Dysautonomia anyone got this ?

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hey im new i have dysautonomia mast cell and me/cfs and whole lot other stuff i will be trying new drug end march when i see my new doctor fludrocortisone it called i have not agreed to alot other meds ended up in hostpital so really nervous but excitected at same time for it to give me a lil or lot my life bk as im only 28 two kids and husband i house bound cant do alot i walk arou d house my heartrate goes up in the 100/150s so ovs i need somthing i use .wheelchair outside the house for appointments etc any advice be helpful hope tday is good pain day for u all

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    I have been diagnosed with dysautonomia also. It just means my autonomic nervous system acts wacky sometimes, particularly under stress or in a food or chemical reaction. I checked my food and chemical allergies and found I had many. When I follow my safer allergy diet and stay away from massive chemicals, I am fine. I take atropine when I have to have a surgery, because it stabilizes the nervous system. (Soldiers use this on the battlefield if exposed to chemical warfare agents) I took it for awhile regularly, and found I only needed it when under duress mentioned above. Good luck finding your answers! You are not alone!

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