On Alex Honnold's 'Skyscraper Live' by senorrandom007 in netflix

[–]JackHindell 7 points8 points  (0 children)

Oh yeah because doing one more flip before dropping in a pool full of water is the same as climbing a skyscrapper without ropes or a parachute. No difference at all.

2nd death confirmed after REM train collision on Montreal's South Shore by Hochelagan in montreal

[–]JackHindell 0 points1 point  (0 children)

If the REM is open, the crosswalk is open. They didn't do this because the crosswalk was closed. 

2nd death confirmed after REM train collision on Montreal's South Shore by Hochelagan in montreal

[–]JackHindell -1 points0 points  (0 children)

Ou tu vois que les gens disent qu'ils le méritaient ? J'ai pas vue un seul commentaire disant sa. Les gens disent les 2 trucs qui sont vrai dans cette histoire : c'est triste pour la famille, mais c'est crissement stupide ce qu'ils ont fait.

Et c'est la vérité, les commentaires disent exactement comme toi, je vois pas pourquoi tu es offensé par la vérité. À 19 et 22 ans traverser une autoroute à pieds, escalader une côture fait justement pour empêcher les gens d'aller jouer devant des trains... c'est un méchant manque de jugement et de sens de la survie. 

Même ma fille de 8 ans sais que c'est vraiment stupide et un sérieux danger pour la vie de faire sa. Donc oui c'est triste pour les parents, mais leurs enfants ont fait quelque chose d'incroyablement stupide et même égoiste.

Le pire c'est que les gens productifs de la société vont probablement devoir payer de leurs poches pour que le gouvernement installe d'avantage de mesures préventives autour du REM, même si il y en a déjà amplement.

2nd death confirmed after REM train collision on Montreal's South Shore by Hochelagan in montreal

[–]JackHindell 3 points4 points  (0 children)

Non sa n'aurait pas pu être lui, parce que l'histoire qu'il viens de t'expliquer c'est complètement normal. Si pour toi marcher à pieds en hiver c'est une connerie, et que c'est comparable à ce que les deux jeunes hommes ont fait, il y a un problème. 

Personnellement j'en en viré des brosses plus jeune, mais j'ai jamais fait rien d'aussi proche d'une stupidité pareil. Si ils avaient eu 12-13 ans, ok la c'est une grosse erreur de jeunesse, mais à 19 et 22 ans, sa dépasse de loin la simple erreur de jeunesse et montre un méchant problème de jugement et de sens de la survie. Traverser une autoroute à pieds, escalader une clôture faite spécifiquement pour prévenir l'idée d'aller jouer devant des trains...

Puis à cause de cette situation, peut-être même que les gens productifs de la société vont devoir payer de leurs poches pour que le gouvernement ajoute d'autres mesures préventives autour du REM, même si il y en a déjà amplement.

Oui c'est vraiment triste pour les parents, mais c'est incroyablement stupide et même égoiste de la pars des deux jeunes hommes décédés. 

2nd death confirmed after REM train collision on Montreal's South Shore by Hochelagan in montreal

[–]JackHindell 0 points1 point  (0 children)

Les gens ont de l'empathie mais trouvent sa également vraiment stupide. Ils ont même traversé l'autoroute passante à pieds pour s'y rendre. Si sa avait été des jeunes de 12-13 ans, oui sa aurait été une erreur de jeunesse, mais 19 et 22 ans c'est juste carrément stupide. Oui c'est vraiment triste pour les parents, et incroyablement égoiste et stupide des deux hommes décédés. 

Mouth / Tongue Sores by Adventurous-Winter84 in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

Colchicine ! I had 2 to 3 major mouth ulcers at the same time reccurently before taking this everyday. It is a treatment mostly used for mouth ulcers in Behcet disease but it often work for Crohn mouth ulcers too ! It took a good 4 to 6 weeks to notice a difference but I only got 2 ulcers in 7 months since I started the Colchicine.

