Her nervous system has become anti fragile and is able to bounce back from stressful events (the war in Israel) and not “crash” as she said… when we can bounce back and forth between stressful events to calm or somewhat calm is a huge healing sign
This is so inspiring! I have a diagnosis of POTS along with ME/CFS (and a bunch of supposedly 'unrelated' chronic symptoms) that has fluctuated from mild to severe over nine years, and I'm finally well into my recovery now after discovering the mind body connection stuff in January of this year. It's my dream that this could be me someday soon! Thank you Manya so much for sharing your story and Dr Yo for your amazing work ❤
Thank you. Another really interesting conversation full of wisdom. I’m learning about the IFS at the moment and it’s helped me. I’m also a recovering co dependent . I think there’s so many similarities between people that are more sensitive and these issues.
The disautonomia component of Manya’s story resonates with me but also the explanation of how IFS helps with trauma processing, memory RE consolidation and inner child healing was very helpful.
Focus on what you CAN Control. There are are so many things in your life outside of the symptoms you do have control over. I guarantee you you can’t control your symptoms. Trying so hard just seems to turn up the volume. When a symptom arises I try to to talk to it and say…I can’t control you and turn to something I can. Realizing there were so many things I could Control in my life was comforting.
Very good conversation and very helpful. As an aside, my youngest daughter is the same age as Manya and I saw the similarities. She’s adorable. So glad she’s doing so well!
Wow this is just like me. Perfect timing I'm just starting to get super into ifs right now. Make perfect sense. Thank you for another amazing interview ❤🎉❤
Thaaaank you for this! I have the exactly same symptoms, especially the in and out fainting but not fainting when sitting in a chair. I have had this body weakness and going out of breath when running since childhood, also feeling tired all the time, oversleeping and having difficulty focusing, but after an urinary infection and kidney surgery everything went downhill pretty fast and within 6 months year I could barely do my own shopping or cooking and cleaning. Went to a bunch of doctors, got humiliated when mentioning dysautonomia (I live in Romania so imagine that continuous learning in the medical field here is almost non existent). After a ton of research I got to the right doctor and got diagnosed with POTS and I also match criteria for Ehlers Danlos but I am not diagnosed with that atm. I was given beta blockers that do next to nothing but I am so determined to get better that I will not stop at the lame excuse "there is no cure for this".
Oh my!! Dysautonomia was my 1st diagnosis! Still working on my healing. Im crying listening to her story. Ive been told salt, compression socks, water. Been on the bets blockers and florinef. Now doctors say its hereditary and my daughter has it at 16! I say Now they tell me VM too. I say No Way! Im going to beat this!!
For so many years with this dizziness. Every day I try to do my best, but I haven't job for years, there are certain places I can't go, especially these last few months are very difficult, I'm very dizzy, I think my boyfriend will break up with me soon. I couldn't be sadder. Sometimes it makes me want to die and end with all. I don't know which specialist to look for, what medicine to take, what exercise to do, which psychologist to go, I've tried everything in these 11 years! I'm very tired, And frustrated, especially today
I am so sorry you are going through all of this. You can see that you are not alone in how you are feeling on this channel. I would highly recommend signing up for my free course. I go over all my recommendations in a step by step format and it is 100% free thesteadycoach.com/free-course. If you need immediate help, please call 988 and they will be able to help you get the resources you need.
Hi again! Im a couple weeks into watching your channel every day. Wanted to say again THANK YOU!! What you said about how we with symptoms recall our previous lives as perfect and symptom free but it’s not entirely true… so true haha I know I’ve always had some TMS type symptom and sensitivities since I was a kid like Manya says. But the dizziness is the scariest and most debilitating by far!
I was hoping this was going to be about someone with pots and constant dizziness. I am dizzy 24/7. I can’t find anything about anyone who suffers from both. I had a concussion in March and then everything went downhill at the end of April.
I was diagnosed with POTS from a cardiologist and diagnosed with general dysautonomia and vestibular dysfunction. Is this all the same as neural circuit dizziness?
POTS and dysautonomia without an underlying medical cause are almost always a neural circuit problem. I would put your symptoms through the ppdassociation.org checklist (ppdassociation.org/ppd-self-questionnaire) so you can see how the characteristics match up with a neural circuit issue.
