Adrenaline spikes: Med detective needed, award given

Posted by sierrawoods @sierrawoods, Feb 20, 2018

I'm desperate for help. If I was rich, I'd pay a million $ to get answers. It's hard to summarize: I am a 59 yr old woman. 8 yrs ago I started having what feels like strong adrenaline rushes during the night and especially in the early morning. They disrupt my sleep making me severely sleep deprived. It used to happen a few times a month but in the last year, has been happening daily. This is not as simple as anxiety. My life is not particularly stressful compared to years ago and I've always handled stress well. Physical symptoms come first, then anxiety from adrenaline comes after. On rare days, If I sleep through the night, I wake with excess adrenaline and will be hyper the whole day and evening. Sometimes, I will have a severe "crash" in the afternoon with all kinds of symptoms that have me couch-bound. I take a tiny dose of Amitriptyline (10 mg) before bed to help with sleep, but it's obviously not working well enough. I am on Synthroid for non-Hashimoto's Hypothyroidism since 1996. Despite being 59 yrs old, I am not yet officially in menopause (last period was May 2017). TSH, fT4, fT3 are normal. Urine catecholamines (epinephrine & norepinephrine) are normal (although that does not necessarily reflect what is in the brain). Plasma ACTH is normal. I've tested negative for autoimmune disorders. Cortisol was high a few years ago (34.3 mcg/dL) but it's currently high-normal. DHEAS normal. Accompanying the start of this was phantosmia and occasional RLS. My diet is excellent, including a few good supplements. Until last yr when it started happening daily, I was exercising 6 days/wk. I cannot tolerate it any more - any exercise beyond mild cardio/aerobic causes an increase in symptoms. I meditate and have tried all kinds of herbal teas. I've experimented with different possible solutions, to no avail. I'm a voracious researcher (only legit sites) and still cannot figure this out. I'm normally a positive, active, happy person who loves to help others but this is ruining my life. I cannot make any plans, cannot get my work done, cannot even visit friends. I had to stop my volunteer work with children. šŸ™ I'm starting to become depressed and hopeless. I've been to a total of about 9 doctors about this problem and they just shrug their shoulders and send me hope with more disappointment. The only help offered was an addictive prescription for benzos but I refuse to be treated for something without knowing the cause. Ideas: an atypical tumor on my pituitary or adrenal glands? Maybe, but I can't get a doctor to order the necessary MRIs. Perhaps not endocrine but a sleep disorder? High A.M. adrenaline is typical for sleep apnea but it should not cause these severe symptoms, and I really do not think I have sleep apnea (I don't have other symptoms). A neurological disorder? Maybe, but I can't get a doctor to order an MRI of my brain to make sure my pituitary gland is okay. If you've gotten through this far and you have any thoughts, please chime in. If your idea leads to a proper diagnosis and I get well (or treated properly) I will be your slave for life šŸ˜‰ Okay, seriously. I'm not in a good place right now.

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@cleacock

This is the graph that shows the levels of severity of hyperstimulation and when cortisol is high and low during the day. Please refer to anxietycentre.com for detailed information. I have no affiliation with them.

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@cleacock Have you ever spoken to someone at the anxiety centre one on one? Do they have specific suggestions for alleviating this problem? Many thanks for your help.

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@neil6

Hello I just read your post and it relates to me totally I'm getting one surge every other day mostly in the morning or during the night. It sometimes prevents me sleeping for hours, or I wake up try to sleep and just as I begin to nod off it flares. It's like my body won't let me sleep as it thinks there's danger. I've been diagnosed with cfs as I was getting energy crashes but they only last one or two days and doesn't relate to half of the CFS criteria as adrenaline will cause same symptoms. ie pots imsonia etc. Also as I have excersise intolerance I thought it was cfs/ me. Not convinced! I'm taking melotonin and somelex but nothing makes me sleep longer or get me through a spike. I'm anxious because of this condition not the other way around. Do you have any advice or updates hacks as my hormone panel came back as normal. kind regards Neil

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You can try extended release melatonin. Or try something stronger like Passion Flower. It acts like s benzo on me. I take a half dose but not every night. It does leave me a bit groggy the next morning and works a bit like a muscle relaxer. I donā€™t like that feeling but it does help me sleep.

