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        <title>Atrial Fibrillation Forum - AFIBBERS FORUM</title>
        <description>A forum for sharing experiences regarding atrial fibrillation and other atrial tachy-arrhythmias.</description>
        <link>https://www.afibbers.org/forum/list.php?9</link>
        <lastBuildDate>Thu, 12 Nov 2026 23:46:57 +0000</lastBuildDate>
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            <guid>https://www.afibbers.org/forum/read.php?9,202065,202065#msg-202065</guid>
            <title>My peer-reviewed article on re-evaluation of magnesium for AF. (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202065,202065#msg-202065</link>
            <description><![CDATA[ Dear fellow members affected by AF:<br />
<br />
I first want to announce the publication of my peer-reviewed article in a medical journal. It can be accessed by adding the following URL to a browser: <br />
<br />
[<a href="https://www.frontiersin.org/articles/10.3389/fcvm.2026.1878314"  rel="nofollow">www.frontiersin.org</a>]<br />
<br />
Some may recognize my pseudonym, Hugging. I am now a retired M.D. in the US and an emeritus professor of clinical immunology. Due to my <br />
<br />
successful conversion of my AF with a protocol I developed, I have recognized some underappreciated observations in the medical literature <br />
<br />
about AF, in particular why oral magnesium (Mg) has not become a standardized addition in the therapy of AF,<br />
<br />
In my opinion, the following observations should prompt cardiology to re-examine the importance of standardizing oral Mg as part of therapy for some individuals with AF. All of these observations are backed up by medical literature citations:<br />
<br />
1. Most individuals with AF are deficient in elemental Mg (Mg2+) in their heart cells despite having a normal blood Mg level. <br />
<br />
2. The half-life of Mg in humans is 6 weeks. That means if you restricted Mg in your diet for 6 weeks, your body would contain 50% of Mg. Hence, if an AF individual has a pre-existing Mg deficiency in their heart cells, it is reasonable to presume it will take multiple 6-week half-lives of Mg to replenish Mg in heart cells. This is a key point: taking oral Mg will take at least 4-6 months before one may observe a reduction in AF.<br />
<br />
3. The daily RDA for Mg2+ in males is 420 mg, and in females it is 380 mg. Mg supplements cannot meet that requirement, as most provide around 7-10% of the weight of a Mg dose; for example, a 500 mg capsule of Mg gluconate provides 35mg of Mg2+. Absorption reduces that amount to about 40%, so one capsule provides 14 mg of Mg2+. That means one or two capsules of Mg supplements alone will not meet the daily requirement; on top of that, if one has AF with a pre-existing Mg deficiency, one needs to consume foods high in Mg (see online).<br />
<br />
4. Choosing a Mg supplement is difficult because almost all do not provide data on the percentage of Mg2+ in each dose and the % absorption. As a general rule, the literature indicates that you should avoid inorganic Mg supplements (Mg oxide, Mg hydroxide, Mg carbonate, Mg sulfate) because they are poorly absorbed and therefore act as laxatives. In contrast, organic Mg supplements are better absorbed ( Mg glycinate, Mg gluconate, Mg aspartate, Mg lactate, etc.) Since there are no professional guidelines, I recommend choosing an organic supplement from a company that manufactures under current good manufacturing practice (cGMP) and that does not contain other ingredients, especially calcium and zinc, which interfere with Mg absorption.<br />
<br />
5. Mg2+ is a physiologic calcium blocker that can interfere with calcium release in heart cells, and by doing so, it inhibits what may turn out to be an important innate mechanism of immunity called the NLRP3 inflammasome, which, when unblocked, releases cytokines (small inflammation-producing molecules) that likely cause inflammation associated with AF.<br />
<br />
6. Since Mg2+ is deficient in AF heart cells, the heart cells have difficulty producing energy from stored energy molecules called ATP. To reverse this deficiency, there is a need to replenish Mg2+, which can only occur over a long period of magnesium consumption with better-absorbed Mg supplements and foods fortified with Mg2+.<br />
<br />
7. Personally, I was able to determine a reduction in my AF by self-monitoring my EKG with Kardia and Apple Watch (3-4 times a day for 30 seconds; total of 2 minutes), but other technology may do the same. If sinus rhythm occurs more frequently, it will encourage continued oral Mg supplementation and foods fortified with Mg.<br />
<br />
The article presents evidence for a needed pharmaceutical inhibitor of the NLRP3 inflammasome, which likely causes the inflammation associated with AF. <br />
<br />
