I have just been diagnosed with a serious heart condition--VF and am obviously so depressed and scared.Someone please be there for me now.I feel so lost right now.I have battled cancer and depression now this.
Hi Rain, sorry to here this. I went through cancer radiation a few years back so i know the feeling of mortality. Being faced with life threatening diseases can be overwhelming. I read that defibbrillation inplants can be a be help. Dont fear life and dont dwell on death. Just take the correct medical direction. The only thing that we have lost with these diseases is the ability to mentally rest in our future. Just live day by day as i believe this is how it is ment to be anyway.
Thanks Dave,and you're right,I have faced many battles in my life and no doubt this is the biggest,tomorrow I found out more as I have an appointment but I have to face reality,one day at a time--thats all I can do from here on in.
Yes NG,I had to be cardioverted more than once,they put me under so when I woke up I had no idea where I was.2 abnormal ECGs and 1 borderline,I am trying to get my head around it all.I thought I was going to die.
Well, I don't understand that, because v-fib is always a medical emergency. It's not like a heart murmur that is a chronic, manageable condition. How did you find this out? How were you diagnosed with it? What kinds of tests did thr doctor do?
I was told it can be life threatening and I fought a battle with cancer which I overcame,sadly my father did not.I had an episode in 2009 where my heart was beating at 160 beats per minute and out of normal sinus beats.I thought I was having a heart attack.They gave me an asprin and other meds via IV drip and 13 hours later they cardioverted me.
That's what I don't understand. It would be rare for a cardiologist to give you that diagnosis and just send you home. You should have been admitted until they decided how they were going to treat it (usually an implantable defibrillator).
If I were you, I would maybe get a second opinion. It just doesn't make any sense.
It was a medical emergency,they did ECGs and they were both irregular,they also took Xrays or images of my heart and they said that it's larger than normal.They did blood tests and said there is damage to the heart,I find out more tomorrow.I am trying to assess all my option,I know a bit about AF but not VF only that it is alot more serious.
Ventricular fribulation and they sent me home after a day,I didn't even stay in the cardiology ward,I will get a second opinion NG because this was through the public health system,I am seeing a private cardiologist and it will be expensive but my life might be on the line here so I will do all I can.You don't realize how precious life is until something like this happens.I'm so scared,I was depressed as it was and now this.I was having more irregular beats today like a flutter in my upper chest--throat,it's a scary feeling.Then it will beat so fast and then slow down.
If you're having symptoms, you need to go get checked out immediately. You had to be cardioverted because you were in v-fib, and they didn't even put you on a cardiac ward? Wow. Something is NOT right!! Witjh the other info you provided (the damage, the enlarged heart), it's concerning.
A-fib and V-fib are two totally different animals. Like I said, v-fib is always a medical emergency, and if left untreated (cardioversion), is not compatible with life.
You need to get this straightened out ASAP. Pick a hospital that is known for their cardiac care, and head there. I don't mean to frighten you, but like I said, something isn't right. Either they misdiagnosed you, or they don't know what they're doing. V-fib isn't something they just fix and send you on your way.
Hope it works out for you. In the very least, hang on to the fact that you're very lucky....many people who go into v-fib are unable to be cardioverted back to a normal sinus rythym.
I asked them what would have happened if I didn't convert back to normal sinus rythym and they didn't answer me.I see the specialist tomorrow,Oh god I hope I get some answers.Somethings just not right,I don't feel well at all.
I saw a heart specialist and she said it's SVT not VF so an error was made at the ER.I was relieved but am still scared as I have a heart condition.I require more testing and I'm glad I got a second opinion.This is why medhelp is such a wonderful site because you people gave me the strength to fight when I really thought I was done.I will have to change my lifestyle and stop stressing--how does one do that?I was so scared and you great people were there for me,It means so much--thankyou.
What about the cardiovert and all those details you shared? They had ALL of that wrong? wow. Sounds like a lawsuit. If they'd treated you as they do the majority of patients that get that diagnosis of VF---- could they have hurt you? I wonder how they got those two mixed up?
glad you got good news that you don't have V fib. That is great.
No,I required cardioversion anyway,more than once they told me,100 js whatever that means and yes they did get it wrong.A few years ago the same hospital sent a man home after he was having chest pains,as he was walking out the hospital doors he had a heart attack and colapsed to the ground.I don't know much about SVT but I'm learning more.Thankyou for your concern,I think having any heart condition makes a person look at their lifestyle--I will try to stress less.
