|
3050 |
L.Hunter |
2018-04-26T17:09:43.357 |
ME-CFS is a terrible ailment and I am completely left to my own devices with it. My GP is so overworked, she doesn't ... |
|
3050 |
L.Hunter |
2018-04-26T17:13:26.98 |
My GP is overworked and received no training about ME-CFS at medical school. She does not have the time to read and c... |
|
3050 |
Sharon Leitch |
2018-04-26T17:31:30.733 |
My friends daughter is affected by this awful condition - it is heartbreaking to see what she goes through everyday -... |
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3050 |
Rhona Laing |
2018-04-26T17:49:31.063 |
People are suffering and nobody cares |
|
3050 |
Jane Moodley |
2018-04-26T19:37:33.677 |
Please research ME |
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3050 |
John Grant |
2018-04-26T20:26:49.497 |
Local dedicated M.E teams in each trust |
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3050 |
Helen |
2018-04-26T20:41:49.04 |
I hope petition helps |
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3050 |
Rosamund Lee-Harper |
2018-04-26T20:45:56.22 |
I have had ME for 10 years. I am not aware of any me nurse in Surrey. I see an immunologist every 6 months..I have ha... |
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3050 |
Christie Love |
2018-04-26T20:49:24.33 |
Please help those who need it so desperately. |
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3050 |
Melanie meston |
2018-04-26T20:59:25.19 |
Signed and shared |
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3050 |
Pauline Ross |
2018-04-26T21:06:58.683 |
It is totally heartbreaking how little research money is available for ME....also the lack of knowledge and understan... |
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3050 |
eileen munro |
2018-04-26T21:15:05.903 |
People have t stop dying or being put under mental health care due to lack of proper medical care or deliberate misle... |
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3050 |
Kim foxon |
2018-04-26T21:26:29.937 |
People with M.E. desperately need support and action now! |
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3050 |
Toni Higgs |
2018-04-26T22:35:44.913 |
Myalgic Encephalomyelitis is as devastating as Multiple Sclerosis, Parkinson's Disease, AIDS and Cancer yet it gets t... |
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3050 |
Richard Shorter |
2018-04-26T22:42:56.75 |
How can it be right that such a severe illness can have no money spent on research when the first thing we were told ... |
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3050 |
Sandra Wilson-Greene |
2018-04-26T22:54:33.58 |
All aspects of general health should be represented whithin our NHS and there should definitely be a specialist with... |
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3050 |
Katrine |
2018-04-26T23:08:34.513 |
Together we will change the world |
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3050 |
Peter Russell |
2018-04-26T23:27:36.303 |
Identification may have improved, but the lack of initial recognition is part of a very inconsistent pattern of care.... |
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3050 |
alan tipping |
2018-04-27T02:09:35.993 |
why is it advantageous for governments to ignore the truth when it comes to complex diseases. these diseases will not... |
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3050 |
Erica Eele |
2018-04-27T07:45:52.147 |
Please invest in biomedical research and support programs for people with MECFS, similar in scale to support programs... |
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3050 |
Ann Courtney |
2018-04-27T08:01:45.523 |
Please treat us with digity |
|
3050 |
Hannah Grundy |
2018-04-27T09:15:51.657 |
I'm signing to help my friends and family in Scotland that have either been affected by this illness or could be in t... |
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3050 |
maralyn hepworth |
2018-04-27T09:55:12.917 |
Things MUST change. It ruins not just the lives of sufferers, but their families to. |
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3050 |
Anna Pratt |
2018-04-27T10:09:16.197 |
GET should never be prescribed as an efficient treatment for any stage of M.E. and I am shocked it still is !! CBT o... |
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3050 |
Brenda Young |
2018-04-27T10:13:50.903 |
Please help m e sufferers and other disabilities. |
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3050 |
Dorothy McNicoll |
2018-04-27T10:51:12.113 |
ME sufferers are desperate for research into the causes and treatment of the disease. Let's have some real action no... |
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3050 |
