Tell me more about PSP: Hi, I am 35 years... - PSP Association

PSP Association

9,658 members11,568 posts

Tell me more about PSP

KokoLu profile image
12 Replies

Hi, I am 35 years old and I notice tremor in fingers on my left hand two months ago. Now I have tremor in my right hand too. Before that I had problems with my vision, every few days I can't see well on my eye or my eyes. Also, I have pain in my neck, shoulders and hips. I have problems with my balance. I take meds for depression and insomnia. I will see my neurologist at Frebruary 29. Please, can you tell me more about PSP, are my simtoms tipical for that or not? Is there anyone so young with PSP? Is it true that meds for PD not working for PSP? Sorry for so many questions, I am so afraid, I have 2 daughters, they are 4,5 and 6 years old, and I notice that here are people related with persons who have PSP, and not persons who have desease. Tnx for patience and sorry for bad English...

Written by
KokoLu profile image
KokoLu
To view profiles and participate in discussions please or .
Read more about...
12 Replies
jillannf6 profile image
jillannf6

hi

i have psp and do not knwo of anyone your age with it

I am 66 and was diagnosed dec 2010

you need ot speak ot your neurologist re the symptoms

love jill

sorry i cannolt be of more help

KokoLu profile image
KokoLu in reply tojillannf6

Jill,

I sent you a message on PD forum... Can you tell me what was your first simptoms?

KokoLu profile image
KokoLu

Somebody else? Please!!

Sue20045 profile image
Sue20045

My dad has had to have various blood tests and scans and sees the neurologist every 3 months and has had a speech and language therapist come out to help with his talking and his coughing when eating

AnabelaQ profile image
AnabelaQ

My mother has 69 years old, she was diagnosed in May 2010, showing symptoms since 2006/07, she began to complain dizziness, trouble with her vision (blurred), and mood change, and her first big fall has happened in Christmas 2007 without reason. I apologize if I could not help you more! But the most important is you remain calm until you speak with your neurologist. Good luck! (And sorry my english is not good enough as well)

KokoLu profile image
KokoLu in reply toAnabelaQ

Tnx a lot!

riosenior profile image
riosenior

Kokolu

I understand your worries but you really must wait until you see your neurologist and then hopefully you will get an accurate diagnosis.

Pinda profile image
Pinda

Hi

My husband has PSP,was diagnosed in June after 4 long years of testing.He is 62.He does not have or had tremors,.He has the eye poblems,balance,coughing ,speech problems and his personality has changed a lot.He also had pain in his muscles all over his body at the start of his symptoms and he has cognitive slowness.Please wait until you see the neurologist and confirm things,It is very hard but try

Good luck.

Kathy profile image
Kathy

Hi Kokolu,

I know you must be very worried but at this stage there are several conditions that could fit with your symptoms. PSP is generally found in people over the age of 50.

See what the neurologist says at the end of the month.

Good luck! We'll be thinking about you

love Kathy

KokoLu profile image
KokoLu

Tnx a lot!!! Do you know anybody with PSP under age of 40's?

jimandsharynp profile image
jimandsharynp

My understanding is that meds for Parkinson's either don't work for PSP or if they work it is only for a short time. They didn't work in my wife who was first diagnosed with Parkinson's, given PD meds, then later diagnosed with PSP.

arwenmark profile image
arwenmark

From all I have read PSP does not start until at least age 60.

Not what you're looking for?

You may also like...

PSP and tracheotomy?

I explain: 12+ years with PSP. 1 year with tracheotomy. Every need covered (Its sucks!) My...
AnisFer profile image

PSP - swallowing questions

Hello...my partner has had PSP for about six years and is having more problems with swallowing. I...
PSPPsP profile image

Spread the word about PSP!

I had to go into London today and my car broke down. Bad luck. But it broke down within 100 meters...
Kevin_1 profile image

Question about eye movement in PSP

This is my first post, not just on this forum, but on any forum, ever.. I've been following the...
Kris539 profile image

Can it be PSP even if there are no instances of falls for 2 years?

Is it possible for someone to have PSP and still not have falls? How early or late does one start...
shobacg profile image

Moderation team

HelenPSPA profile image
HelenPSPAAdministrator

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.