Posts Tagged ‘thyroid literary support’

My Pretty, Bleeding Thorn

dearthyroid | February 8th, 2010 | 10 Comments »

Thorn in my side, thyroid patient letter, Dear Thyroid, thyroid disease support, thyroid blog, thyroid support

Written by THypothyroid Patient

Dear Thyroid,


Because of you I spend my day looking and researching for ways to make myself feel better. I first gave notice to you when I was in my 30’s, and now 20 years later you still haunt me. I recognized that you were not being a friend to me when I could hardly get out of bed in the mornings and all I really wanted to do was sleep the day away. But I had to hold down a full time job as a home health nurse and the bills had to be paid. I discovered you after researching what could be making me feel so bad.


Not being one that just ran to the doctor for everything, I tried to fix me, but nothing was working so I finally dragged myself to see a doctor. I told him that I was sure that I had a problem with you, hypothyroidism. My hair was falling out. I was too tired to get out of bed. I had no appetite, but was very much overweight. Obese to say the least.


The doctor took some blood and tested your function. My TSH was a whopping 76! No wonder I felt awful! He began me on Synthroid in which I did begin to feel so much better.


But because of you not behaving as you should in my body, I will battle being overweight for the rest of my life. I will battle being in the proper ranges of T3, T4 and TSH for the rest of my life. I will constantly be fighting symptoms and trying to figure out “why”. I will always be looking for solutions to fix the many everlasting problems you cause.


You are always trying to get the best of me and think there are some doctors that like it that way. That is why they prescribe synthroid to those who do not respond to it, as is my case. After being on Synthroid for several years and changing doctors for various reasons, I requested to be able to try Armour Thyroid. And it made a world of difference. I must have started not being able to convert T4 to T3 (or is it the other way around?). Whichever it is, you, my dear thyroid are a constant reminder that you cause turmoil.


It was the middle of last year that I had to change doctors once again, because mine was leaving town. And I chose one that did not believe in Armour Thyroid. I’m sure it is a “money” thing. He didn’t give a hoot that I would not feel better on it, and oh, by the way, my dosage was needing to be changed. For some odd reason my TSH had been within range for a long time, but it began to be very low—almost nonexistent at something like .003. I was having awful symptoms. I was losing hair like crazy, wanting to sleep all the time, heart palpitations, tired, no appetite. The only one that wasn’t an obvious hypothyroid symptom was my heart feeling funny. I only have that when you’re overactive. But no luck losing weight, either.


So I finally started going to another doctor who had no problem putting me on Armour. I was so depressed, my hair kept falling out, and I suffered from muscle cramps with the smallest movement. I had no appetite but I was putting on more pounds. I knew that my levels were still not right. But since being changed to Armour, I am feeling much better and less depressed. And by the way, my new doctor did confirm that some doctors along with the pharmaceutical companies pushed synthroid because of not having control of the”natural” thyroid. In other words they don’t make money on it, the bottom line.


I know I will always be at battle with you. You are the thorn in my side. But I will not go down without a fight. I am on constant watch for new procedures that will defeat your fight to put me out of balance. Oh my dear thyroid, look out! I’m on a mission to put you back in your place and have you to be behaving once again.

Signed,

T

How long have you dealt with your thyroid problems, diagnosed and undiagnosed? Did you know there was something wrong long before you went to the doctor, but couldn’t quite put your finger on what it was? What proactive measures do you take to fight back? Let “T” and all of us in the thyamily know in comments!

Silence Has Never Been More Golden

dearthyroid | February 1st, 2010 | 11 Comments »

Michael Wilson, thyroid patient, men with thyroid disorders, thyroid support, thyroid blog, Dear Thyroid letters

Written by Mike Wilson (Undiagnosable Thyroid Patient)

Dear Thyroid,

I haven’t written to you in a long time.  And this is a good thing!  We should both be happy about this fact.  I know I am, and I hope you are.