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Hi
A little over 2 years ago I began having the symptoms you described. The adrenaline rushes woke me every morning around 4am and the intensity of feelings from this began to grow over the next few hours until I was suicidal. This continued until mid afternoon then began to subside until my mental/emotional settled and I felt normal again, although exhausted. No longer suicidal, not even particularly depressed or anxious. Then Iā€™d go to bed and itā€™d happen all over again. Groundhog Day! I dreaded going to bed but was so tired I had to. Only for the cycle to begin again. 2 months went by and Iā€™d tried all the mindfulness and meditation to calm me, was seeing a psychologist but my body was telling me this was physiological rather than mental/emotional. The anxiety and depression were the result of the physical stuff rather than the other way around. Eventually I heard from someone about MTHFR gene mutations that created similar symptoms so saw a GP who specialised in that and Pyrroles Disorder. She ordered the test for Pyrroles and bloodwork to identify high levels of ā€˜freeā€™ copper based on my history and current symptoms. She said I was textbook for Pyrroles and directed me to online resources to better understand it. Sheā€™d studied the condition at The Walsh Institute founded by Dr William Walsh.
She directed me to have the tests asap then after the tests to begin taking high doses of activated B6, magnesium and zinc. Within a week of taking this I began feeling better. We continued tweaking the supplements and adding some others as the main issue is that I undermethylate and have problems detoxing metals from my system. The excess unusable copper in my body (which has a specific way of testing for it) causes the electrically charged feeling in my body. Iā€™ve realised Iā€™ve recently been consuming lots of nuts and seeds high in copper.
The reason for finding your post is that I googled ā€˜adrenaline rushes in the morningā€™ as Iā€™ve began having them again. However, itā€™s also been months since I took the supplements Iā€™m supposed to. So I basically know why Iā€™m having symptoms again but felt the need to do some research just in case it could be something else. After reading your post I realised itā€™s probably not something else! Iā€™ve also recently been attempting to detox with ā€˜clean eatingā€™. As my body releases toxins I have issues with clearing them from my system without correcting the pathways that are dysfunctional. So Iā€™m getting back on the supplements ASAP and wanted to write about it here in case itā€™s helpful for you. Iā€™m in Australia btw and the conditions I mentioned arenā€™t recognised by the general medical profession here. The Walsh Institute is in the US but several doctors here are getting the training as the markers for these conditions make sense to them. Most of them are inundated with more patients than they can handle who are being treated successfully with the right supplements to correct biochemistry. Itā€™s a very fine balance that needs to be supported by blood tests to confirm whatā€™s working and what isnā€™t. Iā€™d say the first step is looking at the information on the Walsh Institute website then finding a practitioner who can test and treat you. Also find Pyrroles Disorder and/or MTHFR support groups on social media for more information.
Best of luck!

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I experienced severe adrenaline rushes at night due to chemical sensitivity to a sick building. I was not able to work in that building or do my job (molecular biology researcher) and had to take disability retirement. That was above 10 years ago. The rushes subsided after I stopped working, but reoccur in response to anything stressful - too much exercise, travel, etc. I got on this forum to try to figure out how to eliminate them. Question for you: have you had new chemical exposures that coincide with your symptoms?

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@gman007

@sierrawoods, Welcome to the group and I hope someone has the solution to your riddle. When you wake up with this high adrenaline, do you have any other physical symptoms? The reason for the question is that I awake feeling as if everything inside my body is vibrating. Yea, I know that is weird, but I can not find any other way to describe it. The best answer I have found in researching is that I am have a panic attack in my sleep. I have no dreams, or at least any remembrance of them. I do not understand how this is possible, but that is the best answer I have found. It is a bit disconcerting, but not really painful, just strange. If you find your answer, I will be very interested in what you learn. Would someone please try to help Sierra find an answer or point in that direction?

