Well, you learn something new here every day. The only time I had ever heard of parvovirus before today was in relationship to dogs. It's in intestinal virus that can be deadly for them, especially puppies.
However, human parvo is quite a different matter and seems to cause a rash and not much more from the little I just read about it. Google "parvovirus B19" to find out more. I don't believe it has a thing to do with the thyroid. My guess is that your high level of antibodies means that you have either had it at some time during your life or have recently been exposed to it. It doesn't sound like anything to worry too much about. I've never heard of this being tested before. Was it part of a thyroid series or more generalized bloodwork?
Does Parvovirus have anything to do with the thyroid?
ok, I just got copies of my labs from the last year, and something I didn't notice before, is that there was a test done just last month on June, 9 2009 that I totally do not understand.
Parvovirus B19 IgG Antibodies - My Result for that was 5.2 HIGH. Normal range is 0.9 - 1.1. What does this mean?
yes, I'm on my meds and have been for about a month now, it just seems that I take something to fix one thing and then that throws something else out of whack. Haven't heard from the referral yet. So frustrating.
I'm sorry to hear you're feeling really awful. Are you on your meds or off? How long have you been back on (if you are)? Any progress with the referral? This is the problem with hypothyroidism...when your meds aren't right, you don't just get one symptom, you get a whole load of them and just feel lousy.
God, I don't know how much longer I can keep going like this. My wholebody is so messed up right now. GRRRRRRRRRR.
Kimmie, you definitely need a new doctor. Your FT4 simply is not normal, and your FT3 technically is normal, but very, very close to abnormal. Furthermore, many people start feeling hypo before their numbers even get out of normal range. Even your TSH is way out of normal range.
I.m glad she brushed up and "discovered" T3 meds!. Best of luck with your referral. I'm glad to hear that you're back on your Levoxyl. When you see your new doctor, don't forget to ask about switching brands to see if that helps you feel better.
My doc said that my free's were normal. I asked her to try me on some T3 meds just to see if they would make a signifigant difference. She said they were not low enough to put me on meds. She does now know there is such thing as T3 meds. She is surely a quack. I told her I want a referral to dartmouth ASAP. I'm going to see a specialist. Got to wait till they review my records and then they will call me with an appt. I've been taking my Levoxyl.
You definitely need to get back on thyroid meds. FT4 is below the range, FT3 barely made it in, and TSH is way over.
What would I do? Well, first of all I think I'd try again to see if T4-only meds will bring up your free's and alleviate your symptoms. And I'd definitely try a different brand name to see if the fillers are what's causing you to feel so bad on the meds. Once you get closer to "normal", you can consider adding some T3 if the T4 alone is not alleviating your symptoms.
This all takes some time, but I think it's worth starting out low, increasing slowly, and only changing one variable at a time so it's easier to know what the cause is if you start not feeling well or have side effects.
Have you made any progress in finding a new doctor?
Oh yeah, my TSH level was 9.27.
I just got my T3 and T4 results, T4 is 0.58 (L-0.61 H 1.12) T3 is 2.55 (L-2.50 H-3.90), any advice?
She sounds scary! Didn't know there were T3 meds??? Wow!
Good idea on the specialist...best of luck.
I think your right, time to find a new doc. I called her and asked her to test my T3 and T4 and to give me meds for the T3 as that is most likely my issue. She was very difficult to convince and at that, she's like well I guess we could do it, but I don't think it's gonna make much of a difference. Then she proceeded to say that she didn't think there was any medication for T3. Hello, and she is a doctor. I told her I have done a lot of research on it, and I really think that this T4/T3 is the solution to my symptoms. At this point, I need to find another doc. I am going to get my T3 and T4 levels tested and search Dartmouth for a specialist that will know what he's/she's doing.
You're right, I don't see FT3 and FT4 there anywhere. TSH is high at 9.27 indicating hypothyroidism (but you already knew that).
I think it's time to find a new doctor who knows how to treat based on FT3 and FT4. I can't believe that with your symptoms and complaints about the meds giving you side-effects, your current doctor chose to run only TSH. Well, I can believe it, but it's irresponsible.
Don't suffer because your doctor,s ignorant...find someone who can help you.
I finally got the results of my blood test. I don't think she even tested my T3 T4 levels.