SVT is supraventricular tachycardia.It is treated with beta--blockers,I am just starting to learn about my condition,I did experience some of the symptoms like the rapid heart rate,difficulty breathing,sweating & the feeling of wanting to throw up.I felt dizzy aswell.There was a flutter in my chest region aswell.The are going to put a holter monitor on me for 24 hours.
Just wanted to say good luck to you and hang in there! I am praying for you and am happy to hear you did the right thing and got another opinion!
Sounds like you are on the right path to a healthy heart.
I want you to Remember... one of the best things you can do for yourself is to be your own patient advocate, always be on the ball if you ever don't 'feel' right again, Next time I'd advise you to do go to the nearest hospital, (preferably one that specializes in cardiology). Or better yet, call 911.
What you were describing sounded like it was life threatening! I was very concerned this morning when I read your post and seen how you were treated at the first Hospital!
So therefore, again I cannot stress enough how important it is to be your own patient advocate when something just doesn't feel right, it is probably because it isn't (right)!
All the best to you and God Bless!
Hey Rain, so your back with us!!! I told you you would be just fine. I read there are 2 types of SVT, one is SNRT and the other EAT. Either way its great news and the only down side is treatment discomfort but that should be a piece of cake considering what you thought was going on. Just courious, and you can a private note if you rather, but what type of work do you do?
Thankyou for your kind words marlene,anything that involves the heart is a scare but I will be working with my doctor & cardiologist & taking their instructions.At present I am having trouble sleeping.Good bless you to.
Thanks once again dave,you have been a great support,I'm a lab assistant & I am also a qualified support worker.I experienced depression when dad passed away in 2005 & I cheated on the best woman I ever had in my life in 2010 & still have not forgiven myself for that.
Sorry about your dad, i lost mine in a horrific truck accident when i was 20 years old. Missed a lot of guidance in my early years. and about the best woman and your guilt, that experience will make you a better person when the next best woman comes along.
You're right again dave & you lost your father at a young age,so sorry about that,my father was everything to me,I miss him so bad.My relationship was very sad because I loved my woman so much & let her down,I'm full of guilt & maybe this explains all my health issues now.
Rain, with all the problems that life throws our way, what i did was to balance them out by being creative. Im not saying this to boost myself up, as i am a regular guy with no special talents, but want to mention it, as is a reality. I created and Patented a very simple product, similar to those you see on TV for" $19.95 and get one free". I knew it would be successful as is a product that is needed by people. I new this because it was part of the industry i am in. You see many things for sale and say " why didnt i think of that". There is something very simple in your work field that you could create and be a big hit. Its so easy its hard!!
And this ER treated you for VF and you indeed have SVT.....that's not good as these conditions require different treatment plans; totally different treatment plans. Then, they sent you home and you weren't converted in NSR? WOW, never heard of that. We NEVER sent a patient home UNTIL they were converted. Sounds like you have a lawsuit on your hands as SM has stated.
Well....anyhow, you should probably be relaxing. You don't have the Holter monitor on yet? What beta-blockers or meds did the Cardio prescribe? Surprised this Cardio did nothing to cardiovert you or is he?
Thanks for the support Londres,I will be going on beta--blockers and I am having a 24 hour HM put on aswell.I was cardioverted,they needed to do it twice they said.I had 2 abnormal ECGs and was given the wrong diagnosis at the ED.I have since seen a specialist & she said I have SVT.I am learning about this condition and doing my best to understand it.Sorry,I forgot you are a nurse,I should have asked you about SVT.Thankyou.
So sorry to hear u are having such stress and unhappiness in your life. U have helped so many people on here and we need to b here for u. Thinking of u. I care and always will. Enjoy today. Find something to laugh about. Take deep breaths. B grateful for everything. Knw u have a support system. Lov hobby
The process is slow here.I get the HM put on this friday & I have the script for the beta--blockers & I have been advised to take it easy.I will put the computer away because I have been googling SVT & it's making more stressed.I think I might be getting treated slowly because of my age--41,most of the people in the waiting room were over 70.
