Jaron,
While you're in Brazil I think you should check out the juices with Acai Berry
in them. I have gotten TREMENDOUS relief from drinking this (new to my area)
juice called Mona Vie that I've even become a distributor. Its some super
antioxidant berry that I am quite sure has
I think the weather you're looking for is in Fijilol
--- On Sat, 12/5/09, CANDIS KALLEY cakal...@embarqmail.com wrote:
From: CANDIS KALLEY cakal...@embarqmail.com
Subject: Re: [TMIC] Back on!!!
To: tmic-list tmic-list@eskimo.com
Date: Saturday, December 5, 2009, 4:25 PM
#yiv31901541 p
I have not gotten any vaccines yet because I was on the fence about it. I have
gotten the flu vaccine in the past and was fine.
However, my MS Dr. told me to get the vaccines, but do not get the kind that
are taken in your nose.
Happy Halloween,
Jill
--- On Sat, 10/31/09, lynne myers
After 6 years and 2 TM episodes I finally got a diagnosis yesterday. I went
from having TM to MS to no MS to Lupus. Oddly enough all normal lupus tests
come back negative, but theres a new and specific one that came back positive.
The crazy part is I was taking shots for MS since March! Good
. I would not even mind a month wait to get into a doctor just because I
know I would not have to live on the street to pay for the treatments needed.
Kathy who is frustrated, hurting, depressed and scared..
- Original Message -
From: Jill Z
To: LadyOwl
Sent: Tuesday, September 15
Jill From Chicago
--- On Sun, 9/13/09, Laura Beaudin laura.beau...@gmail.com wrote:
From: Laura Beaudin laura.beau...@gmail.com
Subject: Re: [TMIC] Looking for TMr's for support groups
To: Catherine camoa...@yahoo.com
Cc: kevin weilacher hwyfli...@yahoo.com, Transverse Mylitis Group
I wonder if this could work for TM? Does anyone take this blood pressure
medicine and notice any difference? Maybe with some blue gatorade and blue
MM's it would work better...hehe
http://www.webmd.com/multiple-sclerosis/news/20090817/blood-pressure-drug-may-help-treat-ms?ecd=wnl_mls_091109
Jim that is great! No pain no gain. Have you been eating blue MM's or
something???
--- On Mon, 8/24/09, Jim Lubin jlu...@eskimo.com wrote:
From: Jim Lubin jlu...@eskimo.com
Subject: [TMIC] able to move slightly
To: tmic-list@eskimo.com
Date: Monday, August 24, 2009, 3:26 PM
The past two
I had that banding feeling when I first got diagnosed 5 years ago also. But
with my second attack in January I didn't have it thank God!
--- On Tue, 8/11/09, pjv1...@chartermi.net pjv1...@chartermi.net wrote:
From: pjv1...@chartermi.net pjv1...@chartermi.net
Subject: Re: [TMIC] That banding
Wim I really like your paintings! What talent. I really LOVE the palm tree
one. That would go great with the decor in my house.
Jill
--- On Sun, 7/5/09, wim from holland wim_from_holl...@hotmail.com wrote:
From: wim from holland wim_from_holl...@hotmail.com
Subject: [TMIC] arts page
To:
Carol,
That is great news! Glad to hear he's on the road to a speedy recovery.
Continue to Keep us posted!
Jill
--- On Sat, 7/4/09, cjb...@aol.com cjb...@aol.com wrote:
From: cjb...@aol.com cjb...@aol.com
Subject: [TMIC] Update on Jim
To: tmic-list@eskimo.com
Date: Saturday, July 4, 2009,
Well said Tracy!
Jill
--- On Wed, 6/17/09, Tracey L. Black tracey.bl...@hnoins.com wrote:
From: Tracey L. Black tracey.bl...@hnoins.com
Subject: RE: [TMIC] Transverse Myelitis Network
To: ladyno...@aol.com, heyjude48...@aol.com, tmic-list@eskimo.com
Date: Wednesday, June 17, 2009, 1:14 PM
I get them with correspondence from my daughter's school. I guess they want to
confirm which parents read the email
--- On Mon, 6/15/09, Grace M. grace...@gmail.com wrote:
From: Grace M. grace...@gmail.com
Subject: Re: [TMIC] read receipts?
To: jharpe...@aol.com
Cc: k...@frontiernet.net,
My doc just told me it's VERY VERY important to take 3,000-5,000 IU of Vitamin
D plus omega oils (either fish or flax) every day. Also anyone over 45 should
be taking a baby asprin everyday.
Fewer broken bones when we get older because the vitamin D helps the body
absorb calcium which is
I'm here too.
