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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>Fri, 12 Jun 2026 01:38:31 +0000</lastBuildDate>
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        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201537#msg-201537</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201537#msg-201537</link>
            <description><![CDATA[ Gloaming: <i>So, it seems that about 50% are going to make it out to the five-year mark, give-or-take.</i><br />
<br />
<br />
Let&#039;s just make it simple and stick to the five-year mark, which you initially brought up.<br />
<br />
Again, According to Winkle et al. 2023 &quot;Very Long-Term....&quot; nearly 68% of PAF patients remained AF free, five years after a single ablation. And the stats are even better in younger patients with fewer comobidities.<br />
<br />
So that&#039;s quite different from the impression one gets from anecdotals on the various heatlh forums.<br />
<br />
Also, keep in mind, AF ablation studies use an extremely high bar for success, per your first link. In many trials a single episode lasting 30 seconds counts as a recurrence. Ok for research maybe, but in the real world, most of us would consider years of normal rhythm, with only a brief or even a not so brief occasional episode a successful outcome. <br />
<br />
For example, I had a 3-hour AF episode, six months after my ablation, but AF free for the last 2 1/2 years. So if I were in one of those studies,<br />
I would not have made it to the &quot;five-year mark&quot;  but is that even relevant? Both myself and my EP consider my ablation a big success.<br />
<br />
So if you add my experience and many others like me, the stats start becoming even more favorable for ablation.<br />
<br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 11 Jun 2026 21:31:11 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201536,201536#msg-201536</guid>
            <title>Ablation scheduled</title>
            <link>https://www.afibbers.org/forum/read.php?9,201536,201536#msg-201536</link>
            <description><![CDATA[ I saw my EP today. He went through the options I have including staying on Multaq, trying tikosyn while being hospitalized for three days, or an ablation. I’m ready to be done with as many drugs as possible and not being blindsided by episodes randomly. It’s not always my thyroid. We scheduled a PFA for October. He will do an ablation for afib and look for flutter and ablate it. I assume he will try to induce flutter? The procedure description says: Afib/atypical flutter ablations. I remember him saying he will look at the areas of my previous ablation to see if it has reconnected. He even said I may be able to go off Eliquis if I’m afib free after one year. But his notes say CHADS score 3 so I’m not so sure I would want to stop it.<br />
<br />
Because I was having severe muscle cramps and spasms on 40 mg. atorvastatin he prescribed Crestor 5 mg. There doesn’t seem to be any follow up on my coronary artery disease. I told him I stopped aspirin after about seven weeks due to spitting blood. His notes say bleeding gums. We can’t actually know that. He also apologized for my portal messages being ignored. I mentioned I sent two KardiaMobile strips the nurse requested but nobody acknowledged them. He seemed surprised and said from now on message him not the NP. My NP was working at the hospital that week and never got my messages. He looked at them today and said flutter. <br />
<br />
I had thyroid labs yesterday in preparation for my appointment next week with my endocrinologist. Normal. They have been normal for about seven months now. TSH went down a lot compared to last labs in March but was still normal. Of course my doctor made a note on the results that we will discuss at my appointment. Usually he puts “good values.” When I researched what the drop might mean it said it’s possible I’m going hyperthyroid and may need to increase methimazole. I’m still taking 5 mg. daily and have been for about a year.<br />
<br />
Pam]]></description>
            <dc:creator>PamelaJean</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 11 Jun 2026 20:53:18 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201535#msg-201535</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201535#msg-201535</link>
            <description><![CDATA[ Good point, Jim.  However:<br />
<br />
[<a href="https://scienceinsights.org/afib-ablation-success-rates-what-the-data-shows/"  rel="nofollow">scienceinsights.org</a>]<br />
<br />
[<a href="https://www.jacc.org/doi/10.1016/j.jacadv.2024.101200"  rel="nofollow">www.jacc.org</a>]<br />
<br />
<br />
So, it seems that about 50% are going to make it out to the five-year mark, give-or-take.<br />
<br />
This is a very interesting article including data on AI-assisted CA:<br />
<br />
[<a href="https://globalrph.com/2025/03/heart-ablation-success-rate-new-study-shows-87-long-term-freedom-from-af/"  rel="nofollow">globalrph.com</a>]]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 11 Jun 2026 15:48:09 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201534#msg-201534</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201534#msg-201534</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>mjamesone</strong><br />
That&#039;s because health forums are subject to selection bias. People with unsuccessful ablations are more likely to post. </div></blockquote>
<br />
