What would you do with extra time each day?

“Thank you Avior Nutritionals for helping those living with MS find a higher level of wellness and for sponsoring this post.”  


An Open Letter to My Friends Living with MS

Caroline Craven - the Girl with MS


To my friends living with MS, 

What would you do with more time in the day?  Even 5 minutes? 

That’s what I’m asking myself now, almost every day.  

I used to rest and take naps in the afternoon.   I never scheduled anything after lunch.  Who knows how I would feel?  

But things are different now. I continue to take better care of myself.  Yoga, gentle living, and healthy eating are just a few things I focus on.  Going to the doctors and taking my vitamins are also kept up on a regular basis.  

And then, last spring, I added Myetin into the mix.  It has been a huge bonus in my life.  The spasms and pain have been greatly reduced.  But most impressive has been this new found energy.  

Myetin is a combination of high-dose biotin and NAD+ made by Avior Nutritionals.

I know that this post is sponsored by Avior Nutritionals, but I am writing from the heart to say that sure do wish I had started this supplement much earlier.   On a daily basis I am amazed at the level of my afternoon energy on any given day.  

Whale Watching Pacific Ocean
Everyone with MS is different. And I am not a medical professional. But, there is scientific research behind high dose biotin and its potential benefits for those living with MS. 

And dang, if they don’t taste great.   I’m grateful that I can’t overdose on them.  As I’ve said before, these are my Scooby snacks.  After my pills, and only after do I get to slowly dissolve my Myetin.  

Please consult your health care provider.  And as always, if you have any question at all, please feel free contact me online at GirlwithMS.com


I still have down days, where a rest is needed after lunch.  But these occurrences are scant compared to the past.  Lately my afternoons are spent with friends, puttering in the garden, cooking for the family or working on MS advocacy.  Wow.  
Enjoying Harvest Festival! 
It’s still a rare occasion that I plan anything too important in the afternoon.  But if it’s necessary I seem to be able to pull through.  

Never imagined this energy would return.  

Thank you Avior Nutritionals for all you do to say #takeTHATms!  

Best, 



Caroline Craven
@thegirlwithMS


This blog post created in partnership with Avior Nutritionals. 

Guest Blog Post: Dr. Terry Wahls Recruiting for Diet Study


TWO MS DIET STUDIES are RECRUITING

MS Diet Study Research Opportunity Worldwide 
Many people with multiple sclerosis (MS) are very interested in dietary approaches to managing MS-related symptoms. 

Unfortunately, there is not a lot of research on which diet people should follow. Research has mostly focused on which supplements to take. Studying food choices and diet is much more complicated and equally as important. 



Right now there are two studies planned to examine if there specific diets that help reduce MS-related symptoms.

To find out the impact of specific diets, we need participants. Please consider enrolling in these two studies. 



  Dr. Terry Wahls  

1st STUDY:  Dietary Approaches to Treating MS-Related Fatigue 
Dr. Terry Wahls does clinical research at the University of Iowa, studying diet in the setting of multiple sclerosis. We are conducting an interventional study to understand how diet can affect fatigue. 

In our study we will be comparing the effectiveness of the low–saturated fat diet (Swank) and the modified Paleo (Wahls Elimination) for reducing the severity of MS-related fatigue symptoms and quality of life.   

The study lasts 36 weeks. We conduct baseline assessments and ask participants to continue eating their usual diet for 12 weeks, during which time there are repeat assessments. Then patients are randomized to one of the two study diets, trained on their assigned diet, and receive coaching calls to help them successfully adopt and sustain the study diet. There are repeat assessments 12 and 24 weeks later. 

We are currently recruiting participants and will continue recruiting through early 2019. Participants must have a diagnosis of relapsing-remitting MS, fatigue, and live within 500 miles of Iowa City, Iowa. This includes the states of Iowa, Illinois, Indiana, Missouri and Wisconsin, and parts of Arkansas, Kansas, Kentucky, Michigan, Minnesota, Nebraska, North Dakota, Ohio, Oklahoma, and Tennessee. 

Individuals interested in being considered for enrollment in this study may complete screening questionnaires and use code JMJPYEJHP. 

