General Health Conditions & Rare Disorders Discussions about general health conditions and undiagnosed conditions, including any disorders that may not be separately listed below.


advertisement
Reply
 
Thread Tools Display Modes
Old 12-27-2014, 03:30 PM #1
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
Default New member with Late Onset Tay-Sachs disease

Hi all!

I just joined and posted in the introduction forum. But was diagnosed with Late Onset Tay-Sachs disease a little over three years ago.

Are there any other LOTS patients here? It's possible, but I doubt it. I'm one of only about a hundred confirmed cases in the entire United States.
John Pollman is offline   Reply With QuoteReply With Quote

advertisement
Old 12-27-2014, 03:44 PM #2
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Wink

John, I answered you on your other thread.

Welcome to NeuroTalk.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
Old 12-27-2014, 03:51 PM #3
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
Default

Thank you for having me!
John Pollman is offline   Reply With QuoteReply With Quote
Old 12-27-2014, 06:39 PM #4
EnglishDave's Avatar
EnglishDave EnglishDave is offline
Magnate
 
Join Date: Dec 2014
Location: Yorkshire, England
Posts: 2,098
8 yr Member
EnglishDave EnglishDave is offline
Magnate
EnglishDave's Avatar
 
Join Date: Dec 2014
Location: Yorkshire, England
Posts: 2,098
8 yr Member
Cool Smirk LOTS Support

Hi John,
Well, your first GP certainly did a number on you! When I read your posts I had to go have a quick recce as to what LOTS is. As you say yourself, it's very rare.
What isn't so rare are the symptoms matching those of fellow Forum members, so there will always be a sympathetic shoulder of someone going through something similar.
I read that LOTS progression can be slowed by certain drugs - although side effects look rough. I trust your current Doctor has you on suitable treatment.
Any time you want to chat…
Dave.
EnglishDave is offline   Reply With QuoteReply With Quote
Old 12-27-2014, 07:18 PM #5
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
John Pollman John Pollman is offline
Junior Member
 
Join Date: Dec 2014
Location: Rochester Hills, MI
Posts: 15
8 yr Member
Default

Hi Dave!

I live about 20 miles north of Detroit, Michigan. But I am currently enrolled in two LOTS studies. One is at University of Minnesota in Minneapolis (about 750 miles away), and another one at the National Institute of Health in Bethesda, Maryland.

I've been to Minneapolis twice already, and I'm headed back there in early March. I'm making my first visit to NIH in mid April.

There is no cure for Tay-Sachs, but they are trying some drugs to hopefully slow the progression of the disease. All I can say is thank God for health insurance. I'm on several different medications. One of them I take three times a day, and it costs $304 per pill! The grand total of my medication cost over $29,000.00 per month!!!
John Pollman is offline   Reply With QuoteReply With Quote
Old 12-27-2014, 08:08 PM #6
EnglishDave's Avatar
EnglishDave EnglishDave is offline
Magnate
 
Join Date: Dec 2014
Location: Yorkshire, England
Posts: 2,098
8 yr Member
EnglishDave EnglishDave is offline
Magnate
EnglishDave's Avatar
 
Join Date: Dec 2014
Location: Yorkshire, England
Posts: 2,098
8 yr Member
Cool Smirk What's a Dollar Worth?

Hey John,
Your distances never cease to amaze me, 750 miles is almost the length of our Country! 30 miles destroys me. To think we once Ruled the World.
As for costs, you are worth far more than the arbitrary Dollar value put on your drugs by some Multi-National Pharmaceutical, at least we have the much-maligned but truly wonderful NHS over here. I certainly wouldn't be here without it!
Good luck with all your travels and treatments.
Dave.
EnglishDave is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
John Pollman (12-27-2014)
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
adult onset Tay-Sachs Stellatum Myasthenia Gravis 9 12-29-2014 12:03 PM
The association between non-motor symptoms in Parkinson's disease and age at onset badboy99 Parkinson's Disease 0 04-25-2014 10:47 AM
Late-Onset Myasthenia Gravis Linked to Higher Cancer Risk Stellatum Myasthenia Gravis 3 07-03-2013 06:14 PM
New gene uncovered for late-onset Alzheimer's Stitcher Parkinson's Disease 0 01-14-2007 03:19 PM


All times are GMT -5. The time now is 12:56 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.