Saturday June 21, 2008, 6:55 pm
first causes of death for M.E./CFIDS is heart attack, stroke and suicide. This however is from the disease itself, which they still tried to hide.

Saturday June 21, 2008, 8:08 pm
'Doctors' in the UK - ordered chronically sick ME CFS CFIDS patient Sophia Mirza to be removed from her home by force (breaking her front door down) and locked her in a mental asylum to 'treat her'.

Days after returning home - she died.

Those in power refused an autopsy and her death would thus have been covered up - had it not been for the intervention of her devoted and loving mother and a helpful MS (Multiple Sclerosis) specialist.

No apology was given, no action was taken by the authorities towards those who did this to her. Her mother and family is left destroyed.

The British Medical Association (BMA) who have the power to strike doctors off their lists for inhumane/damaging behaviour - did nothing.

These 'Doctors'(by innapropriate medical intervention) effectively killed this woman in the name of a belief system. The 'belief' she was insane.

Outside the medical profession, people who do this are called 'terrorists'. (Religion being a belief system).

Despite the autopsy PROVING this young person died of an inflammatory immune disease - there is silence from the guilty and silence from those who can punish.

Sophia Mirza's injust suffering is a prime example of the arrogance and ignorance of the British medical profession when it comes to this awful condition. Doctors to this day, STILL believe they are Gods - despite their privileged knowledge being increasingly opened up to the public. They are not Gods, but they are legally immune - hence their behaviour.

This video post is in memory to her immense bravery her mother speaks of.

May she rest in peace, and never be forgotten.

For the TRUTH on what ME does to people, go to:

http://www.meresearch.org.uk/
http://www.investinme.org
http://www.cfsrf.com/
http://www.ahummingbirdsguide.com
http://phoenix-cfs.org
http://www.ahmf.org
Category: Education
Tags: sophia mirza me/cfs cfs/me myalgic encephalomyelitis me m.e cfids pvfs cfs gene fatigue testing kerr wessely health

Saturday June 21, 2008, 8:21 pm
Rest in peace, Sophia. We will not forget you.

Saturday June 21, 2008, 8:36 pm
YES WE must make sure the medical community DOES NOT, THIS not secondary like heart attack, stroke as usual with M;E/CFIDS, (suicide), this diretily the disease, NEUYRLOGICAL IMMUNE ITSELF AND THEY STILL TRIED TO COVER IT, i hs sgo should have put in FIRST WOMAN KNOWN TO HAVE DIED FROM M.E./CFIDS. I hope this spreads across the world, the more exposure the better

Saturday June 21, 2008, 9:11 pm
there are 3 treatments I know of, 1 is not approved yet for near 15 years or more AMPLIGEN also for HEP C aand CANCER and HIV;AIDS, also, Imuvior tabs in Canada and from Ireland I think, and the best so far I tried was KUTAPRESSION SHOTS from Swartz in the USA , dr. long time ago I paid and he did the apa paper work to ship them up throu health canada, it 6 months of treatments the first trials, this 1994, I had much improvement and quality of life compared to what it was, paint 1 wall and be in bed for 3-4 days, go to store and could be a week, and crash with flu syptoms fm worse, light nosise sound sensory perception,k touch all get even worse. The shots far enough from going back to work, but was more than worth living, it felt more like living not surviving existing a day at a time. No other doctor would get them for me, they didn't want to do the paper work, plus I had to have the money, I have been left like this with no doctor since the malpractice, they are insane. It turns out you have to stay on the shots, and go off for awhile here and ther same with most immune therapies and the imuvior. If you are severe enough they ARE WORTH EVERY CENT IF YOU CAN GET THE MONEY TOGETHER, I tried to get them again and the doctor supposed M.E. /CFIDS specilist didnt' even know about them and refused to do the paper work. I can't wait until I can get some more let alone a neurlogist that is ahead in the field and the damage done, it nurlogical here but they still saying it not most. used to be like that for MS and prior parkisons. nite

Saturday June 21, 2008, 10:15 pm
Thanks Sunshine, I will send this tragic article out. What a shame that it always seems to take an innocent life to wake people and the medical world up.

Sunday June 22, 2008, 7:49 am
thanks so much sunshine for this tragic, but wonderful story... how marvelous for sophia's mother to have been able to do this for her... i am sure she is at peace now, knowing that others may one day benefit from what has been discovered about ME... perhaps the medical world will take notice and others will not have to suffer needlessly with inappropriate treatment as sofia did...:)

Sunday July 20, 2008, 5:29 am
I hope to see major changes soon in the way me/fibro/cfs patients are treated, both medically and emotionally. So many people are suffering alone.. without any hope for relief.

Thank you for sharing this. :)

Wednesday July 30, 2008, 6:04 am
I have RSD and FM and have had to put up with doctors who didn't believe that I had anything physical wrong with me. However, the majority of doctors that I have are very supportive and willing to treat the pain. It has turned me into a totally disabled woman requiring a power wheelchair because I am so weak. I hope this mother continues her fight to have those doctors disciplined and we should try to keep this in the public eye to further understanding.

Thank you Sunshine for bringing this to our attention!

Wednesday July 30, 2008, 8:07 am
thank you for your input, hi Dawn I googled RSD, I can relate with the all the damage I have, and FM, and M>E>, which people have no understanding of it seems unless they have it themsevles and very few specialists understand, most are in the USA. Well you are getting care and treatment now, and I hope to be getting the same sooner rather than later, it's been too long already. see you on the flip side, healing blessings. cheryl/sunshine