For questions, please email MSDietStudy@healthcare.uiowa.edu or call 319-384-5002.



2nd Study:  Complementary and Alternative Medicine in Multiple Sclerosis  
The second study is an observational study being conducted at Bastyr University for people with MS, optic neuritis, or clinically isolated syndrome. The survey asks participants about their diet, complementary and alternative medicine use, current symptoms, and quality of life. 


Participants are asked to complete surveys twice a year. Because it follows people over time, this study can also help answer questions about which diet is associated with better quality of life and fewer MS-related symptoms. 

Also, because this is a survey-only study, people can participate from all over the globe. You can learn more about this study and complete the surveys using this link.

Please consider participating in these important studies and encourage others to consider participating as well. Changing clinical practice so dietary advice is part of the care for people with MS requires research that asks the question, “Can diet reduce MS disease severity?”  

We have two studies asking that question. MS researchers from around the globe including myself and the MS community are anxiously awaiting the results from these studies. I hope you’ll consider participating. 

We’d love to include you! 

A Fresh Start: Job-Hunting After a Major Illness

Guest Blog Post from Rufus Carter: 


Finding a job is often a cause for considerable angst. Some common concerns may include fears of discrimination, how much you should disclose about your injury or illness and gaps in employment while you focused on your wellbeing. While these may be legitimate cause for worry, it’s also important to bear in mind that you are not alone. 
Job hunting after a medical absence is not uncommon, but that doesn’t take away the fears you might fear. But there are many ways to get back in the game. 
Creating your own gig
Sometimes difficulty finding a full-time job presents an opportunity to start your own venture, using your own skills. If you enjoy cooking but don’t have the means or confidence to open a full-blown restaurant, why not try a pop-up restaurant instead? It’s a low-risk, low-overhead proposition that can help you build a clientele, work according to your own schedule and earn income quickly. 
Carefully consider your talents and background. There’s probably something you can turn into money-making venture while you conduct a job search. If you’ve got a talent for making decorative objects, consider selling them on Etsy. Or, if you have a musical background there may be an opportunity to give lessons, either in person or online. Writing is a popular and potentially lucrative online gig these days, whether you’re producing marketing content or writing a blog, it’s a great way to make money doing something you enjoy. 

If you love animals, consider starting a dog walking or dog-boarding service, a growing and successful niche for many individuals who’ve decided to enter the gig economy.
Remedy your resume
Job searching takes place online to a very large degree these days, but that doesn’t mean a sharp, well-written resume is any less important. If anything, that makes it more important to place a coherent, informative and eye-catching account of your work history in front of employers. If you’ve been out of work for a while, it’s probably necessary to do some updating and make sure your most recent work experience is explained, as well as the highest education level you’ve attained. Remember, this is an employer’s introduction to you, so be as thorough as possible. Mention what you enjoyed about your last job, what skills you possess that would be especially valuable, and where you’d like to be five years from now. 
Where to go for help
If you get stuck along the way, there are many resources, both online and in-person, that can help set you on the right path. Many organizations can help you put together an effective resume and locate jobs despite your former health issues. If your illness resulted in addiction, America in Recovery is an excellent resource and maintains a job board that can put you in touch with employers. If you aren’t sure where to even begin, consider reaching out to an employment agency. This is a group that works directly with employers and can coach you through which jobs may be a good fit for you. You’ll have an opportunity to hold a temporary position while you gain experience or walk the direct-to-employment path. 
Finding a new job and readjusting to life after being down can be difficult. Draw on your innate abilities and interests to earn an income while looking for a long-term opportunity. It can instill in you a new sense of purpose and give you new goals to shoot for. Embrace the opportunity, remember what you’ve learned during treatment and reach out for help if you feel overwhelmed and anxious.

Image Courtesy of Pixabay.com.

THANK YOU Rufus!  
For this awesome input about finding work and keeping hope during difficult times.    #takeTHATms!   


Losing Touch, Finding Intimacy - repost from NY Times

Elizabeth Jameson, living with MS, wrote this most beautiful account of finding intamcy.  With her permission we are reposting to share with as many people as possible.  Thank you for helping us spread the word!    This is a REPRINT of NY Times Opinon with permission.