Angela Holm |
2018-04-27T12:46:30.773 |
People are suffering so deeply with so little hope in Scotland. Professionals need to be informed and we must stop t... |
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3050 |
Kim Foxon |
2018-04-27T13:01:19.073 |
People. With M.E. desperately need support and funding for appropriate treatment! |
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3050 |
Alison Orr |
2018-04-27T13:52:09.487 |
Please refer to the International Consensus Criteria for a proper definition of what ME is. Please use Invest in ME, ... |
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3050 |
ann birds |
2018-04-27T15:16:27.013 |
we all need proper treatment for this vile evil illness.. |
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3050 |
Jannik |
2018-04-27T16:27:02.81 |
Without research for ME hundred of thousands people will die the next years due to no treatment or wrong treatment (e... |
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3050 |
Emma Gardner |
2018-04-27T17:02:57.253 |
Vital that funds are allocated for research and appropriate support is given to M.E. patients. \r\n\r\n\r\n\r\n |
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3050 |
FM |
2018-04-27T17:40:46.86 |
Please take action soon. |
|
3050 |
Teresa Kavanagh mckie |
2018-04-27T17:43:48.783 |
A member of my family contracted ME in her teens now 27 yrs old and confined to a wheelchair as classed as too severe... |
|
3050 |
Linda McMillan |
2018-04-27T19:01:18.177 |
For 17 years I suffered in silence because the medical professionals in my area ignored my symptoms and diagnosed me ... |
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3050 |
Bonnie Ruggiero |
2018-04-27T21:36:22.083 |
I have MEand I'm from the United states. I've been suffering for 23 years. We so desperately need funds for research,... |
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3050 |
Leonie watt |
2018-04-28T05:43:41.233 |
Its shocking the lack of treatment people have had in this day and age. About time wrongs were righted. |
|
3050 |
Brenda marshall |
2018-04-28T06:10:53.987 |
I would like to see more care for people with ME in Scotland |
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3050 |
Sarah Cockrell |
2018-04-28T10:21:15.223 |
We need more hands on support. We need GPs to be trained in it. We need it to be taught correctly at medical school- ... |
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3050 |
Suzanne |
2018-04-28T10:37:57.893 |
If Scotland lead England no Ireland will follow\r\nFingers crossed \r\n8 years bedbound\r\nMissing my life |
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3050 |
CJ |
2018-04-28T11:14:14.607 |
This is an extremely important petition to sign. I have had ME for the last 3 years. My GP recommended me GET(Graded ... |
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3050 |
Helen Smith |
2018-04-28T11:54:25.927 |
In 30 years of ME, regrettably doctors, while in my experience empathetic have no idea how to find a care pathway for... |
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3050 |
Carol Mathieson |
2018-04-28T13:08:28.373 |
I would definitely like to see very much improved treatment and care for people with ME in Scotland. |
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3050 |
Miriam Connor |
2018-04-28T13:11:32.4 |
Seven years of ignorance has robbed a family member of her mobility and self esteem. First do no harm... NHS funds wa... |
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3050 |
Lucina Alwyn |
2018-04-28T13:20:15.167 |
I have suffered from this devastating disease for 21 years and it has ruined my life. Yet no treatment on horizon |
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3050 |
J kelly |
2018-04-28T13:40:10.2 |
We need medication like m.s patients get , why are we not treated the same .i have been battling for many ,many years... |
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3050 |
Patricia Brown |
2018-04-28T14:06:31.63 |
There millions suffering from ME all over the world. We need help NOW. Some are dying and others feel like they'd dyi... |
|
3050 |
Sandra Dillon |
2018-04-28T17:39:06.237 |
I think the Scottish Government should be doing more to help fund research in to a cure or treatment to help all thos... |
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3050 |
Richard Brown |
2018-04-28T17:59:38.943 |
Governments worldwide need to wake up to the fact that this illness is real. It doesn't kill large amounts of people ... |
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3050 |
brenda berger |
2018-04-28T19:15:53.673 |
My family member suffers from me in scotland |