Wow....misdiagnosed with VF instead of SVT?? That's like night and day. That would be like a doc misdiagnosing chicken pox as leprosy. I was trying to be vague the other day, but VF usually only occurs during cardiac arrest, or right before (as in it being the cause). Very lethal and NOT something a doctor would diagnose you with and then discharge you, without putting in an implantable defibrillator, or SOME kind of intervention. If I were you, I would be getting on the phone about the ER doc AND the whole medical team involved in treating you for "VF".
You said in your OP that you were "just" diagnosed with VF. When was that that you were in the ER and diagnosed, and what happened to make you end up in the ER, did you pass out? Some kind of other emergent situation? Did they cardiovert you that same day? Do any lab work? Do you recall them testing for cardiac enzymes? I'm honestly just blown away by this...you should have never been discharged, let alone the fact they didn't even put you on a monitored unit. I could see a misdiagnosis, it happens, but the whole TEAM failed you.
When someone is getting moved to a hospital floor, there are several people involved in that process, chooosing the correct unit (ie ICU versus telemetry until vs regular floor), plus who your attending MD would be, etc etc. I can't believe that not ONE person caught that VF was NOT the proper diagnosis, and intervened. Let's put it this way, if your initial dx was right, you'd likely be dead. UNREAL. I'd be mad as a hornet.
The doc who gave you the new diagnosis, how did he come to that new diagnosis? Is he a cardiologist? What did he say about the "damage" you were told about? How did they come to that determination? Through what diagnostic process? The enlarged heart, did they say anything about that?
I'm sitting here shaking my head. I don't think you realize how big of a deal this is. It's HUGE. When you posted (from HOME) that you had been dx'ed with VF, I nearly fell off my chair. I tried not to panic you, but you needed to head back to the hospital. Thank GOD the diagnosis was wrong, because you may not have made it to your follow up appt.
I know NG,It all happened so fast,like I woke Up I couldn't breathe,was rushed to the ER and told to chew an asprin,the moments later was taken to another room,put to sleep for 10 minutes they informed me later and cardioverted twice,the first cardioversion did not put the heart back to normal sinus rythm and the used 100js.When I woke up my heart was still beating like a rabbits but it wasn't out of rythm.The diagnosis was wrong big time but because I was so scared at the time I didn't know what to think,I also asked why they were sending me home they said the cardio ward was full.When I saw the heart specialist she said you have SVT not VF because I my family would be arranging my funeral right now.I am having a HM put on this friday for 24 hours and they either took an xray of my heart because they said it was rather large for someone of my weight and my height.I believe you people have some of the best cardiologists in the world in the USA but the same can't be said over here.I don't know if you have hear of Dr Victor Chang but he was a brilliant heart surgeon becak in the 80's,sadly he was murdered.He performed the first heart transplant in Australia I believe.I am relieved that it's SVT & not VF because VF is deadly if not treated right away.I need to learn more about SVT and learn how to live with it.The fact that I now have a heart condition still scares me but all the stress and insomnia probably hasn't helped.Thankyou for your information from a medical prospective.
You should definitely be celebrating. This is literally like someone telling you you had end stage pancreatic cancer....then changing it to a gallbladder attack.
I'm amazed at the incompetency. VF and SVT on a monitor are night and day. Even the newest of med students/nurses would (should) be able to distunguish between the two a mile away. With VF, the heart is literally spasming, seizing.....very obvious.
You need to be VERY proactive about this. First thing you need to do is obtain a copy of your entire medical record. Find out what exactly they did to you, what tests were run, etc....and what the results were...and you need to be SURE that nowhere on your record does it indicate you had VF. If it's not corrected, you may find yourself coming out of the hospital with an unnecessary implantable defib. Not to mention, like Loundres said, the course of treatment varies a lot, especially in urgency and aggressiveness. You need to make sure your record is correct as you move forward with this new doctor.
You've basically just been given a new lease on life. The people who were on duty that day need to be talked to, educated, evaluated.
I agree with everything you have said,This is why medhelp is a great place for info,I think you & londres would have done a better job diagnosing me but I don't want to condem the public health system but it's really not good enough,I felt like a number not a patient.
I will be writing a letter of complaint thats for sure,it very difficult to start a lawsuit against government hospitals here,they always seem to come out on top in the end,the same hospital sent people home after reviewing them in the ER and then these people had heart attacks minutes after leaving the hospital.It's a nightmare whats going on.
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