Something must be going right.  Don’t stop whatever it is you’re doing (or not doing).

Have you been feeling swollen lately?  No.
Have I been feeling sluggish lately?  No. (Well, not beyond my usual lazy self…)
Have I experienced brain fog?  No.
or Irritable Male Syndrome?  No.
or extremely rapid skin, nail, and hair growth?  No.  (OK, well, the finger- and toenails a little…)

It’s winter… you usually demand a dosage change to support your levothyroxine habit.  But you haven’t (O the joy!)
And I’ve been sleeping well most every night, and it feels good to rest so much on the weekends… actual healthful rest, not “exhaustion recovery”.

No, it’s been smooth, sailing for several months now.  I cannot remember the last time this happened.
I’ve felt good enough to finish my graduate research, kick Masters Degree ass at my thesis defense, do the job of two people at work, start shopping for a house, and I even got almost all of my holiday shopping done today.  I must not be giving you any grief, because you haven’t given me any grief.  This is how symbiosis is supposed to be, right?

I even turned an actual, real pumpkin into two pies for Thanksgiving in just about 3 hours.  That used to take me 2 days in the past.  Yup, we did good, quick, quality work on that orange squash, didn’t we?  It’s these little things in life that make the difference.  Thanks Thyroid for that!

I think you must be pleased that I significantly reduced the caffeine in our diet.  I know now that you had difficulty with it, and would inadvertently make Heart flustered.  I didn’t like that feeling either.  And, I’m wondering if the niacin is helping you out.  Skin hates it, because the flushing feels like mustard gas pumping through his pores, but he’s tough, he’ll get over it.  Not like you, since we’ve established how delicate and fragile and special you are and how much coddling you need.  That’s just how you are.

Anyway, three cheers for at last four months of stable metabolic bliss at an enjoyable level.  Huzzah!  Huzzah!  Huzzah!
In your honor, I shall compose thyku:

I have accepted
My thyroid and all its faults
That’s just how we are

When my thyroid feels
Miserable, unhappy
I know so will I

It’s not thyroid’s fault
Something else made it that way
Common enemy

Happiness and health
Are friends walking hand in hand
Each helps the other

I cannot know all
The things my thyroid needs, but
I do what I can

Here’s a magic word:
Triiodothyronine
Artificial life

Dear Mr. Santa
For Christmas please bring to me
Free liposuction

Mike is a 36-year old male suffering from hypothyroidism of mysterious cause for almost 10 years now.  He believes that knowledge is power, and that true healing cannot happen without fully understanding the entire situation.  Examining the opposing point-of-view is essential to obtain knowledge and understanding.  The greatest discoveries come from thinking differently.

Check out Mike’s website.

My Hate for you Continues, Thyroid of Mine!

dearthyroid | January 29th, 2010 | 18 Comments »

Dear Thyroid Letters, Hypothyroid patient Lori, hypothyroid support, hypothyroidism blog

Written by Lori (Hypothyroid Patient)

Dear Thyroid,

My post holiday shopping was ruined because of you.

My whole family was affected by my bad mood. Why was I in a bad mood? Because of you and your stupid inactivity, why can’t you understand that I am tired of feeling so fat and sluggish?

You know this, I did not eat ONE SINGLE fattening thing over the holidays. I ate all vegan food. I never touched the fudge, cakes, pies, ham, or anything else, so proudly displayed on the table at my mom’s house. Did I lose a single pound? NOT ONE! Your lazy ass decided not to burn any calories leaving me feeling bloated and fat.

So, the bad mood started when I discovered I would have to move up to a 40 C bra. I have never had a bra that big… EVER. The “C” is fine, but NOT the 40. My boyfriend thought he was helping when he pointed out that I should not feel badly because he wears 40 waist pants. Oh wow! That helps a lot, thanks BF. I am almost as mad at him as I am at you, evil thyroid!

