Search the web
Sign In
New User? Sign Up
crohns_n_colitis · This list is intended for those who suffer from the chronic illnesses, Crohn's Disease and Ulcerative Colitis. I hope to be abl
? Already a member? Sign in to Yahoo!

Yahoo! Groups Tips

Did you know...
Real people. Real stories. See how Yahoo! Groups impacts members worldwide.

Best of Y! Groups

   Check them out and nominate your group.
Having problems with message search? Fill out this form to ensure your group is one of the first to be migrated to the new message search system.

Messages

  Messages Help
Advanced
Peripheral neuropathy   Message List  
Reply | Forward Message #4764 of 5061 |
Re: [crohns_n_colitis] Peripheral neuropathy

I wonder myself if I am having neurological problems. I do know that it isn't uncommon to have more than one autoimmune disorder. I was dx'd with ulcerative colitis in 2004, arthritis in 2005, and last October I was told I have autoimmune hepatitis. My G.I. told me that oftentimes a person can have 2-4 autoimmune disorders. I have really bad tingling and numbness in my left toes and above my knee - it feels like I can't lift it or bend my leg at times. Both of my arms fall dead asleep every night regardless of my sleep position, it is so painful that I wake up from it...the worst is when I am sleeping on my back. Lately, I've had blurring in my vision - mainly my right eye. I also have been experiencing dizziness/vertigo once or twice a day and mental confusion - I will lose my train of thought or stumble and slur my words. I'm not sure what to do about these symptoms, and am wondering if I may have MS or something of the like. I found it interesting that you brought this up, I feel like maybe I'm not so crazy.
 
 
Babette
 
 
 
----- Original Message -----
From: Eve
Sent: Thursday, December 04, 2008 6:34 PM
Subject: [crohns_n_colitis] Peripheral neuropathy

I have had colitis for 5 years now. Was doing pretty good until I was
rushed to the ER with what was believed to be a stroke. But it was
not, turned out to be Peripheral Neuropathy.

My question: is there a link between these 2 conditions. It seems
that my immune system is not attacking the nerves on my left side.
Have been searching the web and can not find anything that may connect
the 2. Any information would be greatly appreciated.



No virus found in this incoming message.
Checked by AVG - http://www.avg.com
Version: 8.0.176 / Virus Database: 270.9.13/1828 - Release Date: 12/4/2008 8:05 AM


Fri Dec 5, 2008 4:09 am

babettesdaycare
Offline Offline
Send Email Send Email

Forward
Message #4764 of 5061 |
Expand Messages Author Sort by Date

I have had colitis for 5 years now. Was doing pretty good until I was rushed to the ER with what was believed to be a stroke. But it was not, turned out to...
Eve
ladyshadowma...
Offline Send Email
Dec 5, 2008
1:34 am

Sorry I meant to say that my immune system is now (vs. not) attacking my nerve system. ... was ... connect...
Eve
ladyshadowma...
Offline Send Email
Dec 5, 2008
1:57 am

Sorry, I don't have any info but I wound up with questions because my left leg feels heavy and I am unable to lift in straight while in bed doing exercises but...
Patricia OBrien
pattio1944
Offline Send Email
Dec 5, 2008
2:24 am

It started in my left leg, going numb or tingly. Worked it's way up to my arm and this past week was the left side of my face droops and I'm told I talk like...
Eve
ladyshadowma...
Offline Send Email
Dec 5, 2008
2:47 am

I wonder myself if I am having neurological problems. I do know that it isn't uncommon to have more than one autoimmune disorder. I was dx'd with ulcerative...
A Busy Child Daycare ...
babettesdaycare
Offline Send Email
Dec 5, 2008
4:09 am

Boy that does sound so familiar. My arms and legs would do the same thing at night and the pain would have me walking and trying ice packs heat packs,...
Eve
ladyshadowma...
Offline Send Email
Dec 7, 2008
2:58 am

EVE, FYI....I started having Peripheral Neuropathy symptoms after taking FLAGYL for an extended period of time, to help heal a Fistula due to CD. I had to stop...
hermit_46
Offline Send Email
Dec 16, 2008
7:02 pm

I am on Remicade, and am wondering if that is where my symptoms are coming from. I am not currently taking Flagyl, but did briefly for a hospital stay 2 years...
A Busy Child Daycare ...
babettesdaycare
Offline Send Email
Dec 16, 2008
7:52 pm

Hi, I am new to this group. I used to be on Remicade and it always made me itch like crazy!!! It also caused a rash on my arms and legs. Rhonda ... From: A...
Rhonda
leighhi27
Offline Send Email
Dec 16, 2008
8:13 pm

How long were you on the Remicade before you noticed the itching? I've been on it for 2 years now and I'd say the itching started about 4 months ago...it's...
A Busy Child Daycare ...
babettesdaycare
Offline Send Email
Dec 16, 2008
8:42 pm

I was on Remicade for 18 months when I developed a severe allergy.  24 hours after my treatment, my throat started swelling and closing.  I was at work and...
Patricia OBrien
pattio1944
Offline Send Email
Dec 16, 2008
9:15 pm

Well, I was on Remicade for about 2 years, every 6 weeks. I started noticing the itching about a year into the treatments and the rash was after my last...
Rhonda
leighhi27
Offline Send Email
Dec 16, 2008
9:18 pm

When I first started getting Remicade they did a slow infusion and it took about 4 and 1/2 hours. Then they changed it to 2 hours. I never thought that that...
Rhonda
leighhi27
Offline Send Email
Dec 16, 2008
9:31 pm

I took Humira for about a year.  Again, I might sound like a doomsayer and I don't want to keep people from trying Humira.   It was wonderful.  Maybe it is...
Patricia OBrien
pattio1944
Offline Send Email
Dec 16, 2008
9:46 pm

One of my doctors at Emory in Atlanta mentioned that she didn't really think Humira was very effective. My GI doctor here in Athens wants me to try it. I am...
Rhonda
leighhi27
Offline Send Email
Dec 16, 2008
10:08 pm
Advanced

Copyright © 2009 Yahoo! Inc. All rights reserved.
Privacy Policy - Terms of Service - Guidelines - Help