Contact details for Dr Costantini

[Celtis]

I know that I ought to be able to find these by searching posts, but I have searched unsuccessfully all morning and have decided to just ask.

Also, how do I get to view people's profiles on this site?

Thank you all for sharing so much with all of us. When I was given my PD diagnosis with the news that it is a degenerative disease with no cure I felt quite despairing . It has been heartening to share other people's stories and to see that there are things you can do. (My neuro never mentioned exercise, vitamins or supplements)

[Hidden]

Doc email is listed on my profile which you get to by click on my picture/image

[Celtis in reply to Hidden]

Thank

[Ajssister]

Hi. Did you get it from RoyProp? I can give it to you too. Thx

[Celtis in reply to Ajssister]

Thanks. Ajssister

I have got them, busy getting details of everything to send to him. Hold thumbs for me. This looks so promising. How lucky we are to have someone to help us!

[Ajssister]

Ok. I included my brothers height, weight, age, length of time of symptoms signs, time on C/L, all meds he’s taking and all supplements he’s taking and what type of diet n exercise he’s doing plus water intake. Good luck. God bless. Keep us posted.

[Celtis in reply to Ajssister]

Thanks again! That gives me a good check list. I will post as I go along.