KStenhouse🇨🇦

From my old riding instructor. Aspirin plus hot bath and epsom salts. Stretch every couple of hours. It works every time! No clue if ibuprofen would do the same.

WHY YOUR EXERCISE PROGRAM MAY NOT BE GETTING YOU RESULTS 🧠🧠 Did you know your brain controls everything you do in fitness and rehab? Your nervous system has 3 essential parts: 1️🧠 Sensory Input – what you see, feel, and sense (eyes, vestibular system, proprioception) 2️🧠 Neural Integration – how your brain processes and organizes that information 3️🧠 Motor Output – the actual movement you create (squats, pushups, lunges, corrective exercises) 🧠 THE PROBLEM? Most fitness and therapy programs only train the motor output piece. That’s why so many programs feel incomplete — they skip the brain’s input and integration systems that drive movement quality. ✅A truly effective, brain-based exercise program must include: 🧠 Sensory drills (eye + vestibular training) 🧠 Neural integration (kinetic chain + coordination) 🧠 Motor output (traditional strength + corrective training) This is exactly what I build for you inside The MS Gym — programs that train your entire nervous system, not just your muscles. Because when you train your brain, your body follows. 🧠 #TheMSGym #BrainBasedTraining #NeurologicalFitness #MSWarrior #Neuroplasticity ##movementismedicine #multiplesclerosis #mssucks #neurologicaldisorder

WHY YOUR EXERCISE PROGRAM MAY NOT BE GETTING YOU RESULTS

🧠🧠 Did you know your brain controls everything you do in fitness and rehab? Your nervous system has …

(See alt. txt.)

www.facebook.com/share/v/1Ccd...

#FeedForMSFolk #neurorehab #neurorehabilitation #MultipleSclerosis #TheMSGym.

I agree that this is a strategic move. I also suspect it’s not permanently shelved - it can remain a strategic tool.

My theory is that he was leaving it as a bargaining chip. He wasn’t a fan either - it was from previous admin. Plus being shelved doesn’t suggest permanency.

Multimodal MRI Reveals Consistent Basal Ganglia and Limbic System Alterations in COVID-19 Survivors The long-term impact of COVID-19 on the brain is multifaceted, encompassing structural and functional disruptions. A cohesive theory of the underlying mechanisms of the Post-COVID Syndrome (PCS) remai...

“…suggest COVID-19 is associated with selective structural and functional alterations in basal ganglia–limbic–cortical circuits, with stronger effects in severe cases … in line with symptoms … fatigue, memory impairment, attentional deficits, and insomnia.”
June 20, 2025 preprint
#Covid19

Phot of a Blandings turtle after a rainstorm, making her carapace shiny and almost black - the yellow throat and jaw a stark contrast. She’s sitting on the shoulder with lots of fresh green foliage behind her, trying to cross the road.

Here she is just peeking her head out to look around and find the stream.

Moved this beauty across the road to the stream she was heading for today. She was on the shoulder, right side right after a hill and easily could have been shmucked. Blandings turtles are threatened in Ontario and endangered in the Great Lakes/St. Lawrence area. #Blandings #threatened #endangered

We had more white crowned sparrows pass through than we’ve ever seen before. It’s was crazy!

That’s very cool! I wonder how they were introduced …

High Payoff Workshops Workshops on High Payoff Drills

Three FREE workshops coming up! HIGH PAYOFF DRILLS.

#TheMSGym

Please check the link to determine the best workshop for your mobility level!

Session 1: Sitting Strong, May 19th, 1 pm EST

Session 2: Standing Strong, May 21st, 1 pm EST

Session 3: Moving Strong, May 23rd, 1 pm EST, 11 am MTN

Plus EBV is implicated in at least 6-7 other autoimmune diseases now, not to mention various head and neck cancers. Yes to a vaccine. Which I think could even help someone in my situation.

Doing better than I have since 2018. I’ve thrown everything at it (if scientifically factual!). Having been a research chemist, I have the background to deep dive. symptoms of MS are often caused by other things and too often, symptoms get swept under the MS rug when they are treatable/manageable.

Printed version for both photos: Infectious mononucleosis in childhood (hazard ratio [HR], 1.98; 95% CI, 1.21-3.23) and adolescence (HR, 3.00; 95% CI, 2.48-3.63) was associated with an increased risk of an MS diagnosis that remained significant after controlling for shared familial factors in stratified Cox proportional hazards regression (HRs, 2.87 [95% CI, 1.44-5.74] and 3.19 [95% CI, 2.29-4.46], respectively). Infectious mononucleosis in early adulthood was also associated with risk of a subsequent MS diagnosis (HR, 1.89; 95% CI, 1.18-3.05), but this risk was attenuated and was not significant after controlling for shared familial factors (HR, 1.51; 95% CI, 0.82-2.76). Conclusions and Relevance These findings suggest that IM in childhood and particularly adolescence is a risk factor associated with a diagnosis of MS, independent of shared familial factors.

