This community is blessed with an abundance of highly intelligent and well-informed participants. Many participants have a high degree of experience and expertise on various aspects of the Parkinson's challenge. The community provides a place for people with Parkinson’s around the world to come together and support each other. We know that connecting with others can be of great help in coping with Parkinson’s. We want to ensure that the discussion pages are being used in the best possible way.
Please take a few minutes to familiarise yourself with our Code of Conduct below
This forum is a great resource for PWPs and a place to share useful information that many PWPs can use and it is also a place where members can not only find practical solutions and support, the latest PD related news & updates, but also a place to find moral support when the going gets tough! It will be very nice to keep all of those good qualities intact for years to come!
1: the action of understanding, being aware of, being sensitive to, and vicariously experiencing the feelings, thoughts, and experience of another of either the past or present without having the feelings, thoughts, and experience fully communicated in an objectively explicit manner
also : the capacity for this
2: the imaginative projection of a subjective state into an object so that the object appears to be infused with it.
After the diagnosis I was desperate, alone and without knowing what to do, then I discovered this site. The courage and the desire to fight are back. Thank you Helen.
This forum is one of the hi-lights of my day. I feel so much better now that I read it. I am now getting information aout PD that I didn't know existed, My doctors are not very informed about PD. and sorry to say but the L.A.Parkinson's office is neither........Thank you Helen for all that you do.
This forum, along with Parkinson's News Today and Scott Simon's The Science of Parkinsons are the primary sources of 15 sources that I draw from weekly in building my database named Parkinson's Online - which currently has 3,400 items collected over the past three years.
Parkinsons Online does not have a url, it is accessible only via EverNote software as a Notebook. You download the software, available for no cost at evernote.com. Then I can give you access to the Notebook if you send me your email address.
can you send me access to the notebook? i downloaded evernote. not tech savvy so not sure I've done it correctly? but anyway, my email is sent to your acct. thxs
I have learned so much from this group and have appreciated the discussions and the support we all can provide each other. I am amazed by those with such a strong research focus. Thank you all.
Please note that a number of posts have been deleted this week following complaints by users. Once again I refer you to the code of conduct. Many thanks
My mother (age 75) has Parkinsonˇs illness. She is now in very bad condition. She canˇt walk, she barely eats anything. Doctors gave up on her. They said that she will die soon.
She cant talk, she doesnˇt respond on questions
I have heard for the late dr. Antonio Constantini and his method 's for Parkinson treatment.
Deara Eivovla, I'm very sorry about your mother and I understand your concern, Parkinson's can sometimes be overwhelming for everyone, caregiver , patient and doctors.
However a little help is always possible, but you should write the same message in the form of your personal post and not as a reply to another poster because this way it will work better. This is an easy thing to do and you will have all the help and the solidarity and the answers of the colleagues of this forum. If you have difficulties I can explain it to you better, it's a simple question of form.
can we have the names of the complainants . Can anyone gang up and send multiple complaints and get someone banned ? Is there away the rest of us can have a say or provide input. Is there an appeal process where we can speak for the accused.
Thank you Helen. Here i have come to encounter wonderful, warm intelligent people that makes me feel welcome and valued. I cherish them all. The bits of research are presented discussed and explored. It challenges me to ask questions and share my own experiences, to identify with others, to find solutions together. To realise that we are not alone.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.
Ambroxol in Parkinson's: Results of Phase ll Trial Published
I would like to apologize to members of this forum........
Qigong for PD!!!
Coconut Oil for Parkinson's - "non-clinical" trial. Please Participate
