Jump to content

StandUpSitDown

Members
  • Posts

    42
  • Joined

  • Last visited

Everything posted by StandUpSitDown

  1. Hi - I have moderate anhidrosis with my AAG. When it comes my turn, I plan to get a covid vaccine - but I admit to being worried about the second shot - where some get fevers. I haven’t had an illness with a fever in years. What happens when you get a bug and get a fever, but have some trouble sweating? I am suddenly rather nervous about this, and I don’t know if I even should be nervous. I know I can talk to my doctor but I was wondering if any in the group had a thought. thanks!
  2. I've been diagnosed with POTS since 2005, which was better diagnosed as AAG in 2011. I am lucky. I have an extremely supportive wife, a job that I can do leaningback with feet up, etc. I have learned to live with the difficulties just like most of you. Yesterday, my wife drove us an hour to a planetarium show. My symptoms decided to flare up just as we got there. As I said, I have an amazing wife. But I don't think I've been this blue about my condition in years. Amazing how I can work through day after day of limitations, and it's something absolutely trivial that gets me down.
  3. So the past four years (but last year), my wife and I have visited Disneyland once a year as sort of a break from everything. It's a 6 hour drive from our house, she does the driving. I rent a scooter when there, and the past three times it's been wonderful. I go about on the scooter, from place to place in the two parks here. In the summer of 2011, I even took it down the street to the Anaheim convention center (almost a mile from our hotel), to go to see a day of a Disney fan conference there. I loved how the scooter made me feel so very mobile. It was GREAT. This time the scooter is making me nauseous as heck. Since visiting last time, my doctor changed my beta blocker to one that is far more effective for me (from propranolol to Nadolol), so I don't know if that's causing it. But I am feeling VERY defeated. The scooter was this way I could feel 'somewhat normal' because I could walk with my wife to various rides - I couldn't ride the swoopy/faster ones, but I could go with her out in the parks. Now I can't even just mosey along the parks enjoying the festive atmosphere in the people. I started with POTS in 2005; in 2008 (December) I was able to return to visit, and that was SUCH A SUCCESS for us. We both felt really good about it. Discovered last fall that I have the autoimmune one (titer of AchR-G of 0.08-0.2, fluctuating). Now I feel like this little joy we had found after years of trying to taken away again. I know, I know - we're lucky we can go here at all, and I have an amazingly supportive wife. But I felt so dejected that when she stayed down in the hotel lobby to visit a shop, I just went to the room, and for the first time in a long time, just plain cried. I am so so so very sick of this. Sorry for complaining.
  4. Let me turn the tables a bit, as a guy with POTS. If your husband were as sick as you are - think deeply about this for a bit - how do you think you'd be dealing with it? If he were unable to work; if he needed help with so much. Imagine if you were a guy - and you talk about the lack of sex drive. Imagine being that tired, nauseated and dizzy, and being a guy. I am lucky. I work in a field (computer programming) where I can work from home most days, and do so with my feet up, so I earn an income without much physical exertion at all. Again, I am very lucky. My wife is wonderfully supportive. But she has admitted to me it was easier for her to do this because she still sees me as a provider. Psychologically, that's easier for her. The truth is, we sign up for sickness and health. And my wife honors that. But it sure as heck isn't easy for them, and so I try my best to cut my wife tons and tons of slack. She signed up for life; we made our vows. But nobody expects or wants this. It's hard - not easy. So I take her bad days in stride.
  5. One thing I want to clear up, as I didn't check this thread after I made my post a few weeks ago. The Zio Patch from iRythm *does* record every heart beat. The report it gives also shows 'detected event's from their computer analysis of the recording. But it will also pay special attention to the times you push that EVENT button. But it is indeed a RHYTHM monitor - it shows when beats occur - it doesn't show anything more than that, and it cannot produce the kind of charts a multi-lead holter can.
  6. Tinks - this is entirely a guess: Perhaps the counting backward in increments of 7 is asking you to do something that's not easy, and requires mental concentration. If you are in a fog, or distracted by symptoms, that otherwise aren't significant enough to show up on their monitors, perhaps doing this helps show them stuff. Again, I don't know. If someone is 'good at these kind of numbers games' it may be that they can do this easily no matter what, even if stressed by POTS, whereas someone who has struggled with such number work in their head may find the slightest thing - the test environment itself - may make them stumble. Again, this is all a guess.
  7. One suggestion: see if you can find a doctor who is willing to order this test from Mayo Clinic. It's probably not cheap. http://www.mayomedicallaboratories.com/test-catalog/Overview/89904