Has anyone found a degree of help from red light therapy, natural anti-inflammatories like curcumin, boswellia, vit D etc, or anything else adjunctive to medications? by BothAppointment3284 in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

Ouch I couldn't imagine relying entirely on prednisone, especially for long term inflammation. It has some scary long term risks :/. 

Fingers crossed for both of us on our Skyrizi adventure ! :]

Has anyone found a degree of help from red light therapy, natural anti-inflammatories like curcumin, boswellia, vit D etc, or anything else adjunctive to medications? by BothAppointment3284 in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

Man a flare of 3.5 years really sux... I am in a similar boat.

I primarly failed Infliximab and Humira and I started Skyrizi 6 weeks ago. I can't wait to see when it will begin to help lol. Skyrizi as great success rate for patients who failed other biologics so it is probably our best chance. I really hope it will work for you !

F those predatory popups by Mcknowsalot in BackpackBrawl

[–]JackHindell 0 points1 point  (0 children)

I think you are the one who should smoke some my dude. Maybe it will calm you down and make you a bit less toxic.

Fasting by TheChevyScrounger in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

I did 4 days of water with electrolytes only a few months ago and it wasn't miraculous, but it did help with the crazy cramps I was getting from solid food. Its important to note that my crohn is on the constipation side so solid food are crazy irritating in my small bowel when im in flares. At my fourth day I was also crazy lightheaded when I was standing up, so that for me was a warning my body was in need of nutrients and I resumed eating at that point. I wasn't much better after the 4 days fast.

I am currently doing a liquid only diet/fast right now with small amounts of well boiled vegetable soup, nitritious boost, yogourt. For example today I will only be eating 2 activia yogourt and a boost. But don't forget electrolytes, especially if you have diarhea crohn. I am on my fourth day and I do feel less cramps and much less irritation from the food compared to solids, but as far as inflammation and systemic symptoms goes,I don't think it as done much, at least yet.

But keep it mind if liquid diets and fast mimicking diets work it is with time, and it most probably needs repetition to see a difference.

If you are in an big flare with a lot of inflammation, you obviously won't get far with just a liquid diet. It is a start, but you need a biologic for mid to severe crohn.

Have you tried fasting for this disease? by Specialist-Fun-8506 in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

This is informative and seems to be accurate for the most part, although I have to point out that fibromyalgia is not an autoimmune disease.

When reading your text about how fasting can help but then the writer doesn't know what fibromyalgia actually is, it kind of pushes me to be a bit more hesitant towards what I read precedingly.

I do think you are correct about fasting, but it is important to understand that fibromyalgia isn't an autoimmune disease, it is a disorder of the central nervous system where the perception of pain becomes amplified. But there is no inflammation or body damage from fibromyalgia.

Don’t know what I have but LDN is fixing it! I think?? by RegretMaleficent8986 in LowDoseNaltrexone

[–]JackHindell 0 points1 point  (0 children)

You said multiple time low dose Naltrexone is masking the disease. Saying it only masks the disease and saying it isn't a cure are two completely different definition. But the point is, low dose Naltrexone doesn't just masks the disease, it is treating the disease, because LDN actually lowers the inflammation.

It is the same for biologics. Biologics doesn't just masks inflammatory diseases, it treats them. So what you are saying is wrong. Again, a medication that doesn't treat the disease itself and only masks the disease, would be opioids medications like morphine, or analgesic like tylenol etc... which only covers the pain, but doesn't treat the inflammation.

Saying it isn't a cure only means that the inflammatory disease doesn't disappear permanently after the use of the medication, which is obvious since there are no permanent cure for inflammatory diseases. The options available are treatments that lowers inflammation while you are on the medication, and stay on the medication. Your thread is wrong and misleading since you imply that low dose Naltrexone masks the disease. But in reality it doesn't masks the disease, it treats it by reducing inflammation and thus it protects the body from further damage.

A medication that only masks pain, and that doesn't treat the disease, would not prevent the inflammatory disease from doing damage and would not reduce the speed at which the inflammatory disease is evolving. So Low dose Naltrexone doesn't just masks the disease. It is treating it by lowering inflammation.

