Stephanieann Posted September 1, 2016 Report Share Posted September 1, 2016 So to add to my lovely Pots diagnosis, once my Pots symptoms started to crash (which led to my diagnosis) I started to get weird skin sensations. Pin pricks, creepie crawlies, random muscle twitching ( and it just twitches once, not like consistently like fasciculations) in my fingers and thighs. I feel it in legs, feet, hands, ears, face, pretty much all over and it's very random and doesn't happen every day. It's not painful because they are just quick pin pricks but its annoying more than anything. I mentioned it to my dr today and he said to wait and see because he thinks it could resolve. I have been under a huge amount of stress since my pots started so I almost think it's related to that since it's not following the typical neuropathy pattern since I feel it in my face and ears too. But what do I know, lol. I do not have a b12 deficiency. I do have low iron and vitamin d. All my other blood work has been fine. Anyone else with similar symptoms and found a cause? I feel so upset because my Pots is pretty much under control and I feel great but now i have these symptoms to worry over And i'm a great worrier, lol. Quote Link to comment Share on other sites More sharing options...
MomtoGiuliana Posted September 1, 2016 Report Share Posted September 1, 2016 I get these symptoms from time to time. In fact, for probably a good two decades now--sometimes with POTS symptoms sometimes just on its own. I do think it is part of dysautonomia. Quote Link to comment Share on other sites More sharing options...
MomtoGiuliana Posted September 1, 2016 Report Share Posted September 1, 2016 This list includes tingling/numbness as a possible symptom. http://www.dinet.org/index.php/information-resources/pots-place/pots-symptoms Quote Link to comment Share on other sites More sharing options...
Macca Posted September 1, 2016 Report Share Posted September 1, 2016 Hi - the unusual sensations are often seen with people who have POTS and a related Small Fiber Neuropathy (SFN): https://neuropathyjournal.org/small-fiber-neuropathy/ My understanding is that SFN and POTS are part of the same neuropathy issue. There is a number of earlier posts on the Forum about this - please see examples below: Quote Link to comment Share on other sites More sharing options...
Guest Posted September 7, 2016 Report Share Posted September 7, 2016 Hello, I get all of that too. I also get where a muscle will twitch super fast (I call it rapid fire...not sure what it's really called). I think the times when they twitch once are worse though, because they'll make my finger, leg, etc. actually jerk. It drives me nuts. Quote Link to comment Share on other sites More sharing options...
Guest Posted September 7, 2016 Report Share Posted September 7, 2016 I should add too...I also losing some sensation in my hands. I have a hard time telling if water my hands touch is warm or cool, and they are really losing their dexterity. They are kinda numb a lot of the time. I'm on a never ending wait list for a dysautonomia clinic in Canada, but am sure I must have nerve damage (the neurologist checked for carpel tunnel, but it wasn't that). Quote Link to comment Share on other sites More sharing options...
Jessica Posted October 5, 2016 Report Share Posted October 5, 2016 Stephanie - I have all of these neuropathy symptoms too! They can be so disturbing! Quote Link to comment Share on other sites More sharing options...
Bopler Posted October 5, 2016 Report Share Posted October 5, 2016 On 10/5/2016 at 2:06 AM, Jessica said: Stephanie - I have all of these neuropathy symptoms too! They can be so disturbing! Yeah I get this too if I stay in the same position for too long. Quote Link to comment Share on other sites More sharing options...
Jan Posted October 7, 2016 Report Share Posted October 7, 2016 I get the skin prick feeling and the thumping feeling from time to time. In the grand scale of symptoms I worry about, I just ignore them. My doctor tested me for lots of different deficiencies that could cause it, but none showed a cause. Quote Link to comment Share on other sites More sharing options...
Stephanieann Posted October 7, 2016 Author Report Share Posted October 7, 2016 @Jessica they are very disturbing. Mine calmed down a bit but are still there. Ugh. The fear of wondering if and when it will get worse is the worst! Quote Link to comment Share on other sites More sharing options...
haugr Posted October 26, 2016 Report Share Posted October 26, 2016 I have that too. The pins and needles sensation were very intense when my POTS was triggered, but has been minor over the last few weeks. I get it in the bottom of both feet, and then it kind of moves around a bit in my arms and hands, but it seems to be more prominent in my left side. I also occasionally get it in my scalp. Quote Link to comment Share on other sites More sharing options...
Kriss Posted March 19, 2018 Report Share Posted March 19, 2018 I have the same symptoms. Was talking to my grandmother, she was saying that it might be that i have magnesium deficiency. Also went to the doctor, they thought it might be my metabolism or some ****. Im gonna try to workout and take magnesium/c/kalsium supplements. I'll report back if this works. Quote Link to comment Share on other sites More sharing options...
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