The Life in Spite of MS Blog is our written experience about living with MS. It...
You can even subscribe to our Life in Spite of MS Blog (without giving us your email if you prefer), RIGHT-click on the orange RSS button on the left at the bottom of the NAV Bar. Copy-and-paste the URL of this site's RSS feed into your RSS reader. It's that simple!
Or click on the Facebook or Twitter button at the bottom to share this page with your family and friends.
This is the best way to get your favorites and news RSS feeds brought right to you.
Would You Like To Be Part Of This Blog?
Become part of the Life in Spite of MS Blog! All you do is tell your favorite story by clicking here and choosing one of the links! Your story becomes part of this blog (which shows the site's most recent pages) and a permanent part of Life-in-Spite-of-MS.com for other visitors to read and enjoy!
The hopes and dreams for my life changed forever on that fateful day in May 1999 when I was diagnosed with MS. I can still hear the words the neurologist
As a Spouse Caregiver of someone with MS, the time spent in this role can be overwhelming, as much as it is a blessing.
Hello again! It's been a long time ... but I was one of your interviews (just saw myself on your page). You came up in my Google search ... so we meet
All the LiSoMS Videos in one place! You can find them all right here. Cir's vlogs, yes, that's right - he's vlogging! Let us know how you like them.
...You are a true inspiration to many of us. As for as whom will read this and respond I will thank you all. Hello, my name is Casey Raines, I have MS!
Stem Cell Therapy for MS, or SVF, is a treatment that many people wish they could get. The results have been very positive for those who are able to afford it.
The MS Recipe - what exactly is it? For those who already use essential oils, you may already know. For those who don't, read on...
Hi all! Just wanted to let everyone know that we will be canceling the forum page. We have over 600 members, however, it is just too expensive to keep up without any participation.
Sooo, our solution to this is a new Network - which by the way is free! Click on the link and you'll be taken right there to join. Hopefully this will be better way to engage with one another.
So head on over and join now. The forum page will be closing soon.
MS Mouse would like to share her challenges with you, her fellow MSers. Here you will find blog posts especially for you.
A wheelchair is a fact of life for many MSers. Yet for some, it's something that they hope they'll never need.
MS is the Snowflakes Disease. Want to know why? You may already know. We just found out the reason a few weeks ago.
Are there any essential oils for MS that can help alleviate the symptoms or even slow the progression of the disease? If so, what are they?
A wheelchair ramp is a must if you use a scooter, powerchair, or manual wheelchair. We tried living in one apartment without one and it was not fun.
An accessible kitchen is a must if you do most of the cooking and even if you don't, it's a necessary convenience.
Cir's 4th infusion of Tysabri went well. No video again - hopefully next time. Also, no adverse reactions and still on an uphill as far as feeling more
More African Americans with MS Videos part 3. Here you'll find even more videos of people of color sharing their journey's with multiple sclerosis.
More African Americans with MS Videos 2. Here you'll find more videos of MSers who share their experiences while living with this disease.
Here are African Americans with MS videos. This page contains a host of videos by several African Americans from 14 and up. Enjoy!
The statistics about MS in African Americans may not be true. An article in Momentum, an MS magazine, shows how the myths about what we've long thought about who gets MS, may have been skewed.
MS and diabetes are both autoimmune diseases. If you have MS, you are more likely to develop other conditions as well.
Take a look at the Snapshots of MS Photo Album. It includes people like you, who have MS and have learned to live with it and persevere. It also includes memorial pictures of courageous MSers.
Hi everyone! Cir had his third Tysabri infusion this past week. Our intention was to actually do a short video, however, that did not happen. I will try
Hey there, I write for, play in, sing for, and manage, a local Nashville rock band. We're called Crack Mammoth. I have a hard time standing for more
Our MS Jewelry Shop is where you can find pins, bracelets, pendants, and more - jewelry with a multiple sclerosis theme.
Why can I not find a chat room? When I can't sleep because my hands are on fire, and I just want to rip my hair out, I would like to talk to somebody with
Multiple Sclerosis an Enigma by Terry Crawford Palardy - a Book Review. A woman receives a diagnosis of MS much later in life. This is her story.
Meet Jamie-Lynn Sigler! Or maybe you already have, figuratively of course, as Meadow on the TV show Sopranos!
Respite care is something I didn't know was available for years as a caregiver. There are services that will allow you to have a break from your duties as a caregiver.
Thank you. I was diagnosed with Dystonia in 2001. Had to leave my job as a mechanical engineering designer. Became homeless. But your book gave me hope.
A Tysabri Update - If you've been coming to our site for awhile, you may have read that this medication was one that we didn't feel comfortable with. Well that's changed.
LISOMS on Pinterest! Yes, you heard that right! I love Pinterest and have several boards there. So why not have one for Life in Spite of MS, too? Check it out!
I Fall One neurologist said it's M.S. A specialist said nope; it was when you were rear-ended. It doesn't matter, though, does it? Because I fall. I was
You are very fortunate to over come your MS. My husband is not. I see him going down hill everyday. Was diagnosed in 2000. Now early retirement and having
I read this article about MS and cryotherapy and have met someone with MS who swears by it. Has anyone here tried it? (Clicking the following link will
I'm country singer Vince Smith. Watch for my MS commercial soon. My new cd is out. Vince Smiths Greatest Hits. Love you all, thanks for buying my cds and
My new single is finished, when you purchase it the money goes to Life In Spite Of Ms.
Hi, I have been experiencing foot spasms (primarily at night though do happen during the day) for a few years. I have had radiating spasms in my forearms
When you have Multiple Sclerosis, It is funny; You are not allowed to cry, Wipe those tears Back of your eyes will hurt Like you are getting blind Not
As of this year (2016) February, I finally went to see a neurologist about symptoms I was having. Thinking it was something to do with a pinched nerve,
Dear Me, it’s been a long time since we spoke,you know, heart to heart. I miss you a bunch, I mean it so much. Such strangers we have become, where did