|
3050 |
Angela Miller |
2018-04-28T20:45:43.747 |
We need to move treatment forward. |
|
3050 |
Dale Newlands |
2018-04-28T20:54:32.013 |
I think it is time that the Scottish government funded clinics and a centre of excellence for Me in Scotland |
|
3050 |
Beryl Armstrong |
2018-04-28T21:08:47.877 |
I gave know friends and colegues diagnosed with ME as far back as 1990 and this needs to be recognised as one needs e... |
|
3050 |
Denise Nevill |
2018-04-28T21:38:08.003 |
Patients must be listened too \r\nChange is needed now |
|
3050 |
Celia Bowhay |
2018-04-28T22:25:09.607 |
This disease needs serious research funds . |
|
3050 |
Michaela Sanders |
2018-04-28T22:29:14.823 |
As a patient of this illness, the suffering is indescribable. The fact we are overlooked because of how sick we are -... |
|
3050 |
Morag Thornton |
2018-04-29T00:20:32.7 |
People suffering ME need to be acknowledged \r\nThey need an official diagnosis so they can be taken seriously \r\nPe... |
|
3050 |
Irene. |
2018-04-29T10:04:29.673 |
I'll now over 30 years we appear to be going backwards in treatment and acceptance |
|
3050 |
Diane Smail |
2018-04-29T10:49:07.097 |
Scotland needs more help with M.E, more medical staff, more recognition and support for sufferere's. |
|
3050 |
Elena Gimson |
2018-04-29T12:18:06.437 |
Due to the lack of professional care and told to just push through by doctors a member of my family went from mild to... |
|
3050 |
Sarah Griffiths |
2018-04-29T20:54:47.903 |
M.E. sufferers are treated criminally and if it was any other serious disease there would be an out-dry. M.E. is a mu... |
|
3050 |
Ann Forbes |
2018-04-30T12:35:19.34 |
Please speak to Carol Monaghan MP who has an excellent grasp of this subject.\r\nPlease recommend that GET and CBT th... |
|
3050 |
Sarah McIntyre |
2018-04-30T20:47:38.227 |
ME just appaling. Are there any alternative treatments that work? |
|
3050 |
Kristin Stempf de Vargas |
2018-05-01T02:10:46.973 |
Studies have found that ME places a greater burden on those afflicted with it than do many of the most serious diseas... |
|
3050 |
Sheila Wilson |
2018-05-01T08:56:24.553 |
Stop GET it's left me 90% bedridden |
|
3050 |
Rebecca French |
2018-05-01T11:46:39.843 |
I was first diagnosed with ME in 1998. Since that time I have had no specialist care for the condition. I am housebou... |
|
3050 |
Muriel Mackenzie |
2018-05-01T17:30:48.333 |
I will always sign petitions for neurological conditions |
|
3050 |
Pat Moncur |
2018-05-01T21:37:14.173 |
Scotland has a very good record for good health care and research, but we do need to do more for me sufferers |
|
3050 |
Christine Berry |
2018-05-02T10:10:04.487 |
I have suffered with M.E. for 23 years. I've been through a really bad time for the past two years. I only have two g... |
|
3050 |
Christine Berry |
2018-05-02T10:11:01.69 |
I have suffered with M.E. for 23 years. I've been through a really bad time for the past two years. I only have two g... |
|
3050 |
Marco Cattaneo |
2018-05-02T10:11:38.61 |
A member of my family is affected by this terrible illness, which needs to be recognised as such by governments, heal... |
|
3050 |
David Mcguinness |
2018-05-02T10:13:00.423 |
We need to be as one |
|
3050 |
R L Bradley |
2018-05-02T10:14:06.863 |
Id like to see an improvement in care and treatment of all ME patients worldwide. Start in scotland and show the wor... |
|
3050 |
Emily Burns |
2018-05-02T10:14:48.657 |
As a doctor and a scientist who has worked in biomedical ME research it is clear to me that a review is urgently need... |
|
3050 |
Pam Kent |
2018-05-02T10:16:45.627 |
I would like a similar petition to be presented to the English parliament. |