I suggest sending the reference to your health care provider to see whether they are interested in the concepts and protocol, which you can download, as it is a free, public-access article. <br />
<br />
I hope my article makes a difference for many of you affected by AF, but the protocol includes a caution that you must work with a health care provider to determine whether you are a candidate. For medical ethics reasons, I cannot answer queries from individuals seeking my opinion.<br />
<br />
Lastly, I want to emphasize that I do not receive any financial benefits from this free access peer-reviewed publication.<br />
<br />
Best regards,<br />
<br />
Hugging]]></description>
            <dc:creator>Hugging</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 09 Nov 2026 23:16:05 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202057,202057#msg-202057</guid>
            <title>Cyclobenzaprine. (2 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202057,202057#msg-202057</link>
            <description><![CDATA[ I’m having low back muscle spasms at night that’s really boogering up my sleep. My PCP wants to prescribe cyclobenzaprine. It’s a muscle relaxer.  I asked my regular cardiologist if I could take it and he said I could. But everything I read indicates it’s not a good mix with us Afibbers. I’ve only had 2short bouts of AFib the past year. So my ablation seems to be holding things at bay pretty well. Would appreciate any advice on taking cyclobenzaprine.  My muscle pain in my low back and glutes is wrecking my sleep]]></description>
            <dc:creator>Pokey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 04 Nov 2026 12:54:02 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202052,202052#msg-202052</guid>
            <title>Lyme disease? (2 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202052,202052#msg-202052</link>
            <description><![CDATA[ I&#039;ve been lucky controlling my AFIB for the past almost five years. During this time I&#039;ve had a two month string of weekly episodes when I got the Norovirus. When the norovirus symptoms stopped so did my AFIB, that was almost two years agon<br />
<br />
A couple of weeks ago I found a deer tick on me and pulled it off. I never got the bulls eye rash nor any symptoms but unfortunately the weekly AFIB episodes started two days after pulling off the tick (coincidence). Could I be fighting off the Lyme infection without any symptoms which is causing the AFIB, or is it just a red herring?  Any experience in this would be appreciated.<br />
<br />
BTW, I did have Lyme&#039;s disease 20 years ago, the rash and flu-like symptoms, so I know what it feels like.<br />
<br />
Thanks]]></description>
            <dc:creator>MikeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 02 Nov 2026 22:44:02 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202033,202033#msg-202033</guid>
            <title>Dartmouth called about a PFA (3 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202033,202033#msg-202033</link>
            <description><![CDATA[ I guess hospitals arent immune from employee performance and missing deadlines. I was supposed to be scheduled for Sept and was recently called by a new scheduler stating they messed up my paperwork. Offered me Nov, but I havent been on Eliquis 30 days prior so that was declined. I am also headed to Tx in Dec so wondering if I do decide, would this be a better option with a greater chance of success. I have very little info on Dartmouth success rates with PFA. I ve enjoyed a pretty good ride of nearly 7 months on low dose meds also with one recent short episode. Conflicted at my age of kicking the can down the road much longer.]]></description>
            <dc:creator>hwkmn05</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 30 Oct 2026 20:19:20 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202032,202032#msg-202032</guid>
            <title>Flecainide/Metoprolol or Diltiazem (13 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202032,202032#msg-202032</link>
            <description><![CDATA[ If side effects are worse with Metoprolol, is Diltiazem a better alternative or more dangerous with bradycardia even in low doses?]]></description>
            <dc:creator>hwkmn05</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 06 Nov 2026 01:48:52 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202027,202027#msg-202027</guid>
            <title>Magnesium Sucrosomial (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202027,202027#msg-202027</link>
            <description><![CDATA[ I just happened upon info on this newer form of magnesium which basically breaks down in the intestines rather than the stomach. This attribute is said to increase its absorption. As this forum is ‘keen’ on magnesium, I wondered if anyone’s tried this form.<br />
.]]></description>
            <dc:creator>californiagal</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 29 Oct 2026 15:49:07 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202023,202023#msg-202023</guid>
