Cardiac Arrhythmias :: Who Cured Ectopics With A Natural Xanax?
Jul 9, 2015
I love hearing all your personal stories and cures. Months ago someone cured his ectopics with "natural" form of Xanax as his always went away with Xanax. Please post again or if someone remembers the ingredients, let us know.
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I'll get straight to the point. I have been suffering from Vestibular Neuritis for almost a year, to summarise it, its an inner ear problem which affects your balance and can take years for the brain to compensate for it.
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It has multiple side effects, the most common and most problematic one being anxiety. At the start I had too many panic attacks, I couldn't even leave my room. However, by doing things like yoga, meditation etc. I managed to recover a LOT in terms of ANXIETY. Medication didn't help and as my anxiety got under control along with my brain compensating for the lack of balance, I started to feel better, but all symptoms were still there 24/7 to a lesser degree.
One month ago, I relapsed. I assure you, I did nothing different and have no idea why everything came back. As you can imagine my anxiety sky rocketed again. It took me about 2 weeks for the dizziness to calm down as brain compensated for it again. However my anxiety seemed to be there, I tried yoga etc. again (as it was so successful last time) but it did nothing. I have also noticed for the past 2-3 weeks, my bowels have been very irritated- without going into too much detail, I will just say that the frequency of my toilet visits per day shot up. I assumed (and still assume this was anxiety related) so I continued yoga etc. with not much improvement. I changed my diet to eat only bland, simple food...still not much luck.
My latest problem, and this is the one I need MOST help with. Three days ago, as I was trying to sleep, I started getting palpitations which really scared me- I have never had them before. NOTE: I had EKG, ECHO, Holter done 6 months ago and all was normal, so my heart was fine then and is fine now as I had another holter done last week - HOWEVER this time around it was clear that I had ectopic beats but the doctor said this was normal.. This has really made me feel anxious especially because I never had this symptom last year when my anxiety was at a peak.
Yesterday, the palpitations got really bad, I had to take a 4 hour ferry and then drive 4 hours. iI had a fairly greasy burger on the ferry and about 90 minutes later I started feeling ill and had palpitations again. This was the most scared I have been, I felt the urge to go to the toilet a lot and everytime I went, I felt like I was going to faint. My 4 hour drive later was scary too, I almost stopped at a B&B because I kept getting palpitations. The palpitations I had yesterday was different to the ones I've had for the last 10 days...instead of a 'thud' at the end, I had a sense of radiation warm sensation from my chest to my stomach which was really scary and moments of a feeling where you feel like youve lost consciousness for a split second before being 'shocked' into reality.
Has anyone experienced this? Do you think its anxiety related?- If yes, why has it started to happen all of a sudden?
Or do you think this is something to do with GERD? I seem to burping more and feel more 'wind' and also seem to want to go to the toilet more.
I also feel dizzy because I'm eating less because I get scared to eat any amount as the palpitations are triggered!
Anyone suffer from ectopics? Mine started 3 yrs ago when i was pregnant and are getting worse. Had ecgs...48 hr ecg ( which of course only showed a couple) echo and ct angiogram which i'm waiting the results for but wanted to know how many is normal? For the last 5 days have been really bad and tonight in the space of an hour as i counted them i had 16..just so typical that when i had my 48 hr ecg a few weeks back i was having a good few days so of course the cardiologist said all looked normal. Just wondered if people suffered with these and what the outcome has been? Its really getting to me and worrying me now.
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I've got idiopathic dilated cardiomyopathy. I have Afib with this and keep getting extreme tachycardia which means I have to go to hospital to get it controlled. I have asthma too. I'm in Europe and have good doctors - I was in hospital Saturday night into Sunday - I called my doctor as my heart was beating so fast and irregularly, and it was having long intervals of no beats - I have a stethoscope and could hear nothing at the apex and I've been taught how to auscultate, and I was very very breathless. She was very worried and sent me to hospital. After being stabilised, I saw a a cardiologist who did loads of tests and said my heart was very much more dilated than before. On discharge I've been given 02 to breathe if I feel breathless.
