Page created by: Robert Denotsko

I`m new to this PD & don`t know how the correct way to deal with it . I am currently contesting a disability denial at the moment. I don`t talk with most of my family anymore, partially due to non-recognition of medical issues, both on my part and theirs. Any type of help would be beneficial as I have no income at the moment. It`s very depressing knowing you can not do most things you normally would do if you were healthy.I have no residence other than a friends, but this is only temporary, and difficult to deal with. It`s like being dead inside when you can`t provide for yourself.
Any donations can be received at address::( until an account is set up}
Robert Denotsko
P>O>BOX 172
Hazleton, PA 18201
or to BTC address 1DhNfLHei4UsDBKE1ciheiyUpAykB36p9a
Well, Winter isn`t far off & I`m a bit worried about a place to live and changing Dr`s to a new location again.
When you already have a diagnosis of PD and then receive a letter that states confirmation of Lyme (western Blot)?? There is very little help available for those that have a hard time with memory loss.

Thank You, for bearing with me, as I am new to dealing with this.
Robert Denotsko

I think back now at the things I could have done different & wonder if when I was younger, did I notice the signs of others, with similar medical issues? It`s very difficult feeling that your getting healthy if your memory doesn't always allow you to, but ,waking up every day to the same feeling,,like rebooting your PC, The stress of trying to remember what to do next ,from a waking point,gets others pissy and upset because you have to ask more than a few times. The shaking and involuntary movements just make it that much harder to adjust to relearning whats going on when you have to realize and accept it again and again. Keeping this as a type of journal,Im hoping will help. Maybe it has helped others?