|Chat Schedule||Stories and Pictures|
|MS Canada||Famous People|
|Recipes||Rod's Music Shoppe|
PWMS chat ! - Update:
PWMS Welcomes Barb, FrogFairy, Kevin, Kham7, LenoreKitty. We look forward to chatting with you all again. If it was really busy when you came in, please come back soon. Hopefully we can chat and get to know each other better. We have the best room of chatters online. I am serious about that!
If those flashing avatars and emoticons bother you, you can easily turn them off. Just move your mouse cursor up into gray chat text area and right click your mouse to display a pop up menu. In middle of the menu are two lines with check-boxes for "Show Avatars" and "Show Emoticons." Uncheck the boxes, and the flashing will stop.
We want to welcome Kanga and Wayne as new Room Administrators. They will be hosting chats at times befitting their topsy-turvy world. So Australia's mid-day chats (2-4 pm Sydney Time) will follow directly from North American evening chats. Starting on North America's Saturday Night, Kanga will be hosting DownUnder Mid-Day Chats on Sydney's Sunday, Monday, and Tuesday. Please join her, she welcomes all. And Kanga has an accent you can almost hear in her typing.
Wayne will also shortly start up early evening DownUnder Chats (5 - ? pm Sydney Time). This starts at a late 1AM EST, but a more comfortable 10 pm PST. Hopefully a good overlap. Australian evening chats likely are at an hour few north of the equator are ever awake. (Possibly a few British early-birds)
If all these times and days are driving you bonkers, you aren't alone. Just wait a couple of weeks til Daylight Savings Time kicks in. The Chat Schedule Link on the Chat Log-In page is being revised to clearly show just when somebody is hosting. The Chat Schedule Page is always final word on who's hosting.
Stories and Pictures
Hi, my name is RickÖthis is my story
Iím 48 years old and was diagnosed at 36 with RRMS. 1st exacerbation I lost all feeling in my body, it steadily went numb. Almost a year later the feeling began to return, in reverse of how it started. The end result being only my left hand has remained numb. (Great when needing to get finger jabbed for a blood sample.(more)
Profile: Neville Johnson
My name is Neville Johnson, I live in the foothills of the Rocky Mountains in the City of Calgary, Alberta Canada. I have been dealing with MS since the mid 1980ís. It has not bothered me much (nor I have I bothered ďitĒ) until the past year. Iím not on any meds at the moment except Baclofen for spasticity of my legs. I have three great children, twin boys 29, and a daughter 27. Iím divorced, and was a single parent through my childrenís teen years which accounts for the gray hair. I even have two sweet grand children aged 4 and 2. I believe in having a positive attitude and a good sense of humor.
This could be you
|Your name, story, and
photo in the spotlight, right
here in our newsletter. Just send it along to: PWMS@PeopleWithMS.com
People like to read other stories about MS and dealing with the everyday life with MS. Everyone's M.S. is different and everyone's story is different. Get to know the chatters we chat with.
Hello everyone! My name is Betty or you can call me Betty Jo or Jo or BJ. I might even answer to HEY YOU! just to get my attention. I just wanted to tell a little bit about myself. I am married and have been for 33 years. My husband and I are high school sweethearts. I meet him at the first dance of my freshman year. Sam was a junior. We attended Catholic schools. He went to an all boy school and I went to an all girl school. (more )
NEW BIRTHDAY PAGE
* * * We need someone to keep track of our chatters Birthday's. *
FAMOUS PEOPLE WITH MS PAGE
We're making up a new Famous People Page and we need your input . . . .
So far, we have some semi-famous people. Not really a lot, and not really terrifically famous. Kind of a sad excuse for a list. You're sure to know the name of one or more people that are way more famous. Send us the name of any well known person with MS, and perhaps a one liner about them (like 'World Renowned Chia Rancher ' ) PWMS@PeopleWithMS.com
Preface . . .
"WE GO TO THESE ROOMS TO HELP THOSE THAT NEED IT AND TO FORGET OUR OWN TROUBLES. IT IS NOT A REFERENDUM FOR POLITICAL, RELIGIOUS, OR MEDICAL DEBATE. HAVE AN OPEN MIND...WHAT WORKS FOR YOU MAY NOT FOR ANOTHER." ©copyright 2004 JLS (JEFFS)
Chat Etiquette Reminder
Please make a point to welcome any new chatter that comes in our room. Introduce yourself. Ask if there is anything special they want to ask about, know about. Don't ignore the new chatter. Offer them coffee and a muffin. Make them feel at home. Don't keep chattering about peripheral MS stuff with others, or off-topic stuff.
