The #1 Decision You Need to Make
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- čas přidán 28. 06. 2024
- The #1 Decision You Need to Make
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Valuable Resources:
IsThisPDP.com - place to assess your situation.
DansCZcams.com - archive of daily videos. Over 1800 and counting.
DansFastStart.com - The best place to begin your journey. This playlist really covers what is going on, how to know if it is relevant to you and what to do next. Watch, take notes, implement, repeat.
PainFreeYouSuccess.com - Tons of Success Stories.
PainFreeYouGroup.com - if you want more help and direct access to be coached by me.
paypal.me/DanBuglio - If you wish to donate to support my channel, do that here:
Want to join my private Facebook Group? Come join us here:
/ painfreeyounow
Follow me on Instagram: / danbuglio
Made the decision!!! ❤😁 it Is all TMS no doubt!!! Ty Dan sending you much love and to all of you here on CZcams ❤😘😁🌷🙋♀️
Coming here for reassurance again. I made a terrible mistake of not unfollowing some medical instagram accounts and I just saw a post about pelvic pain/pudendal neuralgia (surgery, procedures, how horrible and untreatable it is), I unfollowed immediately but i can’t stop thinking about it now. I need to be smarter, cause bad thought always stay while good ones are hard to keep.
I want to make this decision but the medical world is still scaring me like a monster under my bed.
I understood it when I saw the first videos about Dr Sarno and I bought the book The Way Out by Alan Gordon this year. But it is your videos that changed everything and I fully got it and the realization kicked in that it's the mindset. My symptoms started one morning and I stayed calm instead of panicking and said to myself this is temporary. Instead of many days of sickness and pain it only lasted 1 day. Amazing ❤
What I believe to be true, is true ( for me) , until I believe "it" no more. So I choose to believe: I AM OK! 😊😇
Yes you are!
@@PainFreeYou 🥰
Scripture concurs… as a man thinks, so is he! 💪👍☝️🙏❤️😎😇🥰
Yes. According to your faith be it unto you ❤ Jesus is the truth. 💯
Yes. I would love to hear more about this. I was “diagnosed” with Small Fiber Neuropathy from a punch biopsy. So all the doctors say the burning sensations that I experience are due to that.. but Dr. Schubiner says otherwise. Similar to MRI’s of the back, lots of people have positive punch biopsies for Small Fiber Neuropathy that do not have any symptoms. This “diagnosis” has been what is holding me back from full commitment. It’s difficult. I’ve worked myself into chronic stress/anxiety. Was even referred to an endocrinologist because they were concerned about how high my cortisol was. After the tests, no other cause for high cortisol other than just stress and anxiety, which is reassuring. It’s hard to “not care” when you have persistent nerve pain, but I must push forward with my life and stop putting it on hold until I “get better”.
That is what the doctors say. How many of the FIT assessment questions do you answer as true? IsThisTMS.com the questions are in the txt of that page. Just read, answer and count the true answers. If one or more, the symptoms are from perceived danger and not the nerves.
I was diagnosed with small fiber neuropathy too, and it ruined my life! Guess what it's reversing! The pain and burning they said I would have forever, is a lie! They don't know all of this crap is mind body perceived danger. Hang in there you're on the right path with Dan.
Retro: me too. Near exact. I did go to a neurologist 4/6/24. He seemed confused. His diagnosis: poly neuropathy? Thats what it said with a ? Im 70 but fit active no meds lift weights
On TMS wiki they talked of SFN : that its total TMS
For me symptoms override logic: numb burning feet up my legs. Dan did a success story with Rita. CRPS. Ive talked with Rita twice. She couldnt wear shoes
In my gut i know im ok. My brain is the problem
Nerve damage is BS. Our nerves are not damaged!
The strange neurologist wanted me back to EMG & biopsy. I canceled
I believe I have PDP but through this long journey, I’ve gotten older and maybe that’s why it’s not going away. It started early sixties, I was extremely active with no pain. I feel like I’m getting more pains in my pelvis and all over my body. The stress that started it, taking care of an elderly patents who had strokes is still
present. I have had days hours where the pain is really low but some days its bad and my whole body is weak.
