My Own Story About Thyroid Disease, Adrenal Fatigue And Chronic Fatigue Syndrome
84
|
Best Doctors and Treatments for Hypothyroidism
Price: $0.99
|
|
Adrenal Fatigue a Complete Look
Price: $0.99
|
|
Chronic Fatigue Syndrome & Fibromyalgia an Audio Study
Price: $0.99
|
|
Improving Quality-of-Life for Thyroid Patients Audio
Price: $0.99
|
My ongoing battle with adrenal fatigue began to manifest even before I experienced the obvious onset of Hashimoto's/Hypothyroidism in early 2003. I began to notice months previous to diagnosis, that my tolerance for stress and my recuperative abilities, to spring back from hard physical activity, illnesses, excessive stressors etc.., was slowly diminishing. When my hypothyroid disease kicked in, the adrenal fatigue hit a peak of severity and the combination of the two really threw me for a loop.
The first Doctors I went to didn't investigate to find the thyroid disease and I was not being treated for it, so in the mean time I had to push myself incredibly hard just to keep going because I also had an extremely stressful job situation, managing property at that time.
Finally at one point, the adrenal fatigue turned into severe "adrenal exhaustion" and I experienced a strange viral type illness that left me with severe hives (these resolved) and swollen neck lymph-nodes that are swollen to this day! This is also when my chemical sensitivities became much worse to caffeine chocolate, alcohol and stimulants of any kind. In other words I had developed increased multiple chemical sensitivities (MCS).
I finally demanded blood tests and as a result, was treated for diagnosed hypothyroidism but the adrenal fatigue remained, re-occurring in flares of symptoms. Over time, I learned the difference between the symptoms of adrenal fatigue/exhaustion and thyroid symptoms. With adrenal exhaustion, I get severe post-exertion malaise and it can take a couple of days sometimes to recuperate from hard physical activity.
I have since been treated for these health disorders and have seen significant improvement in them. I do still experience flares in symptoms, if I venture outside of a diet restricting stimulants or if I do not keep my stress levels under control.
It is my belief that CFS is a type of adrenal exhaustion and that adrenal fatigue can be a forerunner to it in some cases. The most well-established feature of CFS that you find in medical research (also fibromyalgia), are "low cortisol levels" and I do not believe this is a coincidence but something that makes sense because the main purposes of cortisol is regulating stress and controlling inflammatory responses in the body. Two of the doctors I have been treated by since 2003, also diagnosed me with co-morbid CFS.
The adrenals when low functioning, cause more allergy, viral and illness responses to occur, due to the adrenals role in immune system function, being greatly diminished. Cortisol is also our body's natural anti-inflammatory and so low levels give rise to joint & muscle pain and other inflammatory reactions in the body. All of these factors combined, contribute to the symptoms of adrenal fatigue and CFS and can add to the symptom struggles of hypothyroid patients who have these co-morbid conditions.
Many Doctors only recognize the most severe form of adrenal hypo-function called Addison's Disease or full blown adrenal insufficiency and they base whether or not a patient has this life-threatening form, via the "ACTH Stimulation Test". The problem is that many people have a less severe form called adrenal fatigue or adrenal exhaustion and
though these patients nearly always pass the ACTH Stimulation Test, they still have inadequate adrenal hormone levels that show up clearly on lab tests and though it is not life-threatening, it still causes symptoms that can seriously affect quality of life.
Even the National Institutes of Health, while studying Chronic Fatigue Syndrome, found "low cortisol" to be a factor in it as well and in the study, they made this statement; "Doctors have long known that even subtle deficiencies in cortisol can be associated with lethargy and fatigue." (LINK>> www.nih.gov/news/pr/oct96/niaid-13.htm )
The "NIAMS" (arthritis etc...) Division of the National Institutes of Health also recognizes low cortisol in Fibromyalgia. Other studies they've published on the PubMed/National Libraries of Medicine website, also recognize low cortisol in PTSD (Post Traumatic Stress Disorders).
The fact is, adrenal fatigue can be a factor in these and other chronic diseases/syndromes or not be related to anything specific.
One major virus that other NIH studies have concluded as being highly associated with CFS, which also has low cortisol as a feature, is the Epstein-Barr Virus. I had a severe case of mononucleosis as a kid, about age-10 and have always believed there is a connection of it, to both my thyroid disease and CFS.