  
DISABILITY

Losing Touch, Finding Intimacy

I had come to believe I was unable to break through my physical disability. I was wrong.

By Elizabeth Jameson and Catherine Monahon
Ms. Jameson is a fine artist and writer living with multiple sclerosis. Ms. Monahon is an artist and writer.


Sept. 19, 2018

One of my oldest friends is here to visit. For as long as we’ve known each other, we’ve been in sync, weaving in and out of each other’s lives and reaching milestones together. We married our partners around the same time, went through law school and medical school at the same time, got pregnant with our sons in unison and lived as neighbors for years. Although we have visited each other frequently, time has slowly gotten away from us. I haven’t seen her in more than a year.

She gingerly lies down on the sofa while I sit nearby. She isn’t looking good. Thinner than I’ve ever seen her, weak and in pain. “How are you?” I ask.

“Well, I have cancer,” she says plainly. She changes the subject, not feeling the need to linger on her recent prognosis or to specify that it is terminal. All I want to do is hold her hand, rub her shoulders and tell her how much she means to me with a firm, loving touch. I stay distant from her, unable to move. I imagine stroking her hair or giving her a pillow to feel more comfortable, but I cannot do anything.

"Emerging"
by Elizabeth Jameson

Our conversation ebbs, flows, then trickles into silence; there is not much more to say.
She rests her hands on her stomach, where she holds the most pain. Five years ago, I would have bridged this silence with a gentle hug or touch. But I am stuck, immobile, unable to express my thoughts and feelings. I don’t allow myself to cry as we say our goodbyes.

When I lost the use of my hands, I lost my love language. I have multiple sclerosis, which has resulted in the loss of the use of my limbs. My disease progresses so slowly that I am caught by surprise when I can no longer do something. Little did I know I have been losing my range of motion by a fraction of a centimeter every day. Nerve by nerve, I lost the use of my legs, arms, wrists, hands, pointer finger, thumb.

I can’t tell you when exactly I became a quadriplegic, only that I know I am now a part of the club. My paralysis limits me down to my fingertips. I can’t operate my wheelchair, can’t hold a coffee cup, let alone someone’s hand — I can’t actively touch in any way. Like a fortress, my wheelchair is both impossible to leave and difficult to enter. If others want to reach out and touch me, it can be
intimidating to make the first move. It feels like there is a thick pane of glass separating me from the outside world, and because of my physical disability, I begin to believe that I am powerless to break through.

Over the years, I have tried to make a home out of my fortress, my glass bubble, uncomfortably settling into my grief. There are times when I feel connected to others, but in most situations, I become passive. I work hard to forget the joy of touching. I am a positive person, I tell myself, I can deal with this. I set up camp at the base of my Mount Everest and try not to glance up at what I am missing.But I feel the loss of touch as if it were a limb that has been severed from my body, an invisible, open wound I painstakingly cover up each day.

Lisa Jameson, artist, writer and living with MS

I am hyper‐aware of the moments when words are not enough. When touching someone’s hand is the only way I can truly communicate my feelings. When I can’t greet someone familiar by warmly placing my hand on their shoulder. Or when I know someone is sad, and it’s not appropriate to talk about what’s wrong; I can’t reassure them affectionately. It is like not being able to breathe. This loss, in combination with the guilt I feel when I grieve it, is overwhelming. I resign myself to the idea that I will never experience consensual, nourishing, intimate exchanges of touch in everyday life.

It is in this state of numbed resignation that an unexpected crack forms in the thick glass that has been separating me from “normal” people: A ray of light that reveals a world of intimacy I have been overlooking.

I am visiting with another friend at a coffee shop. My voice is weak and hard to hear in crowded spaces, so I use a voice amplifier. The amplifier has a microphone and a headset that make me look like an aerobics instructor who happens to be teaching in a wheelchair. I’ve got my headset in place, but when my friend leans in to hear me, it’s no use. My voice is too faint. I motion with my head toward the dial on the device, which can be turned up to make my voice louder. He tentatively discovers the dial, locking eyes with me to check the loudness of my voice. As I keep talking, he turns the dial up, then up and up some more until, yes, there, he can hear me. We nod and smile in unison, return to our conversation.

