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3050 |
Enid Hobson |
2018-05-03T02:04:22.227 |
Needs to connect up with day of action millions missing May 12. |
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3050 |
Michel Lee |
2018-05-03T03:06:20.447 |
Due to the uniquely multi-symptom, multi-system nature of this disease, research in this area is likely to inform und... |
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3050 |
Catherine Gross |
2018-05-03T03:56:35.623 |
New research shows ME is a systemic break down of the body on a macrocellior level. Look forward to research done i... |
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3050 |
Isabel Sukkar |
2018-05-03T04:33:18.657 |
M.E. sufferers do not bring this illness upon themselves. Why then, should any M.E. sufferer not be taken seriously b... |
|
3050 |
Andrew Burgess |
2018-05-03T05:00:56.16 |
Please take this opportunity to lead the way in showing the UK how to respectfully care for people with M.E. using bi... |
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3050 |
Jacqueline Wilson |
2018-05-03T05:01:03.57 |
ME patients need all the help they can get. We have been neglected & ignored for far too long! ME is a hugely disabli... |
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3050 |
Tom Kaardal |
2018-05-03T05:39:51.073 |
A member of my family has suffered for 12 years. |
|
3050 |
Sarah Osborne |
2018-05-03T06:17:04.597 |
I have ME. I live in Wales but support this initiative |
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3050 |
Heather Tierney |
2018-05-03T07:48:49.823 |
A member of my family has ME and the lack of treatment and support she has received over the years is just shocking. ... |
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3050 |
Lindsey Patrick |
2018-05-03T08:09:52.59 |
We need health care to understand this condition |
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3050 |
A.M.Lane |
2018-05-03T08:31:36.407 |
I am signing this on behalf of a family member wrho has had M.e. for 7 years now and nothing seems to be being done a... |
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3050 |
Amy Keeton |
2018-05-03T08:39:49.657 |
I've been living with Myalgic E for a decade now, and know all too well what it does to a person's life. Sending my l... |
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3050 |
Don Fraser |
2018-05-03T08:55:02.753 |
Important that help & recognition is given to sufferers, not just in Scotland but world wide. |
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3050 |
Michael Poston |
2018-05-03T09:19:55.397 |
I am affected by ME. The best treatment for me turned out to be a respite in warm climate with a carer. I am now well... |
|
3050 |
Mrs Irene Gallacher |
2018-05-03T09:28:09.98 |
I have a relative who has suffered from this illness for a long time and was not able to continue working.\r\nAfter r... |
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3050 |
Helene Lockwood |
2018-05-03T09:46:32.967 |
A member of my family has suffered with M.E. for many years so have to give support to all, wherever they may be |
|
3050 |
Christopher Spalding |
2018-05-03T09:48:55.31 |
We need much more research into this condition. |
|
3050 |
Phil Murray |
2018-05-03T10:35:30.363 |
Improved care & biomedical research for people with MECFS must be a priority for the future. Actiono is needed now. |
|
3050 |
Nancy Wilson |
2018-05-03T11:23:05.803 |
It took 20 years to get a diagnosis of Fibro ME 20years of pain fatigue Fibro fog this should not happen to anyone. |
|
3050 |
Alison Caldwell |
2018-05-03T11:24:59.01 |
I have had M.E for 23 years and hope not to die with it. I'm 62. |
|
3050 |
Lucy B |
2018-05-03T11:25:24.26 |
I have many friends who are living with ME in Scotland who would benefit from access to specialist care. |
|
3050 |
Rose Ann-marie Slavin |
2018-05-03T11:48:13.637 |
I am Scottish but moved to England as a child. I have had ME for 8.5 years. I now realise 2 of my family members had ... |
|
3050 |
Claire Prideaux |
2018-05-03T12:21:32.36 |
I have ME. I've lived with it for decades. The fact that governments have ignored us and worse, forced treatments on ... |
|
3050 |
Iain Gill |
2018-05-03T12:38:29.22 |
