How to NOT Get Better if You Have CFS | CHRONIC FATIGUE SYNDROME

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  • čas pƙidĂĄn 15. 12. 2022
  • 📈Learn how we're helping people recover from CFS, Long Covid, Fibromyalgia, Dysautonomia, and other Nervous System Health Disorders: www.cfsrecovery.co/apply?el=y...
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    --------------------------
    PDF RESOURCES
    RECOVERY FREEDOM FRAMEWORK - WHAT AN IDEAL DAY OF RECOVERING LOOKS LIKE âŹ‡ïž
    www.cfsrecovery.co/freedom-fr...
    BRAIN RETRAINING GUIDE FOR CHRONIC PAIN âŹ‡ïž
    www.cfsrecovery.co/pain?el=yo...
    --------------------------
    Are you struggling with chronic fatigue syndrome (CFS) and feeling overwhelmed by the prospect of getting better? You’re not alone. Sadly, many people living with CFS suffer because they don't have the right information or know-how on how to cope and make positive changes that can improve their health.
    While there are certainly effective steps for making real progress towards wellness, it's also important to understand what NOT to do if you want to successfully manage your condition. In this video, I will share some of these pitfalls so you can avoid them in your own journey of living a happier and healthier life - despite CFS.
    You Are Just One Mindshift Away From Living Life Without Chronic Pain and Fatigue
    ----------------------------------------------------------------------------------
    FOLLOW ME ON INSTAGRAM FOR EXTRA CONTENT âŹ‡ïž
    / cfsrecovery
    Tags: Cns fatigue, cns burnout, nervous system burnout, nervous system fatigue, cns exhaustion, chronic fatigue, cfs, chronic fatigue syndrome, bedridden, housebound, adrenal fatigue, chronic fatigue syndrome treatment, cfs symptoms, cfs recovery, cfs health, chronic pain, chronic pain syndrome, chronic pain explained, chronic pain meditation, post-viral fatigue syndrome, long covid, covid long hauler
    #cfs #cfsrecovery #cfsme #bedridden #anxiety #somaticsymptoms #somatic #panicdisorder #panicattacks #chronicpain #chronicsymptoms #longcovid #postviralfatigue
    DISCLAIMER: I am not a medical doctor or therapist. I am sharing my own experience and research. My video content is for information and educational purposes only. Please consult with your medical professional.

Komentáƙe • 93

  • @cfsrecovery
    @cfsrecovery  Pƙed rokem +1

    WANT TO SPEED UP RECOVERY? APPLY FOR OUR RECOVERY JUMPSTART PROGRAM ⬇
    www.cfsrecovery.co/apply

    • @LisaS1
      @LisaS1 Pƙed rokem +1

      Sorry I don't have the money for this help.

    • @alias701
      @alias701 Pƙed rokem

      Hey Miguel, you said you had a doctor in the hospital who knew what the disease is and what to do every day in order to get better. Was it luck or a cfs specialist? How did you know he is the right choice? For me it is very frustrating and difficult to find anyone who really understands this cfs disease/ disregulation.

  • @jessicalee9531
    @jessicalee9531 Pƙed rokem +14

    I think finding a recovery group that resonates with you personally as an individual is the key to recovery I found watching too many videos from different groups overwhelming and confusing I find these videos extremely positive and the least complex you really are doing an amazing job😊

  • @Inge508
    @Inge508 Pƙed rokem +15

    I found this video really helpful Miguel!
    It’s mindblowing that at 27 years old you have these amazing coaching skills, bravo for that!
    That promises for a very successful future, so well deserved!
    Keep up your awesome work!đŸ€—đŸŒ»

  • @miluda007
    @miluda007 Pƙed rokem +3

    I totally agree that tracking everything doesn't work for most people. I've been told over and over by various people (support groups, a pain clinic, the local post-covid clinic) to track things in complicated charts or by wearing a smart watch, but every time I try doing this it just spikes my anxiety. Sometimes I need to go over my limits a bit (which is fine, for me at least), and I don't feel like I'm able to track EVERYTHING. Life isn't a science experiment! There are a few very organized people for whom micro-tracking works, but not for most people. Thank you for validating my experience on this.

