If you have hashi's, your tsh should be suppressed to a .50-1.0. You are going to continue to have symptoms until you get it down and stay optimum for a while. what was your free t4 and free t3 results?
How long have you been taking the Armour ?
If you remained a long time in a hypo state your adrenals could be giving you some trouble and then Armour will not work the way it should.
Exactly what kind of blood work have you had done?
This would be proper testing for both thyroid and adrenal fatigue
Go have a TSH - free t3 and free t4 test - if you had that please post the labs
I would suggest a 24 hr saliva test but many office will not do them. You may have to just get the blood draw for cortisol and ACTH test.
A vit B test would be helpful too.
Dear all,
My free T3 and free T4 were within nornal limits. My endo is always doing these labs once I am in office.. The only problem I had is TSH levels.
Here is the answers to the above questions,
1. I was placed on Armour in February 2008 - 60 mg /daily. The initial TSH prior to Armour was 4.37. ( I was a year on Synthroid 0.75 with some complications...)
2. Two TSH readings after initiation of Armour were 4.1 and 2.9. I stay on Armour Feb. to June, on the same dose of 60 mg /daily. On my 3d reading, TSH CAME UP to 4.1!!!
I see, she kept me 5 months on 60 mg daily, that was , may be , too long - and she did not increase the dose as she should ...
3. I was increased to 90 mg /daily in August, and in a little over month, my TSH came DOWN to 1.6 as of 09/13!!!
4. My Free T3 and free T4 are ok and I never had any problems with their levels...
Always ok.
5. My late afternoon serum cortisol level is fine. I did not have the saliva test for cortisol or Adrenal check..
6. My antibodies levels on the initial "thyroid" work up were over 600....
7. My BIGGEST 2 problems with Hashi are:
**** brain fogg and forgerfulness, I am mentally slaggush and slow.
*** my fingertips are PAINFUL and numb ALL the time. I cannot perform a simple function of writing or holding the pen... I am SO disable...
My phisical revealed NO other abnormal lab values. Just reccurent allergies , seasonal.
Any more thoughts...
Thanks, everyone for your input.
PS. My brain and hands need big help :)
NO your TSH is not what should be the base line for your treatment you are doing.
your FREE T3 is the most important test to read right now. Normal MAY NOT be normal
If you take a look at all the reseach on taking Armour you will know the level of your FREE t3 usually is HIGHER - Your FREE T4 is moderately in between and the TSH is lower.
If your FREE T3 is "normal???????" then it's not normal for you and needs to be upped.
I also have Hashi's and symptom free and have been for 4 mths. My FT3 is over the top in ranges - I have a low TSH ( Which means nothing)
You being way undertreated and your doctor is not increasing you appropriately the way Armour needs to be. Basically your wasting your time and money. and may need to start all over.
This is how dosing works for Armour.
You start at - let's say your amount - 60 mg
TWO WEEKS later up are upped an extra 15mg
TWO WEEKS again upped 15mg
test. ALL YOUR FREE'S AND TSH.
Then stay on 90mg for two to three weeks
up again 15mg
two more weeks another up 15mg
You will stop increases when your symptoms leave and hypo Hashi is not a burden to you any longer.
I think your symptoms may start to disappear after the 120mg 2 week trial but I would bet you will continue increase possibly up to 3 or more grains.
Only way to know for sure is small med increases and symptom decreases.
You may want to try supplementing with selenium and a low dose of natural vitamin E and C. They work synergistically.
Selenium will suppress TPO antibodies but do nothing for Thryoglobulin antibodies.
Hey, one outta two aint bad.
Don't go over 400 mcgs. Most of our food crops are grown in selenium rich soils here in the states, Carolinas being the exception. So if you eat a lot of produce and are getting it in your multi, further supplementation will not be needed.
Aside from that Fish oil (for DHA and EPA) or flaxseed oils (ALA) will help with mood. These Omega 3s are essential to maintain well being. I like the refridgerated oils as they quickly go rancid at room temps.
Good luck.
Healing from Hashi's in a process, not a destination.
