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Please for those suffering who read this, you CAN heal from this!!! I recorded my healing on my channel and am 90% healed WITHOUT medication!! Please do NOT believe the doctors because there IS hope!! I am writing my book about it as youtube suppresses the truth about so-called "genetic" auto immune conditions. There is no such thing!! You CAN heal. 🙏❤

I can't even GET my multiple doctors in southern MICHIGAN to recognize fibromyalgia as an illness!

Edit to say: I can't even get 6 different doctors in southern Michigan to admit that fibromyalgia is an illness! I randomly had 1 doctor from Detroit admit that I "probably have fibromyalgia", after my primary care doc of 27 years diagnosed me soon before he retired at 68. Suffering right now, had neck alkolising (s.p.?) spondylosis (A. K.) since I was 24, add some several decades and I AM HURTING. Done the most of the SSRIs, done the various opiates... (No prescribed - - or otherwise -- opiates for the past 10+ years because suddenly doctors weren't allowed to treat me so I could work a customer facing/retail job on my feet 9-12 hours at a time. (also couldn't get ANY disability help). This is a diagnosis that is HELL! I would not wish it on my worst enemy (and I can think of a couple horrible managers I've had).

Thank you for this I was just diagnosed at age 30 and I'm female 😭

Antihistamines H1 & H2 have helped a lot

great video except i'd question the 'very rare' statement. Given the sensitivity of the topic i reckon there are many unreported cases.

Pedialyte drink is a great hydration if ur lacking water pick it up at ur local grocery store

What are the best probiotics for microscopic colitis?

I have always struggled with sudden reddness, swelling and pain in my hands (more commen) and feet (less common) when i change temperature specifically or do something that increases my heart rate. im unsure if it is eythromalalgia but its the only thing that matches what im going through. I also only really get mild-moderate pain and it only really happens 1-2 times a day and has been happening to me for as long as i remember but ive noticed it was a problem when i was in high school (3 years ago).

i'll just say that the same people who developed Finasteride also helped develop the covid vaccines and push covid related products.... Merck

Would k2 vitamin help to move the calcium back into the bones? Any ideas on minerals and vitamins?

Great video and thanks for the information. I was diagnosed 3 yesrs ago at the age of 57. Basically was told that I had dish, walking and swimming will help manage the symptoms, goodbye! My symptoms include rib pain and a feeling of a heaviness and dull pain further up my spine. Rib pain varies in intensity and at its worst feels like thete is a giant cable tie around my ribs that has been pulled very tight! So I have tried to manage my symptoms with as many eays as I can. Stretching exercises in the morning, walking, swimming all help. I have also started a kind of bouncing movement which involves bending the knees slightly, stomach relaxed, shoulders back and arms dropped down in front of you, gently bounce like a spring compressing and decompressing. Do this for about 3 mins, 2-3 times per day. My next thing was a game changer for me and that is earthing or grounding. I now sleep with a grounding sheet on my bed and it has really allowed me to sleep at night without any pain killers. Worth trying, but consult with doctor if using blood thinners i would say. Low carb diet also helps me as sugar is very inflammatory,. Happy to discuss more at length if anyone is interested. The more strings to our bows the better in trying to manage this disease! I wish you all well and goid luck in your dish management!

It’s not real

Thanks for the info.

Good information on D I S H thank you lots of regards from chennai India

Thank you for the information. Im actually 49 and was just diagnosed with DISH in my spine and its really bad in my neck. Thats why I went to my doctor. Not really much information on it and what I can expect from it

Finasteride is a terrible disgusting drug

These pills are amazing

Omg i cant even sleep been taking this pill for sometime now.

Hard flaccid caused by PFS or PSSD.

Can you be more specific about the most significant side effects?

For me a low carb diet works to reduce flares.

Why is it that every expert I hear talking about Finasteride is bald??

I look at my hair, and i wish i had took it. Because for those who describing PFS.. i feel worse already because of my bald head.

Open it 🤬🤬

Very thorough. Thank you. Question: I see everywhere the recommendation to avoid aspirin but also the suggestion that pepto bismol is helpful. Is it something other than the salicylate that is a problem in ASA?

1 in 100 risk is not rare, it's common.

I’ve been having swelling in my toes that have been itchy and painful, I have been trying for ages to figure out what’s wrong and I think it might be this, I also think it could be linked to the medication I take as it’s a vasoconstrictor, it’s vyvanse for my adhd, and whenever I take a higher dosage as it became such an issue for me last year that I went down a dose and it helped but I need a higher dose for it to actually be affective and I was just wondering if you thought there could be any link between the vyvanse and Erythromelalgia

Thank you!! Every single article acknowledg

I’ve had this horrendous condition for 8 years.

Please make a video on pssd too

Great information. it’s hard to find anything about this. Thank you!

Of course it can make you dehydrated so therefore to make you dizzy

It is a made up condition. There's already a medical term for it, it's called nocebo. Stop reading reddit shit posts and random youtube videos that spew bullshit after bullshit if you don't want to lose your mind. You're welcome.

this also happens with accutane

I also was put to exercise and I feel good swimming, but now my sugar went up and jardience gave me a numb foot and now I have to go to pediatrist, and neurology 😳☺️

They put me on CYMBALTA 60 mg. And it helps me so much. 😊

I think people that have issues are taking way too much of the drug. I would not recommend taking it every day but every other day. And if you have the 5mg dosage split the pills into 4 peace’s and take 1 peace every other day. By the way I was on it for my hair loss my hair came back and I keep my hair using this drug and I have no issue.

this syndrome is not as rare as you think...just watch the comments below the video and you will see...i have this too...

Absloute grifters just jumping on a narritive of wanting payouts the big pharmaceutical companys havent helped themselves in the early days trying to.make it go away paying some people out without evidence these days after years of intense studies showing no such conditions there claims are rightly dismissed as 20 odd years of widespread use of these drugs these claims without 1 shred of scientific evidence or data apart from the possible side effects which are clearly stated and there are potential side effects from every single medication on the planet . In context its been studied since the late 90s and there is one iota of a metric to use that it can cause this fantasy aliment and once medication stops it is scientifically impossible to have long term effects due to the half life efficency and mechanisms of action of post finsetride levels in the human system ...🤔 .

❤❤❤

On the topic of albuterol inhalers, a rinsing tutorial would probably be helpful to many patients if you haven't made one yet. I know family members who have complained that their inhaler "doesn't work" and when I look inside the mouthpiece, the nozzle is plugged with propellant.

PFS and PSSD is Real, think 100x times before do SSRI'S or Fenosteride

this is real! thanks man

Every person I have spoken to got side affects. Blocking a hormone conversion sounds like ludicrous.

Please make a video about PSSD (Post ssri s3xual dysfunction)

Thanks for covering this topic. But I don't think it's as rare as you say. There is a A LOT of denial by doctors and the medical community about pfs. Therefore, it is massively underreported and untracked overall.

Thank you for listing the amount of side effects that are often swept under the rug. Can you talk about PSSD?

Great info. Can you recommend a cleanser and moisturizer for sensitive skin. A dermatologist put me on finasteride yrs ago and it gave me hyperpigmentation on the face along with other bad side effects😢. Then they gave me hydroquinone cream for hyperpigmentation which made everything worse. Dermatologist really did a lot of damage to me and I'm still trying to get back on track. Your videos are great its like you already know what I'm going through then put up a video about it. Thank you!

I had/have nearly all identical symptoms but from Lexapro. PSSD and PFS are so similar! I think this condition is more prevalent than known, most of these symptoms are “subjective” and are ignored by doctors and blame the patients and tell them it’s psychosomatic and in their head.