Re: Can’t figure out the triggers August 25, 2018 12:37PM |
Registered: 6 years ago Posts: 444 |
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Jackie
However, some forward-thinking doctors have asked...if you block the calcium, where does the excess calcium go? It gets deposited into arteries ... according to a paper presented at European Cardiology Society in Amsterdam noting CCBs caused 85,000 avoidable heart attacks and cases of heart failure each year.
Re: Can’t figure out the triggers August 25, 2018 12:49PM |
Registered: 6 years ago Posts: 444 |
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Jackie
For those on vegan diets, there is more than abundant calcium content in the vegan foods to satisfy the body’s requirements so avoiding dairy isn't really a penalty that requires supplementation with extra calcium. The risks of too much calcium and especially in afibbers is real and correct from a basic, biochemistry standpoint.
Re: Can’t figure out the triggers August 25, 2018 01:54PM |
Registered: 6 years ago Posts: 920 |
Re: Can’t figure out the triggers August 25, 2018 02:27PM |
Admin Registered: 6 years ago Posts: 5,338 |
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jpeters
Scary article on calcium channel blockers:
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CONCLUSION:
Our study demonstrates that CCBs reduce the risk of all-cause mortality compared with active therapy and prevent heart failure compared with placebo. Furthermore, with the inclusion of recent trials, we confirm that they reduce the risk of stroke, also in comparison to angiotensin-converting enzyme inhibitors and do not increase the risk of cardiovascular death, myocardial infarction and major cardiovascular events.
Quote
Conclusions This large population-based study provides strong evidence that CCB use is not associated with an increased risk of cancer. The analyses yielded robust results across all types of cancer and different durations of exposure to CCBs.
Re: Can’t figure out the triggers August 25, 2018 02:43PM |
Registered: 6 years ago Posts: 444 |
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Carey
Scary article on calcium channel blockers:
Until you notice that the newest research they relied on to arrive at the scary article is 18 years old and contradicted by larger, more recent studies. For example:
Re: Can’t figure out the triggers August 25, 2018 04:51PM |
Registered: 11 years ago Posts: 4,222 |
Re: Can’t figure out the triggers August 25, 2018 05:18PM |
Registered: 6 years ago Posts: 444 |
Re: Can’t figure out the triggers August 25, 2018 08:25PM |
Registered: 5 years ago Posts: 45 |
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The Anti-Fib
Did you ever follow up on an Endocrine/Cortisol check-up, as suggested in in your earlier Post? A Saliva Cortisol 4X/day test would tell what is going on with Adrenal output. The fact that you can sense it coming on several hours prior suggests some sort of intermittent Hormonal or Electrolytic imbalance. I had intermittent periods of Adrenal Suppression which triggered AFIB. I felt wiped out and unsually tired for about a day prior to my episodes.
Re: Can’t figure out the triggers August 26, 2018 12:22AM |
Registered: 9 years ago Posts: 1,085 |
Re: Can’t figure out the triggers August 26, 2018 08:48AM |
Registered: 5 years ago Posts: 45 |
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The Anti-Fib
Beardman:
I think every Dr. will want you on Blood Thinners. If it was only an episode every 2 months, then they would be more inclined to accept no Anti-Coagulation. Keep in mind when you are doing your research, that Paroximal AFIB could mean bi-monthly episodes, or 1-2 a week like yours.
The other thing is that you are relatively early in your discovery of your AFIB. You have done well and better than most in understanding this complex condition you have. Patience is warranted here. I still think you should medicate during episodes, and I stand by my post regarding this in your initial Thread several months ago.
Re: Can’t figure out the triggers August 26, 2018 10:16AM |
Registered: 8 years ago Posts: 1,102 |
Re: Can’t figure out the triggers August 26, 2018 11:16AM |
Registered: 5 years ago Posts: 45 |
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wolfpack
Completely understand the frustration. Bear in mind, though, that we are all biologics and not machines. The same set of inputs does not always have to produce the same set of outputs. AF is a progressive disease. It will change over time. As things are today, there are really 3 choices for AF: don’t treat, medicate, ablate.
Eliquis has a reversal agent that was recently approved. It is called Andexxa. Your physician may not be aware of it yet. I’m not sure if there’s a big cost difference with respect to Pradaxa, though. It would be worth asking.
