How PD affects me...

[Ianfrizell]

Hi all

This is a link to my vlog about how PD affects me.

youtube.com/watch?v=y2zWEaZ...(Not working as expected?)

Cheers,

Ian

[Seamus6]

Keep up the good work!

... Wondering if you had any luck obtaining Exenatide? .. Saw my PD nurse this week, she was very upbeat about it - I think it's now in Phase 3 trials.

[Ianfrizell in reply to Seamus6]

I'm still trying to get exenatide. My London neurologist was supportive and was trying to sort it out for me. I'll chase her up when I chase the speech therapist!

Cheers,

Ian

[S70AWD]

Thanks for an honest and heartfelt assessment of your PD status. Knowing what others are going through helps, makes me know I am not alone.

[Enidah]

Thank you for sharing that, Ian. It does help knowing we are not alone in this struggle.

[Despe]

Hi Ian! Keep up with the Thiamine. It takes a while to see improvements, so don't give up. You're an inspiration to all the PwP.

[M1tz1]

Like Despe, I think you're an inpiration to those who contribute to HU. Hang in there, Ian. Praying for you.

[JANVAN]

Hello Ian

Sorry to hear that. What I want you to ask .....so you don't use any of L-Dopa medication ?

Do you then use mucuna pruriens ?