Coronavirus – COVID-19


Coronavirus

COVID-19

 

The past month, Coronavirus has exploded. In the news, in the population and it feels like it’s coming for everyone.

Now, just because it feels that way, doesn’t mean that it’s actually the case.

We’ve all be hearing the data for weeks, so I’m not going to keep harping on it here. I’m going to focus on what we can do to help ourselves instead. I’ve seen plenty of headlines saying there is no way to help yourself prevent it and no treatment, and not much we can do besides hand washing (yes, that is very effective).

But I believe there is plenty we can be doing to fortify our immune systems to hopefully prevent contracting the illness all together, but in the event we do get sick, it will be less of an impact to our health.

Diet

Increasing the overall nutrient density of your meals is going to be super important. Aim for 7-11 cups of veggies a day, and several of fruit as well. Specifically, vegetables belonging to the cruciferous family (including Brussel sprouts, cabbage, cauliflower, broccoli and kale) may help to stop viruses in their tracks; due to a naturally high amount of a compound called indole-3-carbinol (I3C). Clinical studies show that this compound has the potential to interfere with the way many viruses reproduce.

Cooking with garlic and ginger is helpful as well. Both of these have antimicrobial, antiviral effects and also immune-boosting benefits

Supplements

Usually I say check your vitamin D levels and supplement accordingly. However right now, I would say you’re safe to supplement with 2-5k IU daily. Vitamin D is arguably one of the most powerful nutrients responsible for modulating and coordinating the immune system. Always use a product with D3/K2. The K2 will help the D3 be more bioavailable for your body to use. 

Glutathione and Vitamin A can be particularly helpful as well, specifically during flu season and dealing with Coronavirus. Much of the issue with Coronavirus is subsequent pneumonia infections. Low glutathione and low Vitamin A can increase risk of death by pneumonia. Being sufficient in both of these can be incredibly helpful for your overall immune system. 

Zinc is also helpful for your immune system. In our bodies, zinc is used to activate T lymphocyte cells. T cells help the body in several ways. One, by controlling and regulating the immune response. Two, by attacking infected cells.

(If you’re in need of high quality supplements, shoot me an email at info@liss-ms.com. I have an online dispensary account at Fullscript, where I can order supplements for you.)

Vagus Nerve

You might be thinking, the what? Or what does the vagus nerve have to do with our immune system? And in fact, is has a lot to do with it! Our nervous system is in constant communication with our immune system- via the vagus nerve. Studies show that the vagus nerve can modulate cytokine production. Most of us, have low vagal tone. We need to be focusing on actively working our vagus nerve to improve the functioning of the nerve, and therefore communication between the vagus nerve and the immune system. A few ways to do that:

Humming

Speaking

Deep breathing, using and activating the diaphragm

Yoga

Meditation

Cold water rinse, either shower or wash your face

Lifestyle

A few things to consider with your lifestyle. Getting enough sleep is paramount. Try for 7-9 hours. Magnesium is a great supplement to consider if you struggle with sleep. Melatonin can help, but your body can quickly become dependent on it and stop making its own. Melatonin is best in severe cases of insomnia, and only for a short time.

Reduce stress. I know, I know. Seems impossible right now. But stressing isn’t doing your body and immune system any favors. If you’re struggling with increased anxiety due to Coronavirus, it’s ok to turn off the tv. Only check in with the news once a day. Take some time away from electronics and your phone. Get into nature, talk to loved ones, read, color, play with pets!

Get low to moderate intensity activity. This will give your immune system a nice boost, and help to bust boredom, as we’re all stuck at home.

Wash your nasal passages out several times a day. This is a bit more intense, but if you feel like you’re possibly getting sick, or have been exposed, this is a great step to be taking. This cleans your nasal tissue and reduces the virus’s ability to take hold.

How does this affect MS?

Having MS, doesn’t necessarily make us in a “higher risk” category. Same goes for all autoimmune diseases. Our immune systems are actually going off the charts! However, some autoimmune diseases can also be immune deficiency diseases as well (but not always). HOWEVER, many of the medications we’re on, are immunosuppressants. Which do cause our immune systems to be lowered. Therefore causing those on immunosuppressants to be in the “higher risk” category. A little more about that:

Copaxone, Aubagio, Tecfidera, Beta Interferons, and Tysabri

These are likely to be safer than the other DMTs as they aren’t thought to be general immunosuppressive therapies. They are more immunomodulating therapy. 

Lemtrada, Mavenclad, Gilenya and Ocrevus

These are immunosuppressants therapies. They might possibly be putting you at higher risk of contracting Coronavirus (or any virus- as you probably know if you’re on one). 

