Welcome to This Is MS!

     Modules
· Home
· Content
· Downloads
· Encyclopedia
· FAQ
· Feedback
· Forums
· Journal
· Private Messages
· Recommend Us
· Search
· Site_Map
· Stories Archive
· Submit News
· Surveys
· Top 10
· Topics
· Web Links
· Your Account

     Google
Google
Web
This is MS
These ads help pay for the upkeep of our site. They are automatically served by Google and are not affiliated with This is MS.

     Languages
Select Interface Language:


     Who's Online
There are currently, 178 guest(s) and 6 member(s) that are online.

You are Anonymous user. You can register for free by clicking here

     Next Step

From the creators of This is MS comes Experience Project

EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at Experience Project.

Get started by sharing your Multiple Sclerosis story.


     Donations

To remain unbiased, This is MS does not accept corporate sponsorships.

Therefore, we must rely on our users to help support us. Please donate to our upkeep if you have the means. Thank you!


ThisIsMS.com :: View topic - Hello
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Hello

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Introductions
View previous topic :: View next topic  
Author Message
phillo
Newbie
Newbie


Joined: May 05, 2008
Posts: 1

PostPosted: Mon May 05, 2008 4:15 pm    Post subject: Hello Reply with quote

I have been lurking on the site for yrs. DXd 5 yrs ago w/MS; RRMS or PPMS was not determined @ that time but it looked progressive. I had been experiencing symptoms that clearly indicated something was WRONG for 2 yrs before breaking down and dealing w/it. My early symptoms, foot drop mainly after strenuous exercise, seemed like they could indicate not only MS, but ALS or Parkinson's. My feeling was, I am in no rush to be diagnosed w/ any of the above and I simply cannot handle a DX of ALS so just wait and watch. Had a rough couple of yrs emotionally, keeping all that to myself.

As time passed, it seemed more and more like MS, or I should say less and less like Parkinson's and ALS. I finally broke down and went to a PCP after 2 yrs of alarming symptoms. The PCP DXd me w/MS before referring me to a neuro who confirmed the diagnosis (after extensive testing). Living in Boston I have access to the "best" MS Dr.s which is essentially irrelevant.

Anyhow, my well known neuro DXd me w/MS, what kind, well we can only watch, wait and see, but it seemed progressive. I'd been experiencing Lhermitte's intermittently since about age 10 (was 26 @ time of DX) so I think I had very mild RRMS for much of my life before the disease started progressing. So, SPMS, or PPMS, does it matter anyway.

I've been leery of getting into the whole CRABS thing, especially considering the progressive nature of my condition though my 1st neuro kept pushing the drugs. Not feeling up to the drugs, especially since I saw no point I moved to a different well known neuro who diagnosed me w/PPMS and essentially said feel free to touch base once a yr for a reality check but there is no treatment for you. When your condition worsens we'll be happy to prescribe drugs for the symptoms but, hey, whaddya gonna do??

Much of my discomfort w/this condition revolves around the anxiety associated w/becoming "that guy" to everyone around me. Of course, the uncertainty about my future sucks. I find myself watching the gait of strangers and envying the way they smoothly walk, left right, left right. I'm a bit bummed out; @ this point the 1 thing that IS treatable is the debilitating depression I'm experiencing, but I'm trapped. No insurance, though probably eligible for free healthcare in MA where I live but I can't motivate myself to do anything because I'm so depressed. AHHH!!

So, thanks for reading and 'hello'. Looking forward to interacting w/ you guys.

-Phil
Back to top
View user's profile Send private message
Artifishual
Family Elder


Joined: Mar 10, 2008
Posts: 283
Location: Texas

PostPosted: Mon May 05, 2008 4:29 pm    Post subject: Reply with quote

Welcome and it is a pleasure to meet you Phil,
You are in a room full of "those guys" so get comfortable. LOL
Hope the depression gets better and look forward to hearing fom you. There is alot of good info on here.

_________________
"Never approach a bull from the front, a horse from the rear or a fool from any direction."
"If there must be trouble, let it be in my day, that my child may have peace."
Thomas Paine
Back to top
View user's profile Send private message Send e-mail
AllyB
Family Elder


Joined: Apr 23, 2007
Posts: 331
Location: Africa

PostPosted: Tue May 06, 2008 3:59 pm    Post subject: Reply with quote

Hey Phil

Welcome - nice to meet you. I am sorry that you are here though, as this is not a nice place to be (except for the people, of course!). I hope that you will connect with some folks and get some helpful information.

The depression is treatable, lots of folks here have taken or are taking anti-depressants, so it might be worthwhile getting your health care eligibility sorted out, if only for that.
I know that this disease is a horrible reality, but if you are less depressed, you may be able to feel a bit better emotionally - that whole mind body thing - psycho-neuro-immunology!

All the best - look forward to hearing more from you.
_________________
Ally
Back to top
View user's profile Send private message
Loobie
Family Elder


Joined: Sep 12, 2006
Posts: 682
Location: Dayton, Ohio USA

PostPosted: Thu May 08, 2008 6:17 pm    Post subject: Reply with quote

Welcome Phil,

Never feel like a pariah dude. You are still Phil, you just do shit slower than you used to. Really work on 'living in the now' so you can enjoy what may be right in front of you that you wouldn't be able to if you're constantly stressed about the future. Focus on what you can still do and not on what you can't. You can do it man. Your logging on here shows you want to do something, and this is a great place to start. Welcome aboard and I hope you use this board to learn and also to vent when you need to. We can take it all! We are all in this together and that is always a little consoling to me. Good luck and I hope your blues go away!

Lew
_________________
"When you're in jail, a good friend will be trying to bail you out. A best friend will be in the cell next to you saying, 'Damn, that was fun.'"
Back to top
View user's profile Send private message Send e-mail
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Introductions All times are GMT - 6 Hours
Page 1 of 1

 
Jump to:  
You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum
You cannot vote in polls in this forum





Personal Stories about millions of life experience--including multiple sclerosis support, lupus support, depression support . Built by the This is MS team.

Anonymous Confessions | Dream Dictionary
Site Map

This site does not offer medical advice. All treatment decisions should always be made with the full consent of your physician.


Visit our sister site dedicated to Inflammatory Bowel Disease: This is IBD


All logos and trademarks in this site are property of their respective owners. The comments are property of their posters, quoted articles are © referenced source, all the rest © 2002 by thisisMS.com.
PHP-Nuke Copyright © 2005 by Francisco Burzi. This is free software, and you may redistribute it under the GPL. PHP-Nuke comes with absolutely no warranty, for details, see the license.
Page Generation: 0.15 Seconds