As he settles back into his chair, I feel lightheaded. By increasing the volume of my voice, he had turned up the very essence of “me.” The fact that he cared so much to hear me. That he took the time to learn how to connect with me.
I had rediscovered intimacy, without touch.

ORIGINAL ARTICLE

 My mind continued to reel long after we said our goodbyes. Maybe I can experience intimacy, I thought. It’s just that the language of it all has just changed. I had to redefine intimacy for myself. What is it, without touch? The freedom to express myself. The joy of being recognized, seen, accepted, equal. Letting my guard down, no longer burdened by society’s version of me, by my version of me. The feeling when the stigmas of disability and illness are lifted. I eyed my version of Mount Everest, thinking that maybe there was a way for me to fully rejoin the living.

After that day in the coffee shop, intimate moments emerged from the fabric of my everyday life. I began to notice how friends, loved ones and total strangers could make me feel visible and whole in completely mundane ways. Appreciating them took my breath away: that someone driving my wheelchair is making love to me, that someone kneeling to my eye level is giving me a gentle caress, that someone feeding me is a joint experience of pleasure and tenderness.

Within the mundane there are beautiful surprises, too. On a busy day, before work, my husband pauses his morning routine to make me a poached egg, his specialty. Something he wants to make for me — I didn’t ask. A friend tries to feed me a cookie. He does it “wrong” at first, but the process of figuring out the best way is like an intricate dance. Over the holidays, a family member puts on Handel’s “Messiah,” music that I love and everyone else in the family finds annoying. They usually refuse to put it on, but this morning they play it just for me, blasting it so that I can hear the music through my bedroom wall.

I savored these moments, and as I did I was propelled and empowered by them. I realized I could play an active role — I could give as well as receive. So I took my intimacy into my own hands, even though I am still grieving what I cannot do. I leave base camp behind and begin my slow, labored ascent; the fluid, open concept of intimacy spurs me onward.

I have always loved food. I muster the courage to ask someone to join me for a luxurious, two‐ hour pastry‐eating session. We take the time to savor every crumb of a single pastry, eating at the same pace together, and I feel honored, loved.

I start seeing myself in others: I am a part of a tribe. Wheelchair users, people with multiple sclerosis, the elderly with canes and walkers, people struggling with aphasia or spinal cord injury. The list goes on and on. We are everywhere. I lock eyes with a 90‐year‐old man in a crowded elevator. He tips his hat to me with a warm smile. I see a woman with a mobility aide in the street and we grin at each other, comrades. Neighbors. Strangers. Visible, invisible.

I poke fun at my own disability, creating humor where there was once shame. When I’m drinking water, I have no way to stop, so when someone cracks a joke I laugh and spit water down my front. It’s humiliating, but hysterically funny at the same time. I have a damp front more often than not.
I now know intimacy can be everywhere. Moments I’ve noticed, received, created. You and I are sharing an intimate moment right now — because if you’ve gotten this far without turning away, you are a part of that exclusive tribe of people who truly see me.

But eventually, my quest for intimacy brings me back to the beginning. To touch.
My good friend is back to visit. We are trying to see each other more often — with less time left, it’s only natural. She lies on the sofa, and I verbalize all that I kept inside last time — how badly I want to stroke her hair, squeeze her hand, sit next to her. She smiles appreciatively, but moves the conversation along, not one to linger in the spotlight. She directs the conversation back to me.

We talk a bit more, and emboldened by my confession, I ask her if she would take my hand, if it isn’t too painful to move. Slowly, she sits up, and my caregiver rolls my chair as close to her as possible. She extends her hand, resting it in mine. We look at each other and breathe.




Elizabeth Jameson (@jamesonfineart) is a fine artist, writer and former civil rights lawyer. Catherine Monahon (@cxmdesigns) is a mixed‐media artist and writer. She collaborates with Ms. Jameson on writing projects.

Disability is a series of essays, art and opinion by and about people living with disabilities. The entire series can be found here. To reach the editors or submit an essay for consideration, write opinionator@nytimes.com and include “Disability” in the subject field.