  8. I'd actually ask WHY the monitor is being used. In my case, I recently was given a 2-week monitor that still allowed me to take quick showers, and was invisible to everyone but my wife (well, for a guy that's easy as we wear full shirts vs. women who wear lots of clothes that expose their upper chests.) It's a size of a large band-aid, and it was called the "zio patch" from iRhythm. The reason I liked the two weeks duration is that it was only on day *5* that the issue that I felt rarely came up, so I was able to push the event button, and record THAT'S IT - and was relieved to find out it was normal. Further, we decided to change my beta blocker half way through the 2-week monitoring period and the doctor loved that - the 2 week monitor was able to show my better response to the new beta blocker, in detail. Overall, for MY purpose - to detect the value of the beta blocker change, and also to see what exactly that rare event was in me, the 2 week monitor was perfect. Your doctor may have different reasons, so this may not be appropriate for you, but could also your doctor may simply be unaware of this new technology. Now this monitor is only two lead - the two ends of the 'band-aid'. If the doctor wants to see details of your heartbeat, that may not be sufficient. But if your doctor wants to largely measure heart rate, then this was a very cool, very useful thing. *edited to fix typo
  9. I've had autonomic issues (purely POTS - so far) since 2005; I am 51. During that time, I have been able to continue working, although during flare-ups, (such as May-September were for me), I have had to get help from my wife driving me pretty much everywhere. I am blessed in that as a software engineer, I can do almost all my work while sitting with a laptop laying in bed, or sitting up in a chair with a hassock, or talking on the phone or video-conferencing with people from work. As a result, even on the worst days I can continue working, I have been able to fulfill a 'provider role' in my marriage - which has meant so much emotionally to me. I credit this success to first, being lucky in choosing a profession where this was possible, and second, working my tail off all my early career to be seen as a really valued employee so I am considered worth my job and salary even with my odd schedule and working conditions. I hope it doesn't come off as sounding quaint and outdated, but when this disease stripped so much from my life, I find being able to cling to this gender-based traditional 'male provider role' has allowed me to retain some dignity with this disease. I look to that as me providing value to my wife, even though we take only local road trips for weekend/week-long getaways (air travel is horrible for me) and I am not often able to go out to dinners being tired in the evening. But we find ways to manage - I'll choose to work on a Saturday so I can have a mid-week day off with her and we go out to eat at a nice place during lunch and tell them to please 'hurry' with the food so we aren't sitting there too long - and the place stays quieter. We go to a local drive-in to see lots of films, so I can be leaning back in the seat, feet up on the dashboard of the car. Similarly, some other aspects of our relationship are impacted as well because of this disorder, and we creatively find ways to address those. Again, I am blessed with an amazing wife. In a very real way my goals in life have really narrowed down to one, focused thing: I will show my wife that while I am not able to do everything I could when we first married, that I am still doing everything I can. If I have a 'good POTS day' we take it. A couple of years ago, I was blessed with a good POTS week - not sure why it happened - but it was as if I didn't even have POTS that week! I drove us everywhere, we went to a beach hotel nearby, walked all about, etc. If I could somehow figure out what happened that week, I would repeat it. The point is - I took advantage of it. I think if we all challenge ourselves to do everything we can possibly do - and be satisfied we put all the effort we had in it - that we can be okay with ourselves. Rather than measure against a 'normal' life - measure yourself against 'did you make the most of what you can do today?' This is how I make my peace with God as well: I realize that it is VERY unlikely this disorder will EVER go away, and for all I know, it will get worse and worse over time. But, none of us get to choose our circumstances. Some are born in America. Some are born in Somalia. Some are born wealthy, some poor. Some have great health, we have rotten health. I think God wants us to show what we do to lead a proper life in the circumstances in which we are placed, and simply asks us to show love and kindness to each other -- and to do what we can.
  10. For me, I am in the VERY ANNOYED phase right now. For six 1/2 years, from 2005 until 2012 (early), I was slowly regaining capability. I was driving my wife 100+ miles in the car, going out to dinners, enjoying a movie. It was a 'quiet' life compared to life-before-POTS, but it had fun in it and looked to be slowly improving. Then, I did too much May of this year (flew to a relative's wedding, outside in 95 degree heat for hours - did great, but the next morning I paid for it with a huge POTS crash into a big setback, so it's like 2007 again. I hope it doesn't take *four years* to get to where I was before! I'm 51. I think we are making great strides in understanding POTS, but I fear they won't be for my generation.
  11. In reference to the person who mentioned you have to "up" the dosage of Propranolol every six months: It's important to remember that POTS has so many root causes, most of which we understand so poorly, that it is impossible to make any general statement about its treatment. For example, I have been on Propranolol since early 2007 - for the first 3 months, it was 20mg a day, now it is 40, and I have remained on that dosage for over two years, with no lessening of effectiveness. I have good days and bad days, but overall, on my typical day, I feel somewhat better after two years on the drug - not worse. So - the rule of thumb with POTS medicine is - "your mileage may vary"
×
×
  • Create New...