: )
Mzzchief
I still think you should be increasing as I suggested prior above. You were on 60mg too long and that may have you all over the place. now you at 90mg and still brain fog is there. I really think another 15 to 30mgs may help you
The only thing I may be able to compare your ache of your hands and fingers are inflammation.
Many hypo/Hashi patients are magnesium deficient so you may want to consider a mag citrate supplement to see if that relieves the pain. No more than 300mgs
Selenium that I know if is beneficial if you need further assistance to convert your T4 hormone into T3.
I would need to actually see the Free T3 T4 labs to even suggest this may help - but many here take selenium.
Thank you, Guys, for all your postings,
I do appreciate your input. I will defenately look for supplements in the store.
I would like to know how I can improve my FT3? I will post the next time all my labs from last endo visit... Sorry, I am at work now..
So, what would I do for my FT3? Cytomel supplement?
Please, advice.
I ejnoy reading everyone's responses, as this means a lot for my health.
Thanks again.
BTW,
My endo PA thinks that the problems with my TSH up and down is related to Armour medication itself, she stated that " I , probably, had a BAD medication lot # and the Armour ks known to be different from lot to lot ( I guess from bottle to bottle). She told me that Armour is NOT stable medication and all endo docs prefer Synthroid and other "synthetic" meds. I have seen only once my endo DOC since I started going to endocrine people, and this PA has only the scattered info on meds. Seems to be this way, anyway..
PS. I have also requested to write me a note for my work . I work with cancer patients and some of them going through radiation therapy - I have requested to make a note for my manager so I don't have to deal with radiation patients after they receive it - she refused to do so, stating " it is safe for my thyroid...
I was so upset, and told her this is not right.
I am new to this community and I too have been on the thyroid rollercoaster. I have been reading your story. This is what I have learned:
Armour is all natural, and derived from animals, so it will difffer slightly from bottle to bottle..it is my understanding that is short lasting meaning you have to take it a few times a day, and works directly with the T3
Synthryoid is directly for the T4 readings. These reads take over 6 weeks to change in the blood, therefore it is a long working. Levothyroxin is the generic form of Synthyroid.
Cytomel is the synthetic /generic form of Armour and....
they do make custom pills of Synthyroid and cytomel together if the doctor prescribes it.
I hope this helps
One more thing I thought of that you could do. I do this when I am not doing well. I amke this special soup.
Brown one chopped onion in olive oil, add in chopped carrots and celery, and ground turkey meat, cook til browned.
Add in 8 or more cups of water, and enough iodized salt to taste. Add in brown rice, or chopped up potatoes. Cook til soft.
Add in lots of fresh chopped parsely. At the time of serving sprinkle on ground flax seeds, a sheet of chopped up seaweed (the stuff they use to make sushi rolls), and salsa if you are feeling like you need some spice.
This stuff fires me up, so do not eat it at dinner just lunch and breakfast. I love it. It is so rich in iodine and it helps the thyroid. The flax seeds are rich omega 3 &6.
Stay away from spinach in large amounts, and pears.
Bluntly the information on inconsistant lot@'s is absolutely false. I'd like to the the actuatly documentation on these finding.
If we want to debate on the Armour inconsistancies - vs Synthroid recalls your will find Abbott Labs having more situations than Armour.
Raeffaela - your PA is narrow minded and listen to gossiped rumors.
Armour is an extremly reliable thyroid medication. Is has a direct T3 and that is very helpful in people with hypothyroidism symptoms.
In order to boost the FT3 you need increases as I said - There may be a chance you are pooling the t3 and your doctor can run a reverse T3 is find that out.
Cytomel is synthetic T3.
Levothyroxine, Synthroid, Levoxyl, etc. are all similar forms of synthetic T4. Levothyroxine is the generic, and most doctors do not like to perscribe a generic thyroid medication, for good reasons.
Armour is a natural form of hormones in a combination of T4 and T3.
Anyone with thyroid problems should not ingest large ammounts of iodine unless the doctor perscribes it. The iodine will affect your hormone levels temporarily, and that is what you do not want. You want your hormones to be as stable as possible, not shooting up whenever you have a kelp snack.
It may make you feel better for a little while, but in the long run it is not good.
