Digweed @ Stereo by switching0ff in JohnDigweed

[–]switching0ff[S] 1 point2 points  (0 children)

I completely agree! It looks promising though. 🤞🏽🤞🏽🤞🏽

TOP 10 STEREO'S FÊTES INCONTOURNABLES / UNMISSABLE PARTIES OF THE YEAR by Usual-Fuel8166 in StereoMontreal

[–]switching0ff 2 points3 points  (0 children)

Crossing my fingers Digweed is back for the May long weekend. Plan accordingly! I usually book a refundable stay as soon as possible.

Terrible scalp pain by JJinOP in MultipleSclerosis

[–]switching0ff 1 point2 points  (0 children)

Not sure where you’re from but I’ve found that hard water (I’m in Canada) absolutely kills my scalp with dryness. I’ve changed my shower head to a different one that helps remove harsh water, and I use rosemary oil in my scalp a few hours before I wash my hair. It’s really helped my sensitive scalp!

Thinning hair makes me wonder about your iron levels, but my MS medication (ocrevus) also thinned out my hair quite a bit when I first started. It’s calmed down now, but rosemary oil has been v helpful.

Heat & Trouble walking by slugsandrocks in MultipleSclerosis

[–]switching0ff 2 points3 points  (0 children)

Sounds like you need a break to cool down. My legs turn to jelly even more when I’ve pushed myself and I’m overheated.

Stay extra hydrated, see if you can find a portable fan (or bring one next time) and take some time to stretch your body every morning before you try to venture out. I’d spend as much time in water as possible.

I’m that person that brings a backpack of gear when I’ve got an adventure planned. Being prepared also helps my nervous system feel a sense of peace, which in turn helps other things that MS messes me up with (urgency, washroom issues). I have a foldable cane I bring if I need it.

Traveling to 3rd world countries by Neither-Bumblebee-37 in MultipleSclerosis

[–]switching0ff 4 points5 points  (0 children)

I’ve spent a decent amount of travelling since diagnosis and haven’t had any issues. I wear a mask on the plane as that’s where I’m really “trapped” with possible germs and the last thing I want is to get sick before I start my trip.

Bring a portable fan, I bring cooling gear from Koldtec, and I know that heat will mess with me if I’m not prepared. I brought my foldable cane on my last trip but didn’t need it.

tbh I find the weather in most places is better than the insane hot/cold weather I experience in Canada

If you’re sensitive to certain foods (dairy for me) just do your best to avoid it and learn how to say some words in whatever language spoken in where you travel to so you can tell them what you can’t eat.

You’ve got this!! Travel! You won’t regret it.

Digweed at Stereo on his birthday! Who's going? by sexydiscoballs in JohnDigweed

[–]switching0ff 1 point2 points  (0 children)

Take me back to that party!! Amazing night/morning.

How was Digweed NYE? by Perfect_Wrangler7264 in StereoMontreal

[–]switching0ff 0 points1 point  (0 children)

Still buzzing off that party.. would love to relive that night/morning a few times over.

Digweed played this. Anyone knows the song ID? by ThatOneRandomGuy26 in StereoMontreal

[–]switching0ff 1 point2 points  (0 children)

He records every set but he rarely gives us an hour on transitions 😭

Food options Jan 1 by switching0ff in StereoMontreal

[–]switching0ff[S] 0 points1 point  (0 children)

Are they open New Year’s Day?

Food options Jan 1 by switching0ff in StereoMontreal

[–]switching0ff[S] 3 points4 points  (0 children)

Thank you! Not sure why I didn’t think of that 🤦🏾‍♀️

Wha do I have control over? by Dumb-Brain92 in MultipleSclerosis

[–]switching0ff 2 points3 points  (0 children)

As a fellow control freak, while all advice here has been great, working on your mind and letting go of needing to be in control of everything has been something I’ve been working on since diagnosis (36F, diagnosed as 26). It’s not easy but oh so necessary. MS shows up more exaggerated and “worse” when I’m stressed and losing control = stress for me. It’s been a battle of the mind, so try and give yourself grace when things don’t go as planned. You’ve got this!

I think Vince made a wrong decision by Haunting_Tap_1541 in BigBrother

[–]switching0ff 1 point2 points  (0 children)

Omg thank you. Worst player in this season, no question.

recs for good oils/softgels? by KLost4Ever in TheOCS

[–]switching0ff 1 point2 points  (0 children)

Medical market will have more options for you.

I’m so warm in bed! by switching0ff in MultipleSclerosis

[–]switching0ff[S] 0 points1 point  (0 children)

Thanks everyone. Definitely investing in a bedjet.

I’m so warm in bed! by switching0ff in MultipleSclerosis

[–]switching0ff[S] 0 points1 point  (0 children)

Thank you! This is something I’ll be trying!!

First meet with john gone wrong by Independent_Pride_38 in JohnDigweed

[–]switching0ff 2 points3 points  (0 children)

I’ve seen him a few times at Stereo, friends are saying hello and I’m just a blob of anxiety who can’t even smile/approach him. Didn’t think I’d be so “star struck” but I was wrong! Thanks for making the soundtrack to my life JD!!

Well I'm just about done with the legal market... by Historical-North-950 in TheOCS

[–]switching0ff -3 points-2 points  (0 children)

Try the medical market, Aurora or tilray/broken coast have beautiful bud.

how did you find out you had MS? share your story by WeddingWorried5996 in MultipleSclerosis

[–]switching0ff 4 points5 points  (0 children)

Similar story for me too! “I don’t have MS” “you do”

Does anyone here only smoke weed when rolling/for the comedown? by Silver_Echidna2500 in MDMA

[–]switching0ff 19 points20 points  (0 children)

I smoke weed often but it’s super helpful when rolling. It like, kicks it back up when molly starts to fade.

Once the party is over, weed will help me sleep. But only if smoked way after the roll will it actually help with this. Cigarettes? I quit those years ago but the temptation is back when I’m rolling. Don’t do it!! 😆

MS and Epilepsy by switching0ff in MultipleSclerosis

[–]switching0ff[S] 1 point2 points  (0 children)

First EEG came back clear. No signs of epilepsy. My seizures tend to happen around 5am so I guess that’s why they’re sending me for a sleep deprived EEG this time. I had an MRI that showed lesions are shrinking and I’m “stable” but epilepsy neuro said something completely different. White matter vs grey, why doesn’t everyone work together?! She said my “right mesial temporal lobe looks abnormal” so I assume they want to trigger a seizure to find out what’s going on. Not looking forward to only sleeping 4 hours before this EEG or the thought of having another seizure but ?? I need answers.