The other thing to consider as MSers is anytime we get sick, we risk the chance of having a relapse or flare. The increased immune activity can often create more inflammation, and therefore a relapse might occur. This would be a secondary consideration for COVID-19, or any cold or flu.

 

A few supplements to rethink:

Elderberry: Recent research is coming out saying COVID-19 can cause a cytokine storm, which can lead to multi system organ failure. Elderberry increases cytokine activity, potentially making the cytokine storm worse.

NSAIDS: I know, this isn’t a supplement, but many use NSAIDs with fevers, which is common in the flu and COVID-19. More research is showing that NSAID use can increase your risk of developing pneumonia, if you do contract COVID-19. Ibuprofen (and other anti-inflammatories) may dampen the body’s immune response to infection because it is has anti-inflammatory effects.

 

If you do contract COVID-19:

If you think you may have COVID-19, call your doctor first before showing up to the office. They will probably have separate instructions for you on where to go, if testing is needed etc.

For treatments, zinc lozenges, preferably zinc acetate lozenges every 3-4 hours. This can help prevent replication of the virus in mouth, throat and respiratory tissue.

If you’re sick enough to be hospitalized, request IV Vitamin C. This is typically given every 4 hours, to total 6-12 grams of vitamin c, over a 24 hour period. China has utilized this treatment effectively, and currently there are 3 clinical trials running using IV Vitamin C.

 

Obviously this is a very scary and uncertain time. I don’t know what this upcoming week will hold, but if it’s anything like last week, we’re in for a wild ride.

The only things we can control, is our reactions and what we’re doing with our daily life.

In the end, I think we’ll all end up ok.

How are you coping with Coronavirus and COVID-19? What measures have you taken? Have you been significantly impacted? What support do you need right now? Hit reply to this email and let me know. I’ll be answering questions on Instagram and in my FB Group as well. I’d love it if you came over and joined in the conversation!

 

If you’re interested in learning more about what foods are beneficial for Multiple Sclerosis, get my Best Foods for MS Guide here! 

I’M ALISSA!

I help women who have also been diagnosed with Multiple Sclerosis make specific and personalized diet, lifestyle & subconscious changes so that they can begin to heal their body, reduce disease symptoms, and return to a life they love.hey there,

follow along on Instagram:

If we haven’t met yet, Hi! 👋🏼👋🏼 I’m Alissa. 
I’m a Holistic Practitioner & Therapist specializing in Multiple Sclerosis. 

There are SO many tools that we can use to help improve our bodies functioning- which can in turn improve our MS symptoms.

The biggies that have helped me? 👇🏼

🥗Nutrition 
🏋🏻‍♀️Movement
🧘🏻‍♀️Stress management 

Want my most favorite, super short exercise that can help MS symptoms??

Comment: SLAP and I’ll send it to you!!

#lissms #SlapittoMapit #multiplesclerosis #thisisms #becausems

If we haven’t met yet, Hi! 👋🏼👋🏼 I’m Alissa.
I’m a Holistic Practitioner & Therapist specializing in Multiple Sclerosis.

There are SO many tools that we can use to help improve our bodies functioning- which can in turn improve our MS symptoms.

The biggies that have helped me? 👇🏼

🥗Nutrition
🏋🏻‍♀️Movement
🧘🏻‍♀️Stress management

Want my most favorite, super short exercise that can help MS symptoms??

Comment: SLAP and I’ll send it to you!!

#lissms #SlapittoMapit #multiplesclerosis #thisisms #becausems
...

1 0
Comment SLAP and I’ll send you the short how to video!

Your body functioning better so you feel better in 3 minutes? 

It sounds like a stupid infomercial BS claim I know and I roll my eyes every time I type it, but.. it’s kinda true? 

Idk, I’ll let you be the final judge

Comment SLAP and I’ll send you the short how to video!

Your body functioning better so you feel better in 3 minutes?

It sounds like a stupid infomercial BS claim I know and I roll my eyes every time I type it, but.. it’s kinda true?

Idk, I’ll let you be the final judge
...

0 0
Comment SLAP and I’ll send you the short how to video!

Your body functioning better so you feel better in 3 minutes? 

It sounds like a stupid infomercial BS claim I know and I roll my eyes every time I type it, but.. it’s kinda true? 

Idk, I’ll let you be the final judge

#lissms #multiplesclerosis #slapittomapit #betterbrain

Comment SLAP and I’ll send you the short how to video!

Your body functioning better so you feel better in 3 minutes?

It sounds like a stupid infomercial BS claim I know and I roll my eyes every time I type it, but.. it’s kinda true?

Idk, I’ll let you be the final judge

#lissms #multiplesclerosis #slapittomapit #betterbrain
...

