Using Schedule A to find a Federal Job...I was curious if any one had any experience or suggestions about using the Schedule A selective placement program for applicants with...reactions4repliesWork & Employment
Help me sleep...Cannot get more than 90 min per overnight session. Might, if lucky get two sessions in overnight. Have tried MMj - vapourizer...reactions1replyCoping
MY WIFE HAS M.S....Hi, Lorraine has MS and is taken Tecfidera, so much better than the shots. Gradually she is becoming worse and uses a...reactions2comments
MS was the only thing I focused on...I was diagnosed in 2007 with RRMS. I worked 12 hr days 5-6 days a week as a QA Supervisor in a...reactions2comments
It is what it is & I am slowly dealing with it......I am 37 & finally got diagnosed with RRMS after a year of tests and trials. It was a relief to finally...reactions3comments
Lesser-Known MS Evils...I love living in a world where I can Google anything and instantly have an answer at my fingertips. It especially comes...reactions52comments
“That’s Normal, We All Do That!”...You know what really grinds my gears? Since I was diagnosed with Multiple Sclerosis I have been dealing with this and I...reactions49comments
Makes us stronger...I am determined not to let this disease define who I am, but it does define what I am fighting through my...reactions2comments
Strength...I was diagnosed several years ago with the illness. It's funny because if you didn't know me you would think I'm the...reactions8comments
Numbness and tingling in lips...I have recently been diagnosed with a mild case of MS. I have had tremors for years and recently developed numbness and...reactions4repliesSymptoms
JimmyT's post about the holidays and website...In an effort to help people take control of their lives, I've been writing a number of stories for the website. I...reactionsrepliesCommunity Resources
How MS Helped Me See What the Holidays are Really About...Living with MS, there are always three things that I think about whenever I have to go somewhere for any length of...reactions2comments
New at this. Trying to figure it out...I am new at MS. PPMS is now in my vocabulary. Part of my job is being a researcher so research on...reactions2comments
Meghan Pcsolyar...Meghan was previously an advocate on MultipleSclerosis.net. Meghan is an advocate on MultipleSclerosis.net. Meghan, 23 at the time, was on vacation August...
Myoclonus – Why am I So Easily Startled by Sound?...A few years ago it’s like something changed in me. Noise was so unbearable! Specifically, loud and sudden sounds. Everything is so...reactions102comments
Well Meaning Words, "But, You Look So Good!"...After living with RRMS for almost 30 years now, like others that have heard this said to them (But, You Look so...reactions6comments
Trigeminal Neuralgia...I have TN and I was wondering if anyone could tell me how long it lasts. I'm currently on meds to control...reactions3repliesSymptoms
Dying yet living with Love....My story begins very early stage. I will give a short version, as I'm writing a book. No one could understand, why...reactions1comment
Lonely and frustrating...I was diagnosed August 2008 with RRMS. Since that time I have had my ups and downs but always pushed through it...reactions4comments
