|
2964 |
Joan Coverley |
2018-03-30T08:39:55.53 |
I live in a conservation village on the Moray Coast. I had my house painted last year, no change to colours or anythi... |
|
2964 |
Derek Smith |
2018-04-02T13:22:44.473 |
Residents of the garden suburb should not have to pay for planning permission to make small changes to their properti... |
|
2964 |
James Williamson |
2018-04-02T22:02:27.387 |
To deny or charge a householder from say a patio or shed or a decking area or a small summer house is surely an infri... |
|
2964 |
Michael Paterson |
2018-04-04T09:45:58.127 |
Agree with the rationale of the request |
|
2964 |
Michael Paterson |
2018-04-04T09:55:58.927 |
As a member of the committee I agree with the rationale of the wording of the Petion |
|
2964 |
Louise Hunter |
2018-04-08T23:46:23.803 |
Very unfair |
|
3050 |
Ann Forbes |
2018-04-23T21:10:14.647 |
I fully support this petition .\r\n I have contacted Carol Monaghan MP's office to inform of this petition (in case ... |
|
3050 |
Richard Vallee |
2018-04-25T18:02:27.253 |
Please end the discrimination against ME patients. \r\n\r\nNot a single country has found the courage and will to do ... |
|
3050 |
Yvonne Cassidy |
2018-04-25T18:11:14.737 |
I would just like to be treated like an normal human who is I'll and not have people or doctors looking at you as if ... |
|
3050 |
Fiona Culbert |
2018-04-25T19:06:56.213 |
Compared to England ME CFS support is worse than appalling. I have watched my family members health, education and fu... |
|
3050 |
Caroline Cecil |
2018-04-25T19:13:05.4 |
Something desperately needs to happen NOW for ME sufferers - there is basically nothing for us, no treatment, no supp... |
|
3050 |
Maureen McIntyre |
2018-04-25T19:24:31.06 |
For me, the top priority by far is funding for biomedical research. We need to know the cause and, hopefully identif... |
|
3050 |
Louise Ann McAllan |
2018-04-25T19:32:32.123 |
I was recovering from ME and was pushed into Graded Exercise Therapy. It made me bed bound and still doctors conside... |
|
3050 |
Janet Sylvester |
2018-04-25T19:33:26.28 |
There is a desperate need to support people with ME in Scotland. The fact that there is only one specialist nurse (in... |
|
3050 |
Nicky Delacey |
2018-04-25T19:35:09.64 |
Please please please can we have done proper research, support, care and effective treatment for so many people affe... |
|
3050 |
jacqueline miller |
2018-04-25T19:45:43.127 |
If you already know it is bad or wrong, and do it anyway, you commit a sin difficult to redress. |
|
3050 |
Jackie Richards |
2018-04-25T20:41:44.79 |
GPS and other health professionals need to be educated more about treatment and care of ME patients. |
|
3050 |
Helen Love |
2018-04-25T20:49:48.32 |
My family member has ME and this would benefit her greatly. |
|
3050 |
Gregory Cockrell |
2018-04-25T21:01:04.027 |
If Scotland wants to be a world leader. Here is your chance. Look after the downtrodden. |
|
3050 |
Carol Ann McGregor |
2018-04-25T21:30:07.78 |
I have been missing from my life for 25 years. I was bedbound for 7 years and for the rest virtually housebound with ... |
|
3050 |
Karen Shankland |
2018-04-25T21:36:49.157 |
My family member suffers with ME and I have watched him suffer for many years. I have tried to support him with the e... |
|
3050 |
Ann Gammack |
2018-04-25T21:57:37.987 |
Please take action to help people with this devastating condition so that they are no longer missing from society. |
|
3050 |
Aidan McEvoy |
2018-04-25T22:24:10.82 |
This affects a member of my family in Dumfries. Her treatment has been inadequate for many many years. A review is t... |
|
3050 |
Amanda Hamza |
2018-04-25T22:32:40.57 |
I have fibromyalgia with chronic fatigue, during my worst I needed help to do everything but I am thankful to be doin... |
|
3050 |
Shona Forrester |
2018-04-26T06:57:22.923 |
Knowing children that are affected by this condition l do hope this petition can begin to make a difference to those ... |