--- On Tue, 4/7/09, fr...@franksheldon.com fr...@franksheldon.com wrote:
From: fr...@franksheldon.com fr...@franksheldon.com
Subject: Re: [TMIC] Where is everyone
To: rn11...@yahoo.com, tmic-list@eskimo.com
Date: Tuesday, April 7, 2009, 8:21 AM
Everyone is getting ready for
Jim,
Thank you for the link to the video.
As a former fertility patient...My ex husband and I did fertility meds in
'99-2000 and of course they cannot put all of the cells they make inside of
you or you will end up like Octomom. They freeze them for a later date.
In my case we got
I know some of us TMr's turned into MSr's and I was just wondering have any of
you experienced that Lhermette's sign when you bend your neck forward and get
electric down your legs? And does that ever go away???
Thanks,
Jill in Chicago
TM '04
MS '09 :(
Is anyone out there? I'm weaning off my prednisone now and had a few questions.
Thanks,
Jill
.
I still have no solumedrol drip!!
--- On Sat, 1/31/09, lynne myers lynnemye...@yahoo.com wrote:
From: lynne myers lynnemye...@yahoo.com
Subject: Re: [TMIC] Exacerbation? Medrol Dose pack?
To: Jill Z jillybean60...@yahoo.com
Date: Saturday, January 31, 2009, 6:09 AM
I have used the dose
Hi Everyone,
I had another mild episode/exacerbation of TM the other night. I am a little
weaker today than yesterday.(left leg weakness, right leg burning nerve pain)
I couldn't get a hold of my regular neuro, but got a script for the Medrol dose
pack from one of the docs in the ER.
Normally
If it's religious or political and you DON'T like it then just delete it.
Simple and done. No big deal...
--- On Fri, 10/24/08, Sandy Heidel [EMAIL PROTECTED] wrote:
From: Sandy Heidel [EMAIL PROTECTED]
Subject: Re: [TMIC] re:guidelines
To: [EMAIL PROTECTED], tmic-list@eskimo.com
Date:
Hi All,
I'm still on the list but don't have much to say since I had a pretty good
recovery and I'm actually working 2 jobs thankfully and have been super busy.
I do still think of my TM and continue to pray for all of you.
Jill
Jim Lubin [EMAIL PROTECTED] wrote:
Whenever I hear this I
I get a flu shot every year before and after TM and nothing is any different.
Jill
Grace M. [EMAIL PROTECTED] wrote:
I don't get flu or pneumonia shots either. Because my TM was a result of
relapsing Devic's, it's just not a risk that I am prepared to take.
HI Mindy,
I haven't posted lately myself and I'm in about the same boat as you are.
I have had Lhermette's sign on a few occasions in my 2 years of TM. I
actually had it before then and blew it off because it went away.
I have not had ANY symptoms in a while thank God.
I just wanted to
Kevin,
In fact one of my friends from work had Carpal Tunnel surgery yesterday. I
guess the pain in UNBEARABLE at times and she had a spur of the moment surgery
because she couldn't stand it anymore. Some people live with it for years
though.
It's hard to say in our cases with TM as a
I don't mind hearing about people who have other diseases, syndromes,
whateverI have TM and my best friend has MS. Sometimes we compare notes.
It sure doesn't hurt since it seems like we're all in the same kinda boat. I'm
always worried that my TM will come back OR progress to MS?
Happy Birthday May Babies!!
[EMAIL PROTECTED] wrote: Happy Birthday to the May babies!!
If any of the information below is not accurate, please send a correction to
[EMAIL PROTECTED]
If you don't see your birthday here and would like to have it added, please
send the information to
Hi Everyone,
I was wondering if there was anyone out there that has been pregnant and had
a child since they've had TM? Was your pregnancy normal? Did you have any
times where the TM got worse? I have a pretty mild case and am contemplating 1
more child.
Thanks for all your help!
Jill
Great for her!!! Keep up the good work!
Tracey L. Black [EMAIL PROTECTED] wrote: My daughter, Ashlee,
has just permanently given up her wheelchair. She is now using an up n go
walker and her forearm crutches as her only form of transportation!!! She is
coming up on her 2 year
I do too...even if the website is in my favorites..
ROBERT COOK [EMAIL PROTECTED] wrote:I DO, DO THE REST OF YOU ALL?
EVEN IF I KNOW THE WEB SITE.
BOB
- Original Message -
From: Jim Lubin
To: tmic-list@eskimo.com
Sent: 1/19/2007 3:49:16 PM
Happy New Year to you Jude and everyone else on the list. Let's make this the
best year ever!
Jill in Chicago
[EMAIL PROTECTED] wrote:
Happy Birthday December Babies!!
[EMAIL PROTECTED] wrote: I can't believe we're just about into December
already! Where did November go?? Happy Birthday to all the December babies!