Follow The New York Times Opinion section on Facebook and Twitter (@NYTOpinion), and sign up for the Opinion Today newsletter.
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Creating your own health: Using Diet & Nutrition to Treat MS

Probably one of my biggest factors in managing my MS symptoms is the use of diet and nutrition.  During my three years in the double-blind, T-cell study, back in 2001, my hopes were on nutrition and all things alternative.  I willingly went off all DMD in search of a cure for MS.  But then reality set in, and it was all engines forward in the battle of natural ways to fight the progression of this disease.

Sporting my flower peace wreath
There is a lot of incoming research on Diet and MS.  There are also some active clinical trials.

Click this out:  Here is my article on Diet as a treatment for multiple sclerosis.

Diet - or better yet, a nutritional protocol, is essential in my daily battle against MS.  If my daily intake has too much salt, too much caffeine, too much gluten, too many processed foods, then I will pay the price.  And while that price may not be paid that same day, trust you me that it will not forget and will rear its ugly head.  And, more often than not, all of the prices will want to be paid on the same day at the same time, wreaking complete havoc on your life.


Go for color when cooking and creating healthy menus 
Fresh lemon is key!  Use in water, tea, baths, etc.

 #refresh
Click here for my article on Diet as a treatment for multiple sclerosis.

Become friends with your body and find a new level of wellness.  

Welcome to living with multiple sclerosis.   As you know it often does not bode well for us MS patients.  Out diseases are random and progress willy nilly.  But there are modifiable risk factors that we can take into consideration to help us strive for the best life possible despite's our illness.  These risk factors include cigarette smoke, alcohol, nutrition, supplement intake, exercise, and other situations that we have control over.
~if need be - pee on it and walk away~

Cig smoking is bad.  Bottomline, cut it out.  Alcohol is considered OK in moderation.  Consult with your neurologist or medical expert.  Often people find that Vitamin D, B12 and Biotin can all be beneficial supplements.  In addition, the nrf2 activator, Protandim, is found to be great at fighting oxidative stress.

So, that brings us to Diet, or nutritional protocol.   Everyone is different so finding a protocol that works best for you is key.
Gluten free bread is an option.
Here it is paired with home-made soup and fresh salmon salad.
One person who is making a difference with diet and MS is Dr. Terry Wahls and her Wahl's Protocol. I had the great fortune of speaking with Dr. Wahls a few weeks ago for an article I was writing for Healthline.com - "Diet as a possible treatment for MS".   And wow!   So much great information going on with diet and MS.

The Wahl's Protocol is a modified paleolithic diet.  More about it click here. For those who do not know, Dr. Wahls has made diet a form of treatment for progressive MS.  Thank you Dr. Wahls!   I have been following and almost identical diet based on my own experience for over 15 years.  It is the number 1 "go to" when things are going bad with my MS.

And if you don't have fresh flowers, the fake ones are fun too!

First, I ask myself:  How is my diet?  Where am I going wrong?   And most of the time, this usually fixes it for m!   Like I say, everyone is different.  This is one reason I love the Wahl's Protocol - as it suggests elimination type diets to see what you personally are sensitive to and this is BIG!

Here is my article on Diet as a treatment for multiple sclerosis.

Here are some food common sensitivities:

Processed foods
Salt
Gluten
Red meat
Simple carbs
Sugar
Sodas
Diet anything / excitotoxins or NaStY for MS
Dairy....

FYI - I eat dairy.  Cheese.  I tried to take it out of my diet once and my boss told me to add it back as the rest of the staff was complaining about my horrid mood.  That was near 30 years ago and I haven't tried to remove it since~  I don't eat a lot of it but like it now and then.   I will willingly cut everything else out, before the cheese~

Lately I haven't been able to eat much meat.  My body, probably due to the warm summer months, is craving cooling salads and fresh fruit.  Unfortunately I like beer, especially in the summer months.  It's not the alcohol that bothers me but rather the carbs and gluten.  Talk about a weight gainer!  And then if I add bread....Oh dear save me.

Last winter I made the mistake of letting way too much beer, bread and gluten get into my diet.  Showing no restraint at all for about six months eventually led to a 15 pound weight gain, horrid dry skin and then the dreaded MS relapse!   Ugh.

