5 Multiple System Atrophy | Atypical Parkinsonism (DLB, PSP, MSA, CBS/CBD) Symposium
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- čas přidán 29. 03. 2013
- Speaker: Kathleen Poston, MD, MS, Movement Disorder Specialist at Stanford University's Movement Disorders Center. This is part of the October 2012 Atypical Parkinsonism Symposium, organized by Stanford and Brain Support Network.
Videorecording was paid for by a grant from CurePSP and Stanford APDA.
I am not diagnosed as MSA patient as yet but this was the most down to earth explanation of every symptom I've seen. Thanks for making it so understandable!!
Thank you Linda! Best wishes.
Phenomenal talk! Brilliant👍. Crispy clear
Excellent speaker
man o man how i wish she could be my doctor
Wonderful speaker.
Excellent presentation. I wish I could hear the lady reading the questions better
me too !
I heard Dr. Poston say that sometimes MSA patients can have high blood pressure. Did I hear that right? (She seems to have said this about 15 minutes into her presentation. She said the thing to remember about blood pressure issues is a dis-regulation problem. Did I hear that right?
Yes; supine hypertension is common in MSA.
Unexplained pain is likely CRPS - Complex Regional Pain Syndrome. It is caused by the autonomic dysregulation.
So against the muscles pain, what you can do is with anti pain creams, or pain pills
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What about your body temperature. Getting warm or cold.
🧠🙏
My mother has MSA-C, gave her in the same day Lions Mane 1100MG and Amantadine 100MG, the day after she could talk again, move arms fast, and has a clear mind ! She could not do any of these. She can eat with her owns hands. Could not talk, now she can talk some phrases, clearly, clear mind ! THANKS TO the neurologist of my mother Dr. Rubens Salomao (gave the Amantadine) and Paul Stamets that gave me the hint about Lions Mane. . Thank you Paul Stamets ! Some ppl show great reponses on super doses of Vit D3. So keep trying all medications to see change, what works for you. We have tried lots of medicine. Amantadine and Lions Mane reversed her case.
TubeSpoker written. meters
My mom was first diagnosed with parkinsons in feb 2020 progession is faster n she is not responding to levadopa meds. Docs are confused in further diagnosis some say psp some say msa. One doctor gave amentedine since then her speech is better. Learned about lions mane 1100mg from you. What are the alternative tabs
37:20 Levadopa has not worked with my mother wich has MSA-C !
i couldnt do levo either because had to many symptoms already . I was full blown MSA .
Here's the basics of my story . Faces of multiple Systems Atrophy from beggining to end .
photos.app.goo.gl/6PJ9ZXjMW2wrtfXx1
Are their any clinical trials for MSA in Northern California? We are in Sacramento.
Clinical trials carry significant risks, and you seem to gloss over that.
Of course they do, but all medicines a available today in modern medicine are as result of extensive trials.
Except the covid vaccines...
35:50 an exagerated statement ! Thats why we´re so dependent of pharmaceutical mafia industry !