I&#039;ve been making that point for years. People who get successful ablations just go on with their lives. They don&#039;t post to afib forums. Sure, there are people like me and others here who&#039;ve had successful ablations and remain active, but I can&#039;t recall anyone here who had a successful index ablation and is still active here. Same with other afib forums I&#039;ve participated in.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 11 Jun 2026 03:08:31 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201533#msg-201533</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201533#msg-201533</link>
            <description><![CDATA[ Gloaming: <i>But, regrettably, all the hundreds of posts by different patients on several fora dealing with AF suggest that you&#039;re doing well if you get to five years without a recurrence.</i><br />
<br />
That&#039;s because health forums are subject to selection bias. People with unsuccessful ablations are more likely to post. Conversely, those with successful ablations tend to move on with their lives.  According to Winkle et al. 2023  &quot;Very Long-Term....&quot;  nearly 68% of PAF patients remained AF free, five years after a single ablation. And the stats are even better in younger patients with fewer comobidities. <br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 10 Jun 2026 18:33:36 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201524,201532#msg-201532</guid>
            <title>Re: Iodine &amp; AfIB</title>
            <link>https://www.afibbers.org/forum/read.php?9,201524,201532#msg-201532</link>
            <description><![CDATA[ Very interesting George.<br />
I will take alook at all of it.<br />
Thanks]]></description>
            <dc:creator>TomR</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 10 Jun 2026 18:31:25 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201531#msg-201531</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201531#msg-201531</link>
            <description><![CDATA[ Yes, many have gone on to expire from something other than the AF for which they were ablated years earlier....even ten years.  But, because it is a progressive disorder, it tends to reappear inside of 3 years for the heavy majority of sufferers, and maybe the &#039;average&#039; runs out to about 5 years if you take the standard deviation on either side of the curve.  This is NOT empirical...I&#039;m just imagining what the distribution would look like if presented as a graphic curve and my guess is that one standard deviation left of the mean would be around 3 years-ish, and one standard deviation above the mean would be around 5-7 years............................................................ish.  I would love to see veridical data.<br />
<br />
But, regrettably, all the hundreds of posts by different patients on several fora dealing with AF suggest that you&#039;re doing well if you get to five years without a recurrence.  And do keep yer fingers crossed. (:P)]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 16:51:24 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201524,201530#msg-201530</guid>
            <title>Re: Iodine &amp; AfIB</title>
            <link>https://www.afibbers.org/forum/read.php?9,201524,201530#msg-201530</link>
            <description><![CDATA[ I&#039;ve taken around 50 mg (20 drops)/day of iodine as Lugol&#039;s solution (60% iodide, 40% iodine) for a number of years.  <br />
<br />
There are notes I put together uploaded to this post from 2023: [<a href="https://www.afibbers.org/forum/read.php?9,191885,191892#msg-191892"  rel="nofollow">www.afibbers.org</a>] There is a broken link to Dr. Guy Abraham&#039;s papers.  Here is one that works, through the Internet Archive: [<a href="https://web.archive.org/web/20220127105351/https://www.optimox.com/iodine-research"  rel="nofollow">web.archive.org</a>]<br />
<br />
When I consulted with a person that runs an iodine FB group (and is a retired nurse who had been doing an iodine protocol for 10 ish years), he told me a fair number of people who consulted with him had afib and it did help mitigate their episodes.  I can&#039;t say it has made a difference one way or the other for my afib case.  The most potent afib rhythm med is amiodarone, which has an organic (chemically organic in this case) iodine molecule as its basis.  As most know, it also has potential side effects from long duration use.  My logic was that Lugol&#039;s, which does not have those issues, might have the same benefit. <br />
<br />
One thing is that iodine is a halide in the periodic chart.  It will displace other halides.  The big one is bromine/bromide, which is now ubiquitous in our environment.  Getting it out of your system is good, but needs to be done slowly.  There is a salt loading protocol, developed by a US military doc in WWI for dealing with bromine gas poisoning. It should be done for two weeks prior to consuming high iiodine doses. In my uploaded document, there is a list of suggested companion nutrients that sholud be taken with the iodine.]]></description>
            <dc:creator>GeorgeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 15:31:03 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201529#msg-201529</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201529#msg-201529</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Ken</strong><br />
 Two successful ablations, first good for 13 years, the second for 6 years, but unfortunately, there have been some breakthroughs.  Afib will always come back.</div></blockquote>
<br />
13 years and 6 years sounds amazing, though still discouraging to hear &quot;Afib will always come back&quot;.<br />
<br />
Has anyone had just one ablation and remained AFIB free for decades?:)]]></description>
