Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 01-08-2016, 01:07 PM #1
AnnT2 AnnT2 is offline
Member
 
Join Date: Oct 2006
Posts: 148
15 yr Member
AnnT2 AnnT2 is offline
Member
 
Join Date: Oct 2006
Posts: 148
15 yr Member
Default Ominous hints in our past

When you watch a movie, the background music often gives you a hint when something bad is going to happen. I wonder if the same is true for people with Parkinson's. While we didn't have music to warn us, there were possible signs way back in our earlier lives when we walked unfettered and had steady hands that gave us a hint - usually overlooked - that PD was going to set up shop in our bodies.

The medical profession looks for biomarkers to determine who is at risk, but they usually involve blood tests, CAT scans, and MRIs. However, I believe there are signs easily detected by us, the patients. Was your handwriting smaller than that of others. Did people often ask you why you looked so glum . . .even when you were enjoying the party?

These are a couple of signs I had - although I did not recognize them at the time. How about you?

Ann
AnnT2 is offline   Reply With QuoteReply With Quote

advertisement
Old 01-09-2016, 05:34 AM #2
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
Default Yes I remember ...

signs from early days, (5 years old ish).

i) As a child I had OCD, Habits, (such as touching things in an order, etc), and a stammer.
ii) My handwrighting was awful.
iii) We always said I was left handed but my mother (different generation), forced me to be right handed. I was ambidextrous for many things, brush teeth with either hand, left footed, play pool left handed, bat right handed at cricket, etc.
My PD now affects my right hand predominantly, so I am probably right handed but had to do some things left handed due to the PD.
iv) I remember at about 15 running at school and wondering why I was moving slower than others, as I was in pretty good shape and should have been faster than I was.
v) At a martial art I used to do at age 30, (10 years before dx), my right side was harder to stretch, (this is my side affected most by PD).

So I had a number of signs going back all my life. This is why I hope that if I have had PD for so long and am still OK, things can stabalise and perhaps get better.

Love to hear if anyone else had signs.

Take care,
Neil.
aftermathman is offline   Reply With QuoteReply With Quote
Old 01-09-2016, 05:40 PM #3
johnt johnt is offline
Senior Member
 
Join Date: Apr 2009
Location: Stafford, UK
Posts: 1,059
15 yr Member
johnt johnt is offline
Senior Member
 
Join Date: Apr 2009
Location: Stafford, UK
Posts: 1,059
15 yr Member
Default

From childhood I had:
- people telling me to "cheer up", even when I was happy, an early masked face?
- poor posture;
- muscle stiffness, even though I was fit at stamina sports.

John
__________________
Born 1955. Diagnosed PD 2005.
Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg
Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg
johnt is offline   Reply With QuoteReply With Quote
Old 01-10-2016, 05:42 AM #4
Niggs Niggs is offline
Member
 
Join Date: Jul 2015
Location: Guiseley,West Yorkshire,England
Posts: 165
8 yr Member
Niggs Niggs is offline
Member
 
Join Date: Jul 2015
Location: Guiseley,West Yorkshire,England
Posts: 165
8 yr Member
Default

From Childhood,

Severe abducted feet (I wonder about dopa responsive dystonia)
Bad handwriting,like a spider crawling across the paper according to one
motivational Teacher.
Feeling physically awkward compared to others.
Energy seemed to deplete quicker tha my Peers.
Whilst rock climbing my left leg would spasm ,Parkinson's side

Nigel
Niggs is offline   Reply With QuoteReply With Quote
Old 01-10-2016, 07:45 AM #5
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
Default So it looks like ...

a number of us presented PD symptoms from early in childhood.

I read somewhere that PD symptoms are evident when 80% of neurons are not functioning and this typically takes around 10 years elapsed.

I believe the brain regenerates upto around 25 years of age.
Really simplistic view, lets assume this regeneration means PD cannot occur until 26 years old.
Taking the 10 year incubation period this means the earliest PD presents itself is in the mid 30s.

However John was dx'ed at 50 years old and I was dx'ed at 40 years of age.

Our stories suggest we had PD early in our lives.

So what was PD doing in the years between our childhood and the first clinical presentation of symptoms.

I would be interested to get the view of the large PD charities as to whether they believe PD signs can exist in early childhood and if so, do they have any idea what is the process by which it remains dormant until later life. I will chase up PDS UK and MJFF and get back to you.

I have a personal interest in this as my granddaughter is displaying little habits and tics. This may be nothing but then again ...

Regards,
Neil.
aftermathman is offline   Reply With QuoteReply With Quote
Old 01-16-2016, 07:06 AM #6
ronstrong ronstrong is offline
Junior Member
 
Join Date: Dec 2015
Posts: 15
8 yr Member
ronstrong ronstrong is offline
Junior Member
 
Join Date: Dec 2015
Posts: 15
8 yr Member
Default

Quote:
Originally Posted by Niggs View Post
From Childhood,

Severe abducted feet (I wonder about dopa responsive dystonia)
Bad handwriting,like a spider crawling across the paper according to one
motivational Teacher.
Feeling physically awkward compared to others.
Energy seemed to deplete quicker tha my Peers.
Whilst rock climbing my left leg would spasm ,Parkinson's side

Nigel
Much the same (except I'd never climb!)

Dx 2010 45yo
ronstrong is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
hints of MS on MRI years before symptoms Natalie8 Multiple Sclerosis 4 12-23-2008 04:19 PM
Helpful Hints mlomonaco Aneurysm 3 05-05-2008 10:17 PM


All times are GMT -5. The time now is 03:25 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.