Recent comments
Most recent annotations on things by Anthony D Wright
- ssarmca ssarmca: Great Yarmouth - A Borough Not Fit For Heroes Senior Staff Members, Elected Politicians and Council Lawyers face prosecution in the International Criminal Court at The Hague for crimes against... (12 March 2009)
Read annotation | All by this user - Carl Harding: Mr Wright you are quite right to raise this issue, more and more we see the heartbeat being restricted in Great Yarmouth and moving jobs 22 miles up the road only goes to strengthen the fact our... (12 March 2009)
Read annotation | All by this user - ssarmca ssarmca: With the level of homeless veterans and those evicted to make way for European mirgant workers in Great Yarmouth Mr Wright is reluctant to speak up for security of tenure for the over... (30 March 2008)
Read annotation | All by this user - ssarmca ssarmca: How much are these MPs supporting gambling receiving in KICK-Backs from the operators? They seem very keen indeed. How do we find out now they have exemp themselves from the FREEDOM OF... (26 February 2008)
Read annotation | All by this user - The real SSARMCA: Well actually I think that he is doing a great job as the local member for Houndslow. (9 January 2008)
Read annotation | All by this user - ssarmca ssarmca: This man is more interested in bringing gambling to this town than the 155 homeless veterans, another 300 homeless sofa surfing and the lack of affordable housing and European migrant workers... (7 December 2007)
Read annotation | All by this user - ssarmca ssarmca: Not sure how this levy helps the 155 homeless veterans in Great Yarmouth, lack of affordable private rented homes or the 7.500 on the council house waiting list or stop the 150,000 foreign... (23 November 2007)
Read annotation | All by this user - Hazel Edwards: I was diagnosed with MS in March 2001 after many years of not being well and losing my balance. I became paralysed from the neck down and was diagnosed as having MS. My local disablement Forum... (11 June 2004)
Read annotation | All by this user - jean munro: I am also a sufferer of lupus, hypothyroidism,and various other illnesses,my problems have plagued me for 10yrs or more, ruined the quality of my life and that of my family. Prevented me from... (10 June 2004)
Read annotation | All by this user - Jane Wood: The government i feel should do more for people diagnosed with lupus and the recognition of it, more needs to be known and easily recognised and accepted, as people daignosed or not have to fight... (8 June 2004)
Read annotation | All by this user - melody redhead: ALL IASK TO LET MY BODY DO THAT MY MINE TELL IT CAN DO THEN THE SETTEE LOOMS AND I AN EXHASTED IRONING PILES UP POTS PILING UP THE LOO DOEXN'T GET CLEANED I USED TO BE AN OBSEVSIVE CLEANER I... (7 June 2004)
Read annotation | All by this user - melody redhead: WE NEED SOME SUPPORT FROM GOVENMENT MEDIA HELP AS WE DONOT GRT MENTIONED SO MANY PEOPLE HAVE NOT HEARD OF THIS DREADFUL CONDITION (7 June 2004)
Read annotation | All by this user - melody redhead: I HAVE BEEN DISGNODED WITH SLE LUPUS SINCE BEING ILL FOR ALONG TIME IN 2000 IT WAS THE MOST FRIGHTENING TIME TO GO THROUGH LOSING SO MUCH WEIGHT BEING AWAY FROM MY LOVED ONE FOR 4 WEEKS HAVING... (7 June 2004)
Read annotation | All by this user - Fran Horne: I am a sufferer of autoimmune disease. I was dismayed to learn that many, many diseases were notably absent from the Disability Discrimination Bill. I consider it paramount that government... (7 June 2004)
Read annotation | All by this user - K C: I have waited over twenty years to be diagnosed with Lupus, Sjogrens, APS (having been previously wrongly diagnosed with ME some 20 years ago. ME is now recognised by the Government. From the... (7 June 2004)
Read annotation | All by this user - Emma Hickling: I am 27 years old and have had Lupus since the Young Age of 9. As Lupus can be a life threatening Illness I do agree wholeheartedly that Lupus should be recognised with other life threatening... (7 June 2004)
Read annotation | All by this user - Woodrow Fields: Although I am not a UK citizen and live in the US and am not a sufferer of Lupus or any other auto-immune disorder. I would just like to add that In the past few months I have had the... (7 June 2004)
Read annotation | All by this user - Barrie Eitelberg: It is imperative that those of us who suffer with Lupus, Sjogren's, Fibromyalgia or any other chronic illness, know that there are people out there who are fighting for us!! I still don't... (7 June 2004)
Read annotation | All by this user - Valigene Hubbard: I am also a sufferer of Lupus, Antiphospholipid Syndrome and Sjogrens Syndrome. I agree with the previous post about the need to make the classification of our diseases permanent. These diseases... (7 June 2004)
Read annotation | All by this user - carrie hoffmann: I would ask why are lupus/sjogrens/fibromyalgia/etc (ie all auto immune desieses) not classed as 'permenent' disabilities? they can all be as debilitating as multiple sclerosis, which affords a... (7 June 2004)
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