            <dc:creator>Yuxi</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 13:40:25 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201527#msg-201527</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201527#msg-201527</link>
            <description><![CDATA[ I take Taurine daily along with Magnesium and Potassium. Definitely not a trigger and possibly has helped me avoid afib.  Two successful ablations, first good for 13 years, the second for 6 years, but unfortunately, there have been some breakthroughs.  Afib will always come back.]]></description>
            <dc:creator>Ken</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 12:38:04 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201494,201526#msg-201526</guid>
            <title>Re: AFib/HF/Apnea</title>
            <link>https://www.afibbers.org/forum/read.php?9,201494,201526#msg-201526</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>gloaming</strong><br />
Simple PAP is my tern for, as an example, the RESMED AS11 &#039;Elite&#039; model that will afford the wearer some pressure relief in its settings, but it doesn&#039;t have the variable pressures that a Bi-PAP machine or an ASV has.  Or the AS10 &#039;Curve&#039; models with the more fancy algorithm software loaded.  Mine is just straight full-time pressure because my OSA responds best to that &#039;simple&#039; delivery modulus.</div></blockquote>
<br />
Thanks! I will run that past my sleep doc.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 11:36:17 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201525#msg-201525</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201525#msg-201525</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>susan.d</strong><br />
Have you had a recent cardiac MRI? It provides an accurate EF as long as you are in NSR.</div></blockquote>
<br />
My diagnosis is HFpEF.. so HF with preserved ejection fraction. (about 50% of HFis this type)]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 11:35:20 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201524,201524#msg-201524</guid>
            <title>Iodine &amp; AfIB</title>
            <link>https://www.afibbers.org/forum/read.php?9,201524,201524#msg-201524</link>
            <description><![CDATA[ I found this interesting. Am currently at 15 drops of 2% Lugol&#039;s iodine. <br />
<br />
<br />
Cardiovascular System (from Recent Advances in Iodine Nutrition, Michael Donaldson, PhD, on ResearchGate.net)<br />
<br />
Iodine is critical to the heart and arterial system.  Iodine (as well as omega 3 fats) is<br />
critical to the stabilization of the electrical pulses of the heart.  Lack of iodine is related to<br />
atrial fibrillation.  An iodine-containing drug called amiodarone is used to prevent atrial<br />
and ventrical fibrillation and releases about 9 mg of iodine per day. It is a complex, <br />
toxic drug and is stored in the fatty tissues of the body, but part of its mechanism of<br />
action appears to be the iodine that is being released slowly by the drug. <br />
<br />
Bruce West is a chiropractic doctor who has found iodine to be very helpful in helping <br />
patients with arrhythmia problems.  He says, “The body needs adequate stores of iodine<br />
for the heart to beat smoothly.  After close to a year now of using Iodine Fulfillment<br />
Therapy, I can attest to this fact.  Most of the stubborn cases of cardiac arrhythmias and<br />
atrial fibrillation that we were unable to completely correct with our cardiac protocols<br />
have now been resolved with adequate supplies of iodine added to the protocol.”<br />
(West B. Atrial fibrillation, arrhythmias and iodine. Health Alert. 2006;23(6).)<br />
 <br />
Another article is here: [<a href="https://drsircus.com/iodine/iodine-supplements-and-dosages/"  rel="nofollow">drsircus.com</a>]]]></description>
            <dc:creator>TomR</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 03:11:51 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201523#msg-201523</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201523#msg-201523</link>
            <description><![CDATA[ Hi George. I tried that a few years before ablation, and it actually triggers afib for me.]]></description>
            <dc:creator>Shiny Sleeves</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 09 Jun 2026 01:53:22 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201522#msg-201522</guid>
            <title>Re: 2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201522#msg-201522</link>
            <description><![CDATA[ Have an personal friend who has had afib for over 20 years (never ablated). A few years ago he started getting lots of PVCs.  He started taking 2.5 g/day of taurine in divided doses and the PVC frequency diminished materially.  If I remember correctly, he initially went up to 4 g/day and was able to drop bacik to 2.5.]]></description>
            <dc:creator>GeorgeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 08 Jun 2026 14:52:55 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201521#msg-201521</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201521#msg-201521</link>
            <description><![CDATA[ Have you had a recent cardiac MRI? It provides an accurate EF as long as you are in NSR.]]></description>
            <dc:creator>susan.d</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 08 Jun 2026 03:29:51 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201520,201520#msg-201520</guid>
            <title>2 yrs post ablation and now PVCs and thumps</title>
            <link>https://www.afibbers.org/forum/read.php?9,201520,201520#msg-201520</link>