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When I awake from an adrenaline rush, I have all kinds of skin sensations, varying from light vibrating to a feeling of tight skin that almost painful to dramatic ā€œpulsing pricklesā€ that make me think of electricity. Also occasionally a staticky sound in my ears. No sensation of panic though.

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Have you ever studied or practiced desensitizing over a long period of time? I was born with eczema, allergies, and just plain whimpy health and suffered all through my growing up years, and then did the dumb choice of marrying a farmer. I was so desperate and couldn't afford or have the time for trips to the specialist so I did my own thing by gently exposing myself in small doses or amount of time to anything that made me itch, sneeze, cough, or feel bad. No one believed in me and thought perhaps I should divorce, but I was determined to feel better, and with the big garden and well balanced eating I got better in twenty years. In fact my basic health is pretty good despite living with a stressful husband while the marriage was a disaster. But I kept at it, and truly believe that desensitizing myself over the years a little at a time can be an effective cure and can alleviate many chronic problems.
On the other hand, my sister catered to her many "allergies" and died with chronic diseases that she declared were none of her fault. She also blamed the doctors, six of them, when her visits did not result in a fast cure. This is a worst case scenario, but I certainly know what it feels like to itch all over. I only had one panic attack and with the advice of my paramedic son and his friend, taught myself to not do that again without the aid of a psychiatrist. If we are born with sensitive bodies it can be a lifetime of effort to control or eliminate the exposures and to get sensitized to some exposure. Yes, I avoid poison ivy!

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@dorisena

Have you ever studied or practiced desensitizing over a long period of time? I was born with eczema, allergies, and just plain whimpy health and suffered all through my growing up years, and then did the dumb choice of marrying a farmer. I was so desperate and couldn't afford or have the time for trips to the specialist so I did my own thing by gently exposing myself in small doses or amount of time to anything that made me itch, sneeze, cough, or feel bad. No one believed in me and thought perhaps I should divorce, but I was determined to feel better, and with the big garden and well balanced eating I got better in twenty years. In fact my basic health is pretty good despite living with a stressful husband while the marriage was a disaster. But I kept at it, and truly believe that desensitizing myself over the years a little at a time can be an effective cure and can alleviate many chronic problems.
On the other hand, my sister catered to her many "allergies" and died with chronic diseases that she declared were none of her fault. She also blamed the doctors, six of them, when her visits did not result in a fast cure. This is a worst case scenario, but I certainly know what it feels like to itch all over. I only had one panic attack and with the advice of my paramedic son and his friend, taught myself to not do that again without the aid of a psychiatrist. If we are born with sensitive bodies it can be a lifetime of effort to control or eliminate the exposures and to get sensitized to some exposure. Yes, I avoid poison ivy!

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Dorisena, what you were able to accomplish is remarkable! Thank you for taking the time to share it. For my chemical sensitivities I went the route of avoidance, making my bedroom a safe haven from toxic chemicals and being very careful about everything I brought into my house. For a while I had to avoid stores, libraries etc. But after nine years my tolerance has increased and I donā€™t hesitate to go or do most things for fear of chemical exposure. Supplements, too, have helped. But, exposure to smelly caulk yesterday seems to have given me a very bad nightā€™s sleep and a headache, so the problem is not completely gone.

