II has been suggested that Neuroaid iI reduces the symptoms of PD. It is generally used for stroke patients. I would be interested to to know whether this product has been tried by others. Has it been helpful? Are there any side effects?

My brother has Parkinson’s and is finding that at night he has sweats so much so bed is wet. The doctors say that this is a side effect of the medication. Anyone else have this problem

I have hard time swallowing so I build up saliva to the point of having to put my head over the sink.I was told to get a bed that I can raise up so I won't aspirate in the middle of the night I tried botox in the saliva gland and it helped for about 10 weeks I went back at twelve weeks had the shots. but they didn't work so now they want to raise the dosage ..anybody experience this issue

Anyone else find that the corners of their mouths are ever so slightly allowing liquid to occasionally drip out? I've also been inadvertently biting the inside of my lower lip a lot. Just subtle little changes I'm noticing, can anyone else relate?

I have problems with my speech. I tend to slur. I have been at a number of neurologists in South Africa. As I am also moving slower and Carbidopa seems to work, I take 5-6 tablets a day.

I also take Requip 4mg.

Lately I have developed problems with drooling. Carbidopa appears to assist with drooling.

What do you think?

I have 4 major concerns; slowness, speech, drooling and getting up from a chair. I do not have any other “typical” symptoms.

Should I get another medical opinion?

My issue mostly is swallowing anything like bread, crackers etc. the issue is hard for me and I’m having trouble with this because it’s all new and different.
My physician hasn’t discussed this with me. I’m felling lost. She said I’m in early stages. Will this get worse?