|
3050 |
jane Mcnamara |
2018-04-26T07:00:50.803 |
Despite offering support and advice I ultimately feel as a Gp I am unable to offer patients what they need - a second... |
|
3050 |
Arlene Haydock |
2018-04-26T07:27:35.197 |
I have suffered for years with ME. Been disappointed that there is very little know about this illness and no help pr... |
|
3050 |
Alison Cormack |
2018-04-26T08:16:56.53 |
I have had ME for 6 years, am registered disabled, unable to work, have to use a wheelchair when outside and not able... |
|
3050 |
Nancy Wilson |
2018-04-26T09:25:55.167 |
I have Fibromyalgia ME my life is limited although I can manage it's a fight to stay upright and keep going . I was m... |
|
3050 |
Mary Ross |
2018-04-26T11:11:14.143 |
This is a much misunderstood condition and needs more doctors and practitioners to take it seriously. More research a... |
|
3050 |
cait ni cadlaig |
2018-04-26T11:21:08.003 |
I have ME I also have Fibromyalgia .The 'fibro' affects me at times more than the ME But at times both kick in and it... |
|
3050 |
Kate Chaplin |
2018-04-26T11:52:34.953 |
I know someone with ME in Scotland, near Inverness) whose gp doesn't believe him! Intense day and age! With all the ... |
|
3050 |
Jocelyn Turley |
2018-04-26T12:49:55.053 |
As an M.E. patient of 9 years (with more severe symptoms & disability in the past 4 years), I understand first hand, ... |
|
3050 |
Emma edwards |
2018-04-26T12:51:30.147 |
Please support this |
|
3050 |
Chris Afford |
2018-04-26T12:59:52.447 |
Support for ME patients is much needed and long overdue. It would be a real statement of intent were the Scottish gov... |
|
3050 |
Norman Mackenzie |
2018-04-26T13:03:39.353 |
A member of my family has suffered ME for nearly 30years now & doctors still have no idea how to treat this disabling... |
|
3050 |
Claire Ryan Heatley |
2018-04-26T13:05:15.477 |
The old model of treating the patient and the myriad of complex systems involved in this condition in isolation will ... |
|
3050 |
Patricia Davis |
2018-04-26T13:47:29.217 |
CBT and GET do not work and do harm to people with ME. Please remove them from treatment guidelines, and provide pro... |
|
3050 |
Simin Ghatineh |
2018-04-26T13:53:12.203 |
We need proper biomedical research |
|
3050 |
sue m. |
2018-04-26T14:31:51.74 |
I know there is no treatment, but support of the same kind as delivered by Marie Curie or Macmillan nurses would be v... |
|
3050 |
Helen Hyland |
2018-04-26T14:43:06.227 |
Too many lives have been wrecked by this cruel illness. One ME nurse for the whole of Scotland is woeful. These peo... |
|
3050 |
JOSEPHINE |
2018-04-26T14:46:28.79 |
I sign this petition for all future M.E sufferers. In the hope that one day, stigma will be replaced with hope of an... |
|
3050 |
Rob Daley |
2018-04-26T14:49:38.773 |
Present understanding by GPs of the challenges of ME sufferers is disgraceful. Lack of appropriate understanding and ... |
|
3050 |
Mandy Singh |
2018-04-26T15:08:02.697 |
scotland lead the way! |
|
3050 |
Jo |
2018-04-26T15:28:06.123 |
This is essential...it took me over 15 years to get a proper M.E diagnosis....and I had to pay for a private consulta... |
|
3050 |
Julie |
2018-04-26T16:23:03.02 |
Help needed all over the UK. Could Scotland be the leading light? Others may follow. |
|
3050 |
Barbara Lees |
2018-04-26T16:24:39.443 |
I live in England. A family member was born in Scotland.\r\nI have ME.\r\nI have Scottish relatives who have friends ... |
|
3050 |
Barbara Lees |
2018-04-26T16:35:44.773 |
I would like to see improved care for people with ME in Scotland.\r\nI would like to see evidence that the governmen... |
|
3050 |
Sylvie Jourdan |
2018-04-26T16:37:48.837 |
People with M.E need to get real treatment. GET and CBT (based on fake illness beliefs) at best do not work, at worse... |
|
3050 |
Esther |
2018-04-26T16:57:37.743 |
This a terible disease please help us! |