LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » thyroid hormones can cause muscle wasting

 - UBBFriend: Email this page to someone!    
Author Topic: thyroid hormones can cause muscle wasting
Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939

Icon 1 posted      Profile for Pocono Lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm new to the thyroid rollercoaster/merry-go-round. I've been doing research in an attempt to help myself and came across this.

I have had severe muscle wasting/weakness and never correlated it to thyroid.
Thought I would post this in case it may be an issue for others. I've read where the thyroid tests are not a very good indication and also many do MUCH better on Armour Thyroid as opposed to Synthroid.

Again it's all new to me so I'm by far no expert.
Just trying to help myself and others.

http://ajpcell.physiology.org/content/290/2/C650.full
Enhanced levels of hormones and cytokines, in particular glucocorticoids and TNF-α, are likely to be major initiators of protein breakdown. Interestingly, thyroid hormones can cause muscle wasting due to both excess and deficiency by yet-unknown mechanisms


http://www.rightdiagnosis.com/news/thyroid_disorder_underdiagnosed_and_misdiagnosed.htm

--------------------
2 Corinthians 12:9-11


9 But he said to me, �My grace is sufficient for you, for my power is made perfect in weakness.� Therefore I will boast all the more gladly about my weaknesses, so that Christ�s power may rest on me.

Posts: 1445 | From Poconos, PA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
2young2dieMom
LymeNet Contributor
Member # 25434

Icon 1 posted      Profile for 2young2dieMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was taking synthroid for a year before I was diagnosed with ALS. I've had significant muscles loss in my shoulders, neck, chest and hips in the following years.

I stopped synthroid after a year but just started on tirosint. The muscle loss is progressing anyway. I always wondering if these things were related.

--------------------
Dxd ALS 3/2010
Dxd cllinical Lyme 4/2010
Positive for Protomyxzoa but absolutely nothing else in Igenex

Posts: 417 | From central ct | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
AuntyLynn
Frequent Contributor (1K+ posts)
Member # 35938

Icon 1 posted      Profile for AuntyLynn         Edit/Delete Post   Reply With Quote 
Pocono Lyme:

I am diagnosed hyperthyroid. I have managed to get basic tests about every year or two, and it isn't slowing up. (Have not had health insurance in 5+ years!)

The one visit I had with an endocrinologist, he said I've likely been hyper all my life, and when my estrogen levels dropped in peri-meno, it started presenting. Apparently estrogen has a protective effect against thyroxin.

There are inexpensive meds for hyper, but the American medical community pushes radioactive iodine ablation BIG TIME, and I am definitely NOT comfortable with this treatment! It is really difficult to control "dose" with RAI, and people say if you don't like the results, "tough luck" - you're stuck with it.

Most RAI patients go HYPO post treatment, and need thyroid supplements for life!

BTW, other countries use RAI as a "last resort" for stubborn cases only! Of course RAI testing and treatment costs about $20K, whereas the cost of treating with thyroid inhibiting drugs is mainly in the routine blood work. "Go figure."

I have never heard of using Armour or synthroid for Hyper. They are, however, used for Hashimoto's disease, which is a thyroid that fluctuates, between high and low.

There is a wholistic approach to treat hyper - taking L-Carnitine, which blocks thyroxin damage to the liver and heart, but does nothing to limit weight loss and muscle wasting. Dose is allegedly 2-3 gms per day.

Author and thyroid patient Elaine Moore has some great books on thyroid disease. She also has some very good online blogs. I would do a search for her material, as she is very informative.

Another lay author opines that hyperthyroidism is likely caused by a copper deficiency; which might explain why far more women than men suffer this disease. Seafood, especially oysters and crab/lobster are good sources of copper.

Also, it seems apparent that heavy metals poisoning may be implicated.

Let me know what you learn? Thanks!

Posts: 1432 | From New Jersey | Registered: Jan 2012  |  IP: Logged | Report this post to a Moderator
Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939

Icon 1 posted      Profile for Pocono Lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
AuntyLynn,

I understood that to read that muscle wasting could be caused by too much or too little thyroid hormone that our own bodies produce.

I added the synthroid comment as a separate issue. I didn't clarify that. Sorry.
Hoping my adrenal/thyroid treatment will also clarify my brain. lol

I was dx with hypo.

It's got to be really tough to manage hyper and Hashi's.

2young, I didn't know what Tyrosint was and when I looked it up it said it's only T4.
Again, I'm just learning and from what I've read that's a mistake many people(doctors) make.

I don't know your labs etc. and wouldn't be able to advise anyone but I think it is definitely worth you researching.

The site that seems to have the best information is STTM (Stop The Thyroid Madness)

I just went there to find something for you and this was right there on the initial page.
http://www.stopthethyroidmadness.com/
T4-only
Next I would check the status of your adrenals. Mine I'm finding out is a huge factor.
Something I also came across.


http://adrenalsweb.org/index.php



Low Cortisol
�Allergies getting worse
�Body ache - all over
�Clumsy
�Confusion
�Continuing hypothyroid symptoms with a high Free T3
�Dark circles under eyes
�Diarrhea
�Dizziness
�Emotionally hyper sensitive
�Fatigue
�Feeling better after 6 pm
�Feeling of doom or panic
�Flu like symptoms
�Headache
�Heart palpitations
�Highly defensive
�Hypoglycemia
�IBS symptoms
�Inability to focus
�Inability to handle stress
�Inability to interact with others
�Inflammation that doesn't go away
�Irritable
�Jittery or hyper feeling
�Low back pain - in kidney/adrenal area
�Motion sickness
�Nausea
�Rage or sudden angry outburst
�Overreacting
�Paranoid
�No patience
�Shaky hands, internal feeling of shakiness
�Weakness - general or localized