I can’t even mention the size of clothes I had to buy out of desperation to keep warm because, thanks to you, I froze my ass off in Florida. I have never felt so cold to the bone!

So, I guess if I was a pig and ate crap during the holidays, this anger would be directed at myself, but it’s not, it is directed where it belongs! At you! So, it would be nice if you would figure out what you are going to do and get to work and stop being a lazy ass because I have done everything I know how to do.

I hate you. A lot!

Lori

WOW – Lori is angry. Her body has completely changed. She’s become physically unrecognizable to herself, something we can all relate to. Have you made peace with your ‘new self’ or do you feel as angry and frustrated as Lori? Speak up, beautiful babies.

The Dream Of A Thyroid Language

dearthyroid | January 28th, 2010 | 10 Comments »

Sarah Hypothyroid Patient, Hypothyroidism support, hypothyroid blog

Written by: Sarah Downing (Hypothyroid Patient)

Dear Thyzilla,

Had I only known all those years ago when I started gaining weight and being taunted for it by my parents, my sister, my boyfriend(!) at the time and sometimes complete strangers that there was something physically wrong with me or rather you, perhaps then I could have saved myself the years of guilt and self-flagellation that I put myself through. I ate so little, avoided calorie bombs and shelled out on frequent gym memberships. The fact that I had to work my butt off to lose even a small amount of weight only for it to pile back on sooner or later often meant that I would eventually give up going to the gym only to talk myself into trying another form of sport in a desperate endeavor to lose weight and return to the Size 6 I was at age 18. My wardrobe was filled with a department store range of Sizes – from an American 8 to 12 and eventually 14, I had it all and I finally got rid of the smaller ones as I realized it was just futile to try and wriggle my way back into them – despite all my efforts to the contrary.

To make matters worse and illustrate how merciless Germany’s attitude is to women with curves, the biggest available size in most stores is a 12 and this is considered fat. Furthermore, the shops they do have for curvier women tauntingly name themselves things such as “Mode fĂĽr Mollige/Fashion for Chubbies”. Ignorance is bliss and many people are blissfully ignorant – the gynecologist I went to, for instance, because I was experiencing painful intercourse, which I now know is a result of the fact that the thyroid causes dry mucous membranes, including that of the female genitalia. And, of course, the other symptom of an underactive thyroid – low libido – only made things worse! Instead of helping me, the woman patronized me and even made a nasty remark about my weight, but failed to diagnose me!

I then switched gynecologists only to have the same problem. The first appointment went fine, but by the second appointment – six months later – I had found out about my underactive thyroid and wanted to let her know, as it does after all affect the whole body. Despite this knowledge, gyni number 2 once again made a cruel comment about my weight.

What really blew my mind was when a German friend of mine, who for years had made disparaging remarks about my weight gain and was an addict of Weight Watchers and “so relieved she didn’t suffer from any weight problems”, fessed up that she too was suffering from an underactive thyroid, so how on God’s green earth didn’t she know that this can cause weight fluctuations and why wasn’t she more sympathetic to my plight?

And for that matter, why the hell wasn’t my own mother who herself had been suffering from an underactive thyroid for years and only recently found out? The sad thing is that my grandmother had been suffering for even longer with an underactive thyroid and yet nobody bothered to tell her that this runs in families, so she might want to tell her offspring and theirs to get themselves a check-up. The same with my mother – only several years after diagnosis did a so-called medical professional bother to tell her about the family connection, alerting me to the problem and resulting in my check-up and eventual diagnosis.

I was happy and sad at the same time to finally know that there was a reason for me being “fat” – I’m only slightly overweight, but thanks to the people I have crossed paths with over the years – I now do have hang-ups about the way I look and never again will I look at a fat or overweight person in the same way, because I know only too well that it can often be something so much more complicated.

