CurePSP Family Conference in Rochester, MN - PSP Association

PSP Association

9,232 members11,334 posts

CurePSP Family Conference in Rochester, MN

taihde profile image
13 Replies

If anyone is interested I just received notification that the videos of the conference are now available on YouTube. I can post the link for anyone who is interested. The speaker on caregivers was great. Very motivational.

Written by
taihde profile image
taihde
To view profiles and participate in discussions please or .
13 Replies
Pavaga profile image
Pavaga

Hello Taihde,

Yes, I would like to see the conference. Can you please forward the link. Thank you very much, Patty

ninalulu profile image
ninalulu in reply to Pavaga

i like to have a link. thanks

Nanny857 profile image
Nanny857

Hi, I would like to see it too please.

DeDeDickson profile image
DeDeDickson

You beat me to the punch, as I just opened the email as well.

I agree that the caregivers’ presentation was wonderful. And, truthfully, I also enjoyed the one explaining how hard it is to diagnose the Parkinsonism diseases. We all know it to be true but this explains why it seems to take some doctors time to come to a PSP or CBD or MSA diagnosis.

Marie_14 profile image
Marie_14

Please could you send the link? Thank you.

Marie

taihde profile image
taihde

Here is the link:

The videos that were filmed at the Family Conference are now available on our YouTube page here: youtube.com/playlist?list=P...

Kevin_1 profile image
Kevin_1 in reply to taihde

Thanks Taihde

:)

Karynleitner profile image
Karynleitner

Thank you.

taihde profile image
taihde in reply to Karynleitner

Karen, there was a lift mentioned in the last presentation thAt made me think of you. She's a very small lady but was able to manage her husbAnd who I believe she said was

Over 6'.

Karynleitner profile image
Karynleitner in reply to taihde

Thanks. I’ll definitely watch for that. We have a Sabina Sit and Stand which is great, but still not easy. I really can manage it without too much trouble. When he is Unable to bear weight on his legs, we’ll have to regroup. I’m Just getting a little burned out and discouraged .

Thanks for thinking of me.

I hope you are doing well. PSP Is tough. Have a great week. 😃

Yvonneandgeorge profile image
Yvonneandgeorge

Could you also please send me the link. Thank you Yvonne xxxx

taihde profile image
taihde in reply to Yvonneandgeorge

Link already posted above. Let me know if you can't see. We will be out of town for a few dAys at our "home away from home" in the northern woods. Since this disease is so unpredictable we are tAking as much advantAge of the good days that I still have as we can. We have no WiFi there so I'll be out of touch. Reminds me so much of my roots (Scotland) . Some good books, good music and lots of peace and quiet away from the city.

kenh1 profile image
kenh1

Thank's for the link. Very interesting and informative.

You may also like...

Cure PSP Family Conference in Rochester

just wondering if anyone in the U.S. is planning to attend this conference on PSP/CBD/MSA at the end

FYI: CurePSP Conference

Upcoming family conference

Hi Folks, Anyone on here attending the 2015 Canadian Family Conference June 13th? http://www.psp.or

CurePSP at Mayo Clinic

Would love to know if anyone is here in Rochester at Mayo Clinic for the CurePSP Seminar tomorrow....

Summary article from CurePSP

I've just read this article called Best Practices in the Clinical Management of Progressive...