This page is for fans of Jooly's Joint, and online community for people with MS run by Julie Howell. If you'd like to share your experience of life with MS or ask questions, please visit the Jooly's Joint website at http://www.mswebpals.org
Information
- Founded:
- 27 January 2008
Favorite Pages
Photos
2 of 4 albumsSee All
Lunch April 2009Created about 6 months ago
JJ's 10th birthday party!Updated on April 1, 2008 at 2:36pm
4 of 16 fan photosSee All
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Events
1 past eventSee All
- MS Life
Manchester Central
Saturday, March 29 at 10:00am
Karen Hi i am new to this site i have had ms for 13 yrs but only deff for 5 yrs i am pretty good still but the last two yrs things started getting worse and now need to use a dissability scooter out side for longer walks .Have been on capaxone for 18 months without any affect so they now want me to try tysabri is any one out thair on it to help me with info thanks kaz
Roger Chamberlain I've just set up a new site for those of us blessed with MS. Called LAMS based in rural Norfolk, England. Check it out!
Marion Hi all MSER for 4 years anyone here from NJ NY?? Havent been to JJ in a long time but still a member
Lori Hi everyone....I am in north Florida and have had MS for nearly 20 years. I still work full time and am mobile and get around pretty well. I am on Copaxone (although I don't want to be). My MS is progressing slowly, thank God, but I try to never take a day for granted. I would be happy to be a friend to anyone who ...needs one. Please feel free to add my name. I check my FB nearly every day. Have a wonderful day! :0)
Jooly's Joint Nearly 500 fans, I'm amazed! Thank you Margo for doing such a great job here.
Jooly's Joint
To everyone who knew Geno, who was a regular chatter in the JJ's chatroom, and who sadly died recently...
This group is for our memories of him.
This group is for everyone's memories of Geno (Gene Stein) - a one-off, a great friend, and one of the good guys!
Hugh Miller Hi all my name is hugh i'm from stenhousemuir sunny scotland i have had ms for 12 years now .
Sarah Lipson Hey all...my names Sarah and i was diagnosed with MS last yr.I live in Manchester in the UK and i would like to make a young persons group get together of young people with MS,maybe go for a drink etc...if anyone is interested please contact me...keep well.
Todd Bob Miller
HERE HERE, IS THERE ANYBODY IN THE JOINT FROM SILVERLAKE CALIFORNIA????
HOPE EVERYONES DOING KICKIE!!!
Orla Morris Hi all, anyone from ireland in jooly's joint?
Belinda L. Dees-Boyd Good morning to ya. I have MS and would like to meet friends!
Jo Maynard hi all im new lol
Jamie Meyers i dont mean to knock rebiff. but i was on rebiff for a year and a half.. (first meds i was on for MS) and i was in pain of some sort mostly everyday. unable to touch my toes without a tear to follow, i thought i was going to feel that way the rest of my life. after speaking to my doctor (who also figured out that the r...ebif was not doing its job 100% of the time) started me on copaxone.. now i am no sales person, but if i had to sell something, it would be that. the shot maybe everyday, but the ability to stand up straight and the lack of pain.. is worth it.
