What is the ‘CrossFit Open’ you may ask? It is a 5 week long competition, that individuals can register for online. One workout gets announced each week, then scores are submitted. The top athletes go on to compete in Regionals. Then those top athletes go one to compete in the CrossFit Games.
That made this year a no-brainer. Even though I had surgery in September. Even though I hadn’t worked out very much since. Neither of those things mattered much to me, I wanted in. Throughout the 5 weeks of this year’s open, I was able to record my score for weeks 2, 3 and 4 of the workouts. Through a series of unfortunate scheduling events, I never made it into the gym to complete the workout week 1. And week 5? Oh week 5. We’ll get there eventually.
I competed in the scaled division for each week. Which means the movements are slightly easier, and the weight slightly lighter. Week 2 was confusing as hell to explain, but not so bad to complete. It wasn’t the worst I had ever done and it built my confidence. Week 3 was the same, except it was much more straightforward. I was able to execute the movements, which I didn’t think I’d be able to. A nice surprise! Seems so rare in CrossFit, a surprise being welcomed!
Week 4, it all started to go downhill. The workout started with my most favorite lift ever, heavy deadlifts. After that, it was all the movements I hate. One of those movements was a wallball. This is where you are required to throw a weighted med ball into the air and reach a target. These are a MAJOR weakness of mine. I know this is a weakness, I’ve been working on this weakness, but it’s still a weakness. I made it through the deadlifts ok. Then the wallballs were next. That’s where I got stuck for the rest of the workout. They were tough. I missed so many of them. But my judge kept telling me slow down, wait until you are ready. I was rushing so much of the movement, I was missing way more than I should. I finished with only completing 15 of 55 wallballs. But that’s 15 more than I thought I would get. Because patience was key. (First learned lesson)
Week 5. Oh heavens, where do I start? At the beginning I suppose. EVERYONE in the CrossFit community who had done this workout several years ago, was talking about this one. How awful it was, how terrible it was. But going into this workout, I felt good. I felt ready. I felt like I was going to conquer the final workout of the games and end on a high note. My coach started class with a great ‘speech’ to us all. About if we thought the workout will suck, it will suck. Which totally makes sense, mindset is everything after all. Then he went into the second part of his speech. He started talking about the disabled and adaptive athletes. How they would feel happy to move like this, even if we think it is ‘awful’. This really hit home for me. Granted I am not an adaptive athlete right now, but that is always in the back of my head. There was a time when I thought that would be in my near future. That speech of his, brought these issues of mine to the forefront again. Not really the way I had envisioned my workout starting. Anyway, my sister went first. She did great, but also suffered. She struggled, but did well overall. I was up next. To say I struggled is an understatement. It was the hardest workout I’ve done. The weight was hard, yes, I struggled and failed with it many times. It was a weight I KNOW I could do a year ago. I started to get frustrated. I continued to struggle and fail. I succeeded twice, then I would fail. This went on and on. Finally my coach came over. He told me if I kept missing. I would have to lower the weight. Major frustration set in. So did a few tears. Tears? In a workout? Who am I? Ugh. I worked on. I pushed them away. I got mad. I got mad at my body, I got mad at MS. I got mad at not being where I used to be. But that didn’t help anything. I kept up my pattern. Succeed then fail. He came over again. I had to lower my weight. There came the rest of the tears. From where, I don’t know. I am very skilled at stopping tears. But when I am in the middle of lifting heavy weight, I am no match for small puddles of water.
I wanted to quit. I even said to my sister who was judging my workout, ‘I’m done’. But he came right over and said finish it. And I did. I pulled misty self together, lowered my weight and finished the workout. I worked long after class was over, but everyone stayed to cheer me on. And well into the next class that had started, but they all cheered me on. I felt a whole range of emotions. I was exhausted, I was embarrassed, I was frustrated, I was grateful.
I was grateful that I finished, and didn’t quit half way through. I was grateful that I had others around me to cheer me on. I was grateful that I could move like this in the first place, and lift the weight I could after what I’ve been through. This workout was one of the toughest, if not THE toughest I’ve been through. It challenged me physically but, it was the hardest on me mentally. I had to get over my frustrations with my body, my frustrations with MS and my frustrations with my emotions, and FINISH my workout. I know I can handle this in the future. Because I’ve already handled it. (Second learned lesson).
If you want to hear more about my CrossFit journey, join my list here! I’ll be sending out an email about my struggles and progress!
follow along on Instagram:
It’s been a week for me… maybe you too?
Use this short video for a moment of peace and regulation.
What do you notice in your body and about your emotions when you exhale and drop your shoulders?
Or when you hear bird songs?