@@TheSteadyCoach Thank you! Yeah, so far there’s no underlying cause all the heart test came back normal. All my symptoms started after the death of my mom and after getting Covid. I was totally fine before all of that happened.
Hi, I was under severe stress for about 1 year for some reasons, and from the 6th month onwards, I got snowy vision syndrome and palinopsia, fortunately, I was able to control my stress to a great extent and return to a decent state, but I have these vision problems, in addition to diziness and tintinus, is there a way to completely get rid of these symptoms?
I get this is inspiring but 80 percent of people that have this illness from teenage years grow out of it. She said it started in high school. Not as much hope for adults.
I hear you! The real POTS started when I was 18, and I know I wouldn't have grown out of it. The inner work was crucial for my recovery, and it's a life-long journey of taking care of myself. Sending healing wishes on your journey🙏
![Lp. Сердце Вселенной #60 РОЖДЕНИЕ ЛОЛОЛОШКИ [Финал] • Майнкрафт](http://i.ytimg.com/vi/YoR0pAV9FVQ/mqdefault.jpg)
Isn't it funny how you can be so dizzy and then watch something like this and then it calms down!
Her nervous system has become anti fragile and is able to bounce back from stressful events (the war in Israel) and not “crash” as she said… when we can bounce back and forth between stressful events to calm or somewhat calm is a huge healing sign
Thank you so much! Praying it continues upward🙏
This is so inspiring! I have a diagnosis of POTS along with ME/CFS (and a bunch of supposedly 'unrelated' chronic symptoms) that has fluctuated from mild to severe over nine years, and I'm finally well into my recovery now after discovering the mind body connection stuff in January of this year. It's my dream that this could be me someday soon! Thank you Manya so much for sharing your story and Dr Yo for your amazing work ❤
Can you do more success stories with pots im curious to know a bit about it
yes please!!
Thank you. Another really interesting conversation full of wisdom. I’m learning about the IFS at the moment and it’s helped me. I’m also a recovering co dependent . I think there’s so many similarities between people that are more sensitive and these issues.
Thank you so much for your support, Jules! It truly means a lot and helps keep my course free ❤
@@TheSteadyCoach You are very welcome. You are doing really well on here, I hope many more find you.
The disautonomia component of Manya’s story resonates with me but also the explanation of how IFS helps with trauma processing, memory RE consolidation and inner child healing was very helpful.
Thank you for doing this interview and touching upon POTS/ Dysautonomia a lot of the deregulated nervous system mimics POTS!
Sure does!
Focus on what you CAN Control. There are are so many things in your life outside of the symptoms you do have control over. I guarantee you you can’t control your symptoms. Trying so hard just seems to turn up the volume. When a symptom arises I try to to talk to it and say…I can’t control you and turn to something I can. Realizing there were so many things I could Control in my life was comforting.
Yes! Empowerment is the opposite of helplessness. Thank you for sharing.
Very good conversation and very helpful. As an aside, my youngest daughter is the same age as Manya and I saw the similarities. She’s adorable. So glad she’s doing so well!
Wow this is just like me. Perfect timing I'm just starting to get super into ifs right now. Make perfect sense. Thank you for another amazing interview ❤🎉❤
I am so glad you saw this interview at the right time, Lucy ❤
Thank you Dr Yo for this great informative video! I loved hearing from someone with my exact diagnoses! And thank you Manya for sharing your story !
You're very welcome, Tara! I am so glad Manya's story resonated with you.
Thaaaank you for this! I have the exactly same symptoms, especially the in and out fainting but not fainting when sitting in a chair. I have had this body weakness and going out of breath when running since childhood, also feeling tired all the time, oversleeping and having difficulty focusing, but after an urinary infection and kidney surgery everything went downhill pretty fast and within 6 months year I could barely do my own shopping or cooking and cleaning. Went to a bunch of doctors, got humiliated when mentioning dysautonomia (I live in Romania so imagine that continuous learning in the medical field here is almost non existent). After a ton of research I got to the right doctor and got diagnosed with POTS and I also match criteria for Ehlers Danlos but I am not diagnosed with that atm. I was given beta blockers that do next to nothing but I am so determined to get better that I will not stop at the lame excuse "there is no cure for this".