My vertigo and vision got so bad that driving was out of the question...even just to a friends house.  Lethargic and inflamed my life consisted of laying in bed and "trying" to motivate.  Oh how I hate this feeling!   My skin was dry and eczema appeared all over.  Hair loss was abundant and my breath was so bad it even grossed me out.   What have I done?  So healthy last summer and then wowza, what a defeat brought on by my own weaknesses.

Time to make a change!

Feeling the summer spirit, light and fresh!
Nothing huge at first, just cut the carbs back down to no more than 10% of diet or so.  Eliminated processed foods again and removed gluten for the most part.  A little now and then does not bother me.  But a six pack of beer and loaf of bread is not considered moderation.   That's OK, the change feels good.

Back to juicing and healthy eating.  Beautiful summer produce combined with beans and grains cooked fresh are making the table.  Herbs from the garden and cheeses and meats from local farmers inspire this cook to create.


Some of recipes for your enjoyment:

Anti-inflammatory Rice Pudding

Obsessive Gaspacho 

Juice Recipes

Chia Pudding


Words of Advice:

Try different diets.  Work with nutritionists who understand MS and the different trending diets.  This is your health - it is your body.  Do not try whack-doodle eating schemes.  Try stuff that has worked for others, the key word being "try".  Give yourself a chance with different foods and see what you might be sensitive to.  Everyone is different!  

Add color and energy throughout your house with fresh flowers.
Here is my article on Diet as a treatment for multiple sclerosis.

Buy brand-name Prozac online at up to 80% less, from Canada. 100 capsules for just $272.93 USD at YouDrugstore.com. Compare at $1,282.40 from local pharmacies. Save now.

Epic vacation, lost vitamins, fighting a relapse.

Ack.  

Where is my pill box?  

This trip was flawless until now. Everything organized and flowing like a dream.   

Until midway into the last week when my vitamins were nowhere to be found.  Oh crud.  My Myetin was in this box.  Not to mention my Grandmother’s diamond ring. But in reality it was the Myetin I was most concerned about.  

This means five days without my high dose biotin, Myetin  Oops.  Not a good thing when venturing into 100F heat, adventures and time with your boyfriend.  Not good at all.  


The heat hit hard but my MS stayed at bay.  

Fun was had by all.  Mid-State Fair, Dwight Yoakam and great friends.  One couldn’t ask for more.  Except to find their Myetin.  


Energy flows where attention goes.  And I do not have energy to waste.  Putting my lost vitamins aside, we had a beautiful drive to the Central California Coastal town of Harmony.  I’ve been visiting this town since 1985 and the charm never fades.  


After some pottery purchases and selfies with the Cow parade, we ventured on up the road to the unbelievable Hearst Castle in San Simeon.  It’s been years since riding the visitor’s bus up the hill.  And, well, let’s just say my MS had the better of me.  Dizzy, fear of heights, it took everything I had to relax and meditate my way up the historical path.  


These frantic, nervous feelings are new to me.  Prior to MS, my weekends consisted of rock climbing, white water kayaking, racing mountain bikes, and back country skiing in the Cascades of Oregon.   Now I am afraid of a bus ride. 


Then, we arrived at top, and the sun came out.  Not too bad at first and fortunately not a scorcher this day.  But the rooms, those grand rooms of William Randolph Hearst, they got a little warm.  


A once avid adventurer, this girl with MS is limited in many ways unnoticeable to the naked eye. Fatigue, pain, balance issues, spasticity, are just a few to having a nursing, loving caregiver such as Tim, has made all the difference in the world.  My parents have been wonderful caretakers, but traveling with Tim does have its benefits! 

As dizziness rolled over me and the heat related MS hug crept its creepy hands around me, Tim grabbed a chair, a fan and sat me down.  I don’t look sick.  People stared, but only for a bit.   

Do people with invisible illnesses need to wear a sign? 

Often I feel the need to carry my handicap placard with me, hanging it around my neck.  Or to wear some sign that says, “I have MS and might trip and fall on you.”  

Frustrating to be in this position, with an invisible disability, but it is a good reminder to look at other people the way I want to be viewed, with kindness and gratitude in my heart.  To see without judgement.  

