Life in Spite of MS Blog
The Life in Spite of MS Blog is our written experience about living with MS. It...
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Health directory
New Single
My new single is Statue Of A Fool. Vince Smith Reply: That's great, Vince! Thanks so much for letting our visitors know. I am sure they will find it
This is Your Interview
This is Your Interview Page - You can interview your loved one, family or friend - about their MS.
Meet Steven Mueller and his Wife Angie
Meet Steven Mueller and his wife, Angie. Unlike most couples, they both have MS and have agreed to share their story.
Downloading Songs
Hi! Fans, when you download any of my songs, all proceeds go to Life in spite of MS. Thanks alot for being a fan, I sure do appreciate it. Vince
Want to help with MS research?
Hello, My name is Madeline and I work for a consumer insights agency based in Brooklyn, NY. We are currently conducting research about the MS caregiver
19 years living with MS
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
As a Spouse Caregiver of someone with MS, the time spent in this role can be overwhelming, as much as it is a blessing.
MS brought out the Artist in me
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
LiSoMS Videos
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.
Thank you, Montel!
...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 101
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.
MS Recipe
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...
Canceling Forum Page
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.
Desk of MS Mouse
MS Mouse would like to share her challenges with you, her fellow MSers. Here you will find blog posts especially for you.
Wheelchair
A wheelchair is a fact of life for many MSers. Yet for some, it's something that they hope they'll never need.
The Snowflakes Disease - MS
MS is the Snowflakes Disease. Want to know why? You may already know. We just found out the reason a few weeks ago.
Essential Oils for MS
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?
Wheelchair Ramp
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.
Accessible Kitchen
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 Tysabri Update
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
African Americans with MS Videos 3
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.
African Americans with MS Videos 2
More African Americans with MS Videos 2. Here you'll find more videos of MSers who share their experiences while living with this disease.
African Americans with MS Videos
Here are African Americans with MS videos. This page contains a host of videos by several African Americans from 14 and up. Enjoy!
MS in African Americans
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
MS and diabetes are both autoimmune diseases. If you have MS, you are more likely to develop other conditions as well.
Snapshots of MS Photo Album
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.
Cir's 3rd Tysabri Update
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
Expression through music
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
MS Jewelry Shop
Our MS Jewelry Shop is where you can find pins, bracelets, pendants, and more - jewelry with a multiple sclerosis theme.
A plea/question
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 Book Review
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
Meet Jamie-Lynn Sigler! Or maybe you already have, figuratively of course, as Meadow on the TV show Sopranos!
Respite Care for Caregivers
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, Montel
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.
Tysabri Update
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
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"
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
Dear Mr. Montel
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
Has anyone tried this?
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
Dear Friends,
"Life in Spite of MS is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com."
We'd also like you to know it doesn't cost one cent more when you click through the links here on our blog. Not one single penny. And we willl make a little extra cash when you do click through. We'll be ever so appreciative. You also have our word that we'll only link to things that we would use ourselves, (or wish we could have or use.
Sincerely,
Cir & Akrista
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