A friend of mine has a German husband who makes tactless comments about my weight every time we see each other. I wanted to finally nip this in the bud, so I mentioned to him at our recent Thanksgiving party that I had discovered I have a metabolic condition and hence the weight problems. I figured that because he owns a gym, he should be familiar with this kind of thing. Of course, like so many others, he didn’t listen and then proceeded to compare me to this 600-pound British guy who had been in the news a few weeks earlier and couldn’t get out of bed or out of his chair. I had also explained to Mikey – yes, you know who you are, although you may never read this letter – that I am suffering from extreme exhaustion right now, which is almost certainly compounded by the Epstein-Barr virus I was diagnosed with. Because people with an underactive thyroid usually have weakened immune systems, we are more susceptible to infections such as the EBV virus, which 95 percent of people carry in their body at some time, but only when your immune system is weak does your body become unable to fight it off and chronic Epstein-Barr and thus Chronic Fatigue Syndrome may result. Right now I’m on antivirals for this, which will not get rid of the virus entirely because once it is in your body, it remains dormant your entire life, but with a bit of luck, the antivirals will deactivate it and, from what my new and wonderful doctor tells me, once my thyroid receives adequate treatment, my immune system should become stronger anyway.

But I’m getting ahead of myself. Allow me to backtrack to the point in time at which I got diagnosed by my first doctor. I was put on the one-size-fits-all Levothyroxine (my current doc confirmed and I also read that T4-only meds are most often prescribed, as they are cheaper than the T3-T4 combination meds that many patients find to be more effective, which is what I wanted in the first place had I actually been given the choice!) and told to come back in three months. After about a week to 10 days (apparently that’s how long it takes to get into your system), I was feeling phenomenal – I was no longer sleeping till 12 and bright-eyed and bushy-tailed most days at painfully early 8 am. It felt awesome to have so much energy and I finally started losing weight, too. I had decided to invest in a personal trainer because now that I knew the cause of my weight problems, I felt finally able to tackle them and was hopeful that I would succeed. As my trainer is also a physiotherapist, she can write me bills for physiotherapy (which is pretty damn similar to what we do anyway) and the insurance pays, or at least they did so far, but now they too are trying to make my life hell, but more on that later.

After about one and a half months in to taking the meds, I started feeling crap again and had stopped losing weight despite my rigorous workouts twice a week with my personal trainer. I went back to my doctor, but as I was trying to get my insurance to pay for therapy at the same time and needed her to write a report, she fobbed it all off as “emotional exhaustion”. The thing is I have experienced emotional exhaustion before and I was certain that this wasn’t it. We’d gone through the year from hell with my grandfather and my fiancĂ©’s mother dying within months of each other, so I felt that therapy would be beneficial (after making me and my potential therapist jump through several hoops, my insurance company got one of their lackeys to turn down my claim as “not medically necessary” despite my doctor certifying several medical diagnoses in an attempt to get the bastards to pay – but this is a standard process of insurance companies here. Even if your doc states something is medically necessary, they still ignore it half the time and you have to fight it tooth and nail).

Incidentally, I suspect that the year from hell may have brought all this stress and entailing medical problems to the fore (my cortisol levels are now sky-high and this is caused in part by increased stress – adrenal problems are extremely common with thyroid patients), but therapy wasn’t going to help my tiredness and I knew that, so I changed doctors, further empowered by the thyroid websites I had been reading and researching on, which all too often described patients and their doctor horror stories. I didn’t want to be one of those who makes the mistake of staying with the wrong doctor for years. Incidentally, before we switched doctors, I had asked our doc to check Corey’s thyroid because he was tired, irritable and slightly overweight, but moreover because his brother has Hashimoto’s. She did a simple TSH test and pronounced him healthy, just as she pronounced me cured when she took my first TSH test when on the first new meds, despite my persisting symptoms. I was skeptical either way.