Almost ten years of my life were spent in this beautiful Central Coast of California.  I yearn to return to the countryside with Tim.  Have a garden, animals, couple of horses.  But that’s another story.  




A bit of Life before MS

A former horse trainer and ranch hand, I was fortunate to have worked several of the Hearst Ranches.  There were broodmares and foals in Paso Robles at Phoebe Hearst’s Circle 6 Ranch.  This ranch also housed a couple of international vaulting teams and the USET two-up carriage horse team.  This was all fascinating and fun work while studying Agribusiness and marketing at nearby California Polytechnic State University, San Luis Obispo.  

In addition, my ranch work took me to the Estrella Ranch where I exercised cutting horses, rode turn back, worked cattle and witnessed a variety of wildlife while loping across George Hearst’s 17,000 acres.  Also, The Jack Ranch out in Cholame was a beautiful, historical setting to work cattle and hunt wild boar.  Thank you Hearsts and Hearst Corporation for amazing memories!  



Distracted from my lost vitamins, we continued down the Pacific Coast Highway to the beautiful Cliffs Resort in Pismo Beach.  Thank you, Tim, for this wonderful gift and surprise!   



Still no Myetin 

My attitude was all positive but symptoms started to rear their ugly heads.  



First, my vision started to wane.  Try as I might, but it was getting hard to focus.  Fortunately for me, all I had to look at was this incredible view of the beach. This is why my hands are not on the steering wheel.  When it goes, it goes!  


Next, the weeble wobbles.  And, we do fall over, unless there is a cane, chair, or a loving caregiver, like Tim, nearby.  Blessed to have the latter, it was easy to lean on him, both physically and emotionally.  Because let’s admit it, having times like this get us down whether we like it or not.  

The pill box is nowhere.  It must be somewhere in the trailer back in Templeton.  I cant buy my Myetin  at a store.  Hmmmm.  Definitely next time I travel, will pack a backup supply, or two.  Because I really don’t like this feeling and I want my vitamins!   

Tim and I had an amazing adventure.  We tootled on home down Hwy 1, the Pacific Ocean to our right, the burned hills of Montecito to the east.   

Life is good. Very good. And it will be even better when I get to my vitamins.   



Research has shown it’s also important to understand that taking high dose biotin may provide a false positive result on a thyroid test.  For a true thyroid result, research recommends abstaining from it for two weeks prior to the test.  

I shared the research with my doctors. And more importantly, shared my personal results.  


Pain, fatigue, cog fog has reduced to a point of non recognition. Work productivity and energy level are at an all time high.  

My life with MS is thriving at a level I’ve never expected or believed would happen.  

Thank you, Myetin, for creating a product that works for me.   

And thank you, me, for knowing how to research and fine quality interventions to help me and others with MS.    


Back on Myetin.  

My pill box was left in Templeton.  Grateful to know the diamond ring wasn’t lost.  And to know I actually did leave it somewhere and didn’t lose it. Whew.   




Back on Myetin and it feels oh so good!   

It tastes so good.  LOL, I can’t believe how much I actually like this dissolvable tab.  Talk about an easy vitamin to take.  

So, if you read my earlier blog post about Myetin, I call it my Scooby Snack.  Only after all my swallowable pills are taken may I partake in my tasty Myetin.  The things we do to stay on track.  

But even then I tend to rush through my tab.  That’s not the point!   The point is to let the tab take its own sweet time to dissolve under my tongue.  

The problem is, I have no patience.  Literally, none.  Especially for sweet tasting tabs of wellness.  






Take the MyMyetin Challenge!


So, I’ve created the MyMyetin Challenge.  

How long can you take to dissolve your Myetin?   

I’m at .... lets see, I better try one now so I can see what my record it.   Hold on for a sec.   



OK.  One minute!  sixty Seconds!  That is my record for dissolving My Myetin tablet.   

Can you pass the sixty second MyMyetin challenge? 

#MyMyetinChallenge #SixtySeconds #BeatThat #takeTHATms!


CLICK HERE TO PURCHASE MYETIN 

This blog post brought to you by Caroline Craven, Avior Nutritionals, and Myetin, your high dose biotin for MS.   Thank you all for your continued support of GWMS and our mission to say #takeTHATms!


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