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I feel like i have a big ball of anxiety in my chest, like i cant relax it. Sorry sounds weird but i could probably make myself panic right now if i wanted to. Feels like someone shot adrenaline right into my chest. Its awful. Im not sure what to take for it either. I have klonopin but i dont want to be drowsy tomorrow.

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A good POTS friend of mine told me she walks around a little bit when she get's those and it seems to help me too. Claritin helps me too if it's related to some type of food. I know that sounds silly to suggest Claritin but my MCAD type responses feel better with that.

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I get this too - your description isn't weird. It feels to me like a ball of electricity - anxious energy right in the center of my chest. I hadn't had it in a while - but everyday lately. Other than breathing I haven't figured out what to do. I don't think I'm MCAD, but I am hyperadrenergic, and associate it with my wacky sympathetic NS dancing around and acting up. Doesn't feel good - especially right now when I should be asleep! Hopefully some folks will hop on with suggestions :)

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I get this too when I have a flare up. People with POTS either produce and/or have trouble clearing stress hormones from their body from what I understand. Breathing exercises can help me. Breath w/ diaphragm rather than upper chest; breathe in, hold and exhale, slowly. There is guidance for calming breathing techniques in various places including Dr. Weil's materials--perhaps on-line. Exercise/stretching can help if you are up for it. Also making sure I am well-hydrated.

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Spring brings allergies, and my sons suggested could it be all this new pollen? I wish you the best ~

Bellamia ~

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Under "Itchy Adrenaline Surge." Hate to be a broken record...

If you are having MCAD symptoms, claritin will help with BP issues. It needs to be taken daily. Take careful note of how you react to it. Flushing is one symptom of MCAD. It does NOT have to be present to make a DX. Check out: www.tmsforacure.org to learn more. Click on mastocytosis on the top to learn more about MCAD & other mast cell disorders.

Hugs-

Julie

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Thank you so much Julie!

You have given me SO much awesome advise for awhile now LOL. I just dont know how to bring it up to my doctor because he probably has no clue about it. What specialist deals with this?

Sorry I have been so spacey and all over the place, its just so crazy right now beacuse I am in such a rush to hurry and be better. Freak out mode has commenced LOL.

I do have very bad allergies to grass but I dont really leave the house. I have sinus issues too. Is that pretty common with MCAD? The reason I fear benadryl is because i once took nyquil and had a HORRIBLE reaction. I know they are different class drugs, but any liquid thing that can make me tired makes me panic. (so annoying)

thanks again!

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Dani-

Look on the DINET home page; MCAD is listed as a cause of dysautonomia/POTS. Print that page (which has references to research) and show it to your docs to begin the conversation. A mast cell specialist is the best doctor to see, but there are very few. IF you improve on the MCAD regimen that I have previously described, that will be very telling. MCAD is NOT an allergy problem, it affects every bodily system- especially your autonomic nervous system. I have NO allergies and very low IgE.

During an episode, take a zyrtec or claritin if you are so fearful of benadryl. Any H-1 ought to ease things for you. Once again, check out tmsforacure.org to learn more. Click on mastocytosis for a description of MCAD & other mast cell disorders.

Feel better-

Julie

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