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I have some strange feelings and etc for around 6 months. I don't have any panic attacks or anxiety from long time ago, but something is wrong with me. For example in morning I stand up from bed and my heart rate goes to around 130 or when i climb up stairs ( around 20 of them) i get heart rate around 170 per min. That's not normal I know, but I have had heart ECG, heart ULTRASOUND,blood tests and etc and everything is fine. But on left side of chest I have pressure, feels like some organ is swollen or I don't know, maybe lung is pressed or something. I had also lungs x-ray but it came out fine. When heart is beating fast, i feel pain in my upper chest like in my airways, and when my heart calms down i have sore upper chest. 1 month ago i got maybe palpitations but not sure if it's palpitations, happens most when im standing. I get fast squeeze in left chest like my left lung is squeezed, but in this second my heart stops beating and then starts after 1sec beat fast and again slowly. I really dont know what to do, because im sure i dont have anxiety or panic. I was on xanax,citalopram,lexotanil for long time and nothing helped me for that. P.S My left leg is always cold,mostly when im laying down. Sometimes i get vibrating sound in my left chest and i don't know what is this. Mostly im scared if its my heart or what... Doctors said im okay, but i still feel not normal and without full access to live my life.. I had also brain scans,neck x ray and all is fine. All tests I had everything is normal. What do you think I should check? Please don't write about psychology problems, because its not this and im sure its not in my head.
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Let me tell you I had full blown Raynaud's. I'd need roughly one hour recovery from an attack. Blue fingers white fingers, pain - the lot. I've got low blood pressure so I can't take medication. I have to go to hospital for a week for iloprost infusion. Anyway let me tell you what cured me. I take 3 pills. Butcher's broom, odorless garlic and gingko biloba. I had been taking just Gingko (which didn't work) but I was advised to take Butchers Broom in Holland and Barrett, they also said buy fish oil but I didn't like the thought. Anyway, it's only been 5 days but you could describe me as having bad circulation now but not Raynaud's. I've washed my hands with cold water, gone out without my mittens and I'm ok. I went to an event and minutes after entering I was shaking hands. My hands were warm!! You cannot imagine what it feels like to not have cold hands anymore. I was ready to saw my fingers off. This 'spring' has been awful but now I'm no colder than anyone else . Please buy these natural remedies, it'll change your life.
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I am taking Cataflam. I am taking large doses for several days a month. I am interesting about cardiac risk regarding this fact. I have heard that this dosage can be very risky for me. To be honest, I am not sure that these rumors are true.
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I underwent an EPS for cardiac arrhythmia one week ago but it has left me with severe bruising half way down my thigh. It is not swollen and not painful just a little in my groin. I did bleed a bit after the procedure and when i stood to go home and the cardiologist seemed to have difficulty inserting the catheter into my groin.
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has anyone else gone through this after an EPS is this typical?
I was in hospital in 2006 with severe illness. I had gotten up to go to the bathroom yet collapsed on the way there. I was given morphine as I was in extreme pain, however, i began feeling very sick, so cyclizine was put straight into my drip. Literally 20 seconds later, i remember feeling as if someone had put their hands round my neck - I couldn't breathe and my heart was racing - this is the last thing i remember. According to my mother and father, I went into cardiac arrest - blacked out, and then was unconscious. At this point, I was dead. I had no pulse and was not breathing. I was given emergency CPR and was thankfully, revived. I remained in hospital for the next week under strict observation. I was 15 at the time. I have a severe allergy to cyclizine, and never again will I go through this ordeal.
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After doing the best I can to ferret out the risks vs benefits of cardiac catheterization. 92% of my brain says, "No." That niggling 8% is a real pain.
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I am female. I am over 60. I have not had a myocardial infarction, (that they're telling me about anyway). I have some stress wall hypertrophy, but that's pretty much it. If I could get the physicians/cardiologists, to give me better evidence of need for such an invasive procedure, I might consider it...however...