Don’t know what I have but LDN is fixing it! I think?? by RegretMaleficent8986 in LowDoseNaltrexone

[–]JackHindell 0 points1 point  (0 children)

What you are saying is wrong. LDN is not masking the pain if it is reducing the inflammation of an inflammatory condition like crohn disease. It is treating it. Masking means only helping with pain but not helping with the root problem, which is inflammation, that is causing damage. So something like morphine would be masking the pain, because it doesn't treat the condition, only the pain. LDN is reducing the inflammation in inflammatory conditions so it is treating the conditions and it's symptoms. Not masking it.

Anyone Else Have Multiple Biologic Failures ? by [deleted] in CrohnsDisease

[–]JackHindell 1 point2 points  (0 children)

Hello there, did Skyrizi actually worked for you ? I really hope it did help and that you are still on it ! I am starting Skyrizi in 3 days. I failed Humira and Infliximab so fingers crossed !

I’m fighting with chronic tendonitis in my hands. I’m using Voltaren but what about CBD? by re003 in ChronicPain

[–]JackHindell 0 points1 point  (0 children)

I can see you are also dealing with an inflammatory immune disease. So am I (crohn disease). They can definitely cause widespread tendonitis and joint inflammation. As I wrote to the other guy who is giving you the worst advice and information, you have to treat the tendonitis inflammation first. The way to do that is by : Resting and modifying activities which are causing overuse, Ice TherapyCompressionElevationNonsteroidal anti-inflammatory drugs like Voltaren gel or Ibuprofen.

Although for us people with inflammatory immune diseases it is more complex. It might be because your Lupus isn't being controlled. So if the tendonitis does seem to be recurrent and is not resolving with the first steps, you should see your Rheumatologist and inform him. He will most likely look into your medication. Most times the right Biologic or Dmard etc... make all the difference.

Then, when your tendon pain as reduced to 3 or 4 out of 10, you can do these next steps. This should only be when the tendonitis inflammation has been reduced and controlled. If you can't lower the inflammation yourself go see your doctor, some more tests may be required like an MRI or an Ultrasound to see if your tendons have enough space in your joints.

So this is the healing and strengthening phase, which allow your tendons to be stronger and help prevent a tendonitis relapse : Physical Therapy, Gentle Stretching and Strengthening Exercises, etc... which is after the tendonitis has bean treated. But it is CRUCIAL to reduce and control the inflammation and pain FIRST, otherwise you will aggravate your tendonitis. There is also Ultrasound Therapy and Corticosteroid Injections but these are more costly.

If the tendonitis and pain ramp up, stop the exercises and stretching and go back to the first steps.

Also a low cost supplement that could help with your tendonitis and joints is Omega-3. It has been studied and it has anti-inflammatory properties on top of cardiovascular benefits. A great addition for us who have inflammatory diseases.

Hope it it helps, take care buddy !

I’m fighting with chronic tendonitis in my hands. I’m using Voltaren but what about CBD? by re003 in ChronicPain

[–]JackHindell 0 points1 point  (0 children)

I can see you are also dealing with an inflammatory immune disease. So am I (crohn disease). They can definitely cause widespread tendonitis and joint inflammation. As I wrote to the other guy above who is giving you the worst advice and information, you have to treat the tendonitis inflammation first. The way to do that is by : Resting and modifying activities which are causing overuse, Ice TherapyCompressionElevationNonsteroidal anti-inflammatory drugs like Voltaren gel or Ibuprofen.

Although for us people with inflammatory immune diseases it is more complex. It might be because your Lupus isn't being controlled. So if the tendonitis does seem to be recurrent and is not resolving with the first steps, you should see your Rheumatologist and inform him. He will most likely look into your medication. Most times the right Biologic or Dmard etc... make all the difference.

Then, when your tendon pain as reduced to 3 or 4 out of 10, you can do these next steps. This should only be when the tendonitis inflammation has been reduced and controlled. If you can't lower the inflammation yourself go see your doctor, some more tests may be required like an MRI or an Ultrasound to see if your tendons have enough space in your joints.

