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. 🙁 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 😉 Okay, seriously. I'm not in a good place right now.

Interested in more discussions like this? Go to the Diabetes & Endocrine System Support Group.

@jigglejaws94

Apparently you can have normal catecholamines but still have pheochromocytoma.
https://www.ncbi.nlm.nih.gov/pubmed/16982588

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The doctors sure don't think this! I have read plenty of cases but the top doctors literally say it's impossible to have a pheo without high metanephrines.

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@j40

Hello,

Thank you so much @sierrawoods for starting this thread and sharing experiences. Sierra's account of what she endured was almost exactly what I've been experiencing for almost 8 years, especially the adrenaline surges almost every night. I also began symptoms at the same age, 33, and am now 40. All seemed to begin after Epstein Barr, Dr.s were perplexed for a few years, then I "cured" and reversed everything for a couple years--unclear if all resolved due to higher Synthroid dose, sauna, or another unknown factors. All symptoms returned for the past almost 3 years after I had exposure to Aspergillus mold for 1.5 years. However, I have been away from it for another 1.5 years with no improvements in symptoms. I'm female, hypothyroid, redhead, lactose intolerant, healthy diet, no current lactose, gluten, or caffeine. Since the start of this all, I've developed chronic autoimmune hives, mast cell activation, heightened allergic responses, heart palps, unexplained significant weight gain, low A1C, etc.

In any case, I wanted to focus on what seems to be emerging as one of the core issues and see if this resonates with most people writing in now....

While Epstein Barr seemed to have preceded all, the ADRENALINE rushes / surges, mainly all night (sometimes seeping into daytime), seem to be due to REACTIVE HYPOGLYCEMIA. This seems to be affected by Synthroid (levothyroxine) dosing. Also, increased exercise at any time during the day worsens adrenaline at night. While my TSH numbers have often been in near ideal range, tweaks to Synthroid dosing have lessened adrenaline at many points in time, even when they made TSH #s too low (implying too much Synthroid).

My theory is that I have inability to detox due to blockages mold created and/or due to something virus/Epstein Barr-related, so that Synthroid doesn't get to all the sources that need it, even if TSH registers on labs as "normal." (I realize the general TSH range is wide, so by normal I mean very ideal, close to 1.0, with T3, T4 also at good points.) I worry that to have enough Synthroid absorbed to lessen hypoglycemic episodes and resulting adrenaline surges to raise blood sugar, I'd have to take too much Synthroid for my body as a whole, since my TSH has been well under 1.0 when Synthroid worked to lower adrenaline last time. If my theory is correct, then if there is a way to get Synthroid to where it needs to be (e.g., by detoxification from mold) *without overmedicating,* it seems that would be helpful.

I hope those who wrote in have found helpful fixes and are feeling much better. If anyone has confirmed that hypoglycemia was at the core of their adrenaline and, better yet, discovered what the root cause was, that would be very interesting.

@sierrawoods @cehunt57 @lisalucier @kdubois @jigglejaws94 @camik @chocolate5lover @veeravee @libjen @jenniferg27 @astaingegerdm @realanswers @aclmalibu @b808 @adrianyepez

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It sounds so simple, but I’ve found that one of the things that helps the most is eating carbohydrates during the day. It doesn’t have to be much (a sandwich on whole grain bread or some pasta, but it helps me sleep through the night and seems to reset my cortisol rhythm. I think this only works when my T3 & T4 numbers are good though. I take both Synthroid and Cytomel. I also use Estrogel and progesterone cream for HRT after my ovaries were removed in 2014, so when all things are balanced, I don’t get the “adrenaline” or cortisol rushes in the early morning anymore. Carbs really do help me a lot, and it is an easy thing to try, if you are interested. Start with some pasta for dinner and see if it makes a difference for you too! Best of luck finding something that works! Thanks for posting about your experiences.

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I am so sorry to read of all of your suffering. Wishing for you peace and healing. Martha

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@libjen @astaingegerdm

Thanks for your replies.