When I was optimized on thyroid hormone replacement for hypothyroidism but continued to have symptoms, some that were not typical of thyroid (severe post exertion malaise, swollen neck lymph nodes, orthostatic hypotension), I decided to get tested for EBV, just out of curiosity because I had read so much about research that suggests the possibility that EBV like others in the herpes virus family, can flare-up in persons with a compromised immune deficiency (immune dysfunction).
My EBV/IGG result was "218" with the normal range being <20 (less than twenty). This means my EBV count is more than 10 times the normal cut-off range. While a large percent of the population tests positive for EBV (statistics estimate 80%), titers as high as mine are not common, unless a person is actually experiencing active-mono.
For me, the EBV I feel has a connection to both Hashimoto's Thyroiditis (there is also NIH research on this) and CFS.
The most important thing, if you feel you may have adrenal fatigue, is to be tested for it because other hormone imbalances and illnesses cause similar symptoms.
More pharmacies are now carrying "ZRT Labs" saliva hormone kits, including the ones that test adrenal hormones, so you can check around for these.
The passion I have in the area of adrenal fatigue, besides having it myself, as part of CFS, is the fact that far too many studies and reputable organizations recognize it, including the "Fibro & Fatigue Centers", in 15 states, that are staffed by Board Certified MDs from just about every field of medicine, for people to still believe it is just a pseudo-syndrome. This plus the fact that there are U.S. Government health studies also concluding that there are low-cortical syndromes, well establishes sub-clinical forms of adrenal hypo-function, that could all be referred to under the term; "adrenal fatigue".
PrintShare it! — Rate it: up down flag this hub
Comments
I feel so lost with all of this... I've ALWAYS been the "breath of fresh air, or ray of sunshine" abounding with energy and enthusiasm. Thank you for sharing.. I am trying to figure out what to do next... my job nad social life hav been affected. Anwho, thank y ou and continued health to you!
Thanks childofLight and I wish you better days ahead too! Keep searching online, it usually ends up being the best possible way to educate yourself on health conditions, which in turn helps you get the right treatment (and better treatment).
one of the most insightful articles on this complex subject. i agree, from personal experience 1) that these illnesses run in packs, 2) that one can lead to another, and 3) that the cumulative damage can be permanent. so the need to supplement the depleted adrenals and other organs is a matter of neccesity. if one doesn't stop the cycle, these illnesses get nastier and more disabling and painful. All the while, the pain and loss of health is difficult to see in lab tests or anything. That leads to extraordinary social problems & credibility problems.
Geza,
Very good points you make and I agree 100%! Thanks for adding your well-stated view and I'm so glad the article was helpful.
I appreciate you reading!
i pray that you find relief from those diseases. i too suffer from hypothyroidism. i was first diagnosed with hyperthyroidism and later had radiation therapy because my endo. said there was the possibility of cancer with the goiter. now i haven't a thyroid gland and have hypothyroidism :( and stuck on synthroid for the rest of my life.
Jesus_saves_us_7,
Thanks so much for your many very kind comments on my articles. I sometimes feel guilty that I don't comment more on articles myself but my life took a turn for the busier this year with a recent change in occupations, that keep me on the road for most of the week.
Thanks for your good wishes for me and also for sharing the fact of your also being a thyroid patient. I of course believe in God healing supernaturally and have experienced healings on several occassions. I feel God has a wisdom in when healing takes place and that those of us, like you and I can be a fellow-support to people with our same illness, which they can relate to sometimes even better than the support they can recieve from family members and their doctors. While I continue to have these illnesses, I've also had an incredible inward strength at the same time, that I know for a fact came supernaturally.
I believe you too have felt that strength from your experience. If you get a chance to come by my thyroid forum, I'd love to have you. Here> http://forums.bellaonline.com/ubbthreads.php?ubb=p
Great Job!! Your story is well written, both enjoyable to read and educational. I've got Hashimoto's, Lyme, and Non-Addisonian (but possibly still autoimmune) Adrenal Insufficiency. Like you and most other folks with these diseases, I've gotten the run-around from doctors as well as sub-optimal treatment. That is why I thank you for putting your experience out there. Without bloggers like you it would be incredibly difficult for the rest of us to do our own research to try to make sure that our doctors aren't mistreating us. Because let's face it, no one really monitors them except them!