10 5
It’s an easy exercise with a silly name, but it actually packs a punch and can really change how you feel. 

Imagine measurably more energy and feeling more stable and balanced- and even improving a few MS symptoms here and there too?🤷🏻‍♀️ 

Your possibilities are endless! 

Comment SLAP and I’ll send you the short video about how to do it!

#lissms #slapittomapit multiplesclerosis #thisisms

It’s an easy exercise with a silly name, but it actually packs a punch and can really change how you feel.

Imagine measurably more energy and feeling more stable and balanced- and even improving a few MS symptoms here and there too?🤷🏻‍♀️

Your possibilities are endless!

Comment SLAP and I’ll send you the short video about how to do it!

#lissms #slapittomapit multiplesclerosis #thisisms
...

16 4
Take a time out for a literal minute.

It’s amazing what happens when you take the time to care for your body and nervous system. 

#LissMS #multiplesclerosis #nervoussystemregulation

Take a time out for a literal minute.

It’s amazing what happens when you take the time to care for your body and nervous system.

#LissMS #multiplesclerosis #nervoussystemregulation
...

13 1
First year flower garden needed a post. Already looking forward to next summer, maybe a little less yellow? Can’t wait for the zinnias to bloom!
😂🌼💛
What are you growing??

#lissms #cutflowergarden

First year flower garden needed a post. Already looking forward to next summer, maybe a little less yellow? Can’t wait for the zinnias to bloom!
😂🌼💛
What are you growing??

#lissms #cutflowergarden
...

17 0
Thankfully I haven’t heard any of these in a while.. maybe that means I’m getting my point across 🤷🏻‍♀️

But if you’re new here, I value holistic lifestyle medicine (snake oil 😂) but ALSO conventional medicine, I utilize it all after all. 

Yes, what we do as an individual matters for our health.
But so does the health systems we as individuals operate in.

Tomorrow is my MS-aversary, 16 years of having this disease. my newly diagnosed 24 year old self would be pretty shocked that I’m 40 (like in general lol) and also not in a wheelchair.

Here’s to many more years defying what I initially thought to be true about MS.

Comin with me? Hope so. 

#lissms #multiplesclerosis #thisisms #lifewithms

Thankfully I haven’t heard any of these in a while.. maybe that means I’m getting my point across 🤷🏻‍♀️

But if you’re new here, I value holistic lifestyle medicine (snake oil 😂) but ALSO conventional medicine, I utilize it all after all.

Yes, what we do as an individual matters for our health.
But so does the health systems we as individuals operate in.

Tomorrow is my MS-aversary, 16 years of having this disease. my newly diagnosed 24 year old self would be pretty shocked that I’m 40 (like in general lol) and also not in a wheelchair.

Here’s to many more years defying what I initially thought to be true about MS.

Comin with me? Hope so.

#lissms #multiplesclerosis #thisisms #lifewithms
...

35 4
I’ve tripped a few times in the last few weeks.. nothing crazy, but I noticed.

And I noticed my thoughts… is this a “THING”??

Oh the constant wonderings of an MSer… 
is this a regular life occurrence?
Or is this a new symptom? 😂😂

When was the last time you had this thought process??

#lissms #multiplesclerosis #thisisms #becausems #multiplesclerosiswarrior

I’ve tripped a few times in the last few weeks.. nothing crazy, but I noticed.

And I noticed my thoughts… is this a “THING”??

Oh the constant wonderings of an MSer…
is this a regular life occurrence?
Or is this a new symptom? 😂😂

When was the last time you had this thought process??

#lissms #multiplesclerosis #thisisms #becausems #multiplesclerosiswarrior
...

53 3
When you’re living with MS, it’s not that you don’t want to feel better…

It’s just that life keeps interrupting the plan.
Stress, symptoms, fatigue — they throw you off track.

That’s where support, structure, and accountability change everything.

That’s exactly what my membership is for.
✔️ Evidence-based strategies for MS
✔️ Real community and support
✔️ Gentle consistency that actually works

Only the waitlist is getting access as a Founding Member.

Comment WAITLIST and I’ll send you the link to add your name 

#lissms #MultipleSclerosis #MSwarrior #MSsupport #ChronicIllnessHealing #MScommunity #HolisticHealing #NervousSystemHealing

When you’re living with MS, it’s not that you don’t want to feel better…

It’s just that life keeps interrupting the plan.
Stress, symptoms, fatigue — they throw you off track.

That’s where support, structure, and accountability change everything.

That’s exactly what my membership is for.
✔️ Evidence-based strategies for MS
✔️ Real community and support
✔️ Gentle consistency that actually works

Only the waitlist is getting access as a Founding Member.