Just keep in mind the one rule we have: nobody gets to play Doctor in chat. What we mean by that is; don't go diagnosing chatters ailments or recommending medications. Share your experiences, and what any of the drugs have done for you. Don't encourage the idea that any medication is a miracle cure. Or dismiss any, or all, medicines as doing nothing. Even the well known medications have a wide range of effectiveness. The effectiveness of non-traditional and alternative medicines is even less certain. So talk about your experiences, factual studies and medical trials. Offer your opinions with care, and never recommend. Third hand medical testimonials from a friend of your auto mechanic's wife aren't welcome, unless they are really funny.
Also keep in mind that Laws and Health Care options also vary widely both within countries and across the globe. So be sensitive to the personal situations and tribulations chatters face. Don't rub in how great things are for you.
Norma is coordinating all chats please contact her for any changes. All you have to do is look below and find a place that fits when hosting is good for you. Just let her know what you choose!
Chat Hosting Schedule
Please feel free to give us some ideas for chat. Hey, you can even take charge! Do your own weekly, or whenever, chat. Just invite your friends in, have a party. We have many rooms, so you can have your chat in your own room.
The schedule below shows the schedule of a group of regular chatters who are volunteering a couple of hours of their time to host chat on a regular basis. This makes a chat more successful; people knowing there is someone available to provide support at dependable, specific times.
Note: The schedule below is provided as a convenience.
The Chat Schedule Page is always final word on who's hosting.
|Chat Schedule - March 3, 2007|
|Monday||RonB & Norma||4 -6 pm||11 am - 1 pm||10 - NOON||9 - 11 am||8 - 10 am|
|Monday|| Marlene & JackIL
||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Tuesday||Norma & PhilNE||4 -6 pm||11 am - 1 pm||10 - NOON||9 - 11 am||8 - 10 am|
|Tuesday||RonB & Vanessa||6 -8 pm||1 - 3 pm||NOON - 2 pm||11 am - 1 pm||10 am - NOON|
|Tuesday||Deb & MrRED||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Wednesday||Marlene (aka LadyCove) & Nancy||4 -6 pm||11 am - 1 pm||10 - NOON||9 - 11 am||8 - 10 am|
|Wednesday||Deb & MrRED||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Thursday||Lisa & Norma||4 -6 pm||11 am - 1 pm||10 - NOON||9 - 11 am||8 - 10 am|
|Thursday||Deb & MrRED||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Friday||RonB & Norma||4 -6 pm||11 am - 1 pm||10 - NOON||9 - 11 am||8 - 10 am|
|Friday||PhilNE & Kathie||6 -8 pm||1 - 3 pm||NOON - 2 pm||11 am - 1 pm||10 am - NOON|
|Friday||Norma & Rod||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Saturday||Deb & MrRED||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
|Sunday||Deb & MrRED||1 - 3 am||8 - 10 pm||7 -9 pm||6 -8 pm||5 - 7 pm|
Note to New Visitors:
When a scheduled host is logged in, say Hi and hang around a couple of minutes if the room isn't busy -> they're probably just grabbing a cup of coffee or reading e-mail in another window.
When nobody is scheduled to host, take a look on the right side for any other names. If so, say ' Hi' and type their name just as you see it => that'll 'beep ' on their speakers.
Check the 'Connections' Room to see if anyone has stopped by, left a message, and is coming back soon.
Contact us at PWMS@PeopleWithMS.com if you;d like to host on a regular basis.
PWMS Welcomes MSer's from all over
|Wayno has returned from his exotic cruise in the South Pacific this week. He ought to have some great sea and sand stories to share over the next few nights. And perhaps a few pictures.|
|This upcoming week will see the latest online edition of Kanga's Australian Newsletter, Mentioning Stuff. Thank you so much for your hard work. It's a great Newsletter Kanga! You will all be seeing Kanga more in chat. You can read it here http://PeopleWithMS.com/OZ/|
|This is the week we've started on the OzLinks page. If you have any favorite links to resources, now's the time to mention it. . . Post us at PWMS@PeopleWithMS.com|
|Wayno and Kanga are going to start organizing and advertising some Down-Under chats fitting the topsy-turvy times. Their Mid-Day chats are going to pretty much continue right along towards the end of our evening chats. So hang around chat a bit on those nights to help Kanga and Wayno welcome newcomers.|
If you are interested in lending a hand on starting a Canadian Newsletter, let us know. Or let us know where you have seen information we should add to help us build up the Canadian portion of the web site.