Oh my!! Dysautonomia was my 1st diagnosis! Still working on my healing. Im crying listening to her story. Ive been told salt, compression socks, water. Been on the bets blockers and florinef. Now doctors say its hereditary and my daughter has it at 16! I say Now they tell me VM too. I say No Way! Im going to beat this!!
You will!!! ❤
@@barbaraweatherman5340 🙏❤❤ Thanks!
Yes you can! Thank you for sharing and wishing you all the best on your healing journey ❤
Yes! I believe in you!
You can do this! Hope you're doing better today!
Thanks Manya and Dr. Yo!
You're very welcome, Lynn! ❤
For so many years with this dizziness. Every day I try to do my best, but I haven't job for years, there are certain places I can't go, especially these last few months are very difficult, I'm very dizzy, I think my boyfriend will break up with me soon. I couldn't be sadder. Sometimes it makes me want to die and end with all. I don't know which specialist to look for, what medicine to take, what exercise to do, which psychologist to go, I've tried everything in these 11 years! I'm very tired, And frustrated, especially today
And yeah my boyfriend broke with me after 11 years together …… im very very very sad
I am so sorry you are going through all of this. You can see that you are not alone in how you are feeling on this channel. I would highly recommend signing up for my free course. I go over all my recommendations in a step by step format and it is 100% free thesteadycoach.com/free-course. If you need immediate help, please call 988 and they will be able to help you get the resources you need.
@@TheSteadyCoach Thank you for being so attentive Dr. I'm from Brazil and I really wanted to be your friend ❤️
Hi again! Im a couple weeks into watching your channel every day. Wanted to say again THANK YOU!! What you said about how we with symptoms recall our previous lives as perfect and symptom free but it’s not entirely true… so true haha I know I’ve always had some TMS type symptom and sensitivities since I was a kid like Manya says. But the dizziness is the scariest and most debilitating by far!
❤ thanks a lot
You're very welcome, Velsie!
What is the best cure for pots?
Great interview ❤Dr yo when you will be accepting new patients..I need your help 😭
Hi July, please consider joining my VIP coaching group where I hold weekly interactive sessions. thesteadycoach.com/services#group-coaching
I was hoping this was going to be about someone with pots and constant dizziness. I am dizzy 24/7. I can’t find anything about anyone who suffers from both. I had a concussion in March and then everything went downhill at the end of April.
I was diagnosed with POTS from a cardiologist and diagnosed with general dysautonomia and vestibular dysfunction. Is this all the same as neural circuit dizziness?
POTS and dysautonomia without an underlying medical cause are almost always a neural circuit problem. I would put your symptoms through the ppdassociation.org checklist (ppdassociation.org/ppd-self-questionnaire) so you can see how the characteristics match up with a neural circuit issue.
@@TheSteadyCoach Thank you! Yeah, so far there’s no underlying cause all the heart test came back normal. All my symptoms started after the death of my mom and after getting Covid. I was totally fine before all of that happened.
@@TheSteadyCoachMay I ask what do you mean out an underlying cause?
Hi, I was under severe stress for about 1 year for some reasons, and from the 6th month onwards, I got snowy vision syndrome and palinopsia, fortunately, I was able to control my stress to a great extent and return to a decent state, but I have these vision problems, in addition to diziness and tintinus, is there a way to completely get rid of these symptoms?
Yes! I go over this in detail in my free course thesteadycoach.com/free-course
@@TheSteadyCoach 🙏❤
Now which symptoms ur still struggling or have u fully recovered and no limitations
No limitations, living a full life, some sensations still, but mild and manageable.
I have this too ( POTS/ dizziness)..which books do you ladies recommend?
The Way Out by Alan Gordon is a great one!
Did you also get headaches??
Yes I had some migraines and headaches.
I get this is inspiring but 80 percent of people that have this illness from teenage years grow out of it. She said it started in high school. Not as much hope for adults.
I hear you! The real POTS started when I was 18, and I know I wouldn't have grown out of it. The inner work was crucial for my recovery, and it's a life-long journey of taking care of myself. Sending healing wishes on your journey🙏