Just a quick note to say hi! I too was diagnosed with MTHFR. My medical history is extensive. I would like to speak with you if thats ok.
Popping in to say hello! Hope this note finds you well! - shell
LOL that should have read "dysauto community!"
Just a quick note to say hi! Welcome to the dysauto mommunity. Feel free to ask any questions. I was diagnosed with POTS in November 2008 (with fainting - "vasovagal syncope").
Welcome to the Dysautonomia community! :)
Welcome to our community!Just dropping by to say "Hello" and welcome you to the Heart Rhythm Community! We are glad that you have joined us and trust that the benefits, of sharing your experiences as well as finding answers to your questions , will meet your expectations. If I can assist you in any way please don't hesitate to ask. :)
~Adrienne (Co-Community Leader)
Just a quick note to say hi! You are very welcome. It's a tough spot to be in. I know there was nothing controlling my insides.. Had to stay away from anything that stimulated me, coffee, loud convo's etc., it was the only think that helped me through my symptoms. Took about 3-4 mnths for it to simmer. Like you, it's not that you get worked up and you have probs., it's the other way around. And, since you cannot control them, you get more tweaked. Hang in there best you can. All you can do is pace your every day. Was so hard for me as I was use to going full speed ahead w/out a thought. Glad you found us, thank god for everyone on this forum. ttys, Shell
Welcome, I have never spoken to you befor.
I just read your post about how your husband has become unsupportive. Mine has also. I am in the same boat as you. I was dx in June with Complex migraines but certain that is not all that is wrong with me. I have a brother that has MS and a Husband that only hears what he wants. He heard complex migraines and he no longer wants to search for answers. I am in constent pain. muscle spasms, pins and needles you name it. If you ever need any support I am here.
Right now I have not posted as much as I had on the forum due to being so confused as to what I am going through, but I am always willing to give supportive encouragement. Which we all know we can never have to much of.
This isn't as bad as a kidney stone, but it is bad enough. Stay in touch.
You're in my thoughts especially today. Just wondering how your appointment went this morning or if you are even home yet or did you have to go to hospital for testing or what? I am hoping you made out well and found out what this crazy thing is and you will be able to easily deal with it! I will be waiting for your reply my dear!
Lots of Hugs,
I am glad that you are taking Quix very seriously...she doesn't fool around and has literally saved the life of one very dear member not long ago with her advice. Please let us know what the dr. has to say tomorrow ok?
crswin...PLEASE READ THE POST FROM QUIX IN THE MS FORUM! You need to be seen by a physician immediately regarding your fast heart rate! Quix is a retired physician and when she is firm about something she is for a reason and she says you need to be seen right away...Please do so a.s.a.p.!