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Health directory
Since we last met Steven Mueller, a lot has changed in his life. See the updates he has to share with his new wife.
Meet Julie Blackburn, creator of the Spoonie Day App! Learn a little about her and why she created the app for people just like you.
Wow! A neurostimulator to repair myelin sheath may be the next stage in the treatment of MS. One that may restore damage and not just slow it down.
Of Curbs and Cutaways is an essay about an experiece we had several years ago. I hope you enjoy reading it.
It's here! Multiple Sclerosis Awareness Month 2024. What's on the agenda this year? Among other things, mental health.
A plant based diet and MS is not a new thing. To the contrary, it has been around for several years.
The MS Awareness Shop is where you'll find all those accessories to create awareness of multiple sclerosis, one mug at a time
Our MS Jewelry Shop is where you can find pins, bracelets, pendants, and more - jewelry with a multiple sclerosis theme.
MS is SHIT I fucking hate IT I no longer WALK Thank god I can TALK It’s messed up my LIFE I’m no longer a WIFE Trapped in my HOUSE I feel like a LOUSE
Microparticles reversed physical disability in a mouse model at Johns Hopkins School of Medicine
Continue reading "Microparticles Reversed Physical Disability in MS Mouse Models"
In Lola Falana Part 2 you'll be able to watch more of her available interviews, find links to movies or ways to buy them.
I started going to a naturopath after my GP refused to entertain any notion of using LDN, and he started me on it in 2017. I've used it ever since, and
I can't remember the last time I remembered to remember the thing I often forget. I can't remember the last time I recaptured a story from my past and
Hello visitors, fellow MSr’s, and caregivers, this is a somewhat unusual post, however, Cir and I would love for you to share in our excitement for our son’s recent accomplishments. As a child, Cir Jr loved comics, receiving them for gifts and subsequently devouring them. He loved Captain Planet because the character wanted to save the planet and create a sustainable future for humanity.
He loved the format with its action-packed artwork - the story told in words and graphic pictures with all the excitement of a movie in physical form. As a result of his love for this artform, he spent hours creating characters and worlds from his own imagination, ultimately merging his passion for social justice and comics, to give birth to the project he is now promoting via Kickstarter.
The project, a comic book publishing company, called Conjure Comix, and the story behind it, won the local 2019 Knights Art Challenge with a $60,000 grant prize contingent upon raising matching funds of $30,000 to bring his dream to life. As we all know, the following year, 2020. put a halt to many activities, including Cir Jr's dream of starting his publishing company.
The pandemic did add a new perspective to his project when we saw how marginalized groups were disproportionately affected by COVID, including those with disabilities due to conditions like MS, the African American community, the LGBTQI community, and others. He saw a need for an accessible and easy way to learn about social justice issues through comic books, tracts, and graphic novels.
My hope is that you will join us and pledge as we have, to help get his company off the ground and spread his vision around the world. We also hope that you will share the Kickstarter link with your friends, family, and acquaintances as well.
As a child with a parent suffering from MS, Cir Jr, as well as his siblings, faced tremendous odds at a young age as they watched their father deal with the effects of multiple sclerosis. It directly affected them and the choices they’ve made in their lives as grownups. Cir Jr and his siblings have developed empathy for marginalized groups within our society and want to advocate for and make others aware of what it’s like to live with a disability or as a member of one of those groups.
Cir Jr’s contribution was to create Conjure Comix. Please click on the link above or below to read and listen to his story and help support his dream of creating tracts and graphic novels as you are able. Share it with your family and friends. You’ll be glad you did.
Selma Blair is an American actress who has MS. She shares her journey in her documentary, "Introducing Selma Blair".
John King revealed to the world that he had multiple sclerosis on October 19th of 2020. Who new?
Hi Dear Vistor, A quick update on Cir's Tysabri journey. As you can see from the title of this post, Cir has been taking it for about 5 years now. We
Eyes fall from above, Looks intended to show love. Missed connections brought to light, Body and brain continue to fight. Look down, heart pound Grass
Wondering about MS and COVID19? Here is a video to answer your questions by the National MS Society.
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.
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
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 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
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!
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.
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"
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 10 Pages, 10 Most Visited - Here you'll find the 10 Top Pages on our site! Check them out!
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.
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
If you take other drugs for other conditions or symptoms besides MS, then you may run into problems, especially if those drugs are addicting.
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.
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
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
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
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
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
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
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
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