Pamper Yourself on the Good Days, Too...We all want to feel good, right? We want MS to stay in the background and get no where near centerstage. It’s...reactions7comments
MS 2020...Hi everyone. I am feeling not so good today. I am tired, frustrated feeling some pain today. I have always been a...reactions2comments
2000-2020...Looking back at what I’ve been through as I read personal accounts here makes me grateful to be here. It was February...reactions2comments
How I Learned I Have MS...It was Feb 2011, I cut my workday short in a hurry to get home to take my wife out to celebrate...reactions2comments
Not Being Heard...I have been writing about my many experiences with multiple sclerosis (MS) for years, and one thing people have told me from...reactions21comments
Hereditary Spastic Paraparesis...The Marine Corps found the disease in 1986. Sent me home and would not tell me why. The disease came on July...reactions5comments
MS Comic: Making Excuses...Before her MS diagnosis, Brooke used to search for reasons to stay in. Check out her comic below about all the funny...reactions2comments
Feels Like Sinus Pain...I totally understand about the "face pain". I fell and had a concussion 3 years ago. I experienced headaches for almost a...reactions7comments
Keep Finding My Way Just to Lose It All Over Again...I had my first symptom of blurry vision in the right eye back in later 2013/early 2014, when I was still living...reactions2comments
Face Pain Right Side - Not Sinuses...I have had MS since 2006, however, just diagnosed in 2018. Mobility, vision impaired, chronic pain in face which resemble sinuses. So...reactions6comments
The Other Side of Anger...How many times have you been told not to be angry? These words have been said to me often. Hearing the directive...reactions10comments
MS's Constant Assault on Mental Health...Content warning: The following article discusses depression and passive suicidal ideation. Please know that there are many resources available for support including...reactions25comments
Dangerous Mind...I am 63 years old. I have been diagnosed with MS for over three years. I also have a neuromuscular disorder called...reactions3comments
At Long Last...About 25 years ago my 2nd husband and I began designing a garden I could navigate with MS. My SPMS was diagnosed...reactions3comments
MS and COVID 19...I was diagnosed with MS in 2016 but I had the first signs in 1996 overseas. In spite of these signs, I...reactions1comment
Diagnosed as a Teenager...3 years ago, I was 15 and was diagnosed with MS when my right arm went numb. Followed by that my right...reactions2comments
Used to the Notion of Lockdown...I never thought that people would need to get used to isolation. I have friends doing online zoom sessions with me. They...reactions1comment
Give Yourself Permission to Take A Nap...Why is it so hard to just sit down, close your eyes, and allow yourself to sleep, meditate, daydream, or whatever, in...reactions25comments
My Story...I was diagnosed in late 1978 about 3+ months after the birth of my oldest daughter. I won't go into everything but...reactions1comment
My Invisible Friend...4 years ago I made a new invisible friend full of troubles and pain, but I decided to accept because I don’t...reactions1comment