Re: Can’t figure out the triggers August 26, 2018 01:55PM |
Admin Registered: 6 years ago Posts: 5,338 |
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beardman
With the three different cardiologists and the EP that I saw, not one of them even asked about my diet. I was very clear with all of them that I kept very good records of everything and even asked if changes in my diet might help. I always received the blanket statement that eating better is always good for you . . . What is,”better” when you don’t know what I’m eating! Sorry for the vent.
Re: Can’t figure out the triggers August 26, 2018 03:45PM |
Registered: 10 years ago Posts: 1,748 |
Re: Can’t figure out the triggers August 26, 2018 04:09PM |
Registered: 6 years ago Posts: 444 |
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Elizabeth
Most doctors don't want to listen about diet as that isn't their business, they are in the business of handing out pills or (slash and burn) not trying to find out what is causing your problems.
Liz
Re: Can’t figure out the triggers August 26, 2018 08:43PM |
Registered: 9 years ago Posts: 1,085 |
Quote
beardman
Beardman:
I think every Dr. will want you on Blood Thinners. If it was only an episode every 2 months, then they would be more inclined to accept no Anti-Coagulation. Keep in mind when you are doing your research, that Paroximal AFIB could mean bi-monthly episodes, or 1-2 a week like yours.
The other thing is that you are relatively early in your discovery of your AFIB. You have done well and better than most in understanding this complex condition you have. Patience is warranted here. I still think you should medicate during episodes, and I stand by my post regarding this in your initial Thread several months ago.
I understand am trying to be patient with this, but as you all know it is tough. It is especially difficult for me when I appear to be doing to same thing and am receiving different results. I keep a journal of everything that I can think relates to this. My new things to make note of will be the calcium intake also any association with bradycardia and perhaps Hawthorne berry (Iv’e been doing a fair amount of reading on that as well).
From an outside point of view I don’t disagree with the medication. They would have just such a huge impact on my life being that they want me to stop any martial arts at all while on the blood thinners. On top of this, it seems that the pharmaceuticals are only a temporary solution for most people, especially when their younger. Oh, and then their is the huge cost as well. I requested a blood thinner that had a reversal agent, apparently that is only Pradaxa. It would cost around $600/month just for that. I think the flecainide was another $150 or so and I am supposed to take that twice daily everyday.
Re: Can’t figure out the triggers August 30, 2018 09:45AM |
Registered: 5 years ago Posts: 38 |
Re: Can’t figure out the triggers September 01, 2018 06:35AM |
Registered: 5 years ago Posts: 45 |
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Dinodog
Hi Beardman-
I'm sorry you have to deal with this and understand it all too well. I just turned 45 so now how it is to get this diagnosis and feel like your life is in flux to say the least. Take the time to do some more reading, and I think you will likely conclude that an ablation is the way to go. You are young with a structurally sound heart so your success rate with a top EP will be very high. This is the best method of trying to get off these meds, at least temporarily. I've seen lots of people in your age group with years of med free NSR after a successful ablation. You will of course need to continue not to over-exercise and watch all of the other lifestyle factors- but that doesn't seem to be an issue for you. I don't see why you can't do martial arts on a blood thinner. If it's high contact then yes you might be banged up with bruises. The biggest risk would be hits to the head which hopefully isn't part of the protocol. I am snowboarding on a blood thinner. I don't go out on icy days, wear my helmet, and have a medical ID on me. My top EP advised me that the biggest risk is a bad head injury, and if you have one you'd be in trouble even if not on a blood thinner. I'm choosing to live my life with this diagnosis and try to accept it and move on. You are new to this and all of that will take time. But know that you can still do the things you love and will get through this.
Tracy
Re: Can’t figure out the triggers September 01, 2018 08:19AM |
Registered: 8 years ago Posts: 1,102 |
Re: Can’t figure out the triggers September 01, 2018 08:51AM |
Registered: 6 years ago Posts: 18,881 |
Re: Can’t figure out the triggers September 01, 2018 08:57AM |
Registered: 5 years ago Posts: 45 |
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Jackie
Beardman - The support factor is definitely an important part of the forum. Always has been. I'm pleased to see your cutting back on the Ca and arginine helped and as time goes on, you'll probably see continued stability but you also may need further reductions. What are the numbers of the herniated discs?
Jackie
Re: Can’t figure out the triggers September 01, 2018 02:56PM |
Registered: 6 years ago Posts: 18,881 |
Re: Can’t figure out the triggers September 01, 2018 03:05PM |
Registered: 5 years ago Posts: 45 |
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Jackie
Beardman - oh - yeah ...well, too low in the spine.... I was curious to know if the disc issues were higher up and had some impingement in areas of the vagus nerve, but not down there. I certainly wish you every success with the procedure.