            <title>drug &quot;interactions&quot; and no nos... (7 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202023,202023#msg-202023</link>
            <description><![CDATA[ Where does one get GOOD information on drug &#039;cross overs&quot;. Like you can use Epocrates to see &#039;interactions&#039; but for example..  I have some stomach issues. So I am fooling around with PPIs H2s and other things.  I am also on Eliquis and cardizem and a few other items.  The pharmacist and online might say they are ok and don&#039;t interact but I wonder if stomach meds block the heart meds.  I also wonder about products like Maalox or Gaviscon. And then the prescribed one Carafate. <br />
<br />
People will say ask your EP.  Well... I KNOW that Carafate (sucralfate) coats the digestive track and can block absorption I need to be 100% right now on the Elequis.  My EP said &quot;oh you can take it all together&quot;.   My GI said it does coat so I guess there is my answer.<br />
<br />
But I feel like physicians do NOT have a handle on how things interact- especially if it is between disciplines like cardiac and GI.  When I got on dofetilide, I had a cardiac pharmacist.  She picked up my calls for a year or so but I can never get a call back.  I asked EP staff and they said she isn&#039;t really used for ongoing but just onboarding of meds in the hospital.<br />
<br />
This seems like it is somewhat of a crucial issue- or could be...]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 03 Nov 2026 15:00:21 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202020,202020#msg-202020</guid>
            <title>Fluorouracil 5% cream - AFIB? (7 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202020,202020#msg-202020</link>
            <description><![CDATA[ I had a PF ablation about 1 1/2 years ago - everything has been fine and back to normal (77 yo) routine of running/ biking etc. Regular checkups and weekly monitoring with Kardia are fine.<br />
<br />
I saw my dermatologist about a month ago - see him every 6 months because of some actinic keratoses on my forehead and temple areas (previous bouts of basil and squamous cell carcinoma). I was prescribed Fluorouracil 5% cream. This topical cream was to be applied every day for 3 weeks. After about 2 weeks I felt &quot;off&quot; - kardia suggested &quot;possible AFIB&quot;. I sent the finding to my heart doc - She suggested I closely monitor my readings. I stopped using the Fluorouracil and shortly thereafter (few days) my readings Kardia readings went back to normal. Doc said the cream did not cause the possible AFIB. But I still have my doubts (as the skin on my temple area is thin and meds could have easily gotten into my bloodstream?) - I know - sounds crazy - but all is well now. Anyone have an experience similar to mine?]]></description>
            <dc:creator>AJR3</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 31 Oct 2026 12:26:30 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202010,202010#msg-202010</guid>
            <title>Ablatio and Eliquis (5 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202010,202010#msg-202010</link>
            <description><![CDATA[ Had an ablation in Jan 2023. Doc put me on 5 MG of Eliquis twice a day. Last Wednesday, October 21st. I bumped my shin against a moving car. it was hardly noticeable as far as any pain. About 29 minutes later I started to experience pain ad a growing bump. Went home and iced the bump twice in the afternoon before going to a function that evening at 6PM. elevated my lower leg where the bump was twice, also put ice on it twice. As the night wore on, my leg swelled even more and became very painful. Which led to going to th ER at midnight to have this looked at, as it was becoming more and more painful. After getting checked in, the ER Doc came in to see me and asked questions. One of the first was, why was I still on Eliquis after all this time if had not had any AFIB incidents  since operation. Told him I was following DR orders. He also mention to be careful about potential bumping o I take 5 MG twice a day. So I am looking for info from everyone as to the about of Eliquis. DO you or what do you take instead  Looking for feedback, input any advice. Medications. Alternatives. Thank you]]></description>
            <dc:creator>Explorer18</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 29 Oct 2026 00:07:44 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202008,202008#msg-202008</guid>
            <title>Post Ablation questions (4 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202008,202008#msg-202008</link>
            <description><![CDATA[ Hello Everyone,<br />
<br />