  • @alexanderh.8181
    @alexanderh.8181 Pƙed 10 měsĂ­ci +4

    I wanted to thank you for your videos. They contributed greatly to getting me from flatbound to almost normal in a couple of months. Thank you :)

    • @cfsrecovery
      @cfsrecovery  Pƙed 10 měsĂ­ci +3

      You're very welcome! 🌟 I'm thrilled to hear that the videos I create have played a part in your remarkable progress. Keep up the fantastic work on your journey to wellness! 😊🙌

  • @laurela6626
    @laurela6626 Pƙed rokem +8

    Great information. Thank you! I’m working on recovery from Long Covid with dysautonomia which mimics CFS as I understand it. I’m 16 months in. Your videos are helping me 😊

  • @sea_hous
    @sea_hous Pƙed 3 měsĂ­ci +1

    Just having these videos on in the background while trying to walk downtown for 10 feet (back and forth) in the little town I live was game changer.
    I think it gave me permission, and if people were curious why I was struggling to walk or challenging myself, or talking to myself while attempting to walk - - it provided an explanation in the background. Can’t tell you how grateful I am. Thank you.

    • @cfsrecovery
      @cfsrecovery  Pƙed 3 měsĂ­ci

      Wow! This is amazing! Thank you for sharing! 😊

  • @Lars-Ivar
    @Lars-Ivar Pƙed rokem +2

    Thanks Miguel, I am following the principles from your videos and doing so much progress😁. This video gives me some more puzzle pieces to work with 😀.

  • @tomoyukisawada2522
    @tomoyukisawada2522 Pƙed rokem

    Wow, this is one of the best😊 Truly appriciate.

  • @jelenasavic1032
    @jelenasavic1032 Pƙed 9 měsĂ­ci

    Thank you so so much! I have the same symptoms and it took me soo long to find the right docs. Your videos are amazing and help a lot. Love them! 🙌

    • @cfsrecovery
      @cfsrecovery  Pƙed 9 měsĂ­ci +1

      You're very welcome! I'm glad to hear that my videos have been helpful to you. Stay positive on your journey towards better health. If you ever have more questions or need support, feel free to reach out. 🌟😊

    • @dalerobbins4072
      @dalerobbins4072 Pƙed měsĂ­cem

      What kind of dr?

  • @johanngerberding5956
    @johanngerberding5956 Pƙed 11 měsĂ­ci +1

    I wanted to say thank you again for these videos, this should be show to any long covid sufferer!

    • @cfsrecovery
      @cfsrecovery  Pƙed 11 měsĂ­ci

      You're very welcome! 🙌

  • @AlexMentalGrowth
    @AlexMentalGrowth Pƙed rokem +4

    Hi Miguel
    Thank you for the great work you do.
    Maybe in of your next videos, could you also talk about the use of stimulants during periods of adjustment?
    Referring to coffee, taurine, B12/energy supplements....could imagine it's detrimental as CNS seeks rest & peace, but maybe you can share your experience. Cheers

  • @taylorp1330
    @taylorp1330 Pƙed rokem +4

    Omg sooo true w the heart rate monitor when I got POTS I got an Apple Watch now I don’t use it because it was giving me panic attacks

  • @kathygreen6043
    @kathygreen6043 Pƙed rokem +3

    Lost me on the financial part. Anyone who has truly suffered this, who had the solution, would tell the world for free. This is my third bout. First after thyroid storm. Second after a shoulder surgery. Third this past entire year after respiratory virus. It is very devastating. If I knew the secret I would announce it to the world. Thanks for some helpful information, though.