See alt.txt below photo 1 cor image in print form

Looks like the adolescent risk is higher than childhood infection, but the risk is significantly increased for both. Mono (from EBV) as a young adult shows an insignificant increase.

So childhood exposure still not the best plan. I ended up with MS despite that. 🤷‍♀️

I had early exposure. But I also had a career that caused solvent bioaccumulation so perhaps the triggers add up. Every Covid infection triggered an EBV reactivation except for my last - given remdesivir. I just got better from Covid for the first time.
Without prophylactic VCV, MS progresses. 🙃

Association of Infectious Mononucleosis in Childhood and Adolescence With Risk for a Subsequent Multiple Sclerosis Diagnosis Among Siblings Is diagnosis of infectious mononucleosis (IM) in childhood or adolescence associated with subsequent development of multiple sclerosis (MS)? In this population–based cohort study of 2 492 980 individu...

Supposedly it’s having an EBV-caused infection in childhood or adolescence vs older. I never *had* mono but had older siblings so likely had it under age 6 when it was simply a random childhood fever illness. 2018 testing showed both historical and current ab.

pmc.ncbi.nlm.nih.gov/articles/PMC...

My goodness it was so good! I’ve searched old recipe book archives, googled until my eyes bled. Because she called it Busy Day Dessert, couldn’t ever find it. That’s a jello thing lol.

Now, I would probably find it way to sweet now - but I’m gong to try to adapt it. Glad someone else remembers!

🔹 Caramel Syrup Base (Stovetop) 150 g brown sugar (light or dark) 45 g unsalted butter 200 mL boiling water Optional: 1/4 tsp salt or 1/2 tsp vanilla extract (added after boiling) Instructions: In a saucepan over medium heat, melt the butter. Stir in brown sugar and cook for 1–2 minutes until fully dissolved and bubbling. Carefully add boiling water (it may sputter). Stir well and simmer another 30 seconds. Remove from heat. Add vanilla or salt if using. Pour this hot syrup into a greased 20–23 cm baking dish or deep pie dish. Set aside while you prepare the batter. 🔹 Cake Batter (Gluten-Free Sponge Layer) 125 g gluten-free all-purpose flour blend (with xanthan gum) 100 g granulated sugar 2 tsp baking powder 1/4 tsp salt 120 mL milk (dairy or unsweetened plant-based) 30 g melted butter (or neutral oil) 1 tsp vanilla extract Instructions: Preheat oven to 180°C (160°C fan). In a bowl, whisk flour, sugar, baking powder, and salt. Add milk, melted butter, and vanilla. Stir until smooth. Gently spoon or pour the batter over the caramel layer in the dish — don’t stir or mix! Bake for 30–40 minutes, or until golden and puffed on top. A toothpick inserted near the center (but not too deep) should come out with a few moist crumbs. 🔹 To Serve Let cool for 10–15 minutes so the caramel thickens. Spoon into bowls while warm — the bottom should be rich and saucy, with a soft cake layer on top. *** no guarantees! I haven’t tried it yet!

I’ve been trying to avoid AI due to energy usage. But I’ve been searching out a recipe my mom used to make in the 70s to no avail. She’s almost 97 and doesn’t remember making it. Today chat.gpt and I may have figured it out - and made it gluten free. 😭❤️🙏🏼

AI generated recipe in alt.txt!

Sleep is essential — researchers are trying to work out why A typical person spends more than 20 years in a state of dreamy semi-consciousness. But surprisingly little is known about why we need this down time.

#Medsky🧪 #neurosky #publichealth This study shows how researchers are beginning to understand that sleep does more than just give our brains and bodies a respite from the rigours of the day @nature.com

www.nature.com/articles/d41...

WALKING BETTER DOWN STAIRS If you struggle with climbing and descending stairs, you are not alone. Many many people affected with a neurological condition find stairs super challenging. In this video, we are going to work on going down stairs. Descending stairs requires four big things: 1. Ankle / Knee mobility 2. Leg strength 3. Core stability 4. Healthy vestibular function However, trying to slowly lower your body 7.5 inches (18 cm) when you lack any one of the four key elements above can make going down stairs extremely frustrating. Instead of “force feeding” that movement into your brain, which likely doesn’t have that range of motion available, we can progressively improve your joint mobility, muscular strength, core stability, and vestibular (balance) function in smaller steps… literally. You can master the “down stairs” movement using 1 inch (2.5 cm) platforms to build up to a standard step height. This progressive approach will encourage your body to move and train in a way that will not stress out your brain and cause more symptoms. They KEYS to mastering this movement: 1. Use the appropriate level of balance support (wall, walker, countertop, railing). 2. Drop SLOWLY into the movement paying attention to RELAXING your body. 3. Pause at the bottom of the movement and find your balance. 4. Push your body back onto the top of the platform using your quads, glutes, and core. Once you can perform 10-15 reps on BOTH LEGS with less dependence on your assistive device or surface, INCREASE THE HEIGHT of your platform by 1 inch (2.54 cm). If you can aim to improve an inch every two weeks, it is possible that you will be able to walk up and down stair with more ease and confidence within 12-16 weeks. That would be HUGE! #multiplesclerosis #movementismedicine #neurologicconditions #chronicillness #neurologicaldisorder #disabledtiktok #fyp #foryoupage #mssucks

