yes, anxiety is also a symptom of PE, i was getting scared just by a new email notification, the feeling of doom etc, a few days/weeks earlier, and the day i felt the clot moved via my heart to lungs, that day had started chest pain, shortness of breath, dizziness, excessive sweat etc
The real struggle in the UK is how to get a doctor to stop saying "its just anxiety". I am having symtoms of PE but getting knowhere because my GP and A&E are all saying its Anxiety and sending me home. I think I need to actually almost die before the y do actual tests.
Hello i develope dvt with pe after giving birth and i took a medicine for 3 month but there is no result so i start enoxaparin injection for 3 month the clot is on my left upper leg part can you help me by telling me wich exrcise is better please i beg you🙏🙏🙏🙏🙏
I live in the US and had PE twice over a 2 year period I am glad I happened upon your program seeking for an answer to the extreme exhaustion especially in the first 2 months . I fell asleep at the dinner table anywhere. This was quite new despite a history of Pulmonary hypertension Having listened to your discussion I feel extremely relieved because when I tell the physicians about my exhaustion it is dismissed as though it is almost hypochondriac in my opinion This morning I woke up feeling pretty well then here comes this low energy so I decided to search for an answer because I know I am not imagining these episodes I am a go person. This video is extremely beneficial for me. At least I am sure I am normal Thank you very much.
Thanks to this channel & team behind, for this helpful video on blood clots! I used Planet Ayurveda's supplements and saw great results. My friend also experienced fewer complications with their clots. These herbs are effective and natural! 🌿
You are right. Doctor's have their needs and objectives and patients have different needs. Also we sometimes have insights that aren't obvious: I am a 56 year old man and I had BP of 150/80 HR 90. Perhaps for some people that is normal but not for me: my resting HR is 55 and BP 125/80. I worried about the impact on my life during and after treatment. How much of my life will I have to change and is that acceptable to me?
I broke my ribs and then 2 months later I went to A&E (after visiting a walk in centre) with terrible chest pain and shortness of breath. They were laser focused on my heart. They sent me home having diagnosed costochondritis after ruling out a heart attack. A month later I visited my GP with truly shocking chest pain - still no diagnosis so I was sent for an MRI. A week later I was in A&E having coughed up blood: even then the doctor had to push to get me a chest CTPA scan. Only then was I diagnosed with multiple bi-lateral PE and pleural effusion. I had calf pain, not long after breaking my ribs, that felt like cramp. This continued on and off since.
As somebody who is prescribed Apixaban 5mg x2 daily for life long since 2021 I have never had anybody throughout the NHS have any interest in monitoring me once. Any time I’ve asked questions I’m told there is no concerns using Apixaban. Thankfully your video has made me realise I’m being lied to again by so called doctors as you say there’s no studies into it so is there any wonder if the NHS couldn’t even care to document a patient they advised to take such ‘medication’
I broke my ankle 2 weeks after the AstraZeneca vaccine. I then got bilateral PE's 2 weeks after that. My GP refused to consider that the vaccine could have played a part, but reluctantly agreed to give the Pfizer for the 2nd vaccine. Is there any way of knowing? Many thanks
Can I please ask your help and advice on my own personal situation as I can not find anybody at the NHS . I had a myocardial infarction at 42 years old. Then stupidly had the AstraZeneca that caused unprovoked extensive bilateral pulmonary embolism. Been on Apixaban ever since but GP surgery’s keep ignoring all my requests for help. Diagnosed again with Worsening Bilateral PE. Current GP fails to even document my health and I’ve shown no improvement in 3 years . Centre chest pain is now constant and gets really bad at times. Bpm 160 at rest . Blood ox 78 . Can walk 25 metres then can’t breathe. I know my body can’t keep this up yet I’ve no help Please I need advice
Absolutely nothing was said to me by anyone after blood clot diagnosis, after pricedure for stent placement. Nothing. I was 80. Alone. Scared. Nothing said about how I might exercise or continue to live alone. Thank you for your help and educafion. .
SO after having ITP 4 weeks after C19 Vax, my hemotoligist has said probable cause, Ive looked through my records and cant find a P4 test, this was back in March 2021
It's the diagnosis from "medical professionals " with the oh you have pulled a muscle, it's a muscular injury... like yeah I never did anything to do that, but hey you know best right, well actually no, you do not, 2 times I was misdiagnosed and both times had a P E ... more training and listening to the actual patient! People die because of lack of care and knowledge!