I am reaching the 4 month period after my 3rd ablation and Watchman implant (Dr. Natale) Heart rhythm seems to be stable and very few symptoms (rare shortness of breath episodes). Last EKG was normal. Kardia readings show some occassional PAC&#039;s. Overall , I am really happy with the results. No medications for arrhythmia and 2.5 mg Eliquis 2/day. As a 76 year old male, I am considering a procedure for shoulder repair. In, addition, my doctor has suggested a testosterone treatment. Anyone have thoughts about these treatments interrupting my recovery process from the ablations. Thanks.<br />
<br />
Sir]]></description>
            <dc:creator>SSr</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 28 Oct 2026 19:46:18 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202007,202007#msg-202007</guid>
            <title>A New Canadian Procedure (4 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202007,202007#msg-202007</link>
            <description><![CDATA[ [<a href="https://www.msn.com/en-ca/health/diseases-and-conditions/new-canadian-procedure-could-revolutionize-afib-treatment/ar-AA2g1TyB?uxmode=ruby&amp;cvid=6ade8af871fe4ca4b7f9dc5e55afb25c&amp;ocid=edgntpruby&amp;pc=ACTS&amp;ei=15"  rel="nofollow">www.msn.com</a>]]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 05 Nov 2026 09:07:19 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,202001,202001#msg-202001</guid>
            <title>Finding my next EP (3 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,202001,202001#msg-202001</link>
            <description><![CDATA[ Hello Afibbers,<br />
This is my first post so I may do something wrong!  I&#039;ve had PAF for about 15 years treated with 2 ablations,  one in 2019 and then again in 2024.  All came off Flecainide last year, and all has been well until recent months when the afib has started to show up again; sometimes just for a few minutes and other times for 1.5 hours.  I use Flecainide as a PIP 50 mg, and so far the afib has stopped.  My treatment has been at The Cleveland Clinic ever since I was diagnosed.   Lately, I am only getting about 2 weeks between episodes of afib or whatever as arrhythmia this is.  My EP of may years and the one who did both of my ablations was involved in a serious accident last year.  In his absence, I saw another EP who I can&#039;t stand.  I won&#039;t use any names but the EP I dislike I just saw in August.  They did not weigh me, did not take my BP, and he never listened to my heart.  Every concern I had, he dismissed and told me to come back in a year.  <br />
Meanwhile my original EP who I do like is back seeing patients now after a long leave of absence.   However,  he only does cardioversions and sees patients in the office, as he cannot stand to do ablations or pacemakers.I have a chance to see Dr Pasquale Santangeli next month.  He knows nothing about me.  The person on the phone today said I can&#039;t just change from one doctor to the next.<br />
So what would you do?  Go back to the MD who is smart, thorough, compassionate,  and knows your case well, or just start over with an MD who seems to have remarkable credentials??  Thank you for your thoughts.]]></description>
            <dc:creator>Wolfgang</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 24 Oct 2026 14:53:20 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201990,201990#msg-201990</guid>
            <title>Ablation done (5 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201990,201990#msg-201990</link>
            <description><![CDATA[ I had ablation #2 on Monday. EP said my 2013 ablation mostly failed so he redid it. There were hot spots all over and he is confident of his success. I’ll see his NP in December and if everything has been quiet I’ll stop Multaq. That will be the true test! From his notes:<br />
<br />
CATHETER ABLATION FOR ATRIAL FIBRILLATION<br />
 <br />
PROCEDURES PERFORMED:<br />
 <br />
PFA pulmonary vein isolation and posterior wall isolation<br />
RF ablation for typical atrial flutter<br />
HV interval measurement<br />
3D electroanatomic mapping<br />
Intracadiac Echocardiography<br />
Transeptal puncture<br />
Ultrasound guided access<br />
Left atrial and/or coronary sinus pacing/recording<br />
 <br />
My throat is very sore and I’m coughing, but it should start getting better after 48 hours, which is soon. I’ve had a headache since Monday afternoon that isn’t going away on acetaminophen. Of course my groin punctures are sore and bruised but that’s to be expected. One unexpected discomfort was the nurse getting my wedding band off! After 51 years it was practically embedded on my finger! I’ll have it made larger. 😊<br />
 <br />
Pam]]></description>
            <dc:creator>PamelaJean</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 21 Oct 2026 15:17:26 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201982,201982#msg-201982</guid>
            <title>Amniioderone and ablation questions (6 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201982,201982#msg-201982</link>