Here they are:
Hematology Liver Panel
WBC - 6.9 (L=4.80 H=10.80) Total Bili - 0.4 (L=0.20 H=1.2)
RBC - 4.29 (L=4.20 H=5.40) Direct Bili - 0.1 (L=0 H=0.20)
Hgb - 13.3 (L=12 H=16) Alk Phos - 57 (L=32 H=92)
Hct - 39.7 (L=37 H=47) Total Protein - 6.9 (L=6.40 H=8.3)
MCV - 92.5 (L=81 H=99) Albumin - 4.1 (L=3.50 H=5)
MCH - 30.9 (L=27 H=31) ALT - 10 (L=10 H=40)
MCHC - 33.5 (L=32 H=36) AST - 17 (L=10 H=42)
RDW - 12.6 (L=11.50 H=14.50) Indirect Bili - 0.3 (L=0 H=1)
Plt - 208 (L=130 H=400) A/G Ratio - 1.5 (L=1 H=2.50)
MPV - 11.1 H (L=7.40 H=10.40)
NE% - 48.1 (L=42.20 H=75.20)
LY% - 41.2 (L=20.50 H=51.1) Miscellaneous/Thyroid
MO% - 6.6 (L=1.70 H=9.30) CRP(Inflammation)(mg/L) - 14 (<10 mg/L)
EO% - 2.7 (L=0.90 H=2.90) TSH - 9.27 H (L=0.49 H=4.67)
BA% - 1.4 H (L=0 H=0.80)
NE# - 3.2 (L=1.4 H=6.50)
LY# - 2.9 (L=1.2 H=3.4)
MO# - 0.5 (L=0.10 H=0.60)
EO# - 0.2 (L=0 H=0.20)
BA# - 0.1 (L=0 H=0.20)
THANKS FOR THE INFORMATION,I'M GOING TO LOOK INTO FIBROMYALGIA./THROID..BUT I STILL HAVE A BIG PROBLEM WITH HIVES,THEY'RE DRIVING ME CRAZY..AND HELP ON THAT..ANYONE ELSE HAVE THIS PROBLEM..
I had my thyroid removed because had had huge nodules on it, weren't sure if it was cancer, that in turn was messing my throids numbers up way bad, and the doc's at Darmouth were even confused about what my throid results were coming back as. So they advised it really needed to come out. I wish it didn't need to come out. I would recommend you keep it in unless you absolutely have to have it out. At least if it's in there you have some hormone coming out of it, verses having no thyroid, and having no hormone and having to get it all through meds. As far as talking to my doc, useless. I think I need to go find a specialist.
Why did you have your thyroid removed?? I think your best option is to sepak with your doctor, maybe he can change the med brand and stuff.
I often wonder which is better, to have a thyroid with hashimotos or have it romoved, does not having a thyroid cause more problems? sorry for the questions Im not helping much!
I still haven't got my actual tests numbers back, but givin I have all the symptoms when I am taking my meds, I am pretty sure the T3 is what I am missing. I think I'm gonna go see a specialists. I need to get feeling better.
You're right that it's T3 that is used at the cellular level. T4 must be converted to T3 before it can be metabolized by cells.
However, there's an important point that you've missed. No thyroid meds DIRECTLY regulate TSH. TSH lowers as a response to FT3 and FT4 being raised. You don't necessarily have to TAKE a T3 med to have your FT3 levels in the normal range. You can take a T4-only med, and as long as your body is converting properly, the T4 will be converted to T3.
This is why it is so important to have free T3 and free T4 tested along with TSH. If your levels of FT3 (especially in your case with your fibromyalgia) and FT4 are good, no matter what meds you are on, you will be able to evaluate your thyroid status and adjust meds optimally.
I actually was doing some research yesterday and stumble on some helpful information. I have also been told I have fibromyalgia, having that be the cause of some of my symptoms, I put both thyroid/fibromyalgia connection in my search and came upon this:
The meds I have been on Levoxl, Levothyroxin are T4 meds to regulate my TSH level. Which keeps the thyroid level in normal range, but what it doesn't take care of is the tissue metabolism. T3 is what takes care of that and relieves the fibrom. symptoms. So I should be taking both a T4 and a T3 medication. Also found some info that studies say it works better if you take it at night rather than morning. If interested in this info, (as a lot of people that have thyroid problems have fibromyalgia also) go to http://.thyroid.about.com/cs/fibromyalgiacfs/a/fibrothyroid. I am going to discuss this with my doctor and see if this is the info I have been in so much pain for.
synthroid is a synthetic drug,,if you can take that, ask for armour thyroid it is man made
Weight loss and gain requires dose adjustments. I susupect you need and adjustment. You really should have your labs done about every 3 months.
I also suspect you are getting headaches from not having the right dose.
You really need to take your med. Not taking it can even lead to death.
Never mess with your thyroid meds.
Love venora
I would not recommend stopping the medication. You have no thyroid. As you well know, it controls a lot in your body.
Try a different brand.