We changed doctors based on a recommendation from a good friend with Hashi’s and a wonderful website listing German thyroid doctors recommended by patients and organized by zip code. Dr Neufeldt is something else. I have never met a doctor quite like him. Now I try to do some research at least once a day, partly because it fascinates me and partly because it empowers me to be a better patient and increases my chances of getting better. Doctor Neufeldt encourages this and is also extremely knowledgeable. He works with a team of specialists in his building because he knows how a stubborn thyroid – like yourself Thyzilla! – can affect the whole bloody body. Consequently, he found that one of the arteries in my neck is starting to become blocked (occlusive disease) and checked my blood for genetic risk factors. He has concluded that this is caused by my thyroid and is confident that once on the right thyroid meds, this too should go away. He also found the seven gallstones that the other doctor missed and that are exacerbating my bloating and inability to lose weight. And, most importantly, he actually bothered to check for and found the Epstein-Barr, so now I have to take four little white pills a day and they had better kills of this damn virus!

The other thing he found is that my fiancĂ© Corey does in fact have an underactive thyroid. An experienced thyroid doctor can apparently tell just by looking at someone sometimes that they have signs of thyroid problems. Corey has puffy eyelids and is slightly overweight. Doc tested him and, despite a normal TSH, he found that his thyroid problem is even worse than mine and mine had apparently persisted for at least 10 – 15 years! Corey’s fatty liver, which no other doctor had bothered to do further testing for, is apparently also caused by his thyroid – it’s something to do with the body’s impaired lipometabolism and the buildup of fats. The doc also discovered two gallstones – apparently, 90 percent of thyroid patients have these and they’re also due to the messed up lipometabolism. Corey was angry at the number of doctors who had accused him of drinking too much, even though he drank in moderation. Ignorant gits! Even the “snore therapist” he went to to check out his sleep apnea took one look at his BMI and freaked out. And don’t even get me started on BMI – not only am I slightly overweight, but my BMI will never correspond to the stupid tables because of my body type (big boobs, broad frame) – it tells me I am morbidly obese. A case in point, which really cheered me up: Kate Harding Illustrations. Apparently, sleep apnea can be another symptom of hypothyroidism, but in Corey’s case he also has a deviated septum that he’s going to get operated on in January 2010.

Right now I’ve reached the point where I’m doing as much research as possible to help both myself and others. My own mother is obviously under treated, as she is still experiencing tiredness and brain fog. Thanks to Mary Shomon’s Top Docs website, we’ve found recommended private doctors she should be able to see in the UK. Everyone in the UK has health care thanks to the National Health Service, but due to lack of funding, it’s just not always as high-quality as you’d like or need and luckily my parents are prepared to and able to spend out some extra money to see a private doctor to get my mother better. My own sister had been experiencing various symptoms – night sweats, eczema, irritability – the question is whether or not she has also been hit with the family curse. My brother-in-law has also had his share of ignorant doctors, telling him that his overweight and inability to lose it is caused by his overconsumption of beer and lack of exercise. The same doctor tested his thyroid levels the first appointment and told him that they were worrying only to tell him the second appointment that the very same levels were just fine and that he should come back in six months without an adjustment of his medication.

Thanks to Mary Shomon’s Top Docs, once again, we found a recommended doc. We had to travel about two and a half hours to get to her because they live on the Gulf Coast of Mississippi, where many doctors vacated and still are vacating after Katrina and due to the onslaught of the economic crisis. My sister-in-law has been suffering for 10 years from a pitiful laundry list of ailments, notably fibromyalgia and chronic fatigue (CFS), which is caused by the Epstein-Barr she also has. When discussing our symptoms on my new diagnosis, we realized that our symptoms are awfully similar – notably the aforementioned, plus her hair loss and the fact that she went from a Size 6 to a Size 14-16 within a matter of months, has had weight problems her whole life and so did her mother. Thyzilla, we suspect that your twin brother Thyzuki may be creating havoc in her life. Sadly, the hoards of doctors she has been to have been unable to treat her because she is on Medicaid and they either don’t care or don’t know enough. As soon as she gets the opportunity, she too will go to my brother-in-law’s new doctor, who after the first appointment appears extremely promising. I hope to God she can give her some diagnosis other than – oops, you have CFS and there’s nothing we can do – strange that, considering my doctor gave me antivirals for the Epstein-Barr.

