<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <channel>
        <title>TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
        <description> Totally confused and soooo anxious.

This morning I had zig zags and distortions  in my eyes and couldn’t read all the letters on my page.  (It was not symptoms of a retinal tear or detachment) ...I had this once before, maybe one year ago.  Both times I assumed  it was an Aural Migraine and in awhile I would get a headache...but not a huge headache. Tonight I feel pretty tired and still have a lingering headache.

So today, my eye visions lasted about ten minutes, also I think it was only in my right eye...but not sure....anyway ....the eye zigzags stopped and I reading a paper out loud and I couldn’t pronounce the word “oriented.”....I reread it about three times and I knew I wasn’t saying it right and then everytime I read the would administration...I would speak the word “mother”.......and I was realizing that I wasn’t really comprehending what I was reading.  After about 15 minutes ...it was all gone....but I was left with an huge panic attack....most of the day.   I had no other signs of stroke, no weakness, tingling, drooping, blindness....BP and pulse and EKG were normal, etc.

I made an appointment with my Internet’s for 8:00 tomorrow.  If I didn’t have Afib I would think this was an Aural Migraine with Asphagia.....but now I am very concerned about stroke.    

Does anyone have any experience with aural migraines with asphagia?  I wonder if they will have to run all sorts of huge tests to determine what’s going on.

Also,  is a TIA a warning of a larger stroke?