(Please send any additions or corrections to [EMAIL PROTECTED])
12-2-74 Meghan ([EMAIL
I got these
Carol E [EMAIL PROTECTED] wrote:
Have not received any messages for 2 days. Is the list working?
www.greatamericanbeanbag.com
-
Access over 1 million songs - Yahoo! Music Unlimited.
Hi Everyone,
Thanks for the input on the epidural injection. Well I didn't receive it
today but I'm supposed to next Saturday. The doc prescribed Neruontin and
Baclofen for my pinched nerve? I've never taken any of these for TM or
anything else, but I know alot of you are on them. Can you
Sharon, Yes. My left side is the bad side too, and that's how my TM started. My right foot also felt weird too. I was walking like a duck for a long time because I couldn't feel my leg and feet. I think you need to see your neuro. I didn't like the prednisone either, but it's supposed to help
Happy Birthday November babies!![EMAIL PROTECTED] wrote: I can't believe it is November already! Happy Birthday to you all!(Please send any additons or corrections to tmic-list@eskimo.com).11-01-59 Ella ([EMAIL PROTECTED])11-03-60 Gina ([EMAIL PROTECTED]) 11-8 Diane ([EMAIL
I want to thank everyone for their thoughts and prayers about the MRI yesterday. I couldn't wait til Monday and I found out the results today via my friend at work: 1) I have a brain 2) it has no lesions 3) it's unremarkable YAY!!! Now I can go to my halloween party and enjoy myself and have
Ok everyone, I had my 2nd annual MRI of my braintonight. The neuro said I really show signs (upon exam)of MS but let's hope it's negative. I'm a little nervous and I'm gonna be nosey and look up my results myself at work on Monday...Hopefully I won't faint at my desk. I have a tendency to do that
Bernie, Show off those pearly whites! For those who don't want to see you're smile...they can just delete. Sometimes we don't have a whole lot to smile about so go ahead and show it off I say. Jill in ChicagoBernard Pelow [EMAIL PROTECTED] wrote: Hey Folks, A while back I asked for help in
You guys are describing exactly what I've been asking about...A pressure in my head that I can feel all over my head and in my ears and in the top of my throat/jaw. I even told my Dr. it feels like I have encephalitis without a headache! Like a big head and more off balance when this happens.
I'm confused too. I swear something is wrong w/ my jaw and my left side feels weaker and less sensation than the right. My lesion is at T10-11 why the hell am I feeling it in my left arm and jaw and neck and ears??? I see the neuro on 10/18 maybe something else is going on? Anyone else feel this.
I've been getting them too. Some were sent individually to me and not to the whole group so I can't be sure what/if I missed anything.bobby jim hijar [EMAIL PROTECTED] wrote: I've received at least 23 messages since Thursday. I may have trashed others but I can't remember now..;)
Margie, I've had increased symptoms lately BIGTIME. Mine usually get worse around that "time of the month" + I think the full moon doesn't help either. I'm about ready to go on some antidepressants but I'm trying to hold out. A little ativan here and there will hopefully do it. My mornings are
I used to get the banding across the top and arch of my leftfoot as if I had an ankle brace on. I also would getaround on my left wrist.Krissy Z [EMAIL PROTECTED] wrote: My banding is usually my right leg, and some days better than others, the tightness around my ankle and knee...sometimes my
muscles, and have spent a fortune on Rolfing treatments to ease it off. (They didnt work) Thank you for sharing your experiences. Mine is on the right side, from the torso on down the leg, right to the foot.JanetFrom: Jill Z [mailto:[EMAIL PROTECTED] Sent: September 4, 2006 4:49 PMTo
Mine came on gradually also. I thought it was Cauda Equina Syndrome again like my dr. said the first time 2 yrs ago"Butcher, Bernie [SFS]" [EMAIL PROTECTED] wrote: I think mine came on gradually - when I thin back to what happened before I went totally numb, tingly and lame on my left
I think I was on 900mg a day for a while and I swear I felt worse too! I think it made my condition worse. Especially since mine was caused by a virus and prednisone weakens your immune system..I think it made it worse. I'm ok for now though."Butcher, Bernie [SFS]" [EMAIL PROTECTED] wrote:
Hi Everyone, Have any of you ever heard ofa lipoma or a hemangioma of the spine? One of my friends at work has this and has numbness in her arms, constant painand has memory problems etc. Sounds a little like us but her legs and bladder and bowles etc are fineJust thought I'd see if anyone is
Note: forwarded message attached.---BeginMessage---
The following article from the Chicago Sun-Times
has been forwarded to you by [EMAIL PROTECTED] If you wish
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Comments from the sender:
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I'm pretty new to the TM thing and seem to be making a good recovery so far but I was wondering if: #1 - Do any of the women notice their symptoms are a little worse before their periods or ovulation?#2 does anyone ever get a pressure like feeling in their head? It's not a headache but just
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