A magnesium supplement may be helpful, but you should be tested before taking supplements. If you start taking magnesium and you do not need it, you can make yourself sick.
None of this addresses the original post, but it may be helfull anyway.
HI, everyone,
My labs AS OF 08/05
Thyroid Peroxidase Ab 580.0
Thyroglobylin Antibody 32.5
T4, Free 0.98
TSH 4.13
Thiiodotothyronine, Free 2.9 - I think, this is T3, Free
On 09/13 my TSH is 1.6. And this are all labs I have so far.
I am on 90 mg of armour at this time.
Thanks, again everyone for your input!!!
Yup you need an increase. Your T3 level is still quite low, tsh is too high, and T4 is very low. I think I would ask for a reverse T3 test to see if you are pooling. You definately need an increase though. Your TSH needs to be about a .50 to get optimum with the hashi's. This is why you are still so sick. You need to up by a 1/4 grain weekly until you feel good without the hyper symptoms. Blood work with Armour should be done every 4 weeks.
and your last testing did not even include a free T3 test which is extremely beneficial taking Armour - and I believe any thyroid med for that reason./
Those are her labs of 8/05.
The triiodotothyronine, free is a Free T3. Without the lab ranges it is a little hard to guess, but I would agree the Free T3 was probably low on that test.
Her TSH is now 1.6
It's not clear that she needs an increase. Is there a doctor in the house? Did someone just start perscribing a higher dose of drugs? Who issued a perscription pad?
Who's taking responsibility when someone becomes overmedicated?
I also thought the TSH of 1.6 was the most current lab. Personally, I would want an increase, but I would want my doctor to concur.
I agree that a free t3 and free t4 is needed as well with the Armour.
We can't tell someone what dose to take. We can suggest and have the person run that by the doctor.
One should never self-medicate.
Dear ALL,
Hi, AR- 10
You are confusing me... Are you asking me if I have a doctor. I am sorry, I did not understand your posting,
Of course, I have a doctor, otherwise, I would not take Armour.
The rx was written on the pad from the endo PA that I see since February of 2008.
The initial dose was 60 mg , and recently increased to 90.
My last lab was done by the friend that works in the lab, and I have asked her to run just TSH, since this was done " under the table.." The first lab results are from my official PA, and it was done in August, so TSH 4.1 and the rest of the labs are from August month 2008. The vewy RECENT TSH is 1.6 was done by my friend, and this was NOT an official order from MD. I just asked her to do me a favor to see where am I standing at this time - 09/13.
My next OFFICIAL appt with PA is in October, I believe the end of the month.
So, there is a doctor in the house,and yes, there is a presciption and all that comes with it... This is all I have so far. Thank you.
Can someone, please, post on what is the BEST possible lab results/numbers for Hashi - patient?
Just wondering. Thanks a lot :)
Also , what is pooling????
With Hashi or any hypothyroidism, the best TSH is 0.5-2.0 according to the ATA. :
http://www.thyroid.org/patients/brochures/Hypothyroidism%20_web_booklet.pdf
see page 18 in particular
I was not questioning whether or not you were seeing a doctor. I can tell by your tests that you are seeing a doctor.
I am just a little shocked that we are now telling each other how much perscription drugs to take. You should discuss dosage changes with your doctor.
We are here to offer support and suggestions. Share knowledge and new developments. Not tell people to up their perscription drugs without seeing a doctor about it.
Dear AR-10,
Thank you for all posting.. That was the reason I was posting my response - I did not know if this was related to me or just a general statement. I do appreciate your input to any of my postings. Thank you, kindly.
PS. I would be scarry to take anything on my own. But I would not be surprized if many people out there are lonely and without any health insurance that DO order and medicate themselves to best of their abilities and finances..
There are two questions I wanted to ask, one of them is posted.
- What is pooling
- I have up-coming appt with weight management center. Obviously, they going to suggest and prescribe me some appetite suppresants. How do , guys, feel about it? As long as I am within my " medicaly suggested" lab levels, can I take phentermine or meridia? The last one ( Meridia) was offered to me by my primary care provier sometimes ago, but I have refused due to the VERY FIRST TSH levels of > 8.0
Thank you.