advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 03-07-2008, 07:08 AM #2
cricket52's Avatar
cricket52 cricket52 is offline
Member
 
Join Date: Sep 2006
Location: Limboland in northern Ontario, Canada
Posts: 101
15 yr Member
cricket52 cricket52 is offline
Member
cricket52's Avatar
 
Join Date: Sep 2006
Location: Limboland in northern Ontario, Canada
Posts: 101
15 yr Member
Default

Hi bobcat:

You are a very gifted writer, you sum up what many of us feel.

Limbo is not a good place to be, especially when you are a Type A who needs answers. We all need support.

Sadly, many of us can't get the support of those we love. That's why there are these forums. It was my MS neuro who suggested finding a good forum - this is one - and they has been my lifeline. It is where I come for comfort and support and friendship - people on the forum go my speed. I get my questions answered and my bad days, my angry days understood. My family can't help me, they expect me to help them, and I can't always do it.

I don't know what to say except some of us understand. The last 10 years for me have been tough. That's when I went on disability. Living in Canada my medical care and drugs are paid for, I can't imagine the discouragement you must feel, for you deserve decent medical care and without insurance how can you possibly get it?

I can no longer play the piano or organ, or follow a knitting pattern or read a book. I cannot walk the many kms. I used to love. I sleep too much and struggle with pain and the irritability it brings. My marriage ended after 34 years because my husband didn't have the wife he used to. My bowels keep me inside more than I would like. There's more, but what difference would it make? All the tests rule out everything.

So we sit with a dx of possible/probable MS, the uncertainty reminding us daily that our bodies have betrayed us and the medical community has no answers. Sympathy from them? Maybe. Or maybe they think we are part of that group of psychiatric patients who can manufacture symptoms. For me that's how it feels.

Sometimes there are no answers, except that 5% never show lesions. That's not much comfort because we are back at square one - limbo.

Time helps a bit, just not enough. I too want an answer - any answer. Sadly I don't think it will be forthcoming any time soon for me or my friends on the forum I frequent.

Courage isn't a one time thing - it's a daily act of the will, like love. Your gift of writing will help others here and in turn, they will support you.

Hang in there bobcatsrule - you are among friends. I truly wish you had the money to get the help you should have. It's not fair.

Last edited by cricket52; 03-07-2008 at 07:14 AM. Reason: brainfog
cricket52 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
bobcatsrule (03-07-2008)
 


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
Limbo check in 3/5 braingonebad Multiple Sclerosis 20 03-08-2008 02:40 PM
Limbo check in 2/13 braingonebad Multiple Sclerosis 20 02-15-2008 09:08 PM
Limbo Check in 2/06 braingonebad Multiple Sclerosis 18 02-06-2008 08:23 PM
Hi everyone in TOS land flippnout Thoracic Outlet Syndrome 5 06-26-2007 01:07 PM
One of the finest men to have ever lived died today Thelma Parkinson's Disease 5 11-28-2006 04:26 AM


All times are GMT -5. The time now is 03:10 PM.

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.