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +2

      I understand your perspective, and I do provide a lot of valuable information and strategies for handling CFS through my free videos. However, it's important to keep in mind that creating and sharing that free content requires time, effort, and resources. While I offer a ton of free information, I also offer a paid program for those who may benefit from more personalized guidance and support. The program involves additional resources, tools, and one-on-one coaching to help individuals on their recovery journey. It's entirely optional and designed to provide a more tailored approach for those who choose to participate. My intention is to support and empower individuals in their healing process, and yes, there is a price for it as it takes up ALL my time! I hope that helps clarify things for you.

  • @laurabone3228
    @laurabone3228 Pƙed rokem +1

    Good advice here about not falling down a rabbit hole of negativity in support groups. Some are excellent for information if you can overlook the negative and scarier stuff. It is excellent advice to ltreat the bodily system as a whole, such as the nevous system, instead of the 20 symptoms going nuts. Getting to the root cause should be the goal. I do wish though that I had been wearing a fitness monitor after becoming ill a few years ago. As I am now. Because I have noticed that even the past six months, I am improving leaps and bounds. No more daily crashes and naps are now rare. Sometimes you don't notice when you're improving. Such as the absence of pain. Had I been tracking my heart rate earlier though, I think it would have scared me to death.

  • @andrewsimpson7332
    @andrewsimpson7332 Pƙed rokem +1

    Thanks Miguel. I am curious about your thoughts on supplementing with Creatine to help with energy during the later end of recovery.

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +2

      Creatine is definitely not needed! You can use it if you were working out regularly again, and want to increase performance in the gym, but I wouldn’t use it just to get energy to live a normal life. We’re dealing with the nervous system issue, creatine helps with the muscular system.

  • @jamesjohnstone1224
    @jamesjohnstone1224 Pƙed rokem +1

    Hello friend, thanks so much for what you do for us here on your channel..Quick question, did you ever have the symptom of a pounding heart rate, it’s not particularly fast but will rock my body and create movement!
    I can actually feel my headboard rock sometimes, many thanks

    • @jamesjohnstone1224
      @jamesjohnstone1224 Pƙed rokem

      I know it goes against what you’re saying in this video but ..being able to relate this symptom to CFS is important to me

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem

      czcams.com/video/o95e53HK5ig/video.html

  • @farzinsayyadfar3097
    @farzinsayyadfar3097 Pƙed rokem

    hi miguel,thanks for ur videos ,just wanted to know when u have symptoms u do the brain training or u have anxious thouths?

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem

      Brain Retraining Can Cure Your Symptoms: czcams.com/video/BwFLyhU1214/video.html

  • @elainehewitt6813
    @elainehewitt6813 Pƙed měsĂ­cem

    I know all of this having researched and used the principals for a while now but i watched this just in the nick of time became a holistic doctor ALMOST had me convinced to purchase all these supplements like adrenal support etc and all it would have done is emptied my wallet and plugged me in to the hyper vigilance again which is probably what caused all of this in the first place. Thank you!

  • @LisaS1
    @LisaS1 Pƙed rokem +2

    When I go out and try to walk, that's when I get light headed and feel like I'm about to faint. This happens daily so it's like I avoid walking much since I know I'll start to feel faint. Thank goodness I have my son I can grab on to and he helps me walk.

    • @suepete
      @suepete Pƙed rokem

      Ditto!

    • @dalerobbins4072
      @dalerobbins4072 Pƙed měsĂ­cem

      Same. Horrible bc i used to be a jogger. Now walking around the grocery store when i have symptoms makes me feel faint

  • @LisaS1
    @LisaS1 Pƙed rokem +2

    I been worried half to death for awhile now. My lease ends May 31 but I may have to stay a month or more longer. I must give my cat away or find someone who could keep him awhile - I'm very, very worried about his safety. I'm so scared for him. I feel no joy daily. I hate everything - how some people are, my location, this entire area, and my life (no life) in general. I think I got the chronic fatigue. I'm light headed all the time. I'm fatigued all the time. I can't go out by myself. I get to where I feel faint - happens daily. Sometimes I feel suicidal although I wouldn't act on it. I fear when I take off from this place in 1-2 months things will go wrong and I'll end up homeless. To many worries.