High Cortisol
�Bruising easily
�Fluid retention
�High blood pressure
�Moon-shaped face
�Obesity
�Severe fatigue
�Spare Tire - increased belly fat
�Weak muscles and deterioration
�Increased fat in the back of the neck and upper back area (hump)


Symptoms of Low Aldosterone
�Low blood pressure
�Low blood volume
�High pulse
�Heart palpitations
�Dizziness
�Lightheadedness when you stand
�Fatigue
�Craving salt
�Frequent urination
�Getting up many times during the night to urinate
�Sweating
�Excessive Thirst


Symptoms of High Aldosterone
�High blood pressure
�Low potassium
�Weakness (caused by low potassium)
�Tingling (caused by low potassium)
�Muscle spasms (caused by low potassium)
�Frequent urination
�Water aversion

[ 10-24-2012, 09:39 AM: Message edited by: Pocono Lyme ]

--------------------
2 Corinthians 12:9-11


9 But he said to me, �My grace is sufficient for you, for my power is made perfect in weakness.� Therefore I will boast all the more gladly about my weaknesses, so that Christ�s power may rest on me.

Posts: 1445 | From Poconos, PA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
fourwinds
LymeNet Contributor
Member # 14114

Icon 1 posted      Profile for fourwinds     Send New Private Message       Edit/Delete Post   Reply With Quote 
I initially was diagnosed with Graves' in 1998

(alternating between being Hyper and Hypo).

I, due to my lack of knowledge, let them ablate

(RAI) my thyroid. So, now I am permanently hypo and within the last three months, discovered I

now have Hashi's as well.

You can still have high antibodies without a thyroid.

The interesting part is, quite a few of the

extreme joint pain issues I was having were

"cured" when I increased my thyroid (I take

natural dessicated) dosage.

One of the causes for Hashi's is not getting enough thyroid.

I had been on the same dose for too long (many years) which can cause your antibodies to kick in.

Lyme causes the whole HPA to get out of whack and it is sometimes difficult to balance during

treatment. My adrenals got hit hard in the beginning.

I know NOW that my original issues were most likely triggered by the Lyme and Co's.

PoconoLyme, glad you found the

stopthethyroidmadness site helpful!

(And yes, adrenals should always be addressed FIRST... but most doc's don't [Frown] )

Posts: 396 | From EAPennsylvania | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
nefferdun
Frequent Contributor (1K+ posts)
Member # 20157

Icon 1 posted      Profile for nefferdun     Send New Private Message       Edit/Delete Post   Reply With Quote 
I posted about LDN under 2Young2Die's topic about thyroid.
If you have auto immune disease, it will halt it. I am normal now.

--------------------
old joke: idiopathic means the patient is pathological and the the doctor is an idiot

Posts: 4676 | From western Montana | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
poppy
Frequent Contributor (1K+ posts)
Member # 5355

Icon 1 posted      Profile for poppy     Send New Private Message       Edit/Delete Post   Reply With Quote 
A lot of people have low or high thyroid functioning and do not have muscle wasting.

My sister in law had the radioactive ablation done for what was diagnosed to be thyroid storm. She has to take thyroid pills the rest of her life now and had her liver damaged from the radiation...that particular process is no longer used.

My suspicion is that it might have been her thyroid flaming out, high on the way to a crash, which does happen, and would not require an ablation at all.

Posts: 2888 | From USA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
fourwinds
LymeNet Contributor
Member # 14114

Icon 1 posted      Profile for fourwinds     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tried, and could not take LDN,...

You shouldn't if you have any type of yeast issues

And 2) because of my adrenal issues, it made me feel REALLY bad -- I crashed severely... something about it uses the same receptors as the adrenals...

@poppy "that particular process is no longer used." It is... it just depends on the endo (and whether or not the patient educates themselves to question them.)

I have NO faith or trust in endocrinologists....

But, as an aside... I have not had muscle wasting just fibromyalgia-type pains and the severe joint pain (that went away with the dosage increase).

Posts: 396 | From EAPennsylvania | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939

Icon 1 posted      Profile for Pocono Lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
fourwinds, Thank you for all of your help. Yes the STTM site is quite helpful.
You've certainly been through a lot with thyroid issues.

Interesting that your pain went away with increased dose of thyroid. I just got started on HC and my long standing neck and shoulder pain isn't there today. Because I said that, wait until tomorrow. [bonk]

I found a good descriptive term for it. Coat hanger pain.

Poppy, I agree that a lot of thyroid patients don't have muscle wasting but I find it interesting that weak muscles and wasting is a symptom of high cortisol.

I'm hoping to come across something to explain and help 2young's symptoms etc. and learning at the same time.
Lyme and company is bad enough let alone adding in the collateral damage.

I'm wondering since 2young is replacing T4, if by chance it can make her cortisol high.

From
http://www.virginiahopkinstestkits.com/cortisolzava.html
Too much cortisol, caused by stressors, over a prolonged period of time, results in excessive breakdown of all structural tissues of the body including muscle, bone, skin and brain


Too much cortisol, again caused by the adrenal glands� response to excessive stressors, causes the tissues to no longer respond to the thyroid hormone signal. It creates a condition of thyroid resistance, meaning that thyroid hormone levels can be normal, but tissues fail to respond as efficiently to the thyroid signal. This resistance to the thyroid hormone signal caused by high cortisol is not just restricted to thyroid hormone but applies to all other hormones such as insulin, progesterone, estrogens, testosterone, and even cortisol itself

--------------------
2 Corinthians 12:9-11


9 But he said to me, �My grace is sufficient for you, for my power is made perfect in weakness.� Therefore I will boast all the more gladly about my weaknesses, so that Christ�s power may rest on me.

Posts: 1445 | From Poconos, PA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.