In addition, we suspect various friends of ours may be suffering from thyroid problems (considering one in three people do, it’s a pretty common, but horribly misunderstood disease). Like my sister-in-law, one friend has also been diagnosed with CFS and fibromyalgia and these days, it seems many docs believe CFS and fibro to be just another symptom of an underactive thyroid, our current doctor being one of them. We persuaded my friend to go and see our doctor as she has already suspected problems with her thyroid and we’ll be going together some time in the future. Another German friend blatantly has a thyroid problem – they even saw it on the sonogram, but because her TSH is normal (G-damn!) a whole range of doctors have refused to treat her, so she continues to lose hair, gain weight and suffer horribly. We found a new doctor near her on the German site I mentioned above and I hope she will go to her at some point, but seeing as she has just lost her father, that might take some time.

To add to all this turbulence, my German private health insurance are trying to turn down every claim under the sun by having their oh so unbiased “experts” claim that treatments are not medically necessary despite the doctors saying they are. My worst gripe is that it doesn’t take a genius to figure out that a year’s worth of intense stress such as this, an underactive thyroid (known for causing joint pain) and an active case of Epstein-Barr, which merits administration of the same antiviral drugs given to AIDS, cancer and chemotherapy patients, very likely would cause constant back problems and pain akin to my current symptoms. They are refusing to pay for the chiropractic the contract states they will pay for, so the New Year will start with a letter to the ombudsman (who mediates between policyholder and private health insurance – he has a lot of cases right now because when the economy is suffering, they try to cheat their patients and breach their contracts) to fight them for all the treatments they are obliged to pay for. I’ve been to this guy before though and I know he is good and fair, so I trust he will help me again this time. My thyroid doc is outraged and also on my side, as he is writing them a letter to tell them just how sick I am or rather how sick they are!;-). Insurance companies shouldn’t get away with treating chronically ill patients this way and, in my case, I will do my utmost to ensure they won’t.

So right now, every morning, we each take half a tablet of the new T3/T4 combination medication (Novothyral) that Dr Neufeldt has prescribed us – he tells me it is the practice in Germany to start out with low dosages and then slowly up them . He said it was the other way round in the US, but having no experience of treatment in the US (yet), I can’t really comment. I think we may need our dosage increasing, but we’re jetlagged – we just took a 12-hour flight from Germany to Mississippi, or rather two flights – just recovered from a cold and a 24-hour stomach bug and are also excited about our recent engagement. Corey proposed to me on 25 December, so now we really are in this together through sickness and in health. And, on a positive note, my father who had taunted me for years about my weight gain actually went so far as to apologize when I explained to him that I have a metabolic disease.

My name is Sarah. I’m a 32-year-old English translator and writer living in DĂĽsseldorf, Germany, with my American fiancĂ© Corey. We just recently got engaged (last Christmas Day) and were also both recently diagnosed with Hashimoto’s . We’ve started on thyroid meds and I’m also on antivirals for Epstein-Barr right now. It sucks that we are both ill, but I am glad that we can support each other in this fight to get better and fortunate that we are among the lucky few to actually get diagnosed. Thank you, Dear Thyroid, for giving us the opportunity to express ourselves and hopefully help each other by doing so.

Sarah Downing -

Get to know Sarah, follow her on Facebook and read more about her at her Translation and Journalism Website. Sarah has also started a discussion in the forums, which we encourage you to join “Inadequate Health Care for UK Thyroid Patients“.

Like so many thyroid patients, Sarah has bared her soul and shared her experience of her disease with us. How does her story relate to yours? How does Sarah’s story make you feel? How would you extend support to Sarah? Let us know in comments!