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A Physician's Guide to Progressive Supranuclear Palsy ( PSP ) Part 1 

PSPAssociation
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A guide to aid the dignosis of Progressive Supranuclear Palsy for medical practitioners.
PSP is a terminal degenerative brain disease which robs those affected of their ability to walk, talk, eat and see. The PSP Association provides help and support for those living with PSP, whilst funding research into the causes, treatments and eventual cure for the disease.
www.pspeur.org

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16 окт 2024

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Комментарии : 35   
@landonlawhead7764
@landonlawhead7764 5 лет назад
for the longest time we were under the assumption my father had parkinsons + this helps a lot with such and uncommon disorder im so glad you had this video many thanks
@dramymagdy
@dramymagdy 11 лет назад
Thanks for shedding the light on this subject, and helping us doctors in being more efficient.
@helencheadle5285
@helencheadle5285 4 года назад
Why did ten people put their thumbs down I wonder! ? This man was only talking about what they knew at that particular time, and illustrated Cases. Understanding and treatment has to start somewhere! Sad though it all is. I have a friend whose just been diagnosed, so I want to absorb as much information old and new as I can,to understand and try to support and help my friend. I have to admit I’m surprised PSP isn’t mentioned or included in medical information more than it is. Until now I’d never heard of it, and it’s a dreadful disease. So sad for people with, and people who are part of their lives. So please don’t just thumbs down without explaining why you felt that way, so we can all understand your view and reasoning.
@Mdanamd
@Mdanamd 8 лет назад
Thank you great doctors for such efforts to help us diagnose and understand this disease.
@blackgrl71
@blackgrl71 7 месяцев назад
Just found out an immediate family member was just diagnosed with PSP. Obviously were devastated, especially once we read upon it. They initially thought it was Parkinson's.
@13oct1992
@13oct1992 7 лет назад
Thank you doctor. My mother had been diagnosed and has been suffering from this disease for the past 4 years. She cannot walk, talk, eat or move much. It is very hard on all of us.
@omovses
@omovses 6 лет назад
13oct1992 i feel you. My dad is diagnosed with PSP and hes bed bound now , not talking nor eating (feeding tube placed) not moving Ita devastating to see that...
@lawrencebayon7556
@lawrencebayon7556 5 лет назад
My mother also have been suffering from this disease any tips you can recommend it just keeps on going worst each day my mom is 64 years old i feel that i am taking care of an elderly person of the age of 90+ or something it has really been tough for my family
@kimboslice9445
@kimboslice9445 3 года назад
I feel for all of you. My mom has had it for about 6 maybe 7 years. I remember the exact day I notice the way she was walking. It took years to determine psp. We aren’t to the bed phase but we all know that’s part of it. Walker wheelchair bed. Unless choking or a fall gets them. I already can’t believe it.. I can only imagine being in yalls position. I’m sure nothing can prepare me for that. Prayers for all and your loved ones.
@harshitdubey274
@harshitdubey274 2 года назад
ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-c8YAlDHlvNU.html
@harshitdubey274
@harshitdubey274 2 года назад
just wanted to help 😊
@andrewm514
@andrewm514 Год назад
I've PSP, these doctors should live our life's ! So many skip the net! And are left without help. Seven years before diagnoses! Seven years of thinking your going mad!
@MyLife2020
@MyLife2020 8 лет назад
the side effect of psp 1. can't move eyes 👀 down ⬇ 2. hard to talk and understandable 3. difficulty in eating 4. can't walk alone and need to wheelchair ♿ for distance more than 30 meter. 5. fast sweating and need to cool air always 6. Can't sleep without taking Sleeping pills
@ujalatareeza
@ujalatareeza 7 лет назад
Sayed Moh'd Sayed Jawad
@MyLife2020
@MyLife2020 7 лет назад
Ujala tareeza ujalatareeza yes?
@lawrencebayon7556
@lawrencebayon7556 5 лет назад
My Life any tips to deal with psp my mom can't even stand properly i always her whenever she need to go to take a bath or going to bed all of the symptoms you've mentioned was experienced by my mom i hope you can help thanks
@kimboslice9445
@kimboslice9445 3 года назад
With my mom you are spot on. Only thing.. she’s cold a lot.. u think the sweating might be a side effect of medication?
@kimboslice9445
@kimboslice9445 3 года назад
@@lawrencebayon7556 I wish I had tips. I know u keep asking but honestly it’s psp. It’s only going to progress.. unless they figure out something but so far not much. I’m my moms caretaker. It’s hard on them and us. My tips would be have some breaks or help. Take care of yourself too. Burnout is a huge thing. Love on her a lot.
@abossomss496
@abossomss496 5 лет назад
Thank you very much ...glad to see Dr.Steel himself describe the syndrome bearing his name 💜💜💜
@doczak69
@doczak69 9 лет назад
Great video and explanation, many thanks
@drew9312
@drew9312 5 лет назад
Great video- thank you
@DavidOlsen-e3n
@DavidOlsen-e3n 7 месяцев назад
My name is David a Olsen. I was diagnosed in 2017 with Parkinson’s disease but lately and my eye movement is not good. I don’t move automatically up or down I have to move. My head reading is very difficult because my eyes don’t move from one line to the to the next I must move my head so sometimes I go back and reread the same line by accident, very frustrating. Also, my balances isn’t good I don’t fall but I have the tendency of leaning backwards when I get up sometimes and it’s very frustrating and sometimes when I’m just standing still, the tendency to move backwards becomes regular I don’t know if my diagnosis with Parkinson was correct, I hope I don’t have PSP but is there any help you can give me or information on how to getto find out if I was diet knows properly thank you for any help you can give me. Thank you for your last video was very helpful.
@farehazahid5986
@farehazahid5986 3 года назад
Thank you so much for this video
@toddiloddi
@toddiloddi 11 лет назад
Very informative video!
@borntobewilddz
@borntobewilddz 6 лет назад
Dr Steel ^^ one among those who described STEEL-richardson-Olszewki
@dhirajjha8942
@dhirajjha8942 6 лет назад
Thank You,Great clinical help
@cliforbragatassinari404
@cliforbragatassinari404 6 лет назад
Impactante,bem a real dessa maldita doença
@MyLife2020
@MyLife2020 8 лет назад
any solution for this problem I mean if there is any treatment?
@omovses
@omovses 6 лет назад
Sayed Moh'd Sayed Jawad i dont think so. I’ve done lots of research since my dad is diagnosed with PSP Docs cant do anything
@DoBetterEachDay
@DoBetterEachDay 5 лет назад
May I ask, how long has your father been battling with PSP? I recently found out that my mother has it also, but it took many years for her doctors to figure it out. They've pretty much washed their hands of her now since they can't do anything either.
@lawrencebayon7556
@lawrencebayon7556 5 лет назад
Sara H. Been dealing with the same problem at first we thought it was parkinson's disease but later on we just experience difficulty in swallowing food or any liquids it has been really tough having to feed my mom for atleast an hour or two hours just keep getting worst each day the doc can't even seem to find a solution also
@elizabethreynoso2820
@elizabethreynoso2820 Год назад
My daddy has this 😢
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