The neural pathways can be overwritten. You've already started on the pathway to a pain free you. Keep going. 👏
Can damaged nerves repair themselves? Almost 3 years and still burning, pain from fall injury. Tms tests just below threshold. All injuries heal?@1STBUCKLEY
Doctor says hamstring injuries don't fully "heal". That is where my fear and pain originated. I need to make the decision. It is hard!
How many of the FIT assessment questions do you answer as true? IsThisTMS.com the questions are in the txt of that page. Just read, answer and count the true answers. If one or more, the symptoms are from perceived danger and not the nerves.
How many of the FIT assessment questions do you answer as true? IsThisTMS.com the questions are in the txt of that page. Just read, answer and count the true answers. If one or more, the symptoms are from perceived danger and not the nerves.
I may be wrong but isn't everything a mind-body condition even if you flunk the TMS test? Because the symptoms in your body affect the mind and the mind (thoughts) affects the body.
Thank u for helping all of us u r the man dan 🙏🎉 appreciate your reassurance and help and the videos are awesome
Yes there's no downside after all your not giving pills your telling us what to do how to act with no medication ❤
I needed this SO much. I had a normal EMG/NCS a normal SFN biopsy. Mild reduces sweat in two places on QSART adrenergic response was normal and POTS via tilt with no change in BP yet I’m dx SFN w autonomic involvement and it scares me so much. Thank you for this. I have SO many symptoms and I’m trying so hard to come back and trust that I’m ok. I’m terrified all the time.
Doctors are trained to medicate and operate. And that's the problem because if all you have is a hammer, everything starts to look like a nail.
You often say to live more fix less….
100% Amen...🤜🏻💥🤛🏻🔊💨🕺
I took all the tests. They say highly likely tms. I am have a time of upheaval. 8 months...I really want to feel better. I have been to doctor, on probiotics. They keep trying to put me on restrictive diets. I never in 59 years had any problems with food. I refuse.
You can do it!
Maybe the probiotics are causing more issues. They really need to be tailored to the individual. Upheaval will cause anxiety which interferes with digestion. Brain/gut axis. Used to eat everything then my mum passed young, I did get a stomach ulcer heli co bacteria. Course types of antibiotics. Was still left with food issues. Am under top London hospital gastric. Dietician says I'm getting all the nutrients I need. I found oats made with water ( natural probiotic)and then a treat of jam has settled most IBS. Definitely flares when life gets stressy. But I know mine is PDP.
I panicked when a doctor told me in addition to hamstring will never heal completely and cause nerve pain. Additionally, severe arthritis in knees that he said in near future will need To be replaced. Panic set in, trying to turn it off is difficult
Will this work for hpylori
Dan, what about nba players or other celebrities who had surgery to repair herniated discs and fully recovered?
Nobody told them about tms?
Just wondering why few people believe in tms.
When you watch you tube herniated discs videos, so many views for different exercises, surgery reviews, etc.
We need more tms success stories especially for back, neck conditions
Success rates for back surgery are maybe 50%. Sometimes a surgery can act as a placebo. There's actually a book "Surgery, the ultimate placebo". While nobody told them about TMS, the perception of danger was resolved by the surgery.
If you have sciatica or stenosis and already have difficulty walking are you still gonna believe tms?how long do u have to wait or give the mind body approach, before you go for surgery? In your case, you had sciatica.was it mild and did you have symptoms of difficulty walking?
@@onildilig60 I would evaluate how the symptoms behave. If they behave like a MindBody condition I would never consider surgery. If it’s MindBody the. The body isn’t the problem. Http://IsThisTms.com
How my syptoms behave suggest tms , but the symptoms of herniated discs as explained by doctors, are also like the tms symptoms.
That is why herniated discs or spine problems are the hardest to fix, even by the tms approach.
Mind body can work especially when nothing is wrong with your MRI. Just my opinion.spine problems can really play funny games with your mind and especially your body.