Notice what makes you feel more calm, relaxed and at peace.
Do more of that..
It’s been a week for me… maybe you too?
Use this short video for a moment of peace and regulation.
What do you notice in your body and about your emotions when you exhale and drop your shoulders?
Or when you hear bird songs?
Notice what makes you feel more calm, relaxed and at peace.
Do more of that..
I get it… I was once in paralysis by analysis for years!!
I’m creating a Masterclass/Workshop experience in August to cover this exact topic: what and how to eat for MS.
BUT!! I need your help to narrow down what we’ll be talking about.
Which of these options sounds most helpful?
Comment the number below!!
Workshop ideas:
1. Simple Nutrition for MS: what you need to know about eating for healing
2. Create Your Own MS Diet: How to know what is best for YOU, while also helping MS symptoms
3. Education into Action: How to put the knowledge you have into action steps that make progress
4. Blend of it All: Education, steps to finding your own MS diet and how to get started
Want something else?? Tell me 👇🏼👇🏼
I get it… I was once in paralysis by analysis for years!!
I’m creating a Masterclass/Workshop experience in August to cover this exact topic: what and how to eat for MS.
BUT!! I need your help to narrow down what we’ll be talking about.
Which of these options sounds most helpful?
Comment the number below!!
Workshop ideas:
1. Simple Nutrition for MS: what you need to know about eating for healing
2. Create Your Own MS Diet: How to know what is best for YOU, while also helping MS symptoms
3. Education into Action: How to put the knowledge you have into action steps that make progress
4. Blend of it All: Education, steps to finding your own MS diet and how to get started
Want something else?? Tell me 👇🏼👇🏼
FYI- This process took several YEARS for me . So please stop beating yourself up if you’re not here yet.
Tbh- I needed to go through the scared, intimidated, rebellious no way before I got to the heck yes.
It took me being at rock bottom, symptoms out of control and knowing I needed something else.
So I didn’t really “do anything” to be ready.
I just was when I was.
If you’re feeling ready to make diet changes to help your MS symptoms, I created an Eating for MS guide just for you!
Your guide includes:
- The best foods to be eating when you have MS
- Several ways to get started
- Fast and easy meal ideas
- And so much more!!
Comment GUIDE below and I’ll send you the link to download!
FYI- This process took several YEARS for me . So please stop beating yourself up if you’re not here yet.
Tbh- I needed to go through the scared, intimidated, rebellious no way before I got to the heck yes.
It took me being at rock bottom, symptoms out of control and knowing I needed something else.
So I didn’t really “do anything” to be ready.
I just was when I was.
If you’re feeling ready to make diet changes to help your MS symptoms, I created an Eating for MS guide just for you!
Your guide includes:
- The best foods to be eating when you have MS
- Several ways to get started
- Fast and easy meal ideas
- And so much more!!
Comment GUIDE below and I’ll send you the link to download!
I get it- it’s really easy to shame yourself into changing something, especially your diet/the foods you eat. And especially when we feel there are other things we “should be doing” because we know “it’s better for us”.
But that is NOT my wish for you.
Hi 👋🏼 my name is Alissa and we do things differently around here.
My goal is to empower you with the knowledge and tools necessary to make informed decisions about your dietary choices, tailored to your unique MS needs and preferences.
This is why I wrote my Eating for MS Guide the way I did.
I did not give you foods to fear or messages of ONLY EAT THIS FOOD FOREVER OR ELSE.
I’m giving you the tools to be confident in the choices you’re making, because you know it works for YOU. Not because you “should” do it this or that way.
If you’ve been wanting:
- to eat in a way that supports your body with MS, but are confused about all the different messages online
- to feel empowered about your choices, not shamed
- to do it all in a gentle, slow way, not a crash diet..
My guide is for you!!
Comment GUIDE below and I’ll send you the link to download!!
I get it- it’s really easy to shame yourself into changing something, especially your diet/the foods you eat. And especially when we feel there are other things we “should be doing” because we know “it’s better for us”.
But that is NOT my wish for you.
Hi 👋🏼 my name is Alissa and we do things differently around here.
My goal is to empower you with the knowledge and tools necessary to make informed decisions about your dietary choices, tailored to your unique MS needs and preferences.
This is why I wrote my Eating for MS Guide the way I did.
I did not give you foods to fear or messages of ONLY EAT THIS FOOD FOREVER OR ELSE.
I’m giving you the tools to be confident in the choices you’re making, because you know it works for YOU. Not because you “should” do it this or that way.
If you’ve been wanting:
- to eat in a way that supports your body with MS, but are confused about all the different messages online
- to feel empowered about your choices, not shamed
- to do it all in a gentle, slow way, not a crash diet..