Comment WAITLIST and I’ll send you the link to add your name

#lissms #MultipleSclerosis #MSwarrior #MSsupport #ChronicIllnessHealing #MScommunity #HolisticHealing #NervousSystemHealing
...

16 2
But seriously.. this isn’t too far off 😂

Life handed me a lemon that was a MS diagnosis at 24. 
Life handed me a lemon that was multiple relapses and MS progression by 30.

Then I snatched those lemons, made some healing lemonade, and feel night and day different than I did 10 years ago when my symptoms were at their worst. 

I could do it, my clients are doing it, I know you can too.

That’s why I’m so passionate about doing what I do. I know it’s possible for you to feel better in your body and be able to do the things you want to do. 

Like go for a walk or hike with your spouse, say yes to a spontaneous night out with friends or get up and down off the floor playing with your kids. 

That’s why I want to invite you to the waitlist for what I have coming.

Think, somewhere to go online, where you can: connect with others who have MS, get questions about MS answered, get tools that can help your symptoms, support & accountability to help with actually doing those things.

Comment WAITLIST below and ill send you the link to join the list 

#lissms #multiplesclerosis #multiplesclerosiswarrior #becausems #thisisms #communityheals #mscommunity

But seriously.. this isn’t too far off 😂

Life handed me a lemon that was a MS diagnosis at 24.
Life handed me a lemon that was multiple relapses and MS progression by 30.

Then I snatched those lemons, made some healing lemonade, and feel night and day different than I did 10 years ago when my symptoms were at their worst.

I could do it, my clients are doing it, I know you can too.

That’s why I’m so passionate about doing what I do. I know it’s possible for you to feel better in your body and be able to do the things you want to do.

Like go for a walk or hike with your spouse, say yes to a spontaneous night out with friends or get up and down off the floor playing with your kids.

That’s why I want to invite you to the waitlist for what I have coming.

Think, somewhere to go online, where you can: connect with others who have MS, get questions about MS answered, get tools that can help your symptoms, support & accountability to help with actually doing those things.

Comment WAITLIST below and ill send you the link to join the list

#lissms #multiplesclerosis #multiplesclerosiswarrior #becausems #thisisms #communityheals #mscommunity
...

17 2
I have a saying about dealing with MS (and any other autoimmune/chronic illnesses) that inevitably comes up in my work with clients:
“You don’t get it, until you get it”

Meaning, you don’t understand living life with MS (or any of the above), until you live in a body that has it.

Which is why living with MS can be so tough and lonely, because its hard to find people that truly understand what you mean when you say you’re exhausted, or brain foggy or “fine”.

This is also why I believe that having a community of others who get it is invaluable.

I’ve seen countless times over where someone new to one of my groups is able to feel fully seen and heard for the first time, and that is priceless for them and their healing.

They walk away feeling validated, understood and at home, which are hard to come by at the doctors office 😂🙄

You’re not too much
You’re not alone
You’re not lazy
You’re just talking to the wrong people.

If you wanna talk to the right people, I’m creating something for you..

Think, somewhere to go online, where you can: connect with others who have MS, get questions about MS answered, get tools that can help your symptoms, support & accountability to help with actually doing those things.. 

BUT- only the waitlist is going to hear about it. So- if you want to be notified and involved in creating whats coming, comment WAITLIST and you’re in 

#lissms #multiplesclerosis #multiplesclerosiscommunity #thisisms #becausems #multiplesclerosissupport

I have a saying about dealing with MS (and any other autoimmune/chronic illnesses) that inevitably comes up in my work with clients:
“You don’t get it, until you get it”

Meaning, you don’t understand living life with MS (or any of the above), until you live in a body that has it.

Which is why living with MS can be so tough and lonely, because its hard to find people that truly understand what you mean when you say you’re exhausted, or brain foggy or “fine”.

This is also why I believe that having a community of others who get it is invaluable.

I’ve seen countless times over where someone new to one of my groups is able to feel fully seen and heard for the first time, and that is priceless for them and their healing.

They walk away feeling validated, understood and at home, which are hard to come by at the doctors office 😂🙄

You’re not too much
You’re not alone
You’re not lazy
You’re just talking to the wrong people.

If you wanna talk to the right people, I’m creating something for you..

Think, somewhere to go online, where you can: connect with others who have MS, get questions about MS answered, get tools that can help your symptoms, support & accountability to help with actually doing those things..

BUT- only the waitlist is going to hear about it. So- if you want to be notified and involved in creating whats coming, comment WAITLIST and you’re in

#lissms #multiplesclerosis #multiplesclerosiscommunity #thisisms #becausems #multiplesclerosissupport
...

14 3

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