Disclaimer: This page may contain affiliate links. We may earn a small commission for purchases made through links in this post, at no extra cost to you.
Life in Spite of MS Blog
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!
And I'll even tweet your Web page at my Twitter account, too!
Health directory
MS and COVID19
Wondering about MS and COVID19? Here is a video to answer your questions by the National MS Society.
A Vaccine for MS
A vaccine for MS is currently in the works. Wouldn't it be great if there were a vaccine that could prevent and possibly reverse MS? Find out about it here.
Balancing MS
The balancing act of life with no balance. Adjusting to PPMS with tragic optimism. Since being diagnosed, I have thought a lot about the duality of
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
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
MS Poll of the Month
Here's your MS Poll of the Month! Come by and take a new poll every month. Find out what others have answered from past polls. Come on, it'll be fun!
Thank you, Montel, very much!
I watched your blender ad a few years ago and was impressed. I had no idea you had a medical condition you were grappling successfully with at the time.
Mothers of Tacoma Washington Next Chapter Family
Dear Mr Montel Williams, I am writing to you on behalf of our single homeless moms in Tacoma, Washington - the moms of Next Chapter Family, that opened
Continue reading "Mothers of Tacoma Washington Next Chapter Family"
Agent Anonymous
My journey has been long and arduous. I am hanging in there, though. It takes every ounce of my inner strength to get through each day. I have been challenged
Top Ten at Life in Spite of MS
Top Ten at Life in Spite of MS, Top 10 Pages, 10 Most Visited - Here you'll find the 10 Top Pages on our site! Check them out!
CCSVI is Ineffective Update
CCSVI is ineffective according to Dr Zamboni. He recently published a paper in JAMA, showing that, after doing a double blind study, CCSVI doesn't work.
When MS knocks at your door
Life comes with many opportunities, it all depends on one’s choice on how to design or weave it. You either choose to fight or surrender, this is a story
With great admiration
Hi Steven - Up in the middle of the night and couldn’t get back to sleep. Got my cellphone and started bopping around EBay. I tend to have a unique chain
Other Drugs and MS
If you take other drugs for other conditions or symptoms besides MS, then you may run into problems, especially if those drugs are addicting.
MS Awareness Shop
The MS Awareness Shop is where you'll find all those accessories to create awareness of multiple sclerosis, one mug at a time
MS Jewelry Shop
Our MS Jewelry Shop is where you can find pins, bracelets, pendants, and more - jewelry with a multiple sclerosis theme.
My VoxxLife Socks
Here's My VoxxLife Socks Story...., so far. If socks are your thing, then you're in for a treat when you hear my story.
Recently diagnosed
Hi Montel, I've just been diagnosed with RRMS. I was looking at the medications the other night and the side effects scare me. I was just wondering if
Thoughts of you
How could I have thought How could I've ever known That when I first laid my eyes upon you That my feelings would be so strong Strong and what I believe
MS Dropout
My ms story started very early in my childhood. I always knew there was something wrong with my health, even when no one believed me. The headaches I experienced
Get a hobby, I do videos
Since my brother has had MS he does videos with his dog, he is an amazing trainer and his dog is super smart. View videos on YouTube, they are funny and
Live with purpose
Every time I see an interview that someone has done with you, I find it very inspiring. I love that you live your life with purpose and intention. The
Thank you Montel and a request
I am a volunteer veterans advocate in upstate New York. I want to say thank you for your service to our country. My late husband was a Navy Vietnam veteran
Colors
After being diagnosed with multiple sclerosis and having a terrible accident that severely damaged the use of my left hand, I found my therapy through
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.
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.
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're also part of the Ebay Partner Network, another affiliate program."
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 will 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
You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!
Privacy Policy ~ Advertising Policy ~ Disclaimer ~ Contact Us ~ About Us
New! Comments
Have your say about what you just read! Leave me a comment in the box below.