P.S. I also agree with the PTSD and adrenal link. I was finally diagnosed months after a head-on collision with a drunk driver after which I had PTSD. I also learned that the pain medication I was given, hydromorphone, increases growth hormone but lowers cortisol. In fact, I found one case study in which hydromorphone induced adrenal insufficiency in a woman who had been taking it long-term, as had I. Add that together with PTSD and undiagnosed autoimmune and contagious diseases . . . and well you're likely to crash.
DominicaScot,
Thanks so much for adding your testimonial and great comments. You make some very good points and have that first-hand experience that really drives your points home!
Holy moly!!!!!!!!! You have described my personal 9 year journey of suffering and frustration almost to a T. I wish I had found this webpage years ago. How ironic that literally TODAY I figured out exactly what you discovered ears priot. I was diagnosed with CFS 7 years ago. It got worse every year to the point I had to quit my job. I also had a EBV reading 10X higher than everyone else!!! Any kind of hard exercise took me days to recover from. Got to the point I could only do moderate exercise once a week. It would take me a full week to recover from that and would put me into "sleeping coma's" for hours at a time, the fatigue was so bad. Id pass it in the middle of the afternoon every day as if I was heavily drugged. Only difference is, my testosterone levels were falling off a cliff in addition to my recently discovered hypothyroidism, and adrenal fatigue. My T levels got low enough that doctors started taking me seriously. Got put on Testosterone replacement which made me 70% better. Then when I was put on thyroid medication IT DESTROYED ME. Thats when I learned about adrenal fatigue, and that adding thyroid with weak adrenals makes you worse. I got my saliva tests back last week, and I was below range all day long, except in the morning. So the puzzle was solved literally a week ago, and I started on ISOCORT to support my adrenals. Already feeling better. Recovering from exercise much better. Late afternoon fatigue way down. After I get my adrenals healthy, im going to attempt another thyroid experiment and see if I can handle it.
My life has been ruined for at least 5 years. Docs are CLUELESS about this stuff. Im so happy that I finally solved this puzzle. PLEASE spread the word more! Your pages are AWESOME!
Jason,
Thanks so much for sharing that! I read it with great interest. Your story has many similarities to mine and I agree with your comments.
Thanks again!
I have celiac disease. Celiac disease is very connected to thyroid disorders. In fact, true to statistics, my thyroid disease was diagnosed YEARS before my celiac was diagnosed. I, too, have had adrenal exhaustion, diagnosed by the ZRT test. It's an understatement to say that celiac is connected to other health issues. Now, I think ALL people with a thyroid disorder, adrenal fatigue, abdominal distension, unexplainable yellowing teeth, OR itchy blistering rash, should be celiac tested, even if there are no visible GI issues. My endocrinologist could have helped me get diagnosed years ago. My dentist could have helped me get diagnosed years ago. I should have been diagnosed, but it wasn't a common practice to test for it, and celiac is still the most under-diagnosed disorder today (1 in 100 have it). Celiac, a genetic auto-immune disorder, might not even cause GI upsets if you have silent celiac. Undiagnosed, you can get thyroid disease, adrenal fatigue, diabetes, osteoporosis, and so many other health problems that are avoidable up to a certain point in time. I diagnosed myself by reading a medical journal and Google. My doctor refused to give me the blood tests. So, pro-actively got myself a new doctor. I urge everyone to be their own health advocate and DEMAND a celiac blood test. If your three blood tests come out positive like mine, you definitely have celiac. If your blood tests come out negative, you might have a false-negative and need an intestinal biopsy to prove celiac-related damage. Read about why so many people are testing negative, even though they really have it- celiacdisease.com gig.net celiac.com celiac.org .
Super-good post & I agree with you 100% Denise!
I actually believe I have celiac problems and have come very close to getting tested a number of times.
I in-fact have articles on this connection of thyroid disease to celiac.
I've also found in the U.S. that if a doctor is stubborn about ordering tests I want, I use one of the blood-draw set-up firms that require no doctor visit. HealthCheckUSA is one of those.
Thanks for reading and commenting!






Barefoot in MN says:
14 months ago
Thanks for sharing your story ! It gives me hope that I may yet get a more complete diagnosis, myself.