I know me. Just having the procedure would be psychologically, and, therefore, physically, ruinous. I think I understand - but who can understand this really - that choosing not to have the catheterization, and whatever may happen as a result, means I might sign out quite unexpected. But is this a better way to live? I think so.
I have not felt "well" for at 7 years. (I'll spare you the ailments). However, I don't get colds, flu (no vaccinations)...I don't have hypertension. I'm told I have angina, but I am convinced that the post-meal sensations I get are due to gastric/diaphragm...more on that order of things. I don't have frank chest "pain."
I'm figuring that it will be a complete crapshoot to refuse the catheterization, but I am 100% certain, that there is a better chance of me surviving an invasive procedure if I don't die before I have it, then lending myself to what looks like a never-ending routine of invasive procedures.
What I'm currently hoping for, but have been unable to get, is a cardiologist who will agree to fully monitor me; one who truly understands the various medications available and who would find one that is best suited for this particular body, and who considers cardiac catheterization, et al, a last resort, rather than a first. (Nice fantasy).
So far, I've had the general practitioner I see, attempt to scare the hell out of me without telling me on what evidence he was doing so. (I would change to another GP if there was another one around). That kind of tactic is not only useless, but demoralizing. When it comes to "heart," demoralization can, without a doubt, lead to "heart trouble."
When I went in for a routine pelvic exam, I tested positive for Chlamydia. I immediately received treatment, and informed my partner that he needed to be tested and treated as soon as I was able to, which was 5 days after. Of course he wanted to have sex (even after I told him the news) and I finally agreed, but only with a condom on. He then got treatment the following day. We were informed by our health clinic to abstain from having sex at least 7 days after receiving treatment, but of course like the absolute idiots we are, we didn't. Because I am the big idiot that I am, I had to receive a second round of antibiotics which meant him and I both took them the same day following intercourse with protection. Not sure what our issue with being celibate for 7 days is exactly, but we had sex this past Tuesday with protection, but only a day after taking the antibiotics. I felt a little bit of discomfort when urinating afterwards, but assumed it was due to having sex. Just this morning, he prompted me to have sex again, and we did with protection, but afterwards he continued to try to have sex this time without a condom. I don't need anyone to tell me how idiotic it was to allow him to have sex with me without a condom, but I can't change what happened now. After having sex a second time, unprotected, this morning I had the most excruciating pain while urinating. I wanted to cry it hurt that bad. My partner has also experienced some discomfort while urinating after having sex this morning. I guess what I would like is some guidance, answers, suggestions, possible diagnosis? I am currently assuming the worst that him and I have indeed re-infected ourselves, but just wanted to throw my predicament out there for some outside opinions.
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I cured my BV by drinking LOADS of water. Maybe 4/5 litres a day.
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I tried everything I could afford to try as a broke student. So from garlics to yoghurt to antibiotics to overpriced creams. I visited 4 doctors and none of them helped me much. I burnt the inside of my vagina with all the nonsense I did. My vagina got so bad that I couldn't want for longer than 5 minutes because I would be in so much pain and desperately need to scratch. I used to spend all day in my room with my legs wide open because my genitals wore swollen and they hurt so much. I even remember crying and not being able to sleep. LOL! It was horrible!!
Anyway I started noticing the only time my vagina felt half decent was when I was weeing. So I started drinking more water so I could wee more and the more I weed the less I itched. I drunk 4/5 litres of water for 3 days and really tried to flush out my system and then it just stopped. No more itch. No more discharge, no more stink.
The sad news is I have it again. It's quite mild at the moment but I'm going to start drinking water like crazy again. Hopefully it works again.
I have suffered for years with bv and tried just about everything! Here's what worked for me, it kinda happened by accident but I've been bv free for almost two months, I have been sexually active and even after my period it has not returned. There is no douching of any kind in my cure. Hopefully this helps all or some of you as I take into account that every body can react differently. Best wishes and relief to you all!
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Upon waking (before eating) have large glass of water with a good squeeze of fresh lemon. Take a femdophilus pill with water.