There are some specialists in this area that are injecting special forms of what I'll call "collagen" for lack of a better term...into areas to help regenerate discs which are the 'cushions' between the bones of the spine. The results are said to be amazing. I have no personal experience... just hearing from others. You definitely want to get those repaired as minimally invasive as possible...so you can get back to a normal, active life. Keep us posted.
Best to you,
Jackie
Re: Can’t figure out the triggers September 06, 2018 09:57AM |
Registered: 5 years ago Posts: 45 |
Re: Can’t figure out the triggers September 06, 2018 11:19AM |
Registered: 6 years ago Posts: 444 |
Re: Can’t figure out the triggers September 06, 2018 11:48AM |
Registered: 5 years ago Posts: 45 |
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jpeters
"Calcium is especially important for athletes because they are more likely to lose calcium, as well as other minerals, through perspiration."
[www.uofmhealth.org]
Re: Can’t figure out the triggers September 06, 2018 01:09PM |
Registered: 6 years ago Posts: 18,881 |
Re: Can’t figure out the triggers September 06, 2018 01:43PM |
Registered: 5 years ago Posts: 45 |
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Jackie
Beardman - Good you are getting rid of the excess calcium since anytime there is too much intracellular calcium... which is almost always the case with afibbers, there is also the finding that intracellular magnesium is low. The ratios of calcium-to-magnesium and potassium-to-sodium are established by fundamental biophysics... along with the calcium-to- sodium ratio that is often out of balance in those with hypertension.
Low magnesium causes many more health issues than arrhythmia... but like low magnesium causing muscle cramps, it definitely is attention getting.
Keep up the good work.
Jackie
Re: Can’t figure out the triggers September 06, 2018 02:19PM |
Registered: 6 years ago Posts: 444 |
Re: Can’t figure out the triggers September 06, 2018 02:50PM |
Registered: 5 years ago Posts: 45 |
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jpeters
I have noticed a fair amount of muscle cramps lately, but I attributed that to my increase in biking at the gym. I swapped out running because of my back/leg issues for biking.
"Without enough calcium you may experience muscle cramps."
Re: Can’t figure out the triggers September 06, 2018 03:57PM |
Registered: 10 years ago Posts: 1,748 |
Re: Can’t figure out the triggers September 06, 2018 04:10PM |
Registered: 6 years ago Posts: 444 |
Re: Can’t figure out the triggers September 06, 2018 08:56PM |
Registered: 8 years ago Posts: 1,102 |
Quote
beardman
I have noticed a fair amount of muscle cramps lately, but I attributed that to my increase in biking at the gym. I swapped out running because of my back/leg issues for biking.
I do take a magnesium supplement and I also cut way back on my supplements, so maybe something there is off too. I am now taking
Nattokinase (2,000 FU 1x day)
Taurine (1,000mg 3x day)
Hawthorne Extract (300mg 3x day)
Chelated Magnesium Bisglycinate (200mg 2x day)
Re: Can’t figure out the triggers September 06, 2018 09:21PM |
Registered: 5 years ago Posts: 45 |
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wolfpack
I have noticed a fair amount of muscle cramps lately, but I attributed that to my increase in biking at the gym. I swapped out running because of my back/leg issues for biking.
I do take a magnesium supplement and I also cut way back on my supplements, so maybe something there is off too. I am now taking
Nattokinase (2,000 FU 1x day)
Taurine (1,000mg 3x day)
Hawthorne Extract (300mg 3x day)
Chelated Magnesium Bisglycinate (200mg 2x day)
How about potassium? I had a hypokalemic paralysis event about 7 years ago and, in hindsight, it was preceded by several weeks of severe muscle pains.
Re: Can’t figure out the triggers September 09, 2018 09:16AM |
Registered: 6 years ago Posts: 18,881 |
Re: Can’t figure out the triggers September 19, 2018 06:25PM |
Registered: 5 years ago Posts: 45 |
Re: Can’t figure out the triggers September 06, 2019 03:21PM |
Registered: 7 years ago Posts: 218 |
Re: Can’t figure out the triggers September 07, 2019 09:05AM |
Registered: 5 years ago Posts: 45 |
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hwkmn05
Cardiologist, Thomas E. Levy, MD, JD, in his book, Death by Calcium
Another great read by Dr. Thomas Levy is "Hidden Epidemic". A personal story of his own root canal teeth he believed to be the direct cause for his heart attack and other health issues until removal.