I was a physiotherapist, retired many,many years ago before I heard of PSP. Now I have PSP. I wondered whether any of you could tell me whether any of your sy.mptoms were stirred up by the jab .I never had any problems with the Flu or Covid 19 jabs before the diagnoses of PSP. I am new to this forum. I found the PSP helpline helpful by directing to this page. They said that they were unable to answer medical questions but could send me a book which I could pass on to my G.P, all about PSP.
love to everyone.
eilcod.
Written by
eilcod
To view profiles and participate in discussions please or .
I am a great believer about the toxicity of the Covid 19 vaccine - both my husband and I had the 3 vaccines but we will not have any more or the flu one due to various things that happened after the jabs. I have not found any medical person who was willing to ‘diss’ the vaccine - didn’t want to jeopardise their job I think, apart from one nurse in A&E who was SO vociferous about it that she was ready to quit if all med staff at that time were compelled to have the vaccine. All I will say is that my husband’s PSP seemed to accelerate after the third jab.
My wife did not have any issue with vaccinations and PSP.Logically, when you first had a COVID jab you would have also had PSP as it usually takes a few years to diagnose and for the symptoms to show more, there may be other factors too like drugs you take now that you didn't then.
My wife had 4 Covid-19 vaccine Jabs and we didn't see any aspect of PSP change. Having said that PSP does not progress regularly but progresses irregularly. There a moments of very slow progress and then there is sort of a big step, then again no real changes and again a big step. Some times there are even some reversals... my wife couldn't speak for 6 months then started speaking again, but just for a week. What I'm saying here is that its normal in this disease that symptoms increase by steps, and if one of those steps occurs close to a vaccine jab you will tend to associate the 2 facts but in reality there is no correlation between the 2 facts.
byw, since you know the usefullness of physio, do as much as you can. I Believe it to be one of the biggest game changers in how one lives with PSP. If I could go back in time I would double up on physiotherapy specialy if PSP is diagnosed at young age
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.
Sub -types of PSP
Sad? Devastating!
Awareness of PSP
Confused
