Aprilmarie52 Posted April 13, 2004 Report Share Posted April 13, 2004 I only have POTS, or at least I have only been diagnosed with POTS, but it seems like alot of people on this message board have other problems as well. I am curious to see how many people have "just POTS" and how many have other medical problems as well. Quote Link to comment Share on other sites More sharing options...
MightyMouse Posted April 13, 2004 Report Share Posted April 13, 2004 POTS, NCS, Celiac/Sprue, Ehlers-Danlos III, Asthma, severe medication allergies, gastroparesis & reflux, migraines, ...and I'm probably missing a few on this list because of brain fog. Quote Link to comment Share on other sites More sharing options...
Deb Posted April 13, 2004 Report Share Posted April 13, 2004 I have asthma, rhinitis, and eczema which are all caused by allergies. Along with POTS, I have IBS which was probably caused by the POTS. Quote Link to comment Share on other sites More sharing options...
Sue Posted April 13, 2004 Report Share Posted April 13, 2004 Hi AprilI have noticed that too. I have NCS. I am wondering does POTS cause all of these other problems??? Or has POTS been the results of everything else?? Quote Link to comment Share on other sites More sharing options...
MomtoGiuliana Posted April 13, 2004 Report Share Posted April 13, 2004 I have Hashimoto's thyroiditis and POTS Quote Link to comment Share on other sites More sharing options...
MightyMouse Posted April 13, 2004 Report Share Posted April 13, 2004 Certain things are known to be a result of autnomic dysfunction, such as GI motility & bladder function. With others, the relationship is not clear, such as with asthma and allergies.In my case, it's likely that having Ehlers-Danlos (collagen is too stretchy) predisposes me to have problems with blood pressure, such as POTS and NCS.In others, POTS may show up after an illness, such as a viral infection. There are still too many unknowns with regard to how one ends up with this constellation of symptoms, but there is quite a bit of research going on at places like NIH, Vanderbilt, etc.Nina Quote Link to comment Share on other sites More sharing options...
aPerfectCircle Posted April 14, 2004 Report Share Posted April 14, 2004 I dont have POTS, I have "dysautonomia" whatever that means I also suffer from migraines. I also have aspergers syndrome which is a sort of autism. they thought my dysautonomia was related to that as one of the major symptoms is sensory confusion and hightened/lowered senses. for instance i can barely smell anything, some foods i cant taste, and some foods overwhelm me. the worst for me is the sense of touch. i cant stand the feeling of things against my skin, even before it was burning....so who knows, maybe i am just crazy Quote Link to comment Share on other sites More sharing options...
Merrill Posted April 14, 2004 Report Share Posted April 14, 2004 I just have plain ol' boring POTS (the non-fainting kind). Allergies too, but that's not related.m Quote Link to comment Share on other sites More sharing options...
Deb Posted April 14, 2004 Report Share Posted April 14, 2004 I can't help but think that someday someone will find a correlation between people with allergies and people who contract dysautonomia. I have all sorts of allergies and am super-sensitive to so many things that it just seems to me that getting POTS is somehow related to my over reactions to things. Perhaps in time we'll find out. Quote Link to comment Share on other sites More sharing options...
DawnA Posted April 15, 2004 Report Share Posted April 15, 2004 These are the diagnosis that I have received in the past two years since the diagnosis of dysautonomia. I beleive I have had POTs for a long time. My symptoms became debilitating two years ago. POTS, small fiber neuropathy, OH, mild cervical stenosis, asthma, gastroparesis, GERD, asthma, ataxia, depression and as of today myopathy. They suspect a possible mitochondrial myopathy.I also have allergies. I have always wondered if allergies and autoimmune diseases were connected!Dawn Quote Link to comment Share on other sites More sharing options...
Reputta Posted April 16, 2004 Report Share Posted April 16, 2004 I have just been diagnosed with POTS 3 months ago. Two years I was diagnosed with Graves disease (overactive thyroid) and received radioactive iodine to destroy my thyroid. Thats when the POTS symtoms came along. They were off and on till about 9 months ago and then they decided to stay. I can't help but think there is some link there. Hope to find out soon. Quote Link to comment Share on other sites More sharing options...
danelle Posted April 16, 2004 Report Share Posted April 16, 2004 I'm not really sure. I just recently got the dx of POTS and I go see Dr Grubb in a few weeks. I'm hoping he will have lots of input on exactly what is going on with me!!Danelle Quote Link to comment Share on other sites More sharing options...
denabob Posted April 19, 2004 Report Share Posted April 19, 2004 POTS & NCS with yeah... you guessed it! ALLERGIES! I'm super- sensitive to all drugs and most perfumes ...can't use any soap except ivory or dove and cant get in the same room with a cat or even where it use to be!Migraines-which I believe are a symptom of POTSa "Mild mood disorder" which also I feel is as a result of POTSProbably more but brain fog presumes! Quote Link to comment Share on other sites More sharing options...
