Not expectingWhen I was 14 winter was coming so my mom was talking about getting a flu shot. I thought that'd be a good idea especially with being in school. So... By fred281 min readBookmark for laterReactions0reactionsComments1 comments
MS, no way!I hate to be negative, but I'm not adjusting well to my MS and I've had it 18 yrs. At least 18 yrs ago I was dx'd with MS. I... By dianedee3 min readBookmark for laterReactions0reactionsComments0 comments
Living with MS for 14 years.I have MS for the past 14 years. I was diagnosed May 20 1999. It was not easy I couldn't walk without a walker and do what I just normally... By zonia11 min readBookmark for laterReactions0reactionsComments0 comments
Traveling with MS~My main MS issues involve my cognitive functions. I get easily distracted, my short term memory is non existent and anxiety is very much a part of my everyday life... By ernurseohio2 min readBookmark for laterReactions0reactionsComments4 comments
MS for over 20 yearsI've had MS so long I take things as they come. I try to do the best with what I have. But no longer work and they are a pain... By msallen1 min readBookmark for laterReactions0reactionsComments0 comments
I was 17 It was the second day of my senior year in high school when I really told anyone what was going on. About a week before I had woke up at... By babyfirefly3 min readBookmark for laterReactions0reactionsComments4 comments
Time Your Battles WellLet me start off by saying that sometimes I have what I call a quirky MS misadventure. A recent pre-nocturnal, unanticipated, escape artist of sort’s incident, which threw me for... By lexine-darden3 min readBookmark for laterReactions0reactionsComments5 comments
My Relationship with Medical CannabisMy purpose in writing this is to share my experience and relationship with cannabis as an MS suffer. I am "coming out of the closet". I am 59, a mother... By tesoroms4 min readBookmark for laterReactions0reactionsComments12 comments
My quick journey from advocate to hospital patientAs a RRMS 47 year old I have years of experience with Multiple Sclerosis. I also have the same with advocacy and activism. Last Wednesday I had the honor of... By 1 min readBookmark for laterReactions0reactionsComments2 comments
The Road to diagnosisIt was a cold, dark February morning in 2005 and once again, my eye and facial pain was back. The antibiotics my old GP gave me the week before did... By billie737 min readBookmark for laterReactions0reactionsComments0 comments
Staying strongi was diagnosed about 4 yrs ago and other than numb legs i was coping well. i have gone through some horrific stressful times at work recently and it brought... By eelborno1 min readBookmark for laterReactions0reactionsComments0 comments
Challenge MS~Make it Your BlessingThere is not one person I know who asked for MS. I certainly know I didn't! However,I challenge all of you to turn your anger,sadness,bitterness or whatever negative feelings you... By ernurseohio3 min readBookmark for laterReactions0reactionsComments0 comments
My perspective..My story is….I have had a lot of medical problems in my life so I felt that what I kept experiencing was just going to my normal. I was fatigued... By magent7 min readBookmark for laterReactions0reactionsComments0 comments
My Life with MSI was diagnosed with MS in 1998. I had been teaching school for 13 years. A job that I loved! I had gone to college when our two daughters were... By juneofark1 min readBookmark for laterReactions0reactionsComments6 comments
The DiminisherA fading fifteen years it has been since my diagnosis of MS was confirmed. However, little did I realize at the time, my denial of the ever present possibilities of... By lexine-darden2 min readBookmark for laterReactions0reactionsComments4 comments
Finding InspirationInspiration. With it we can overcome the steepest of obstacles yet without it we are left feeling utterly incapable. While its etiology is as varied and individual as the people... By bucalu3 min readBookmark for laterReactions0reactionsComments1 comments
My experience with what Ashley Ringstaff calls "Cog-fog"NOVEMBER 11, 2013 AT 4:40 PM Cog-fog. Thanks for putting a name to it. It has been difficult to explain to people who are at the receiving end of my... By tesoroms2 min readBookmark for laterReactions0reactionsComments2 comments
My story about MS and employment.Many people on this site have expressed the challenges of MS and employment. I would like to add another experience that was not so positive. My initial strategy for dealing... By tesoroms3 min readBookmark for laterReactions0reactionsComments1 comments
Frustrated and in PainLet me start by telling you a little bit about myself. Back in I don't know maybe 2003 or 2004, maybe even earlier, I would get this weird tingling feeling... By soccermom0811052 min readBookmark for laterReactions0reactionsComments0 comments
Stress Isn't BestStress is my honorary four-letter word. Yes, I can count to six and know it’s not necessarily a bad word but if you have MS it can be downright lethal... By bucalu3 min readBookmark for laterReactions0reactionsComments3 comments