            <description><![CDATA[ I have an ablation this month. They were talking about doing amnioderone during the blanking period.  I have exhausted all other rhymes drugs except that and Sotolol.  I have heard horrific things about amnioderone.  It would likely be for a short time (3-6 months) but have heard even getting off it can be difficult. They will make that decision game time depending on how things look.   The ablation is primarily for a-flutter but probably some fib.  Multiaq is supposed to have been a better cousin but I had such horrible abdominal side efffects I had to quit.<br />
<br />
Also I am on rate control drugs.  diltiasem.  Last weekend I was in flutter so I took (as prescribed) metropolis. when I went back in sinus my HR went to 40 at one point.  It recovered pretty quick.  So before the ablation they are stopping the rate control drugs.  I just feel that I could be in serious trouble. I take the short acting 60 mg every 6 hours.  I also have a CT 2 days prior.  If I am off then and I have gotten super nervous at these before, I can see it shooting up.  Anyone have any thoughts here? questions for me to ask the team?]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 15 Oct 2026 02:33:11 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201981,201981#msg-201981</guid>
            <title>Chia seeds (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201981,201981#msg-201981</link>
            <description><![CDATA[ This is just FYI<br />
I met a man from Singapore recently and he told me that he&#039;d had a heart rhythm problem since he was young. He was now retired, so I guess in his early 70&#039;s. He said that he hadn&#039;t had an ablation and wasn&#039;t taking any anti-coagulants. Perhaps it wasn&#039;t a very serious rhythm problem. But what I found interesting was that he said that for the past 2 years he&#039;d been soaking chia seeds in water over night and eating them the next day. He said that from taking the chia, his heart rhythm had improved a lot.]]></description>
            <dc:creator>TomR</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 08 Oct 2026 20:51:30 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201975,201975#msg-201975</guid>
            <title>Is there any connection between ocular migraines and Afib? (7 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201975,201975#msg-201975</link>
            <description><![CDATA[ After 10 years of Afib, I had an extensive LAA ablation with Dr. Natale in 2013, and 9 months later, a Flutter ablation with him as well. I also got the Watchman on my birthday (!) in January of 2023<br />
<br />
In May of 2014 I had my first ocular migraine, and have since had many episodes.  I rarely get a headache, but I do get the shimmering watery look or a colorful kaleidescope of colors.  It goes away after 20-30 minutes of shutting my eyes.<br />
<br />
When I Googled what causes ocular migraines, it mentioned that they might occur from abnormal electrical activity - which is pretty much what Afib is too, isn&#039;t it?  Hence my reason for asking if there might be a connection...I always tell people who ask about AFib that it&#039;s nothing really wrong with the heart, but it&#039;s an electrical problem.<br />
<br />
Any thoughts on this?  Barb]]></description>
            <dc:creator>BarbB</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 19 Oct 2026 01:43:36 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201965,201965#msg-201965</guid>
            <title>Two Years Post PVI for Atrial Tachycardia (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201965,201965#msg-201965</link>
            <description><![CDATA[ I am almost exactly two years post PVI ablation.  Many of you know my story. Since my ablation in October 2024, I have had not even a single PAC.  I have recently begun to have very short episodes of SVT lasting 20-60 seconds, rates 150-160s that start and stop abruptly with dizziness.  It isn&#039;t really super concerning, although they are slightly more frequent. Is it even worth mentioning to my EP, or do I wait until they are more bothersome?  Is this a normal occurrence?  I&#039;m not really super alarmed by them but it does give me pause after all the trouble I have had.  Just curious what others have experienced late post-PVI.]]></description>
            <dc:creator>MeganMN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 04 Oct 2026 07:05:46 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201955,201955#msg-201955</guid>
            <title>Can Covid vaccine trigger an afib episode? (12 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201955,201955#msg-201955</link>
