home
a-z of conditions
forums
news
about us
See all conditions
Nerves & brain
Parkinson's disease
Forum
Resources & Information
Subject index
Credits
Full list of topics
Discovery :
Early symptoms
Path to diagnosis
Getting the diagnosis
Telling others
Information
Causes of Parkinson’s disease
Treatment :
Levodopa
Dopamine receptor agonists
Managing medication
The operation: Deep Brain Stimulation
Professional help
Self help
Parkinson's symptoms :
Tremor, loss of control
Movement
Embarrassing symptoms
Mental disturbances
Living with Parkinson's disease :
Redefining yourself
Keeping going
Work, career, benefits
Driving and journeys
Support and support groups
Parkinson’s UK and Parkinson’s disease nurses
Now and the future
Caring, care and carers
Advice to others
Search the whole site
Search in this condition
Parkinson's disease
Subject index
Topic
Nerves & brain
>>
Parkinson's disease
>>
Parkinson’s UK and Parkinson’s disease nurses
>>
Parkinson’s UK and Parkinson’s disease nurses
Parkinson’s UK and Parkinson’s disease nurses
>>
Parkinson's disease
>>
Parkinson’s UK and Parkinson’s disease nurses
>>
Parkinson’s UK and Parkinson’s disease nurses
Parkinson’s UK and Parkinson’s disease nurses
Clip
Nerves & brain
>>
Parkinson's disease
>>
DBS
>>
Joe - Interview 32
>>
Joe had found the PDS very helpful, if a bit unrealistically upbeat, when things were very difficult for him before he had Deep Brain Stimulation.
Joe developed Parkinson’s disease while in his 40’s. Deep Brain Stimulation when he was 60 produced a dramatic improvement in his symptoms.
Nerves & brain
>>
Parkinson's disease
>>
3-4 years
>>
Peter - Interview 11
>>
Peter got the PDS to help him put together an information pack for people joining his local branch.
Peter was diagnosed six years ago. He experiences tremor, freezing and rigidity and considerable problems sleeping at night. He takes slow release Sinemet and Amitriptyline.
Nerves & brain
>>
Parkinson's disease
>>
3-4 years
>>
Angela - Interview 10
>>
Angela admires the PDS and questions the value of a proliferation of separate organisations all trying to find a cure for Parkinson’s Disease.
Angela was diagnosed in 2004 with Parkinson’s Disease. She takes Ropinirole, Orphenadrine and Requip. Acupuncture has helped her symptoms.
Nerves & brain
>>
Parkinson's disease
>>
5-7 years
>>
Karen - Interview 12
>>
When Karen first joined PDS she thought she was the only person around with early onset PD. PDS helped her to set up a group which now has 40 members.
Karen was 34 when she first started having symptoms down the right side of her body. She experiences a lot of freezing and festination and some dyskinesia.
Nerves & brain
>>
Parkinson's disease
>>
3-4 years
>>
Peter - Interview 11
>>
Having campaigned for a specialist nurse Peter describes his feelings now they have one.
Peter was diagnosed six years ago. He experiences tremor, freezing and rigidity and considerable problems sleeping at night. He takes slow release Sinemet and Amitriptyline.
Nerves & brain
>>
Parkinson's disease
>>
8-12 years
>>
Ruth - Interview 26
>>
Ruth described the brutality of the original delivery of her diagnosis, her immediate reaction, ways in which people have been able to help and how th
Ruth was diagnosed 9 years ago. She has tremor, stiffness, difficulty sleeping and tiredness. She has to pace herself. Some days are easier to cope with than others.
Nerves & brain
>>
Parkinson's disease
>>
5-7 years
>>
Fiona and John - Interview 09
>>
Fiona found the helpline discretely sensitive to her needs and its trained nurses helpful and sympathetic.
Fiona’s husband was diagnosed in 2003 at the age of 42 with early onset Parkinson’s Disease. He has continued to work full time.
Mail to a friend