My guide is for you!!
Comment GUIDE below and I’ll send you the link to download!!
Or for when you’re trying to talk yourself out of being sick.. 🙋🏻♀️🙋🏻♀️😂😂
Even if you feel fine, try saying a few of these out loud. Feel what happens to your body when you do.
Do you feel an expansion or lightness in your chest?
Does breathing get a little easier?
Just notice the shifts in your body.
I’m not saying we can talk ourselves out of it (illness, flares etc) … but… our body and cells respond to our thoughts.
So how we think about ourselves is definitely in the conversation of how we can take care of ourselves overall.
🧡🧡🧡
Or for when you’re trying to talk yourself out of being sick.. 🙋🏻♀️🙋🏻♀️😂😂
Even if you feel fine, try saying a few of these out loud. Feel what happens to your body when you do.
Do you feel an expansion or lightness in your chest?
Does breathing get a little easier?
Just notice the shifts in your body.
I’m not saying we can talk ourselves out of it (illness, flares etc) … but… our body and cells respond to our thoughts.
So how we think about ourselves is definitely in the conversation of how we can take care of ourselves overall.
🧡🧡🧡
IDK if it’s hot where you live, but where I live, it’s been hot AF.
And you know what that means, you might be seeing an increase in MS symptoms too.
I’ve been using all the cooling methods, but I wanted to see if there was more I could do.
Did you know you can use the food you eat to help cool your body temperature too?
Food can help you stay cool by helping to regulate your body temperature and promoting hydration and sweating.
Some of the foods that help:
🥒Water rich veggies: like cucumber, tomatoes, zucchini, celery etc
🍓Fruits: like berries, melons and tropical fruits
🥥Coconut water and coconut milk
🌿Herbs: mint (mint water is 💯), dill, rosemary, lavender, lemongrass, chamomile
🌶️Spices: paprika, cayenne, peppers etc
If you tolerate them, add these to your next shopping trip and I hope you stay cool!!
PS— I just dropped my new Eating for MS guide!!
If you:
👉🏼 are confused about what to eat to help MS symptoms because of all the mixed messages online..
👉🏼 are stuck in paralysis by analysis because of said confusion, which makes you do nothing cause you’re afraid you’ll do it “wrong” anyway..
👉🏼 know you want to eat differently, but the thought of “starting a diet” sends you into a spiral..
This guide is for you!!
Comment GUIDE below and I’ll send you the link to download!!
IDK if it’s hot where you live, but where I live, it’s been hot AF.
And you know what that means, you might be seeing an increase in MS symptoms too.
I’ve been using all the cooling methods, but I wanted to see if there was more I could do.
Did you know you can use the food you eat to help cool your body temperature too?
Food can help you stay cool by helping to regulate your body temperature and promoting hydration and sweating.
Some of the foods that help:
🥒Water rich veggies: like cucumber, tomatoes, zucchini, celery etc
🍓Fruits: like berries, melons and tropical fruits
🥥Coconut water and coconut milk
🌿Herbs: mint (mint water is 💯), dill, rosemary, lavender, lemongrass, chamomile
🌶️Spices: paprika, cayenne, peppers etc
If you tolerate them, add these to your next shopping trip and I hope you stay cool!!
PS— I just dropped my new Eating for MS guide!!
If you:
👉🏼 are confused about what to eat to help MS symptoms because of all the mixed messages online..
👉🏼 are stuck in paralysis by analysis because of said confusion, which makes you do nothing cause you’re afraid you’ll do it “wrong” anyway..
👉🏼 know you want to eat differently, but the thought of “starting a diet” sends you into a spiral..
This guide is for you!!
Comment GUIDE below and I’ll send you the link to download!!
The soil you grow your tomatoes in matters.
Well, the soil you grow everything matters.
(This is also a metaphor for your mind)
Rich nutrient dense soil = healthy plants
Soil full of sticks, rocks and a tiny bit of nutrients = unhealthy plants
The foundations on which you build a garden (or a mindset) really matter in the end.
Which would you choose?
PS- My new Eating for MS guide is here!!
If you’ve ever been confused on what to eat to help MS symptoms, this is for you!!
Comment GUIDE and I’ll send you the link to download!!
The soil you grow your tomatoes in matters.
Well, the soil you grow everything matters.
(This is also a metaphor for your mind)
Rich nutrient dense soil = healthy plants
Soil full of sticks, rocks and a tiny bit of nutrients = unhealthy plants
The foundations on which you build a garden (or a mindset) really matter in the end.
Which would you choose?
PS- My new Eating for MS guide is here!!