            <description><![CDATA[ I am on Steve Carr&#039;s potassium regimen and until last night I was doing fine (some short episodes since I started in April). So at 3 am afib woke me up - like usually I am getting my episodes at night. I am wondering whether it got triggered by the covid vaccine two days ago. I didn&#039;t have any strong reactions in the past, except for some pain and stiffness in my arm, but this time I got a fever and felt pretty bad all around. In the past I got the Pfizer, but this time I got the Moderna mNexspike. My question is, should I take a micro dose of Flecainide (12.5mg) for the next couple of evenings to prevent another afib episode? I think George managed his reaction to Covid vaccines like that. <br />
And now I am also reluctant to take the Flu vaccine (never got one before, but I am now 70 years old and maybe it&#039;s time), and how would I manage that? Taking Flecainide in the days before and after and how much? (Female, 110 pounds). I usually only take Flecainide as PIP when I get episodes.]]></description>
            <dc:creator>Edda</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 30 Oct 2026 11:46:32 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201952,201952#msg-201952</guid>
            <title>Looking for people w/ afib to interview (3 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201952,201952#msg-201952</link>
            <description><![CDATA[ Hey all!<br />
<br />
I&#039;m a college student doing a project and I need to interview a few people diagnosed with afib, preferably with a monitor. Voice is required (assignment requirement, sorry) and it must be within the next week or two. It will be recorded, but I will be the only one who will access the recording. I&#039;d prefer doing it over Discord, but I&#039;d be able to set up a phone call or Zoom meeting if need be. Please let me know if you&#039;re interested!<br />
<br />
Disclaimer: The project is based around marketing for a new afib monitor. I will not be trying to sell you anything, rather I am establishing &quot;jobs to be done&quot; for the consumer base.]]></description>
            <dc:creator>Kenny</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 05 Oct 2026 23:59:45 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201944,201944#msg-201944</guid>
            <title>Smoked Food &amp; AF  ??? (3 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201944,201944#msg-201944</link>
            <description><![CDATA[ I&#039;m fixin to get a used once smoker for free. Has anybody out there ever had any AF issues eating smoked food ?<br />
I am also looking at a Freeze Dryer. Any AF issues eating freeze dried food ? <br />
 3K to 4K for 1 year supply going price out there. 3K for a  freeze dryer.]]></description>
            <dc:creator>Todd</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 25 Sep 2026 18:29:06 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201939,201939#msg-201939</guid>
            <title>Metoprolol vs Multaq (2 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201939,201939#msg-201939</link>
            <description><![CDATA[ Flutter is my game (not afib).  After 6yrs of increasingly frequent episodes, in 2023 Natale did an ablation that was mostly successful - didn&#039;t address a point near the appendage.  I was then good until recently.  August this year, after 3weeks of continuous flutter, was cardioverted.  <br />
<br />
So now maybe a second ablation - but that might include a watchmen.<br />
<br />
QUESTION:  I was recommended to stop metoprolol (25mg x2) and switch to Multaq 500mg x2.<br />
<br />
What is the experience of folks here?  Which is better to prevent afib/flutter?  Metoprolol or Multaq?<br />
I don&#039;t have a bad reaction to either.  I was good for 2.5 yrs with metoprolol.<br />
<br />
Thanks for any words of wisdom<br />
<br />
-Sven]]></description>
            <dc:creator>swhanson</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 21 Sep 2026 20:51:37 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201938,201938#msg-201938</guid>
            <title>Anticoagulation in AF and One Stroke Risk Factor: A Choice, Not a Prescription (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201938,201938#msg-201938</link>
            <description><![CDATA[ I am hoping in my lifetime there may be a definitive answer. I personally made the choice (with many discussions with my EP and Cardiologist) not to go the anticoagulation route after having surgical closure during my mini maze many years ago.  <br />
<br />
[<a href="https://www.medscape.com/viewarticle/anticoagulation-af-and-one-stroke-risk-factor-choice-not-2026a1000xio?ecd=a2a"  rel="nofollow">www.medscape.com</a>]]]></description>
            <dc:creator>sldabrowski</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 21 Sep 2026 13:06:38 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201937,201937#msg-201937</guid>
            <title>NOACs Linked to Slower Cognitive Decline in Comorbid AF and Alzheimer’s Disease (no replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201937,201937#msg-201937</link>