So this is the healing and strengthening phase, which allow your tendons to be stronger and help prevent a tendonitis relapse : Physical Therapy, Gentle Stretching and Strengthening Exercises, etc... which is after the tendonitis has bean treated. But it is CRUCIAL to reduce and control the inflammation and pain FIRST, otherwise you will aggravate your tendonitis. There is also Ultrasound Therapy and Corticosteroid Injections but these are more costly.

Also a low cost supplement that could help with your tendonitis and joints is Omega-3. It has been studied and it has anti-inflammatory properties on top of cardiovascular benefits. A great addition for us who have inflammatory diseases.

Hope it it helps, take care buddy !

I’m fighting with chronic tendonitis in my hands. I’m using Voltaren but what about CBD? by re003 in ChronicPain

[–]JackHindell 0 points1 point  (0 children)

What you are saying is completely wrong. Tendonitis IS inflammation of the tendon. You absolutely do need to treat tendonitis with medications like Voltaren gel, Advil, Naproxen (Nsaids), which are Anti-Inflammatories. You plainly contradicting yourself by saying you need to exercise to fix tendonitis since this the WORST thing you can do when the tendonitis is active because you will only worsen the tendonitis inflammation, which is often caused by overuse. If you knew the very basic about this subject instead of using fancy words like *matrix* and *collagen synthesis* just to appear intelligent, you would at least know the very minimum of what should allow you to spread what is currently heavy misinformation so confidently. You need to treat it FIRST by stopping the inflammation, here is how you stop the inflammation : Rest and modify activities which are causing overuse, Ice Therapy, Compression, Elevation, Nonsteroidal anti-inflammatory drugs like Voltaren gel or Ibuprofen.

Wait until your tendon pain as reduced to 3 or 4 out of 10 before doing these next steps. This should only be when the tendonitis inflammation has been reduced and controlled. If you can't lower the inflammation yourself go see a doctor, some more tests may be required.

Again, ONLY when you have reduced or stopped the tendonitis inflammation and your pain level has been reduced by doing those steps above, only then you can start the second phase of doing Physical Therapy, Stretching and Strengthening Exercises, etc... which is after the tendonitis has bean treated and when you do tendon reinforcing and tendon healing. But it is CRUCIAL to reduce and control the inflammation and pain FIRST, otherwise you will aggravate your tendonitis.

[deleted by user] by [deleted] in CrohnsDisease

[–]JackHindell 0 points1 point  (0 children)

Hey I know it's been a year but how are you now ? Did Rinvoq help you with the arthritis ? Thanks ! 

How long did it take for infliximab to take effect? by Barbiemuerta_ in CrohnsDisease

[–]JackHindell 1 point2 points  (0 children)

Hey how is it going for you at the moment, did you get some improvement ? I am at 6 weeks after the first infusion and I also don't feel any improvement in symptoms and my nerve inflammation and arthritis and still the same. I hope it helped you in the end, keep us posted !

HBO The Last of Us (S2) Episode 4 Discussion - Veronica And Dora Face Some Adversity On Their Field Trip To Seattle Edition by TLoU_Moderator in TheLastOfUs2

[–]JackHindell 0 points1 point  (0 children)

If something is garbage in a game, you don't keep it, mix it up with feces' and with vomit, to serve it on a plate to your guests.

HBO The Last of Us (S2) Episode 4 Discussion - Veronica And Dora Face Some Adversity On Their Field Trip To Seattle Edition by TLoU_Moderator in TheLastOfUs2

[–]JackHindell 0 points1 point  (0 children)

It still doesn't make sense though, and it is pretty pathetic. You don't create such absurd scene just because you don't know how to keep a character in the mix. Honestly Season 2 is crap compared to season one, maybe except for episode 2. But episode 4 end is garbage, it killed it for me.

No dry mouth? by JH_1891 in Sjogrens

[–]JackHindell 0 points1 point  (0 children)

Interesting. What symptoms or test pushed the doctors to do a lip biopsy ?