            <description><![CDATA[ I *think* I&#039;m having PVCs. My new GP says 2 years post ablation is a common time for PVCs to increase. He says it is a time of increased stroke risk. Anyone have anything to say about this? <br />
<br />
I&#039;m wondering what I can do about this and is this a prodromal sign of a returning afib? I&#039;m thinking it&#039;s time for a Holter monitor to see what my burden is. It has a lot to do with my digestion and I think my heart rhythm is closely tied to my hiatal hernia too; famotidine seems to help on occasion. Also this seems to have something to do with my HR slowing down; when my resting HR was high after the ablation, I had a steady rhythm. Now that&#039;s back to my normal 60, I&#039;m experiencing PVCs. My heart rhythm is best when I&#039;m walking or working around the house actively and my HR is up.]]></description>
            <dc:creator>Shiny Sleeves</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 08 Jun 2026 02:50:25 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201519#msg-201519</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201519#msg-201519</link>
            <description><![CDATA[ Thanks all.  Yea I did a lot of research today on open evidence AI.  (my EP NP actually recommended it as doctors us it.)  I put in my other conditions and ... well.. the AV node ablation can get complicated for me.  I know they will try a regular one first.  And my last ones I would deem a success.  Tomorrow we discuss meds, ablations etc.  Mostly I used AI to gear me with a lot of questions which I also am taking info from here. Thanks again folks.<br />
<br />
I am going to Cleveland for HFpEF (preserved ejection fraction) in August. I don&#039;t want to wait until then for an ablation if I can help it.  And you can&#039;t get into an EP at Cleveland until another cardioglost recommends you. I may be able to have my functional cardioglost take a stab at that appointment.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 08 Jun 2026 02:22:24 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201518#msg-201518</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201518#msg-201518</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>GeorgeN</strong><br />
susan.d had one.  Here is a search on her posts on the topic [<a href="https://www.afibbers.org/forum/search.php?9,search=node+ablation,author=susan.d,page=1,match_type=ALL,match_dates=0,match_forum=ALL,match_threads=0"  rel="nofollow">www.afibbers.org</a>]</div></blockquote>
<br />
It’s saved my life. No more tachycardia flutters<br />
<br />
It’s the last resort. Make sure you exhausted all other options. I wouldn’t worry about pacing induced cardiomyopathy. You can always get a third lead (2 V, 1 atrium) new pacemaker. I just keep an eye on my EF. I used to go to the ER 26 days of a month and hospitalized while they failed to convert me. Now I have a steady 70hr. My battery will last 5 more years.<br />
<br />
Yes you will feel your afib but it’s now not as dangerous because your ventricles are controlled. In fact, you can get pacemaker boost therapy programmed and for me my PM converts 25-27% of my afib/VT/AT.<br />
<br />
It’s a permanent nuke ablation. Make sure you ran out of options before having it done.]]></description>
            <dc:creator>susan.d</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Mon, 08 Jun 2026 01:05:56 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201517#msg-201517</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201517#msg-201517</link>
            <description><![CDATA[ My understandiung is that AV node ablation disconnects the atria signals from the ventricles.  Hence the ventricles are not subect to the potential high rates and irregular beats that the atria in fibrillation can present.  It does not stop the atria from fibrillating or fluttering, or any stroke risk that goes with the fib or flutter.  You are then pretty dependent on a pacemaker.   Susan has experienced issues with side effects from atrial rhythms subsequent to her AV node ablation.]]></description>
            <dc:creator>GeorgeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 07 Jun 2026 23:34:12 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201516#msg-201516</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201516#msg-201516</link>
            <description><![CDATA[ Was AV Node ablation recommended and why? Because it not, it seems like you jumping too far ahead after only one failed AF ablation. It often takes more than one ablation to get it right. <br />
<br />
Without knowing your EP, hard to comment, but I&#039;m a big fan of second and perhaps even more opinions (I had five) especially in hard to treat cases, which your cardiologist&#039;s inferred. And ideally they should be at a top ten or top 15 cardiac hospital that does high-volume ablations. Those centers see more, know more, and have better results. <br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 07 Jun 2026 21:57:48 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201502,201515#msg-201515</guid>
            <title>Re: Edema</title>
            <link>https://www.afibbers.org/forum/read.php?9,201502,201515#msg-201515</link>
            <description><![CDATA[ Thanks, Carey!]]></description>
            <dc:creator>allofus</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 07 Jun 2026 12:14:23 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201494,201514#msg-201514</guid>
            <title>Re: AFib/HF/Apnea</title>
            <link>https://www.afibbers.org/forum/read.php?9,201494,201514#msg-201514</link>