            <description><![CDATA[ May be quite some time to really know if this is the case. <br />
<br />
[<a href="https://www.medscape.com/viewarticle/noacs-linked-slower-cognitive-decline-comorbid-af-and-2026a1000smf?ecd=WNL_trdalrt_pos1_260820_etid8618363&amp;uac=323219MR&amp;impID=8618363"  rel="nofollow">www.medscape.com</a>]]]></description>
            <dc:creator>sldabrowski</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 21 Sep 2026 12:53:47 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201929,201929#msg-201929</guid>
            <title>Early AF diagnosis via eye examination (2 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201929,201929#msg-201929</link>
            <description><![CDATA[ Wonder if that is commonly used/looked at in the USA?<br />
[<a href="https://www.news-medical.net/news/20260914/Eye-scans-detect-signs-of-atrial-fibrillation-years-before-diagnosis.aspx"  rel="nofollow">www.news-medical.net</a>]]]></description>
            <dc:creator>Joe</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 20 Sep 2026 01:05:23 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201919,201919#msg-201919</guid>
            <title>Colonoscopy. .. ablation 3 weeks later.  blood thinner questions (10 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201919,201919#msg-201919</link>
            <description><![CDATA[ I just went off Multaq. I had to cancel two colonoscopies / endoscopies this year b/c of afib episodes. I am now not on Multaq (abdominal issues) And I used some connections to get on the October 2 sechdule for colonoscopy/endoscopy. but I have an ablation scheduled October 23. 3 weeks apart. I will (and have been) certainly talk to my docs but have gotten different pieces of advice on if this is Ok b/c I will have to hold the eliquis for colonoscopy. Also there is the question of me being in and out of afib. I was told that I had to wait 30 days after my &quot;self conversion&quot; mid august for a 8/31 date I had and had to cancel. But people with afib I assume get these tests. I may or may not be in it at that point. I for sure am having more arrhythmias since off Multaq but not tracking them. Also I am having an LAA CT 3 days prior to the ablation and a TEE right before. <br />
<br />
So my questions<br />
1) thoughts on the timing for the eliquis hold <br />
2) thoughts on the whole may be in afib of may have been in afib?  before the hold and self converted.<br />
<br />
Thanks  I have a pretty extensive cardiac history.  I will be talking to my adult congenital doc tomorrow and EP NP on Monday.  But wanted opinions here or questions to ask them]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 20 Sep 2026 12:12:01 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201914,201914#msg-201914</guid>
            <title>Nightmare Experience (9 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201914,201914#msg-201914</link>
            <description><![CDATA[ Imam 76 year old female. Had afib for around 20 years. 10 years I didn’t know ….this is what rhythm guy said. The past six I have been in permanent. Two conversionsno ablations. I have always felt pretty good…no breathing problems nothing. Been on eliquis and metoprilol for six  Years. Then I came down with PMR which is a form of inflammatory arthritis. Took prednisone very short time then nothing. Worst symptoms are leg weakness and fatigue…….just like a stroke. About five months ago I was pulling out of a business in my hometown. Some roads converge and one is a one way. I got confused and went in the wrong way. Knew instantly what I had done  and got turned around. Was worried a little but figured it was old age. Then on August 6 I drove 90 miles one way to a city for appointment, have driven in this city for decades and was very familiar with this area. When I left an appointment I reminded myself to watch for the north freeway and don’t take south. Somehow got confused again and got on wrong freeway. This is a freeway known for very high speeds and a lot of traffic.at the exact moment I got on had a complete attack if  anterograde amnesia. When I woke up, iwas in downtown area I felt nothing weird except I was extremely worried that I might have caused a wreck. Got turned around and headed home. Three scans and an mri later diagnosed as Tia. They also found old ischemic chronic infarction in right cerebellum. The only thing different in my meds is b12 shots and prescription vit d cause they were a bit low. One doctor thinks my extreme driving anxiety pushed me over edge. Another thought the fact that I took my meds right before I got on freeway had something to do with it. After this too long story , do I just sit and wait ! I know I will never drive in a city or on freeway again. It doesn’t matter if it was TGA or epilepsy or a  stroke….it was the most terrifying feeling I have  ever had.<br />
<br />