COME ON CANADA - HELP US OUT HERE!
|Some of you have met Rod, one of our Florida chatters. He has been also been known as our DJ ! He has a very large collection of music. Rod has offered to do his best to find any song you're looking for, and email it to you. He needs the obvious: Name of singer ! Name of song ! He's not a mind reader LOL ! You can email him your requests at: LINGRAM1@TAMPABAY.RR.COM|
MS BRACELETS OF HOPE
One of our chatters is making MS Bracelets of Hope. She is selling them and donating part of the proceeds to the MS Society. I have to say, they are the very best I have ever seen. Excellent quality sterling silver with Swarovski crystals. The Women's one is shown to the left. The Men's one is sterling silver with wooden beads. She has started a web site http://www.freewebs.com/msthings/ If her web site is down you can email her at firstname.lastname@example.org
Inspirational pages called thePoetry Pages
Please Email us with any poems you would like to share with us PWMS@peoplewithms.com
Our Wednesday evening > Healthy Eating support group has started out so well that we added 3 pages to our web site, and more to the pages. You can find a print out journal, recipes, and check out the exercise page.
We will meet every Wednesday evening - check below for your local time
|Check out all of the recipes on our web site that chatters have shared with us|
Please Email us with any recipes you would like to share with us PWMS@peoplewithms.com
Our objective is to provide an informal, supportive site for people seeking on-line information about Multiple Sclerosis. We aren't doctors, we aren't experts. We just live it everyday. We formed this site to share what we have learned, provide a focal point for exchange of information, and give back to the community.
Support is a very big word when it comes to MS. Doctors can only tell you so much during an office visit. Leaving unanswered questions, concerns and issues. People with any disease can often learn best from each other. To this end we provide a chat forum to share information and suggestions, posting of the latest news, and links to authoritative sources of information.
There are many informative sites out there. Visit them all! You can never have enough information. We do not intend to compete with any other sites. Like coffee shops, each has it's own unique atmosphere and clientele. There can never be enough of them.
Our chat is open for anything that has to do with MS. Some topics are not pleasant. But need to be talked about. If you have a problem, no matter what it is, chances are there is someone in chat that can help you. The one thing that PWMS will not accept is being laughed at for any MS problem. We expect all chatters to be considerate of others.
We have appointed Norma, Marlene, JeffS and JackIL room administrators. They have been using the chat. They walked through the set up with us. They can help you if you need help.
is Multiple Sclerosis?
Multiple Sclerosis (MS) is believed to be an autoimmune disease which primarily causes central nervous system problems. In MS, the insulating fatty material surrounding the nerve fibers, also known as myelin, which functions to speed signalling from one end of the nerve cell to another is attacked by cells of the immune system causing problems in signal transduction.
Sclerosis is the most common of demyelization disorders, having a
prevalence of approximately 1 per 1000 persons in most of the
Onset may occur at any age, but predominates in ages 20 to 40 years. An appearance of MS in childhood or after age 50 is relatively rare. Women are more often affected than men with an estimated ratio of 2 to 1 (DeGirolami et al., 1994). There is a silent, asymptomatic form of MS which is estimated to vary from 5% to 20% of all cases (Netter, 1986) and may be responsible for many cases going unreported.
etiological agent for Multiple Sclerosis has not been identified but it
is known that there are several contributing factors. Transmissible
agents have been proposed in the pathogenesis of the disorder (HSV-6,
EBV and retroviruses) but all attempts to identify a well-characterized
virus has been unsuccessful. Some data suggests an environmental agent
in the pathogenesis of this disease. Genetic influences are also clearly
evident. The risk of developing MS is 15-fold higher when the disease is
present in a first degree relative. One study in
TERMS: Tovaxin™ for Early Relapsing Multiple
If you've been following the development of the drug Tovaxin, you'll be happy to know that www.tovaxin.com is up and running. It contains a description of the study and how you can participate, etc.
What is the TERMS study?
The TERMS (Tovaxin for Early Relapsing Multiple Sclerosis) study is testing Tovaxin™, an autologous T-Cell vaccination in patients with Clinically Isolated Syndrome or Relapsing-Remitting Multiple Sclerosis. An autologous T-Cell vaccine, is made from the patient's own myelin reactive T-cells and is unique for each person. This type of therapy is hoped to attack the underlying cause of MS, not just the symptoms.
this Sunday on Depression in MS
Depression is common in MS. It is also treatable. Join this webchat to learn more from the Director of Neuropsychology and Psychosocial Research at the Bernard Gimbel Comprehensive MS Center at Holy Name Hospital in Teaneck, New Jersey. Frederick W. Foley, Ph.D.
This Sunday, March 4, 2007, 5:00 p.m. EST
Montel Williams is promoting the new prescription program
" Partnership for Prescription Assistance " :
call 1-888-477-2669 / 1-888-4PPA-NOW
There are over 150 different programs that can help you get your meds for free, or at a low cost. Check it out ! ! !
We also have some links up on our web site that may help. Check it outPatient Assistance Programs
If anyone has anything they think ought to be added to the weekly news letter, please email me at email@example.com.