If you’ve ever been confused on what to eat to help MS symptoms, this is for you!!
Comment GUIDE and I’ll send you the link to download!!
I shoulda just dunked myself lol.
But save this post to have these tips at the ready.
If you’re an MSer.. you know an increase in temperature can cause our already compromised neurons to work even less effectively than normal.
While we may feel like 💩, there usually isn’t new disease activity causing the symptoms. Rather a worsening of current symptoms, which is also called a pseudoexacerbation.
(Now, if you’re feeling extra 💩💩, and some new symptoms crop up, a call to your doc might be in order.)
There’s a few things I have found helpful for managing the heat:
BE PROACTIVE: Instead of waiting until you’re about to melt, use cooling strategies before you really need them.
Hopefully this way, you’ll never get to the point where you feel like you may burst into flames.
CREATE AN OASIS: If you don’t have central AC, make (at least) one room in your house a cool oasis where you can hide from the heat.
ACCESSORIZE: Get alllll the cooling products. @koldtec scarves, @releafpack cooling packs (amazing for the back of the neck), an awesome water bottle that keeps water ice cold, personal fans or popsicles!
For me, I can feel ok in the heat until all of a sudden I don’t. Using my proactive cooling has helped a ton.
Also, my heat tolerance has been improving since I have been taking so many steps to improve my health.
I rarely feel tingly in my legs which used to be a warm weather staple for me.
But most of all, make sure to advocate for yourself and your comfort.
You deserve comfort as well as any other person.
Please don’t let fear of “ruining” a summer day keep you from saying what you need.
🧡🧡🧡
I shoulda just dunked myself lol.
But save this post to have these tips at the ready.
If you’re an MSer.. you know an increase in temperature can cause our already compromised neurons to work even less effectively than normal.
While we may feel like 💩, there usually isn’t new disease activity causing the symptoms. Rather a worsening of current symptoms, which is also called a pseudoexacerbation.
(Now, if you’re feeling extra 💩💩, and some new symptoms crop up, a call to your doc might be in order.)
There’s a few things I have found helpful for managing the heat:
BE PROACTIVE: Instead of waiting until you’re about to melt, use cooling strategies before you really need them.
Hopefully this way, you’ll never get to the point where you feel like you may burst into flames.
CREATE AN OASIS: If you don’t have central AC, make (at least) one room in your house a cool oasis where you can hide from the heat.
ACCESSORIZE: Get alllll the cooling products. @koldtec scarves, @releafpack cooling packs (amazing for the back of the neck), an awesome water bottle that keeps water ice cold, personal fans or popsicles!
For me, I can feel ok in the heat until all of a sudden I don’t. Using my proactive cooling has helped a ton.
Also, my heat tolerance has been improving since I have been taking so many steps to improve my health.
I rarely feel tingly in my legs which used to be a warm weather staple for me.
But most of all, make sure to advocate for yourself and your comfort.
You deserve comfort as well as any other person.
Please don’t let fear of “ruining” a summer day keep you from saying what you need.
🧡🧡🧡
Growing your own fruit or veggie is a great way to eat more of them!!
It may seem daunting, but it’s actually pretty easy.
Some easy things to grow if you’re just starting out:
🥬Leafy greens (I’m harvesting my kale here!)
🫛Peas
🍅Tomatoes
🍓Strawberries
🫑Peppers
🥒Squash & zucchini
🫘Beans
I’ve grown some type of veggie for years now, usually squash, peas and tomatoes (for Scott lol).
Do you have a garden? That can be in ground, raised or even containers like me.
What do you like to grow?? Tell me below!!
PS- need something to do with the veggies you grow??
I just dropped my new Eating for MS Guide, where I talk all about what foods are best for MS and give you some recipe ideas so it’s super simple for you to find symptom relief through food too.
Comment GUIDE below and I’ll send you the link to download!! (And it’s free!!)
Growing your own fruit or veggie is a great way to eat more of them!!
It may seem daunting, but it’s actually pretty easy.
Some easy things to grow if you’re just starting out:
🥬Leafy greens (I’m harvesting my kale here!)
🫛Peas
🍅Tomatoes
🍓Strawberries
🫑Peppers
🥒Squash & zucchini
🫘Beans
I’ve grown some type of veggie for years now, usually squash, peas and tomatoes (for Scott lol).
Do you have a garden? That can be in ground, raised or even containers like me.
What do you like to grow?? Tell me below!!
PS- need something to do with the veggies you grow??
I just dropped my new Eating for MS Guide, where I talk all about what foods are best for MS and give you some recipe ideas so it’s super simple for you to find symptom relief through food too.