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@radeles

Hi
A little over 2 years ago I began having the symptoms you described. The adrenaline rushes woke me every morning around 4am and the intensity of feelings from this began to grow over the next few hours until I was suicidal. This continued until mid afternoon then began to subside until my mental/emotional settled and I felt normal again, although exhausted. No longer suicidal, not even particularly depressed or anxious. Then Iā€™d go to bed and itā€™d happen all over again. Groundhog Day! I dreaded going to bed but was so tired I had to. Only for the cycle to begin again. 2 months went by and Iā€™d tried all the mindfulness and meditation to calm me, was seeing a psychologist but my body was telling me this was physiological rather than mental/emotional. The anxiety and depression were the result of the physical stuff rather than the other way around. Eventually I heard from someone about MTHFR gene mutations that created similar symptoms so saw a GP who specialised in that and Pyrroles Disorder. She ordered the test for Pyrroles and bloodwork to identify high levels of ā€˜freeā€™ copper based on my history and current symptoms. She said I was textbook for Pyrroles and directed me to online resources to better understand it. Sheā€™d studied the condition at The Walsh Institute founded by Dr William Walsh.
She directed me to have the tests asap then after the tests to begin taking high doses of activated B6, magnesium and zinc. Within a week of taking this I began feeling better. We continued tweaking the supplements and adding some others as the main issue is that I undermethylate and have problems detoxing metals from my system. The excess unusable copper in my body (which has a specific way of testing for it) causes the electrically charged feeling in my body. Iā€™ve realised Iā€™ve recently been consuming lots of nuts and seeds high in copper.
The reason for finding your post is that I googled ā€˜adrenaline rushes in the morningā€™ as Iā€™ve began having them again. However, itā€™s also been months since I took the supplements Iā€™m supposed to. So I basically know why Iā€™m having symptoms again but felt the need to do some research just in case it could be something else. After reading your post I realised itā€™s probably not something else! Iā€™ve also recently been attempting to detox with ā€˜clean eatingā€™. As my body releases toxins I have issues with clearing them from my system without correcting the pathways that are dysfunctional. So Iā€™m getting back on the supplements ASAP and wanted to write about it here in case itā€™s helpful for you. Iā€™m in Australia btw and the conditions I mentioned arenā€™t recognised by the general medical profession here. The Walsh Institute is in the US but several doctors here are getting the training as the markers for these conditions make sense to them. Most of them are inundated with more patients than they can handle who are being treated successfully with the right supplements to correct biochemistry. Itā€™s a very fine balance that needs to be supported by blood tests to confirm whatā€™s working and what isnā€™t. Iā€™d say the first step is looking at the information on the Walsh Institute website then finding a practitioner who can test and treat you. Also find Pyrroles Disorder and/or MTHFR support groups on social media for more information.
Best of luck!

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@radeles Wow! I think I may have the pyrolysis condition you describe. I want to get tested but have some concern about going off my supplements. I routinely take 30 mg Cu every other day and 175 mg B6, because general metabolic testing showed that I am a very poor methylator. On this I have felt fairly well, but any extra stress will set off the adrenal rushes and it will take a lot of resting up to get back to ā€œnormalā€.

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I have had this on and off for about 8 years, and after seeing 70+ doctors - even at very prestigious medical centers of excellence like the Mayo Clinic and Cleveland Clinic - I finally found a physician that could explain (using lab results) why this was happening to me. My physician is trained in the Ritchie Shoemaker, MD protocol called CIRS (chronic inflammatory response syndrome). Dr. Shoemaker found that, by being exposed to mold, some peopleā€™s bodyā€™s canā€™t detoxify/clear the mold and abnormal adrenaline/cortisol zaps can occur. Roughly 20% of the population cannot detox mold because their detox pathways are blocked. It turns out that the basement in my office has tons of mold due to my company having had multiple floods over the years. Iā€™ve been with my company for 11 years and for the first 3 years I experienced very weird symptoms which I couldnā€™t explain. Then I began awakening multiple times each night with jolts of adrenaline/cortisol for about six months. After about six months I started to have lots of other symptoms that felt like MS, however MRIs did not reveal MS. For two years I went from specialist to specialist trying to get help. I then saw an integrative internist that identified that I was hypothyroid and had a TPO of about 1000 (so I had Hashimotoā€™s). When we began to treat with thyroid hormone, I did much better for about 5 years, but they my symptoms returned when my internist put me on low-dose Naltrexone (to try to eliminate the Hashimotoā€™s). Mold and other toxins suppress thyroid function so some of the zaps/jolts can be caused by insufficient thyroid hormone production, but according to Dr. Shoemaker, adrenaline surges can also be caused by an accumulation of toxins as they throw off the bodyā€™s normal processes. The Shoemaker protocol revolves around taking cholestyramine and other binders to remove toxins to get the body working again. Check out surviving mold dot com to learn about this and then either find a recommended practitioner on Dr. Shoemakerā€™s site or ask around to see if any practitioners in your area follow the protocol but just maybe are not Dr. Shoemaker-endorsed. By the way, Dave Asprey, the founder of Bulletproof, had Hashimotoā€™s and other scary symptoms similar to ours due to toxic mold exposure and he, too, used the Shoemaker protocol to cure himself. He's got lots of information about this on his website, bulletproof dot com as well as interviews with Dr. Shoemaker and other healthcare practitioners that understand how to actually cure it. I hope this helps!