A member of my family has had ME for over 20 years. I totally agree with the petition. I recently had 12 weeks chemot... |
|
3050 |
Eilidh Hewitt |
2018-05-03T13:48:46.513 |
I was struck down with severe ME 30 years ago it came like a bolt from the blue. Then I was profoundly shocked to fin... |
|
3050 |
Jeff Sumida |
2018-05-03T13:56:27.42 |
In the first few years, doctors didn't believe me. They said that if you aren't going to exercise, then I can't help ... |
|
3050 |
Suzanne Chadwick |
2018-05-03T15:04:52.663 |
It is really INSANE that anyone would think that this disease could be fixed by behavioral therapy. INSANE! How about... |
|
3050 |
Catherine Velez |
2018-05-03T15:37:19.683 |
I'm 53 years. I have ME for 30 years. My hope is to have a treatment or a cure. |
|
3014 |
Clare Chalmers. |
2018-05-03T15:39:43.03 |
So many families have been abused by unlawful data sharing. Practitioners remain confused to this day and still abus... |
|
3050 |
Catherine Velez |
2018-05-03T15:43:09.827 |
I'm 53 years. I have ME for 30 years. My hope is that I can have a treatment to give relief or a cure, and the same f... |
|
3050 |
Ms. K. Stewart |
2018-05-03T16:03:55.237 |
I love Scotland and while attending school there I was in the beginning stages of fibromyalgia, later being determine... |
|
3050 |
Debby Smith |
2018-05-03T16:31:34.957 |
As a former Scot living in Canada afflicted with this condition, I support the three petitions to Parliament. |
|
3050 |
Elizabeth Laird |
2018-05-03T17:52:58.577 |
There are many people living with this condition, but would greatly benefit from treatment. I have several friends w... |
|
3014 |
Tristram Llewellyn Jones |
2018-05-03T18:00:33.377 |
This whole slippery business of extracting personal information needs to be comprehensively stopped.\r\n\r\nWhy not h... |
|
3050 |
Julie Crampin |
2018-05-03T18:39:54.037 |
I have had ME for 25 years. I support my fellow sufferers wherever they are. |
|
3050 |
Ms karen price |
2018-05-03T19:25:40.48 |
This is such a debilitating disease, I was diagnosed with M E in 2001 but now I am awaiting an mri scan as lumber pun... |
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3050 |
Tricia M |
2018-05-03T19:44:00.39 |
ME is a serious and debilitating illness that deserves serious research funding. Patients have been in desperate nee... |
|
3050 |
Jo Bruce |
2018-05-03T21:30:22.047 |
I have always been a supporter of the NHS but the biggest barrier I have faced, apart from ignorant employers who bre... |
|
3050 |
Ann Higgins |
2018-05-03T21:54:58.613 |
Care for the unfortunate people with ME |
|
3014 |
Catherine Stirton |
2018-05-03T22:27:41.633 |
Well done for highlighting this issue and for standing up to the Scottish Governments half baked attempts at deciding... |
|
3050 |
Angela Barnard |
2018-05-03T23:09:01.45 |
Signing on behalf of my friend who is suffering from ME-CFS. I have watched her decline and am humbled by her resolv... |
|
3050 |
Jennifer Murray |
2018-05-03T23:15:30.513 |
I'm not a citizen of Scotland, but as someone who was a productive citizen of the U.S. until I became ill 22 years ag... |
|
3050 |
Anna Maria Woynillowicz Kemp |
2018-05-04T00:00:43.567 |
I lived in Scotland for one and half years. The medical professionals need to be much more aware of current research ... |
|
3050 |
S Lauryn Douglass Hayden |
2018-05-04T04:12:16.67 |
This is a terrible disease with a viral basis. Numerous US studies have shown the biological basis for compromised me... |
|
3050 |
DS George-Jones |
2018-05-04T04:59:08.2 |
Please find a treatment for ME. It is a human rights issue. We are tired of suffering in silence. |
|
3050 |
Elizabeth Edwards |
2018-05-04T05:29:57.72 |
Please help. |
|
3050 |
Tamara Anderson |
2018-05-04T06:38:15.623 |
It is necessary and remains without cure and mainly impacts women and we will become lost without the research. The l... |
|
3050 |
Myrtle Little |
2018-05-04T08:56:43.757 |
I have had ME for 20 years, it makes me cross and sad about people and especially children not being believed and pun... |
|
3050 |
Kathleen Anderson |
2018-05-04T09:34:48.65 |
Please put more research into ME! |
|
3050 |
Martin Dillon |
2018-05-04T12:15:57.83 |
The present treatment options for people will M.E.are almost non existent and often harmful. The approach from G.P. v... |