Comment GUIDE below and I’ll send you the link to download!! (And it’s free!!)
⭐️Changing my diet!!⭐️
First, like and save this post so you can come back to it if you need.
It took me years to finally be ready to consider changing my diet to help MS symptoms.
It actually took a pretty bad rock bottom moment, but that’s a story for another day.
I get it if you feel like this process is hard and daunting.
Start here:
⭐️YOU DONT HAVE TO CHANGE EVERYTHING AT ONCE
⭐️Pick a meal to switch up, include a few different foods a week or increase protein.
⭐️Get curious about how the foods you’re currently eating are making you feel
Those are just 3 suggestions to get you started.
Want more information about Eating for MS?
Like what (imo) you should include in your diet, how to eliminate foods, and meal ideas??
So that you too can feel so much better in your body and get your life back?
I just dropped a new Eating for MS Guide, full of all the info you need to get started on your own food journey.
Comment GUIDE below and I’ll send you the link!
🧡🧡🧡
⭐️Changing my diet!!⭐️
First, like and save this post so you can come back to it if you need.
It took me years to finally be ready to consider changing my diet to help MS symptoms.
It actually took a pretty bad rock bottom moment, but that’s a story for another day.
I get it if you feel like this process is hard and daunting.
Start here:
⭐️YOU DONT HAVE TO CHANGE EVERYTHING AT ONCE
⭐️Pick a meal to switch up, include a few different foods a week or increase protein.
⭐️Get curious about how the foods you’re currently eating are making you feel
Those are just 3 suggestions to get you started.
Want more information about Eating for MS?
Like what (imo) you should include in your diet, how to eliminate foods, and meal ideas??
So that you too can feel so much better in your body and get your life back?
I just dropped a new Eating for MS Guide, full of all the info you need to get started on your own food journey.
Comment GUIDE below and I’ll send you the link!
🧡🧡🧡
Or, comment WAITLIST to be notified when it’s ready!!
I’ve been talking to many of you about your questions regarding eating for MS.
There’s lots of confusion about what is “right” and “wrong”.
Lemme tell you, I’ll answer this in the guide for sure- and it prob won’t be the answer you’re expecting?
Drop any other questions below and I’ll answer them!!
Or, comment WAITLIST to be notified when it’s ready!!
I’ve been talking to many of you about your questions regarding eating for MS.
There’s lots of confusion about what is “right” and “wrong”.
Lemme tell you, I’ll answer this in the guide for sure- and it prob won’t be the answer you’re expecting?
Drop any other questions below and I’ll answer them!!
:: first, comment WAITLIST below to be notified when my new Eating for MS Guide is available!::
When I was first diagnosed with MS I didn’t even think to ask if anything else besides medication would help me.
It didn’t even occur to me that changing my diet or managing stress would also play a part in my disease.
It took a few years, several relapses and failed medications for my BOYFRIEND (now hubby) to ask my neurologist if any diet would help.
And even then, my neuros answer was 🤷🏻♂️.
If you also haven’t considered it, let me be the first to tell you:
✨IT’S ABSOLUTELY POSSIBLE✨
to decrease your symptoms and influence your long term prognosis by implementing lifestyle changes.
What we eat
How we move
How we manage stress
Our toxin burden
Our hydration status
Etc etc etc
all go a long way in helping us MSers live better with MS.
I lived this transformation; from totally exhausted and unable to get off the couch to hiking mountains or playing golf,
I KNOW it’s possible for you, too.
I’m in the final stages of putting together a comprehensive resource on Eating for MS, comment WAITLIST and I’ll let you know when it’s ready!!
:: first, comment WAITLIST below to be notified when my new Eating for MS Guide is available!::
When I was first diagnosed with MS I didn’t even think to ask if anything else besides medication would help me.
It didn’t even occur to me that changing my diet or managing stress would also play a part in my disease.
It took a few years, several relapses and failed medications for my BOYFRIEND (now hubby) to ask my neurologist if any diet would help.
And even then, my neuros answer was 🤷🏻♂️.
If you also haven’t considered it, let me be the first to tell you:
✨IT’S ABSOLUTELY POSSIBLE✨
to decrease your symptoms and influence your long term prognosis by implementing lifestyle changes.
What we eat
How we move
How we manage stress
Our toxin burden
Our hydration status
Etc etc etc
all go a long way in helping us MSers live better with MS.
I lived this transformation; from totally exhausted and unable to get off the couch to hiking mountains or playing golf,
I KNOW it’s possible for you, too.
I’m in the final stages of putting together a comprehensive resource on Eating for MS, comment WAITLIST and I’ll let you know when it’s ready!!
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