            <description><![CDATA[ Simple PAP is my tern for, as an example, the RESMED AS11 &#039;Elite&#039; model that will afford the wearer some pressure relief in its settings, but it doesn&#039;t have the variable pressures that a Bi-PAP machine or an ASV has.  Or the AS10 &#039;Curve&#039; models with the more fancy algorithm software loaded.  Mine is just straight full-time pressure because my OSA responds best to that &#039;simple&#039; delivery modulus.]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 06 Jun 2026 22:15:38 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201513#msg-201513</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201513#msg-201513</link>
            <description><![CDATA[ Have not had one, but I have read many posts by those who had little other recourse over seemingly intractable rhythm problems of one kind or another.  They invariably come back and report that they have their lives back and are grateful.<br />
<br />
One buzzing fly in the ointment, though: an AV node nuke and ICD/pacemaker installation doesn&#039;t guarantee a correction to all AF cases.  Sometimes it works, and you would be a fully grateful and relaxed wearer of a pacemaker.  For others, the AF continues, but at least they don&#039;t also have RVR and so many symptoms.]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 06 Jun 2026 22:11:43 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201512#msg-201512</guid>
            <title>Re: Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201512#msg-201512</link>
            <description><![CDATA[ susan.d had one.  Here is a search on her posts on the topic [<a href="https://www.afibbers.org/forum/search.php?9,search=node+ablation,author=susan.d,page=1,match_type=ALL,match_dates=0,match_forum=ALL,match_threads=0"  rel="nofollow">www.afibbers.org</a>]]]></description>
            <dc:creator>GeorgeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 06 Jun 2026 13:55:37 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201511,201511#msg-201511</guid>
            <title>Av-node ablation</title>
            <link>https://www.afibbers.org/forum/read.php?9,201511,201511#msg-201511</link>
            <description><![CDATA[ Yes I know this is a big deal.  I am wondering who has had them.. what they have experienced.  I have a long cardiac history.  And afib wise I have had 2 ablations. First one for afib and then a few months later for flutter. That was 4 years ago. Was doing well until life got really difficult this year.  Flutter and fib and cardioverison but I&#039;m in and out and signed up for an ablation.  My 3 cardiologists (including an EP) say the flutter is EZ but the fib is not.  But what about AV-Node? I know the atria part of the heart will still be fibbing away.  Im not sure what the means for heart failure ??  I know fib isn&#039;t great for it... and also thinking continual ablations isn&#039;t great for the heart failure either (HFpEF... preserved ejection fraction).  I was a pest and I have an appointment on Monday with the NP in the EP group to discuss all this. I was also told that an AV node ablation isn&#039;t the easiest given my anatomy.  I know only the docs can really chime in on this for me but wondering peoples experience.  I realize I would be pace maker dependent for life (I&#039;m just shy of 60).  But in my reading this might really help if we can&#039;t get the fib under control.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 06 Jun 2026 03:22:35 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201502,201510#msg-201510</guid>
            <title>Re: Edema</title>
            <link>https://www.afibbers.org/forum/read.php?9,201502,201510#msg-201510</link>
            <description><![CDATA[ It doesn&#039;t always require surgery, but vascular surgeons are the ones who diagnose and treat the condition. You should follow-up on that referral.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 06 Jun 2026 02:36:34 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201502,201509#msg-201509</guid>
            <title>Re: Edema</title>
            <link>https://www.afibbers.org/forum/read.php?9,201502,201509#msg-201509</link>
            <description><![CDATA[ One doctor did refer me to a vascular surgeon, guess I need to learn more about this.  This really requires surgery?!  <br />
Does vascular surgery stop this from happening in the future?]]></description>
            <dc:creator>allofus</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 05 Jun 2026 23:51:07 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201502,201508#msg-201508</guid>
            <title>Re: Edema</title>
            <link>https://www.afibbers.org/forum/read.php?9,201502,201508#msg-201508</link>
            <description><![CDATA[ Compression stockings will probably help a lot. And don&#039;t get them online. Go to a place that sells real ones that have to be measured to fit you.<br />
<br />
One way to tell if it&#039;s simple edema or if it&#039;s veinous insufficiency is whether the swelling extends to the tops of your feet (where your shoelaces are). If so, it&#039;s edema. If not, it may be peripheral vascular disease and you need to see a vascular surgeon.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 05 Jun 2026 23:15:44 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201502,201507#msg-201507</guid>
            <title>Re: Edema</title>
            <link>https://www.afibbers.org/forum/read.php?9,201502,201507#msg-201507</link>
            <description><![CDATA[ Yes, ankles.]]></description>
            <dc:creator>allofus</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 05 Jun 2026 22:01:52 +0000</pubDate>
        </item>
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