Linda</description>
        <link>https://www.afibbers.org/forum/read.php?9,173066,173066#msg-173066</link>
        <lastBuildDate>Mon, 24 Aug 2026 01:19:10 +0000</lastBuildDate>
        <generator>Phorum 5.2.23</generator>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173499#msg-173499</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173499#msg-173499</link>
            <description><![CDATA[ I had ocular migraines before my AFIB diagnosis, but also probably had AFIB then. This is going back 10 years. After my first ablation, the frequency increased dramatically, continuing through a Watchman 18 months ago. Post Watchman they decreased in frequency. 6 months ago when i switched from Eliquis to low dose aspirin, there was a dramatic drop-off in frequency. For me, in hindsight, there appears to be a connection taking Eliquis and frequency of episodes. When on full dose Eliquis I had them most often. I don&#039;t recall with certainty, but during the time I was on full dose Eliquis and before my first ablation, I don&#039;t think I had them any more often. Just after the ablation(s).<br />
<br />
So is it transeptal punctures and Eliquis related? Dunno.]]></description>
            <dc:creator>AB Page</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 22 Feb 2020 13:44:20 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173455#msg-173455</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173455#msg-173455</link>
            <description><![CDATA[ AB Page:<br />
<br />
Do you have a Watchman, and did you get the Aura Migraines after the Watchman was implanted?<br />
<br />
Liz]]></description>
            <dc:creator>Elizabeth</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 20 Feb 2020 20:12:57 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173452#msg-173452</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173452#msg-173452</link>
            <description><![CDATA[ I too have posted about aural migraines, pre and post ablation(s) and Watchman. <br />
<br />
The most surprising situation for me is that last July when I switched from low dose to Eliquis to aspirin, I didn&#039;t have an episode for almost 4 months. And since then only 3.<br />
Prior to that I went through a sort of bell curve frequency - stretches w/o, and then periods where I often had several a week. All lasting about 20 minutes.<br />
<br />
One constant is the apparent trigger of high intensity, tightly focused light sources, many times from the sun glint off of a window or chrome bumper or similar.]]></description>
            <dc:creator>AB Page</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 20 Feb 2020 13:16:55 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173425#msg-173425</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173425#msg-173425</link>
            <description><![CDATA[ I developed Aura Migraines for the 1st time about 4.5 years ago 1 week  after my 1st ablation.  You an go find my old posts.  I still have them to this day usually about 2 per month.  Prior to that I was never even a headache guy and did not know the term Aura.  I thought I was having a stroke on my 1st one and that sent me the the ER.  All these years later, I take an Sumatriptan at 1st sign and just go on best one can.]]></description>
            <dc:creator>Fibrillator</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Tue, 18 Feb 2020 19:25:45 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173326#msg-173326</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173326#msg-173326</link>
            <description><![CDATA[ Thanks Liz<br />
<br />
I have been suffering quite severe dizziness and nausea for some time now, so maybe it&#039;s all part of that. I see my neurologist in a few weeks so will run it all by him again.<br />
<br />
What really frustrates me is that my GP and  Er Dr suggested I may be depressed or anxious and wrote scripts for antidepressants which I declined. <br />
<br />
I said to the Cardio in ER (not my regular guy)  &quot;of course I&#039;m anxious and miserable with a HR of 160+ for 12 hours, and on other days so dizzy and nauseous I can&#039;t walk straight, wouldn&#039;t you be?&quot;<br />
<br />
I&#039;ll do a bit of reading up on the Migraine. I also think my neck may be causing some problems as I have bulging discs and bone spurs which can make me feel as if I&#039;ve had a electric shock if I move my head the wrong way.]]></description>
            <dc:creator>JoyWin</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 14 Feb 2020 12:23:52 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173183#msg-173183</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173183#msg-173183</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Elizabeth</strong><br />
Daisy:<br />
<br />
I have never had an ablation, but, you know I have had a Pace maker installed about 20 years ago and I have had more of these Aura migraines since then.  Could there be a connection or is it because of my AF and family history?<br />
<br />
Liz</div></blockquote>I don&#039;t know. I had a pacemaker implanted a year and a half ago and didn&#039;t get auras, but I did get them with the trans-septal puncture. I have had the very occasional non-migraine auras for about 20 years (before Afib) but I suppose there could be a link between the tendency to get auras and a predisposition to Afib?]]></description>
            <dc:creator>Daisy</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 08 Feb 2020 22:15:16 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173181#msg-173181</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173181#msg-173181</link>
            <description><![CDATA[ Daisy:<br />
<br />
I have never had an ablation, but, you know I have had a Pace maker installed about 20 years ago and I have had more of these Aura migraines since then.  Could there be a connection or is it because of my AF and family history?<br />
<br />
Liz]]></description>
            <dc:creator>Elizabeth</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 08 Feb 2020 21:15:02 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173179#msg-173179</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173179#msg-173179</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Elizabeth</strong><br />
There is also on this site a topic about people having these Auras and also AF, Carey has said that he got it after his ablation and a few others have said that as well.</div></blockquote>It seems that any cardiac procedure that involves a trans-septal puncture (as ablations do) can set you up for auras. I had a mitral valve repair that involved a trans-septal puncture and, sure enough, the auras started the next day. They diminished as the puncture healed though going from about one a day to one every two weeks, to none.]]></description>
            <dc:creator>Daisy</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 08 Feb 2020 20:52:18 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173178#msg-173178</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173178#msg-173178</link>
            <description><![CDATA[ Joy<br />
<br />
I really hate these Aura Migraines, I sometimes hate them worse than AF.  There are all kinds of symptoms that can happen with these Auras, I have read that a numbness sometimes happens in your left arm and face, it is scary.  The numbness has happened to me twice which did scare me as I have gotten these Auras off and on throughout my life, but apparently this can happen and it is due to the Aura Migraine, I have read this when I googled it.  I have since had blood work done plus an echo and everything is good.  So, I try to relax and lie down when I get one plus I take an aspirin which helps.<br />
<br />
My mother and grandmother had these migraines so I guess it is something they passed on to me, it has happened once to my daughter, I hope she will be spared.<br />
<br />
There is also on this site a topic about people having these Auras and also AF, Carey has said that he got it after his ablation and a few others have said that as well.  I will try to find that topic.<br />
<br />
This thread has a lot of info:   Aura Migraines/AFIB<br />
<br />
Liz]]></description>
            <dc:creator>Elizabeth</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 08 Feb 2020 20:19:23 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173172#msg-173172</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173172#msg-173172</link>
            <description><![CDATA[ Hi,<br />
<br />