WALKING BETTER DOWNSTAIRS
#MultipleSclerosis #NeuroRehab #neuroplasticity #rehab #FeedForMSFolk

www.facebook.com/share/v/1RSw...

I had to start with a single magazine! 🙃🤣

See Alt-Txt for full description.

Worth the work and the time! #MS

Researchers link the “clock” hormone melatonin to seasonal MS relapses Background Multiple sclerosis (MS) relapse activity follows the seasons; MS attacks are generally more frequent in the spring and summer and quiet down in the fall and winter. Although the reason for ...

mscanada.ca/ms-research/...

pmc.ncbi.nlm.nih.gov/articles/PMC...

Look at the research for seasonal relapse.

The thought is that it involves circadian rhythms.

Back before DMTs I pretty consistently relapsed spring and August.

Canada Excellence Research Chair Positions Western University, in vibrant London, Ontario, delivers an academic and student experience second to none.

Any of my colleagues want to come to Canada? uwo.ca/research/cer... [One priority area is Neuroscience and Brain Health. We have awesome facilities and people]. @westernuwin.bsky.social

YouTube video by World Health Network How COVID Impacts the Brain: Danielle Beckman and David Joffe

My presentation with @davidjoffe64.bsky.social on COVID's impacts on the brain is already the most watched video on the @thewhn.bsky.social platform 🤯! Thank you to everyone who supports our research! We are now writing a physician's guide for #NeuroCovid #LongCovid 🤓
www.youtube.com/watch?v=soJX...

I would love to hear the strategies. Anything coming from doctors or government would not affect the folks I know. 🤷‍♀️ are there websites?

There is no effective way to fight the a anti-vax narrative. I know many folks. Public health training would do nothing. They should all watch the Pitt. Which wouldn’t really help all of them if the parents respond like the pair in Texas.

Hair loss? Could happen with Mavenclad as well. I didn’t lose hair with either but have lost due to B vitamin deficiency and thyroid issues. So keep an eye on thyroid and a good methylated B complex is your friend. Make sure you join the Mavenclad group!

What @italoromeno.bsky.social said lol.

I can’t say outright it treats MS. It treats the thing I don’t know I had when progressing without lesions in 2018. I showed an immune system actively responding to EBV - zero EBV symptoms, all MS progression (supposedly). Valayclovir turned me around.

Many people I know can’t get vaxxed now (no live vaccines on MS medications for instance).

My gp refused titres last fall but thankfully MS neuro reinforced my need for titres. Neither my mom or I remembered any measles aside from German measles when I was young.

Photo of legs and feet of a motivated person with MS using trekking poles on a pathway. Additionally you can see the title of the workshop which is The MS Gym: Walking Strong.

This Workshop is FOR YOU if: - You can walk for 2 minutes or more at a time. - You use a walker, crutches, or poles to perform daily activities at home. - You experience foot drop, leg weakness or balance problems. - You are wanting to improve walking strength, balance, and endurance. This Workshop is NOT for you if: - You use a chair, scooter, or are seated on a rollator to perform your daily activities. - You find it difficult to sit without slumping or falling to one side. - You cannot stand fully upright using an assistive device for 2 minutes. - You cannot walk more than 2 minutes. ** If you fall into this category or feel you are “on the fence,” please know I have several upcoming workshops designed for specifically for you. ( If you can't attend live, a replay will be sent following the event for those who register. )

Upcoming MS Gym Workshop: Walking Strong
#MS #neuroplasticity #walking #rehab #neurologicalendurance #balance

Please check photo 2 for criteria for workshop
suitability.

Please register here:

themsgym.mykajabi.com/walking-stro...

Jagmeetus interruptus. 🤦‍♀️

"I haven't followed Canadian politics closely, but when a politician talks of limiting free press, activities at universities & defying the courts, it's the canary in a coal mine for autocracy"

- Harvard University Professor when asked his opinion on Pierre Poilievre.

#Canada
#cdnpoli
#elxn45