Thank you very much for all the advice given. As a post DVT patient I was afraid how should I start doing exercises. But you smart ladies gave me the confidence and guidance to get on the track once again overcoming the anxiety. Thank you so much.❤❤
Some doctors can be useless. I had what seemed like a heart attack. I was sweating and gasping for air, my body was paralyzed almost. I had been very stupid thinking it was something eaten so I didn't call an ambulance but went to my cardiologist the following day. He did an ECG and ultrasound and said I was all good. I continued working for a month but with chest neck and arm pain till one night I had an episode that almost killed me. I called the ambulance but because of lack of oxygen the operator could not make what I was saying, I could not even walk to open the door for the ambulance team. Once at the hospital, I was diagnosed with a big PE on both lungs. I was told this was very serious I was in ICU for almost 2 weeks. I'm still having palpitations and some pain. Conclusion if you have pains in your chest and breathing issues insist that you see a pulmonologist and cardiologist.
I was diagnosed with blood clots throughout my body and three pulmonary embolisms in October of 2023. I lost my job due to my health. Now, I have to use a shower chair and a walker to get around. I run out of breath very easily. I'm from the US, and they told me the only treatment for me is a blood thinner. I've tried to tell them my condition is worse, but they don't listen, so I've accepted my fate.
No, this is not your fate.. you decide your fate.. be proactive- be up to date with newest knowledge on your conditions.. be up to date with new medical technology… critique your health and improve it every sec, min, days, months, years… neverthelesss give up on your fate, best of luck
Thanks. That’s really helpful. I have a couple more questions eg flying long haul on DOACs and natural alternatives to DOAC. What’s the best way to raise these?
Important topic which is not really discussed with patients if my own experience is typical. I had a DVT 2022 and the subject of PTS was not discussed with me nor the measures I could take to best avoid it. This needs to change.
Exactly the same happened with me. Every person who has suffered a DVT should be given this advice and then be offered a Duplex Vein Mapping Scan. I lost eight years of my life suffering the same leg ulcer and only being offered compression hose. I was and still am an extremely fit and athletic runner, yet I still suffered with venous leg ulcers. I no longer suffer them because if the procedures I had at a specialist vein clinic in London. I hope you got all of my other comments because they’re all disappearing from my end 👍🏼
our video is very beautiful. I like it a lot. I have been trying to talk to you for a long time. I am waiting for your response. Please give me a chance to talk to you. I am a professional digital marketer and RU-vid marketing expert.👍
I was just diagnosed with PE 5 days ago after a 15-hour flight. When I got home, 8 hours later, I had the worst pain in my left chest. It hurt every time I breathe in. Went to the hospital and did a CT scan and they found peripheral pulmonary embolism. I am now discharged and they put me on anticoagulant. Doing good so far.
Thank you very much. Back to gym Gradual approach is the way. Playing safe from kitchen cutting and chopping Anxiety killed me. Advantage is I was active at.
Im currently in recovery at home. I got out of hospital last Wednesday after 7 days in hospital. Im 27 and have no health problems. It was a complete shock when I got taken to hospital and told me I have two massive clots in my lungs. They said if I didn’t come in that day it would of been a different story. Im feeling a lot better but it still does not feel real to me even after being discharged.
Hi Paul, I suffered an unprovoked pulmonary embolism 4 years ago and whilst I haven’t had a panic attack I do have significant problems with concentration , memory loss and generalised anxiety to the point where I experience a heart flutterings. Could these long term symptoms be common years after the PE?
I have Bilateral PE's. I have a heaps of clots in my right lung, and "only" a couple in my left lung. It's such a struggle and has caused me so many extra health problems on top of that.
@@toralora Firstly, I'm so sorry that your family member has been diagnosed with this. I wish them well and a speedy recovery! 💙 Well, I personally have a heart related issue now because of it. I had to have oxygen masks and tubes in regularly. Shortness of breath has been an issue during and after. I got fluid on the chest & lungs and needed it all drained out (which was the most painful thing I've ever experienced) I still experience pain, and have some lung damage from both the clots and the draining procedure. If I think of anything else, I'll add it. I hope that helps! 🙏🌺
I lost 4pregnancis because noone in UK wants to help me. I had one baby only because doctor from Poland gave me medicines I needed. So how come in Manchester someone can show you what to do and how when you in a risk group and I went through all this miscarriages and they didn't do anything even when I told them about conditions
I was in the situation so I translated my test results from private clinic abroad and took them to the GP and told them about my condition and they recorded it and referred me to a consultant who gave me the treatment and monitored me during pregnancy.