Sak Posted April 19, 2004 Report Share Posted April 19, 2004 My diagnosis is orthostatic tachycardia; it's never been investigated, but I strongly suspect mine is what's called "partial dysautonomia," caused by lack of venous constriction; my system tries to right this by flooding me with noradrenaline. This would explain a number of things, esp. why opiates floor me and stimulants help.I'm also bipolar; unrealted, but the two conditions together have not made for an easy time over the last decade. Quote Link to comment Share on other sites More sharing options...
Louby Posted April 19, 2004 Report Share Posted April 19, 2004 i've ticked the not sure box, as i am due to find out this week if i have EDS, as well as POTS. Quote Link to comment Share on other sites More sharing options...
Brwneyedchica Posted March 23, 2005 Report Share Posted March 23, 2005 As far as I am aware, I just have POTS (but that's enough for me) Quote Link to comment Share on other sites More sharing options...
LindaJoy Posted March 23, 2005 Report Share Posted March 23, 2005 Hi. I also have a lot of allergies and low tolerances to drugs and chemicals. (I was diagnosed with POTS ten years ago, but have an appointment in April to test for whatever else I may have along with it. Hopefully, that's it.) I didn't the allergies and insensitivities that strange since I read the article, "Postural Orthostatic Tachycarida Syndrome: Patient's Report on Causes, Symptoms and Treatment," found at http://home.att.net/~potsweb/POTS.htmlHow many of you have read this? I think it's good. It gives a great deal of information. In it, the author, Christopher Calder, who suffers with POTS himself, talks about many POTS patients having "common allergies, uncommon food allergies and are highly drug and chemical sensitive." Further along he writes, "Patients with a history of bad drug reactions should be doubly cautious when considering drug therapy."If you've read his article, what have you thought of it? If you haven't, it might be worth your while to peruse it. It helped to ease my mind a little about all the weird stuff I experience with POTS. Let me know what you think.LindaJoy Quote Link to comment Share on other sites More sharing options...
lalalisa Posted March 24, 2005 Report Share Posted March 24, 2005 Hello!I have POTS but recently my neurologist said that he thinks my fatigue is caused by CFS. (I could have just POTS and this causes the fatigue or I have POTS and CFS....who knows!)Oh, allergies for me too! Interesting stuff!Lisa Quote Link to comment Share on other sites More sharing options...
worththewords Posted March 26, 2005 Report Share Posted March 26, 2005 POTS, thyroid problem (I had a toxic thyroid nodule destroyed by radiation treatment - i now take thyroid replacement medication), Polycycstic Ovarian Syndrome (PCOS), Insulin resistance (goes along with the PCOS), Asthma, enviromental allergies, allergic to beta blockers , and I tend to have opposite reactions to medication. That covers it and that's more than I'd like to have. Quote Link to comment Share on other sites More sharing options...
Ernie Posted March 26, 2005 Report Share Posted March 26, 2005 Hi,I also have IBS, low blood sugar, many food allergies, and regular allergies, migraines, tinnitus, etc.Ernie Quote Link to comment Share on other sites More sharing options...
morgan617 Posted March 26, 2005 Report Share Posted March 26, 2005 I have meneires, inflammatory bowel, cfids, fibro, non fainting pots, arthritis, barrett's esophagus, osteoporosis, you name it. morgan Quote Link to comment Share on other sites More sharing options...
brethor9 Posted February 19, 2012 Report Share Posted February 19, 2012 I have been diagnosed with POTS/ severe Orthostatic Intolerance, moderate Dysautonomia, beta hyperadrenergic sensitivity, Hypovolemia, Raynauds Syndrome, Chronic Migraine Syndrome, IBS, severe allergies and now suspected MCAD/ Mast Cell involvement, suspected Chronic Fatigue ( but who wouldnt have fatigue with this list Bren Quote Link to comment Share on other sites More sharing options...
lillybits Posted February 20, 2012 Report Share Posted February 20, 2012 lots more han just pots also. ........suspected mast cell also..... Quote Link to comment Share on other sites More sharing options...
TCP Posted February 20, 2012 Report Share Posted February 20, 2012 POTS, ME/CFS and Autonomic Neuropathy. Quote Link to comment Share on other sites More sharing options...
TCP Posted February 20, 2012 Report Share Posted February 20, 2012 It seems that POTS and ME/CFS have blurry boundaries, as do Fibromyalgia and ME/CFS. The involvement of the nervous system can incorporate many conditions or they may be one and the same. Quote Link to comment Share on other sites More sharing options...
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