After breakfast take an Alive Once Daily women's ultra potency multivitamin.
Drink water with fresh lemon throughout the day at least 3 large glasses.
That's it! Also, Try not to eat tons of sweets or too much red meat.
About a year ago I asked my doctor to diagnose the episodes I had been having most of my life.
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These episodes that made me feel detached, listless, dizzy and sometimes short of breath, would last for 10 or 20 minutes or sometimes two hours. The doctors, I had previously presented to, could find nothing wrong with the lungs or heart. I was once sent to specialist who thought it might be a type of migraine.
Anyhow my doctor thought it might be atria palpitations of the heart so I asked him if the next time I was in town, and had an episode, could I come in to see him. He arranged for an alert to be put on the receptionists' computers so I would get a ECG reading/printout immediately.
And so it happened, the resultant reading showed the heart beating 140 bpm ( should be 70 bpm for me)
“Ahh SVT!” the doctor cried, - Supra Ventricular Tachycardia, the electronic pulse finds a quicker way to go but in doing so causes the heart to beat faster.(Not as serious as Atria Tachycardia.)
“Don't drink any alcohol, coffee or tea.” said the doctor.
There are techniques on how to reset the heart back to normal.
I found the best way was to just lie down on the carpet for 10 minutes or so. It was a relief to actually know what the condition was at long last. I could live with it, or so I thought.
There were times when I couldn't reset it and it would last longer and made me feel completely debilitated.
Not wanting to go through the ablation surgery or have a pacemaker fitted, (not having any faith in these procedures), being a Christian I decided I should pray about it and leave it at that.
With a busy life and everything happening, now that the family had arrived from England and living with us, I had forgotten about that prayer time. Then one day, about three or so weeks later I said to my wife “ you know I haven't had an SVT episode in over three weeks?”
So in my next prayer session I thanked God in faith for the healing.
That was six months ago, and, praise God, I haven't had another episode. I drink the occasional glass of wine with my meal and drink coffee and tea every day.
I sometimes get the flutter in my 'solar plexus' area, that previously would indicate to me that an SVT episode was about to start, but now it just stops.
The only cures I have seen offered are ablation, dietry, drinking lots of water and taking a supplement of potassium. I didn't try any of these.
I haven't read of any 'spontaneous healing's for SVT, such as mine, have you?
So I do believe that God can heal you. It just takes honest fervent prayer.
does anyone get cured
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I was getting severe leg cramps several times a week. Since being prescribed one quinine tablet before going to bed, they have completely disappeared. The cramps were sometimes in my calf muscles but mainly in my ankles, feet and the muscle at the side of my leg.
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I don't post a lot on here but wanted to share with everyone the miracles that exist now for treating Hep C. I saw my doctor on Friday and she let me know that my 12 week post treatment labs after 24 weeks of Harvoni came back with a negative viral load and that I am now cured (12 Week SVR). This was my 3rd treatment and thanks to God, it worked. There is hope for all of us. I have had Hep C for 30+ years and am a Genotype 1A, with a Fibrosis level of 3+. As a 3+, I still have an increased risk for HCC, so I will continue to get lab work done every 6 months, ultrasounds every 6 months and a CT scan every 18 months. I encourage everyone to keep on treatment - we are at a place where so many of us now have a chance for a cure!
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My new girlfriend, who I like very much, was very open with me about the fact that she had a blood transfusion as a baby for several surgeries she had to have, which left her HCV positive. She and I were about to move into the sexual part of our relationship, so we both got tested for STDs to show each other we had a clean bill of health. Well as it turns out, her bloodwork showed she was HCV positive again...this is after achieving SVR (not sure for how long she had achieved this yet). She told me and was very upset, so I obviously just gave her a hug and held her. No other way to respond she was so upset. I'm curious, does anyone on here have any experience with this? Possibility for false positives or possibility for her to need to seek additional treatment? I hope you can forgive any questions that may seem ignorant. I am mostly focused on her health, but naturally I'm also concerned about the implications for our future relationship (I understand it is very low risk to pass it to me through sex, but still, I'm human, and I'm just carefully looking at this situation). If anyone can shed some light on her situation, I'd love to hear it. She's a great woman and I'd like to get any info for her that could help.