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@realanswers

I have had this on and off for about 8 years, and after seeing 70+ doctors - even at very prestigious medical centers of excellence like the Mayo Clinic and Cleveland Clinic - I finally found a physician that could explain (using lab results) why this was happening to me. My physician is trained in the Ritchie Shoemaker, MD protocol called CIRS (chronic inflammatory response syndrome). Dr. Shoemaker found that, by being exposed to mold, some peopleā€™s bodyā€™s canā€™t detoxify/clear the mold and abnormal adrenaline/cortisol zaps can occur. Roughly 20% of the population cannot detox mold because their detox pathways are blocked. It turns out that the basement in my office has tons of mold due to my company having had multiple floods over the years. Iā€™ve been with my company for 11 years and for the first 3 years I experienced very weird symptoms which I couldnā€™t explain. Then I began awakening multiple times each night with jolts of adrenaline/cortisol for about six months. After about six months I started to have lots of other symptoms that felt like MS, however MRIs did not reveal MS. For two years I went from specialist to specialist trying to get help. I then saw an integrative internist that identified that I was hypothyroid and had a TPO of about 1000 (so I had Hashimotoā€™s). When we began to treat with thyroid hormone, I did much better for about 5 years, but they my symptoms returned when my internist put me on low-dose Naltrexone (to try to eliminate the Hashimotoā€™s). Mold and other toxins suppress thyroid function so some of the zaps/jolts can be caused by insufficient thyroid hormone production, but according to Dr. Shoemaker, adrenaline surges can also be caused by an accumulation of toxins as they throw off the bodyā€™s normal processes. The Shoemaker protocol revolves around taking cholestyramine and other binders to remove toxins to get the body working again. Check out surviving mold dot com to learn about this and then either find a recommended practitioner on Dr. Shoemakerā€™s site or ask around to see if any practitioners in your area follow the protocol but just maybe are not Dr. Shoemaker-endorsed. By the way, Dave Asprey, the founder of Bulletproof, had Hashimotoā€™s and other scary symptoms similar to ours due to toxic mold exposure and he, too, used the Shoemaker protocol to cure himself. He's got lots of information about this on his website, bulletproof dot com as well as interviews with Dr. Shoemaker and other healthcare practitioners that understand how to actually cure it. I hope this helps!

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Thank you so much for taking the time to share your story. I think I have a kind of parallel case, but with copper toxicity. I am scheduled to see Dr. Mensah in his clinic near Chicago. From what Iā€™ve read, he is an expert in this area. I think that the information and resources that you provided will help when I start detoxing copper. Iā€™ve already had a taste of that when I tried part of the detox protocol on my own - really intense adrenaline surges ( but not as bad as when I was suffering from a sick building.) So I will read up on what Dr. Shoemaker recommends. Quick question - have you tried massages, along with the other things? Thank you for your help and I will keep you posted.

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