Unmatched Information! : I don't know where... - Cure Parkinson's

Cure Parkinson's

26,583 members27,897 posts

Unmatched Information!

Don_oregon_duck profile image
5 Replies

I don't know where I can go to get such great information and advice and feel very comfortable about it, than this Health Unlocked Parkinson's community. I sure hope the other HU communities are as knowledgeable, friendly and kind as this group is, but I don't know that.

I do know how our great circle of support, really gives me piece of mind that about every treatment program available, for Parkinsons', is represented here.

Think about this. I tell my wife, I am going to post my question on HU Parkinsons' asking if anyone is treating their health issue like I am, to see if I am normal. 50 people respond, each with the solution that works for them and none of them are like mine. I turn to my wife and say, "I am normal. I am just like every one else. Nobody treats their issues like I do." That certainly makes having this disease a little more bearable, don't you think?

Written by
Don_oregon_duck profile image
Don_oregon_duck
To view profiles and participate in discussions please or .
5 Replies

The only drawback I see here is the high rate of information flowing through HU.......it is so fast sometimes that I miss a lot of great posts!

Art

Don_oregon_duck profile image
Don_oregon_duck in reply to

The ones you missed probably would not have worked for you anyway. That is why you were directed to the ones you did read. Hee hee

jeeves19 profile image
jeeves19

Anther frustration is that we learn so much together then try to explain or share with our clinicians but they just stare at you as if you’re talking another language! My neuro exclaimed in my last visit that exercise could definitely not reverse elements of the disease despite many anecdotal tales and academic studies suggesting otherwise.

Don_oregon_duck profile image
Don_oregon_duck

Do not forget. The doctors must strictly follow the approved treatments as allowed by the FDA. And the FDA obtains the clinical trial findings from the drug companies that sponsor them. They can't listen to you and me, at least officially they can't. Many begin to see the trap they are in and try to find ways to use alternative treatment programs. If a drug company paid for a study to determine if exercise helps, they, most likely, would find that it does, then your neuro could agree with you.

Springfield78 profile image
Springfield78

So grateful to all of you! Supportive info from around the world...thank you!

Not what you're looking for?

You may also like...

Relationships

My wife and I got into a fight yesterday. I don't even know what it was really about, but I think...
Joealt profile image

Driving and DVLA

I recently informed the DVLA of my condition atypical parkinsons received a reply within a few...
steph02 profile image

Ketogenic diet resource website on the Internet

Since I was diagnosed as having Parkinson's eight years ago, like many PwP's I did a lot of...
Norton1 profile image

Subjective thoughts on the Gloves

Many of us are very concerned about building these gloves for our loved ones. But how do the folks...
Furch profile image

What's up Doc

I am very fortunate to have an amazing care team. A trio that includes my Doctor, my Neurologist...

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

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.