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I've had BV for 20 years, but have found that it's got worse over the last 5 years. Balance activ controls it until I next have sex, or have my period, then it inevitably returns with a vengeance. I've tried folic acid, fem dophilus (which worked but is too expensive for me long term)salt water douching etc.
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However, on this occasion, I douched with salt water for 2 nights before bed to kill the bad bacteria and followed with a balance activ pessary to nurture the good, the next 5 nights I only used the pessary. I only wash with plain water, have taken folic acid and vitamins c and d and I'm eating a fage Greek yogurt with honey (from asda) every day as it contains L.Acidophilus probiotics. I've also reduced my sugar intake.
i recently just became sexually active in September. since September me and my partner has had sex each month until December. I've only been with one guy. i noticed bv started a few weeks after i lost my virginity but it would always disappear before i thought it was problem. January came and i noticed my bv was really bad, this was just a few days after me and my partner had relations. it was a watery discharge and i had a horrible fish odor. it was getting so bad that i became embarrassed to sit next to people.my panties would become really wet from the discharge and stunk so bad. i am a very clean person. i take showers everyday and night and right after sex too. i wash with summers eve and that usually helps with any odor, but not this time. i went to the obgyn and she said it would clear up on it own in a few days but it didn't. i started using baby powder down there. it did help the discharge and the odor but it wasn't helping get rid of my problem.i then switch to anti fungal powder which did help but i always had to reapply it. so i began to look for home remedies online. i created a mixture of white vinegar, apple cider vinegar, and 2 to 3 drops of tea tree oil and put it in a spray bottle. every other night i would spray the mixture between the lips of vagina, i would then put a hot towel on my vagina for five minutes then hop in the shower. this did bring relief to me but i had to do it every week, butt hat's not healthy for your vagina. i am 18 years old but my mothers does not know i am sexually active so i told her i was having a real bad yeast infection. she then told me to take a tampon and soak it in coconut oil, the kind in the squirt bottle (liquid), and after my shower, insert the tampon and go to bed. after THREE DAYS i went back to normal THIS WORKED PERFECTLY. i no longer feel shame to sit next to people nor do i smell anything !!!! i do not do this every night but for the first week i did. ihaven't had sex in two months andunfortunatelyy me and my partner have taken a break so idon't know if my bv would flare up after sex but it doese flare up after my period. i do the coconut oil thing and after three days the discharge and odor is gone. everyone is different so don't know how others will react to this but i encourage you ladies to try this method. when it flares up i take a hot shower with summer's eve then after getting out the shower i wipe my vagina with a regular baby wipe, im a clean freak lol, i then take my tampon and put it in the oil and while its soaking i take a q-tip and dip it in the coconut oil and then trace the inside of my vagina with it and in my hole as well. this stops the smell and discharge, do this before bed that way to the oils can really cheap in and help your vagina.
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quick tip * before sex I recommend you take a shower but don't insert the coconut oil soaked tampon, of course, trace the inside of your vagina with a q- tip and coconut oil. make sure you get inside your hole too, the coconut oil works immediately and mask the smell very well that way your partner wont be able to smell the odor you'll be comfortable, at the most your partner would think you smell like coconuts lol and they smell pretty damn good!
quick tip* i do spray my mixture still once a month just because it makes me feel even more fresh. Like i said ive only been with one guy, my hole is still tight but i do know that vinegar and masturbation can help strengthen your vagina muscles and get it back tight if the vagina has became loose.
1 cup apple cider vinegar
1 cup white vinegar
2 to 3 drops of tea tree oil
directions: spray inside of vagina then put a hot towel on it for five minutes then take a shower. i would do this while the shower is running or in the shower DO NOT DO MIXTURE METHOD EVERY NIGHT YOU CAN HURT YOUR VAGINA DOING TOO MUCH
Has anyone out there with CRPS managed to return to work?
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