I reported it to the state police because I was so afraid I had caused problems. Anything I shoukd be doing since my pcp didn’t have anything further to add. Thank you if you got this far]]></description>
            <dc:creator>Erin</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 03 Oct 2026 15:42:43 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201913,201913#msg-201913</guid>
            <title>AFib in Endurance Athletes: New Heart Science + Strength Training Best Practices (1 reply)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201913,201913#msg-201913</link>
            <description><![CDATA[ Such a complicated topic, but I found this very interesting - not only for athletes.<br />
<br />
[<a href="https://www.youtube.com/watch?v=vxMhgF6QIrM"  rel="nofollow">www.youtube.com</a>]]]></description>
            <dc:creator>AJR3</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 17 Sep 2026 22:08:08 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201902,201902#msg-201902</guid>
            <title>Back on Flecainide? (10 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201902,201902#msg-201902</link>
            <description><![CDATA[ Hey guys,<br />
<br />
It&#039;s been a little over 5 months since my ablation and I have been off of Flecainide for about 2 weeks but I have noticed a dramatic increase in ectopic beats again.  Has this happened to any of you?  Instead of stopping Flecainide abruptly, which they said i could do, I decided to taper off of it instead for 4 weeks before finally stopping it altogether 2 weeks ago.  My cardiologist said I could start back on it and suggested cutting the 150mg dose in half since I had mentioned I had plenty 150mg tablets leftover.  I was really hoping to be done with Flecainide for a while at least.<br />
What I don&#039;t like is, is I get more ectopic beats during exercise so we&#039;ll see what my cardiologist wants to do.<br />
<br />
Eric]]></description>
            <dc:creator>EricY</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 25 Oct 2026 11:55:38 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201893,201893#msg-201893</guid>
            <title>AF ablation relationship to Pulmonary Hypertension tradeoff experience (5 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201893,201893#msg-201893</link>
            <description><![CDATA[ I have been on this forum for quite some time. Diagnosed with AFIB at age 30, now 77. Over the years I have experienced every treatment option. Had a Wolf procedure back in 2007 with LAA closure- which is still closed to this day. 2 &quot;touch up&quot; ablations over the years the last in May of 2025. <br />
<br />
After a recent routine ECHO, my Cardiologist told me I had mild PH. Since I have no symptoms, I was surprised.  That started a cascade of testing to determine why and level. I won&#039;t go into detail about all the tests. After consulting a top specialist in Interventional Cardiology and Pulmonologist at the Pulmonary Hypertension center (I finally consented to a RH/LH cath) it was determined that the mild PH is a result of the multiple ablations and scarring. My pulmonary functions were normal, heart function normal, no stenosis etc; I walk about 3 miles a day and strength training once a week. If it was significant issue, I could not do what I do, was the feedback.<br />
<br />
The cardiologist who did the testing told me, for some, having ablations that keep you in rhythm and improve QOL can be a tradeoff for asymptomatic PH. Which would you rather have had? -  a lifetime of AFIB or a mild case of PH with no symptoms if the AFIB ablations were not performed. No further medical intervention required at this time, other than keeping an eye on it.   <br />
<br />
For me, my decisions over all these years is a no brainer. Still a mystery why so young having this. The EP I last saw told me you will drive yourself crazy trying to determine why, you made it this far - a testament to your advocacy and care.   <br />
<br />
My two cents.]]></description>
            <dc:creator>sldabrowski</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 15 Sep 2026 17:03:09 +0000</pubDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201891,201891#msg-201891</guid>
            <title>Does AF Ablations work? Outcome of Sham PVI study (2 replies)</title>
            <link>https://www.afibbers.org/forum/read.php?9,201891,201891#msg-201891</link>
            <description><![CDATA[ Presented at European Society of Cardiology Congress<br />
<br />
<br />
[<a href="https://www.medscape.com/viewarticle/does-af-ablation-work-s-question-after-sham-pvi-af-2026a1000uli?ecd=wnl_conf_cardio_ESC_NON-SPON_260913_mscpedit_etid8679267&amp;uac=323219MR&amp;impID=8679267"  rel="nofollow">www.medscape.com</a>]]]></description>
            <dc:creator>sldabrowski</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 13 Sep 2026 16:59:00 +0000</pubDate>
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