@@onildilig60 Most people have bulges and herniations. 2/3 of people my age with NO pain have bulges and herniations. If the symptoms behave like TMS, in my opinion, that is what they are and should resolve once you decide that what you have been shown on the MRI are NORMAL abnormalities. Watch this. czcams.com/video/czVW8wD-mHc/video.htmlsi=dAhWYwzmuD1tGwsx
I can’t remember Dan but why does the pain or symptoms get triggered by activities you love doing ?
Ok here is a good one for you....After having a herniated disc, I know after 2 months it has now more or less healed. Do I continue to strengthen my back to try and prevent a physical problem happening again or can I just get on with life regardless and just leave it. At 43 I've never been in the gym and am an average weight etc...Thanks
I have an important question Dan - my doctor is no longer in my health plan and I need to go to a new doctor - now my previous doctor did a million test and says I am healthier than most 20 year olds and he could not find anything wrong with me - Same with the doctor before him. So he knows I have TMS only because I diagnosed myself and he agreed that I was probalby right and that it is TMS. - But going to the new doctor how do I explain what this is in medical terms - because I still have painful digestive symptoms, muscle spasms, chronic fatigue etc. - and I want to establish a clear communication with my new doctor to be able to recognize moving forward if it is still TMS or something else if something else comes up. My old doctor understoond why I did not want to pursue a gastroenterologist or a nerve doctor etc but how to establish communicating with my new doctor my fight or flight brain situation. I do need a doctor for real issues that may arise in the future - and the new doctor may not even agree with my TMS diagnosis and I may have to move onto one that does but in the meanitime how do I communicate this TMS in simple succinct terms to any new doctor?
My explanation is simple. I believe symptoms are created by a brain perceiving danger. Stress induced symptoms. I wouldn't get into Sarno's whole theory of repressed emotions. Stick with stress illness type of language. And if the doctor is open, they can watch the first video in my fast start playlist. DansFastStart.com
I couldnt wait long enough for your decision
Dan, thanks for the vid. I'm getting better. What does it mean if i can do the activites that cause me pain when i take a low dose of xanax? I do meditation, breathing, safety messages but nothing ever gets close to the relief of a low dose benzo. I can play my instrument and focus only on that, even if i try to worry about pain it doesn't come. Im so confused
It means you have a tool that will help you through this journey. Don't look for a deeper meaning. Take it until this mindbody work allows you to no longer need it. View the med as a measure of self kindness. We don't have to interpret a meaning behind your experience. You are blessed to have something that helps. Watch my fast start playlist to learn what is going on and what to do about it. DansFastStart.com
@PainFreeYou Dan you are so amazing. Thank you for your reply. I will use it as a tool of kindness without thinking too much and I will trust my brain to learn what I'm trying to teach it.
Mike
What do you think about polyneuropathy? I never ever had any problems in 8 years (the year i diagnosed with genetic polyneuropathy with EMG) until i found myself deep in depression. My doctor tells me numbness is the result of polyneuropathy but i dont believe it in my heart
That is what the doctors say. How many of the FIT assessment questions do you answer as true? IsThisTMS.com the questions are in the txt of that page. Just read, answer and count the true answers. If one or more, the symptoms are from perceived danger and not the nerves.
@PainFreeYou omg, thank you so much! Yes, it seems the problem isn't my nerves but not feeling safe
One question dan can this help with vax injurys I asked alot sorry any one use this method to heal
I will point you back to the FIT assessment to determine if a symptom behaves like TMS. If yes, then you can be helped with my suggestions. If it does not behave like TMS, then there may be true injury. Regardless - how you respond (fear or calm) will influence the intensity of the symptoms. IsThisTMS.com
@@PainFreeYou I took the pain test and got 36 out of 50
@@roddog4386 That would indicate TMS and not V-injury. You are in the right place. This approach can help.
Thanks dan these sxs came up after vaccination and docs put me on benzo now off benzo 7months so going thru alot of fear and the labels and doing this TMS work U provide to help cause I wanna give up but can't cause of my four kids I'm solo dad
@@roddog4386 there is ZERO downside to deciding you will be fine and teaching your brain safety.