@libjen -- That's wonderful that you've found ways to feel better and that carbs also help. While I'm gluten-free now, I've always had a good amount of carbs. You're right that they do seem to be a mediating factor in keeping adrenaline better controlled. What's strange is that the first time I had all of these symptoms, including adrenaline surges, esp. at night, I went on the Plant Paradox diet (with very low carb intake) for months. If anything, it seemed to help at this time (perhaps with the increase of Synthroid that was able to be metabolized correctly without mold/liver toxicity, which I likely have now). But the last time I tried to cut carbs, I had a massive increase in adrenaline. Since then I went back on more carbs, as usual, plus resistant starch close to bedtime with protein. This seems to help a bit, but isn't nearly enough, as I still wake hungry, weak, and with adrenaline that follows.

To answer @astaingegerdm, yes, I've had tests for cortisol, adrenaline, testosterone, etc., even recently. Years ago my DHEA was high, but in many recent years, all tests have been in normal range. Of course, certain ones like cortisol and adrenaline (like blood glucose) are snapshots in time, so don't show the surges unless blood is taken at the time of a significant drop or spike. When I have my labs done first thing in the morning before eating, most of these have crashed, risen, and leveled to normal by the time they're measured, unfortunately. My A1C is ~4.6 (glucose 83) and my fasting blood sugar is often around 100, so also implies crashes. I also used the Freestyle Libre 2 sensor for a week and it illustrated how I have blood sugar crashes around midnight, 3-4am, and other times during the day and night.

Again, I'm not sure if fructose intolerance is playing into all of this. Some doctors felt it might be.

Thanks again for your thoughts and help!

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I am in the same fight as you..only I started out like you but.. just last April my blood pressure shot up to 208/111 and heartrate of 185 then after that I went through 3 days of the worst lower leg pain of my life that it was unbearable...and now I'm left with muscle breakdown and can barely walk. I also have an elevated urine cortisol which I've tried to get into the Mayo clinic to see an endocrinologist and have been declined. I cant find help at all and I am losing hope which I'm terrified of being in a wheelchair or worse bedridden. If your in Minnesota their guidelines are different than other states and yes what insurance you have does matter to them. But everyone is quick here in this state to put you on whatever pain pill you want without addressing the real issue. There is a Doctor in Canada..Dr. Andre LaCroix hes brilliant and gets it, look him up..I would give anything to see him, if you have the means to go there.. Do it! Minnesota Drs. Are useless.

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Hi Sierra woods. I just found this group and I'm hoping that by now you found relief. Your symptoms are so much like mine. I recently started seeing a nurse practitioner who specializes in hormone balancing. In fact that's the only thing she does. Also, she only uses bioidentical hormones. There is a demonstrable difference between synthetics and bioidentical, including thyroid. I'm having some improvement in my sleep, primarily in relation to adding an iodine supplement to my regimen. I can recommend Dr Brownstein's books. They are an easy read, and cover bioidentical hormones, iodine supplementation, salt, etc. He's written several books and I bought three, used, at thriftbooks. There is also the estrogen dominance support group, which has a wealth of information. Wishing you the best.

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I am very late to this but I have the same symptoms did you ever find a resolve?

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@sierrawoods

@jigglejaws94 LOL! I have two doctor friends and they both told me NOT to tell my doctor that I have doctor friends because they will instantly be on guard and think you are checking every diagnosis and script with your friends. I have listened to their advice. 🙂

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Hi I am suffering the same thing. Its gotten wirse after menopause. Did you get any solution. Please let me know. My email is pariemail at yahooDotcom. I have this power surge. I feel like i have seen a tiger face to face. Tingling in feet. Butterflies in stomach. Its terrible. I am even scared to travel. Have had it for last 10 years. Please help. These days its daily affair. I am 61 years old from India

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@jenlang

I am very late to this but I have the same symptoms did you ever find a resolve?

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Could you share your other symptoms. Also are you post menopausal? I have a knotted feeling in the throat, butterflies in the stomach, tingling in hands and feet, palps sometimes and recently high bp with these adrenaline surges, feel low on sugar every few hours. On bp medications for last 4 months. Prior to that nil medications. 61 years old now

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Did you recover? I’m going through these spikes right now, that wake me with a jolt. I have subclinical hyperthyroidism, but my Endo says I should not have these symptoms. He is so wrong.

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