|
3050 |
Lavinia Capogna |
2018-05-02T10:17:56.253 |
Solidariety with M.E patients in Scotland |
|
3050 |
Gill Harrod |
2018-05-02T10:20:03.74 |
Please give appropriate support to ME suffers. Making them exercise can cause worse pain. More research into this con... |
|
3050 |
Alex Cheung |
2018-05-02T10:20:54.99 |
Scotland could lead the way for the rest of the UK to find solutions to this very debilitating chonic condition. Fres... |
|
3050 |
Raymond Henderson |
2018-05-02T10:21:53.897 |
Urgent reviews of this debilitating illness required to help us ME sufferers |
|
3050 |
Arthur B. Ranken |
2018-05-02T10:24:54.003 |
I am an activist for the Australian Government to fund research, treatment awareness and publicity into this this sho... |
|
3050 |
Marian Anderson |
2018-05-02T10:28:55.363 |
M.E. deserves a break! Not enough research, no treatment or cure. Failed management strategies have been harmful to... |
|
3050 |
Nicky Delacey |
2018-05-02T10:30:53.6 |
Please let us have recognition, support and an effective treatment nationwide for people with cfs me |
|
3050 |
Julia Reid |
2018-05-02T10:32:10.927 |
Justice for people with ME means a fair allocation of funding commensurate with the burden of disease in research, me... |
|
3050 |
Sharon goodwin |
2018-05-02T10:36:13.333 |
This suffering as gone on too long . We need help . |
|
3050 |
Lyn Bowman |
2018-05-02T10:39:22.663 |
Congrations on this initiative. |
|
3050 |
Laura Steckler |
2018-05-02T10:41:32.913 |
desperately needed! |
|
3050 |
Edwin Thwaites |
2018-05-02T10:41:58.46 |
Scotland has an opportunity to be the world leader in ME research and care. Take it |
|
3050 |
Sam Pearce |
2018-05-02T10:43:30.723 |
I was born in UK but moved to South Africa when I fell ill with ME 25 years ago as I could not access benefits and wa... |
|
3050 |
Susan Grundy |
2018-05-02T10:49:46.523 |
A member of my family lives with this debilitating condition which is still very much misunderstood. More research in... |
|
3050 |
Christine Knott |
2018-05-02T10:55:38.273 |
American researchers have found something in the plasma are shutting energy cells down. The UK are way behind in thei... |
|
3050 |
Keith Bradbury |
2018-05-02T11:02:57.477 |
I am a sufferer of 33 years |
|
3050 |
Jonathan Myall |
2018-05-02T11:11:18.637 |
Would be so good for Scotland to take a lead but would be good for the UK as a whole too |
|
3050 |
Brendan W Robinson |
2018-05-02T11:17:22.467 |
Why has this vile disease been left for only the patients and their families to deal with? Where's government help in... |
|
3050 |
Fred Vintner |
2018-05-02T11:19:39.823 |
30+ years of my life with this condition and healthy politicians have little interest or curiosity about how one in a... |
|
3050 |
Penelope Evans |
2018-05-02T11:23:00.967 |
M.E. is a very debilitating illness affecting thousands of people.Funding for medical research must be allocated to t... |
|
3050 |
Ruth Wiegratz |
2018-05-02T11:26:03.073 |
I've suffered long enough. |
|
3050 |
Michael Field |
2018-05-02T11:30:17.667 |
A member of my family has been diagnosed with a MILD degree of ME.. When I see how even this level of the disease has... |
|
3050 |
Roseann Airens |
2018-05-02T11:35:28.623 |
I have had M.E. for almost 20 years. We need more research into this misunderstood illness and support to help us adj... |
|
3050 |
Betty |
2018-05-02T11:38:00.703 |
Get rid of the harmful GET and CBT program. Many people are permanently disabled because they did this program! Fund ... |
|
3050 |
Deborah Causer |
2018-05-02T11:38:49.813 |
People with ME want justice and ethical science. |