE diagnosed in 2009 took my GP 24 years to diagnose, 2009
Places
Map of the places this user has livedMap of the places this user has livedMap of the places this user has lived
Currently
LEICESTER
Previously
LEICESTER, SCOTLAND , GOSPORT, PORTSMOUTH,PLYMOUTH
Terrible and they treated me bad too. Pension I paid into is rubbish and wont pay all am owed unless am dead knowing I nearly died in 2010
Public - a year ago
reviewed a year ago
5 reviews
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Good natural cod liver oil impressed
Public - a year ago
reviewed a year ago
hes a man whos making trillions out of drugs via commisions
Public - 2 years ago
reviewed 2 years ago