    • @atesah
      @atesah Pƙed rokem

      That sounds very stressful, sending you strength and love. Day to day life can be so painful and challenging

    • @martinepeters9891
      @martinepeters9891 Pƙed měsĂ­cem

      If you read it, I wonder how things are going with you.

  • @noreguibi5568
    @noreguibi5568 Pƙed rokem +1

    What's the doctor's name?

  • @ishouldbesleeping1354
    @ishouldbesleeping1354 Pƙed měsĂ­cem

    Do people really DO the bizarre tracking and obsessive stressing about it as you mention in this video? I’m too exhausted to write more than a shopping list twice a week! Get a dog when you feel well enough. I went on Cymbalta for pain and Meloxicam for unresolved inflammation. I go to work a few hrs a day to get out of my head, pay bills, and chat with people. Someone to care for, something for pain, and souls to connect with DO help. I have GOUTY arthritis, Fibromyalgia, and Chronic Fatigue. Surviving cancer and COVID the first 6 months it hit the U.S. worsened my CFS. My internist suggests I try a stimulant so I can make it beyond hitting a wall after 3 hrs of work.

  • @Coliekokker
    @Coliekokker Pƙed rokem +1

    Recently I added some new activity and may have overdone it. The next day I suddenly had problems with my balance and had vertigo. For me this is a new symptom and it scared me as I am not used to it. Do you think it was an adjustment period? It's less now.

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +2

      100% percent that was an adjustment period đŸ‘đŸŒ

  • @Raj-kr2vo
    @Raj-kr2vo Pƙed rokem +1

    What are those all the other illnesses we need to crossed off ?

    • @megsh651
      @megsh651 Pƙed 11 měsĂ­ci +1

      Your doctor will do tests based on your symptoms. For example, I dealt with a lot of tingling, pins and needles in my hands and legs, so the Dr. ordered brain MRI, brain MRA and cervical MRI. I also had CT scans.
      For the palpitations I wore a heart monitor for 10 days, had many EKG's, echocardiogram, ultrasound of arteries (heart and neck).
      So the Dr. will or should order tests, based on the symptoms to rule things out.

  • @jft3038
    @jft3038 Pƙed 6 měsĂ­ci

    I have been extremely tired and fatigue because of arthritis. Can your rewireing strategy also help me?

    • @cfsrecovery
      @cfsrecovery  Pƙed 6 měsĂ­ci +1

      Great question!
      It will work for other issues as well as chronic pain as so much energy is consumed in coping with pain that it doesn’t leave anything leftover, therefore we feel fatigued or have foggy brains. The more we can incorporate relaxation and mindfulness into our routines, the better our sleep will be, the calmer our autonomic system will be and the faster we will heal.
      This will indirectly help other symptoms + fatigue. Reducing pain takes off stress on the nervous system, mainly from the emotional and mental aspect.

  • @FatbikerChinoy
    @FatbikerChinoy Pƙed rokem

    Just wondering, is long covid considered as CFS? The symptoms are really similar

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +3

      I have not caught Covid yet! But there have been many people in the program who have caught Covid during their recovery journey, and they've been able to bounce back using the same principles we teach. GRANTED, as long as there is no damage in the body, that is detectable, essentially Covid is like a really bad flu for them, which wreaks havoc on the nervous system. But if they can learn to allow their body to rest physically, but more importantly mentally and emotionally, they bounce back. Basically getting Covid is like going through a massive adjustment period.

