A Physician's Guide to Progressive Supranuclear Palsy ( PSP ) Part 3
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- Опубликовано: 4 окт 2011
- A guide to aid the diagnosis 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
Fortunately my recent medical condition is good.
The main training I currently do at a day-service facility is as follows. : To begin with, I ride an exercise bicycle for 30 minutes at 25 km / h. 2ndly, I do squats 100 times. The third is walking training using a treadmill and I walk for 30 minutes at a speed of 2.5 km / h, 3 times a day. (90 minutes in total)
I went to the hospital three days ago and had an medical exam by a neurologist.
When I said to the docter that I was doing the training I wrote above, he said that in my case it may be a late progressive subtype rather than a typical PSP (PSP-Richardson type).
P.S. I take one Madopar tablet each day after breakfast and after dinner. I think this is the biggest cause of maintaining good condition.
Excellent video and speakers. Diagnostic criteria particularly helpful.
I received an examination of MRI on August 8 of this year in order to grasp the progression of PSP, and I went to the university hospital yesterday to hear the result of the examination. Unfortunately the result was not good. I confirmed that the form of the image of tegmentum mesencephali was bill of a hummingbird.
My medical condition has deteriorated considerably since last summer. I can only use the treadmill for 10 minutes at a speed of 2.0 km / h. And it's dangerous for me not to grab the bar in front of my body. So the distance I walked is displayed, but it is for reference only. I realized that when I went to a dentist late last year. It took 2 hours 05 minutes to walk just 1.2km one way.
Im so sorry to hear.
My name is Dave Olsen. I just wrote a comment and I just reread it. My words don’t come out right and And I’m sorry for that. This is part of my problem. What I’m thinking doesn’t come out the way I speak. I’m sorry if you can give me any help cause I think maybe I was misdiagnosed. Thank you again for all that you do and God bless. Thank you.
Someone with PSP is physical therapy and white boxing like we do for Parkinson’s. Is that recommended for people with PSP I was diagnosed in 2017 with Parkinson’s disease, but since I’ve been to therapy and boxing it’s been better but I have some of the symptoms my eye movement is very bad. I must move my head whenever I have to look up down or to the side reading is a real problem for me, so I don’t know if my Parkinson’s diagnosis was correct or if I have something else I do have an appointment for a nuclear ophthalmologist to go over my symptoms but reading has been difficult ever since I was young I must move my head whenever I have to look side to side or up or down. Is there any information you can give me? Thank you so much I enjoyed your, your video my name is David a Olsen thank you very much
my frends now 75 years now is very ill. but5 i thinks his the ferst symptons was have 7 yeras before
I am a Japanese man in 60s. I underwent an operation in neurosurgery of the University hospital for idiopathic Normal Pressure Hydrocephalus one year ago. My symptom improved for a while, but turned bad again. And so, a doctor of department of neurology of the same hospital pronounced last month that my illness may be PSP. I'm at my wits' end. May one suffer from not only Hydrocephalus but also PSP?
While I was in the University hospital a year and a half ago, I received Dat-scan, and it was said that there was not the possibility of my PSP.
my mother was diagnosed psp but im sure the imbalance was caused after a doctor damaged her vestibular while puncturing her eardrum because of an inflammation behind it. To me it was clear this inflammation was caused by Tolbutamide also called Orinase en.wikipedia.org/wiki/Tolbutamide
wich was banned in the usa in 1970 i hope this helps btw. my mother got the tobutamide prescribed for a melitis she didnt even had.
My name is David A, Olsen I was diagnosed in 2017 with Parkinson’s but my eye movement has always been bad. Even as a child my eyes don’t move automatically from left to right or up and down. I have to move my head when I read and sometimes my eyes, they don’t move down to the next line and I start rereading what I’ve already read. It becomes very frustrating, now that I was diagnosed with Parkinson that I’ve read up on PS P I am wondering if I was misdiagnosed I have the tendency when I’m standing still for a while I start to walk backwards and then I catch my ball. I catch myself I haven’t had too many. I haven’t had too many falls lately, but in the beginning I had I had two or three falls, and now it’s tendency tooling to go backwards and I’m stuttering. I have spit up when I eat. I was just wondering if there’s a chance I was miss diet know if there’s any help you can give me or information it would be greatly appreciated. thank you and I enjoyed your video. Thank you so much for any help you can give me.
come si può rallentare la malattia e i farmaci
Do pacients keep falling with psp?
Yes. That is a danger that one wants to avoid to extend the life of an individual with PSP.
My mum would fall, unable to extend arms to protect herself. She lasted 9 years, I remember well, in the last few years, knowing she was in there somewhere and hugging her as if if could bring her back by that act. It is a tragic thing.
in this moment i was not understein it his diagnoz was beagining when he was folldown very offen. it was about 4 years before now he is very ill have a big troublle with the YES NOT CAN GOINGS AND VERY VERY TIRED. HIS DAY BEAGINING AT 7 AND GOING SLEEP AT 6 PM. BUT FROM 3 4 PM HE IS VERY TIRED. THE DAys for him are sorter and sorter. i going to him from poland do germany ever 3 weeks for some days and the last time its 3 weeks is for me szoking. the ill goings now very qucly. i seeing it oll but for me its the most not understending not so much i knowing english. very bed that not transeit it for the polish l
Does Donald Trump have this?