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Multiple Sclerosis, lived out loud

Living boldly with Multiple Sclerosis, one honest story at a time

I'm the voice behind MS with Moxie — sharing my real journey with MS, practical advice for the hard days, and the latest updates on treatment and technology, including CAR-T therapy.

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Real talk, real MS Stories & advice from someone actually living it

Follow along on Facebook: MSwithMoxie

Stories from an MS Warrior, not a textbook

Updates on CAR-T & emerging MS treatments

Why people stay

Support that actually understands MS

Real, unfiltered stories

No sugar-coating — just honest accounts of diagnosis, flare-ups, treatment, and the wins in between.

Advice you can actually use

Practical tips for symptom days, appointments, and conversations with the people who love you.

The latest in MS technology

Clear, plain-language updates on emerging treatments and technology, including CAR-T therapy.

How I can help

Ways to work with MS with Moxie

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1:1 Peer Support

A judgment-free space to talk through your diagnosis, fears, and questions with someone who's been there.

See how it works
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Speaking & Advocacy

Talks and panels on living with MS, for clinics, workplaces, and community groups who want the real story.

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MS Tech & Treatment Updates

Plain-language breakdowns of what's new in MS care, from disease-modifying therapies to CAR-T.

See how it works

From the community

You're not doing this alone

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Finding this page the week after my diagnosis changed everything. I finally felt like someone got it.

R
Rachel M.Newly diagnosed, 2023
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The CAR-T updates were the clearest explanation I'd found anywhere — and I've read a lot of medical journals.

D
Dana P.Care partner
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My sister has MS and this page helped me understand what she actually needs from me. Grateful for it.

J
Jordan T.Sibling of someone with MS
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About me

Hi, I'm the moxie behind MS with Moxie

I started sharing my MS journey to fill a gap I couldn't find filled anywhere else — a place that was honest about the bad days, hopeful about the good ones, and serious about the science. What began as a Facebook page has grown into a full community.

Read my full story

You don't have to face MS alone

Join a community that gets the diagnosis, the flare-ups, the small wins, and everything in between.

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About me

My diagnosis didn't get the final word — my story does

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My story

My MS journey started the way most do — with symptoms nobody could quite explain, and a diagnosis that rearranged everything I thought I knew about my future. I remember sitting in the parking lot after my neurologist appointment, googling everything and understanding almost none of it.

MS with Moxie started as a way to process what I was going through. It turned into something bigger: a place where people newly diagnosed, deep into treatment, or supporting someone they love could find honesty instead of pamphlets.

I decided early on that MS could take a lot from me, but it wasn't getting my sense of humor or my hope.

Why I do this

My mission

To make sure no one navigates multiple sclerosis feeling as lost as I did on day one — by sharing real stories, honest advice, and clear information on where MS treatment and technology are headed next.

What makes this different

Why people come back to MS with Moxie

✓

Lived experience, not just research

Everything I share is filtered through what it's actually like to live with MS day to day.

✓

Science made understandable

Treatment and technology updates — including CAR-T — explained in plain language, not jargon.

✓

Room for family and friends too

MS affects everyone close to you — this space is for them as much as it's for you.

Ready to be part of the story?

Reach out, follow along, or book time with me directly — however you want to connect, I'd love to hear from you.

Contact Me

Services

Support built around real MS life

Whether you want someone to talk to, a speaker for your event, or the latest on MS treatment, here's how we can work together.

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1:1 Peer Support

Private conversations for you, or someone you love, to ask the questions you can't ask a doctor and feel heard about MS.

Speaker addressing a small audience at a community event

Speaking & Advocacy

Talks for clinics, workplaces, and support groups on what living with MS is really like, and how to support someone who has it.

Medical technology and research imagery

MS Tech & Treatment Updates

Regular, plain-language breakdowns of new research, disease-modifying therapies, and CAR-T developments.

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Community Workshops

Small-group sessions on managing flare-ups, talking to family, and building a life that MS doesn't get to shrink.

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Family & Friends Guidance

Resources and conversations for the people around you, so they know how to actually help — not just say sorry.

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Curated Resource Library

My personal, vetted list of trustworthy MS resources, from clinical trial trackers to advocacy organizations.

Getting started

How it works

1

Reach out

Send a message through the contact form or Facebook with what you're looking for.

2

Free intro chat

We hop on a short call so I can understand your situation and what would help most.

3

A plan that fits

Whether it's ongoing support, a one-time talk, or resources, we shape it around you.

4

Ongoing support

I stay in your corner — check-ins, updates, and a community that remembers your name.

Questions

Frequently asked questions

No. I'm not a doctor — I share lived experience, emotional support, and plain-language information. Always talk to your neurologist about treatment decisions.

Yes — a lot of what I do is specifically for the partners, parents, and friends of someone with MS who want to understand and help better.

It's an emerging treatment approach being studied for MS that reprograms a person's own immune cells. I cover ongoing developments in plain language on the blog and Facebook page.

Use the contact form and mention "speaking" — include your event date and audience, and I'll get back to you within a few days.

Let's figure out what you need

No pressure, no sales pitch — just a real conversation about what would actually help.

Start the Conversation

My story

The moments that made this journey mine

A look inside my life with MS — the hard days, the breakthroughs, and everything in between.

DiagnosisPerson looking thoughtfully out a window
The beginning

The day the numbness had a name

What it actually felt like to hear "multiple sclerosis" for the first time, and what I wish someone had told me.

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TreatmentMedical lab setting representing CAR-T research
Treatment update

What I learned exploring CAR-T therapy

Breaking down the emerging science in plain language, and how I decided what was right for me.

Read more
CommunityGroup of friends laughing together
Community

The support group that changed everything

How finding my people online turned isolation into one of the strongest communities I've ever had.

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LifestylePerson hiking a scenic trail
Lifestyle

Traveling with MS: what actually works

My honest packing list, pacing strategy, and the trip that taught me both the hard way.

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DiagnosisOpen journal and pen
Early days

The questions I wish I'd asked sooner

A running list I built after my diagnosis appointments — steal it for your own.

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TreatmentDoctor discussing treatment options with a patient
Treatment

Choosing a neurologist who actually listens

The red flags I ignored the first time, and the questions I ask every new provider now.

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CommunityHands stacked together in unity
Community

What my family needed to hear from me

The conversation I kept avoiding, and why having it finally brought us closer.

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LifestylePerson stretching outdoors during a gentle workout
Lifestyle

Building movement into a body that fights back

How I redefined "exercise" on my own terms, flare-ups and all.

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Want the next chapter as it happens?

New stories, treatment updates, and community moments go to Facebook first.

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Contact

Let's start a conversation

Questions, support requests, speaking inquiries — whatever brought you here, I'd genuinely love to hear from you.

Send a message

Thanks for reaching out! Your message has been received — I'll get back to you soon.

Contact details

Emailhello@mswithmoxie.com
Phone(555) 012-3456
Based inUnited States · connecting worldwide online

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