I have recently experienced a similar event, but mine was slightly different . I get AF 5-6 times a month, HR up to 180, 6-12 hours. I’ve recently been put back on Isoptin and low dose Flecainide and Eliquis.<br />
<br />
I was standing in a queue in the supermarket when I felt a numbness run down the side of my head and face, I felt nauseated and shaken  and  could only stagger to a seat to sit down.<br />
 Taken to hospital by ambulance, WAITED 11 hours and gave up and went home. <br />
<br />
Next day feeling very seedy, went to GP who insisted I go back to ER. Waited another 12 hours....stayed overnight, had a cat scan next day and bloods, physical and neurological tests. <br />
They said not a TIA  (but was outside the window of opportunity for bloods.) diagnosis...migraine or BPV. I’m not impressed but I am concerned.I have been freaking out ever since.]]></description>
            <dc:creator>JoyWin</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 08 Feb 2020 10:19:57 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173117#msg-173117</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173117#msg-173117</link>
            <description><![CDATA[ Linda:<br />
<br />
I have read that during the Aura Migraine you can have a tingling in your arm and even your mouth, I have had that twice in my lifetime, it is also a part of what some people can experience during these attacks.  I know it is scary but just know it does happen.<br />
<br />
Liz]]></description>
            <dc:creator>Elizabeth</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 07 Feb 2020 00:06:16 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173115#msg-173115</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173115#msg-173115</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Elizabeth</strong><br />
IDS 001<br />
<br />
Sounds like an Aura Migraine to me---I get those, I have since my early 20s and I am now 80.  I got only a couple a year until I started getting AF then I might get a couple a month now, I can&#039;t take some supplements as they will give me those Aura Migraines.  Yes, they start with a zigzag flashes of light and depending where it hits you in your eye they can obstruct your vision.  They usually last about 20 min. to a 1/2 hr. and you can have a little headache, during the attack and a little while afterwards sometimes you can be a little out of it like you said.  They are nasty and I hate them but they are not TIAs, they are Aura Migraines.  There is a couple of posts about Aura migraines on this site and some have said that they have gotten them and AF as well.<br />
<br />
Liz</div></blockquote>
<br />
Thanks Liz....yes exactly....except I also had this weird speech thing....and I felt I was out of it.  I did NOT like the feeling.  I would be hard pressed to figure out stroke or TIA.....I probably wouldn’t take any chances. ‘<br />
<br />
Linda]]></description>
            <dc:creator>lds001</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 23:22:30 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173113#msg-173113</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173113#msg-173113</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Carey</strong><br />
Glad to hear that. It probably is just a migraine but better safe than sorry!</div></blockquote>
<br />
<br />
I totally agree...My MRA was normal.....I still have a headache/nausea....ugh.   My Doc said if it should happen again to go to the ER<br />
<br />
Thanks!<br />
<br />
Linda]]></description>
            <dc:creator>lds001</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 23:20:10 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173108#msg-173108</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173108#msg-173108</link>
            <description><![CDATA[ IDS 001<br />
<br />
Sounds like an Aura Migraine to me---I get those, I have since my early 20s and I am now 80.  I got only a couple a year until I started getting AF then I might get a couple a month now, I can&#039;t take some supplements as they will give me those Aura Migraines.  Yes, they start with a zigzag flashes of light and depending where it hits you in your eye they can obstruct your vision.  They usually last about 20 min. to a 1/2 hr. and you can have a little headache, during the attack and a little while afterwards sometimes you can be a little out of it like you said.  They are nasty and I hate them but they are not TIAs, they are Aura Migraines.  There is a couple of posts about Aura migraines on this site and some have said that they have gotten them and AF as well.<br />
<br />
Liz]]></description>
            <dc:creator>Elizabeth</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 20:57:26 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173090#msg-173090</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173090#msg-173090</link>
            <description><![CDATA[ Glad to hear that. It probably is just a migraine but better safe than sorry!]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 16:42:31 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173078#msg-173078</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173078#msg-173078</link>
            <description><![CDATA[ Carey, I saw my doc.....she feels I had a complex migraine...however she is going to have me go and have a stroke protocol MRI......today.  Thanks for your help!]]></description>
            <dc:creator>lds001</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 15:07:30 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173074#msg-173074</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173074#msg-173074</link>
            <description><![CDATA[ Carey,I just saw your email. It’s 8 AM and I am sitting at my internist office. My EP,s office is on the floor above me so one way or another I will make sure I get the appropriate urgent care needed]]></description>
            <dc:creator>lds001</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 14:12:07 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173067#msg-173067</guid>
            <title>Re: TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173067#msg-173067</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>lds001</strong><br />
Also,  is a TIA a warning of a larger stroke?</div></blockquote>
<br />
Yes, Linda, it is, and I think you should seek immediate medical care. A 911 call would be a perfectly reasonable thing to do right now.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 06:04:12 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,173066,173066#msg-173066</guid>
            <title>TIA or Aural Migraine.....Sleepless in the Midwest.....</title>
            <link>https://www.afibbers.org/forum/read.php?9,173066,173066#msg-173066</link>
            <description><![CDATA[ Totally confused and soooo anxious.<br />
<br />
This morning I had zig zags and distortions  in my eyes and couldn’t read all the letters on my page.  (It was not symptoms of a retinal tear or detachment) ...I had this once before, maybe one year ago.  Both times I assumed  it was an Aural Migraine and in awhile I would get a headache...but not a huge headache. Tonight I feel pretty tired and still have a lingering headache.<br />
<br />
So today, my eye visions lasted about ten minutes, also I think it was only in my right eye...but not sure....anyway ....the eye zigzags stopped and I reading a paper out loud and I couldn’t pronounce the word “oriented.”....I reread it about three times and I knew I wasn’t saying it right and then everytime I read the would administration...I would speak the word “mother”.......and I was realizing that I wasn’t really comprehending what I was reading.  After about 15 minutes ...it was all gone....but I was left with an huge panic attack....most of the day.   I had no other signs of stroke, no weakness, tingling, drooping, blindness....BP and pulse and EKG were normal, etc.<br />
<br />
I made an appointment with my Internet’s for 8:00 tomorrow.  If I didn’t have Afib I would think this was an Aural Migraine with Asphagia.....but now I am very concerned about stroke.    <br />
<br />
Does anyone have any experience with aural migraines with asphagia?  I wonder if they will have to run all sorts of huge tests to determine what’s going on.<br />
<br />
Also,  is a TIA a warning of a larger stroke?<br />
<br />
Linda]]></description>
            <dc:creator>lds001</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 06 Feb 2020 05:44:21 +0000</pubDate>
        </item>
    </channel>
</rss>