    • @FatbikerChinoy
      @FatbikerChinoy Pƙed rokem

      @@cfsrecovery thank you.. i am considered as a long hauler (symptoms caused by covid) its been 21 months since the start of cfs synptoms, looking to try out your recovery program

  • @karenduey9675
    @karenduey9675 Pƙed rokem +1

    So funny, I did a video on my channel yesterday about this.

  • @iamthefiremanjj
    @iamthefiremanjj Pƙed rokem +2

    What are your opinions on caffeine?

    • @denisebraisby4251
      @denisebraisby4251 Pƙed měsĂ­cem

      I've just reduced my caffeine intake during flares especially in the mornings, it was revving up my nervous system too much and making systems worse

    • @iamthefiremanjj
      @iamthefiremanjj Pƙed měsĂ­cem

      ​@@denisebraisby4251 yah I don't use it amymoreb

  • @sharonashley1008
    @sharonashley1008 Pƙed rokem

    Hey I was wondering did you do DNRS or your own type of brain retraining?

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +1

      Brain Retraining Simplified, Step-by-Step Guide *WORKS FOR CHRONIC PAIN* [2022 UPDATED]: czcams.com/video/_jOYvPkyE_o/video.html

    • @sharonashley1008
      @sharonashley1008 Pƙed rokem

      Yes I added this in. Is this the only brain training exercise you did or did you do visualizations also? And when you do this brain training for chronic pain do you expand and dim the entire time like for example breath in and expand then breath out and dim? Never dimming completely right? Trying to get the hang of this new brain training I’ve added and that’s got me a little confused. Appreciate all your help đŸ™đŸŒ

  • @vivianeclarin2555
    @vivianeclarin2555 Pƙed rokem

    This is sooo helpful!

  • @LisaS1
    @LisaS1 Pƙed rokem

    When people "Crash" what happens to them? Do they get dizzy and have to go lay down?

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem

      This video will help clarify the 'crashing aspect' czcams.com/video/DNg7ipW5uNM/video.html

  • @ttilles
    @ttilles Pƙed rokem

    How much is your program?

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem +1

      In terms of the cost, it really depends on a number of factors, and I have to see if we can even help you first. I always recommend going through the questionnaire and if you qualify, booking a strategy call to see if you're a good fit for the program! www.cfsrecovery.co/apply

  • @Magnocalabro
    @Magnocalabro Pƙed rokem +2

    I have Long Covid and my body feels so heavy and weighed down all the time. It's like I have a ton of bricks holding me down all the time and even sitting upright or lying in bed feel so unsettling. What can I do about that?

    • @5000NATE
      @5000NATE Pƙed rokem +3

      Hello my name is Nate I went through this in February I'm still not 100% but follow the principles of keeping your mind calm I know it's going to be tough some days but you'll get through it many blessings

    • @kimitriwright
      @kimitriwright Pƙed rokem +2

      That's common, it gets better as your system normalises. Just try not to fear it.

    • @cfsrecovery
      @cfsrecovery  Pƙed rokem

      Check this out czcams.com/video/imO8ALQB-GM/video.html
      Also, in terms of overcoming fatigue watch this video - czcams.com/video/Sv9NTv2KkCE/video.html

    • @ezza1236
      @ezza1236 Pƙed rokem +3

      I got sick again or covid again and got set back to where I was before, but I know I’ve gotten better before and I can do it again, is it common to see people get long covid twice, for example you recover and do well but then get covid again.

    • @KatieBarboza
      @KatieBarboza Pƙed rokem

      @@ezza1236 this happened to me too

  • @hellethun3995
    @hellethun3995 Pƙed 4 měsĂ­ci

    ❀❀❀❀❀

    • @cfsrecovery
      @cfsrecovery  Pƙed 4 měsĂ­ci

      đŸ˜Šâ€ïžđŸ˜Šâ€ïž

  • @ivannovoselac3518
    @ivannovoselac3518 Pƙed rokem

    I dont have cfs but generalised anxiety, seems the principles are same.