Mission accomplished

I did a set change this morning. The stream or words that escaped my mouth as the needle shot into place, right by a nerve, went something like this:

Motherfructosewalnutnephronkinaseoesophaguseggmanmitosisketoacidosiswalrus!!

I was trying really hard not to swear. also, this may make more sense if you know that i had an amazing biology teacher in high school who would introduce new terms to us as suitable substitutions for swear words. I think she would have been proud of me.

Diabetes and --- (aka losing faith in my immune system)

This post is a little overdue (by 6 months), but whatever- my stories, my schedule. Or something... The thoughts and emotions remain valid..

So in one of my previous posts i mentioned that my last bunch of lab tests were... Interesting. Everytime i get blood drawn for an appointment with my doctor, she tests my HbA1C, my lipid profile, and my TSH (thyroid stimulating hormone) levels. Once a year or so she tests for a whole bunch of other stuff. But for my regular blood draws, those are the golden three. I had tests done towards the end of last year and lipids and TSH came back normal and my HbA1c was hugely improved (yay!). Fast forward a few months to my next bunch of pre-appointment tests at the end of april this year: my TSH levels came back high. Like, 10-times-what-they-should-be high. Like, good glory, how-are-you-not-falling-over-puffy-skinned-and-where-is-your-goitre?? kind of high... (and with it some less than ideal lipogram results, and an unchanged HbA1c- well yay for that at least?). Some more tests (which I had to pester my doctor for a bit more than i would have liked, surely confirmatory tests should be normal before you make a diagnosis? Otherwise it's just an assumption? A well educated guess?) confirmed that i did indeed have elevated antibodies against my thyroid, and lowered T3/T4 levels. 

Well hi, hashimoto's hypothyroid, nice to meet you...

I know that this is not, technically, a big deal. I know that hypothyroidism is relatively common among women in general, and that a lot of people with type 1 diabetes have hypothyroidism. And i know it's easily managed. A pill, once a day, every day for the rest of your life, and you're A-OK. Please, in comparison to testing blood sugar 8-10 times a day, multiple injections or pumping insulin, lowering highs, raising lows, watching what you eat and making sure to get regular exercise- and avoiding lows in the progress? In comparison, one pill a day and regular blood tests (which i do anyway) is nothing. Really. 

I am not overly upset or stressed about this. Exhausted, maybe, at the thought of having one more thing to deal with. Exhausted, just in general? I confess, there is something particularly disconcerting about realising that , despite all your efforts to control a pre-existing chronic condition (diabetes), your current lifestyle is so unhealthy, so high-paced and high-pressured and so sleep-deprived; that you assume it's perfectly reasonable and normal to feel as crap as you do, to be permanently exhausted, emotional, stressed out and on-edge, that you don't even recognise the way you feel to be symptoms of a disease state. Surely, surely, there's something wrong with that? And, perhaps, something wrong with the post-graduate research system, or the research community, and maybe even society, that we encourage and reward people who live like this? Maybe? (ok, perhaps that's a tirade for another post).

Aside from my exhaustion, there is a slight sense of mourning, a sense of loss that doesn't particularly make much sense. I'm already used to having one endocrine gland that doesn't work all that well, and resigned to living with it for the rest of my life. So the life-long aspect of hashimoto's is not a big deal for me. Maybe its more just the fact that i was so young when my pancreas died that its just always been my "normal" for me. This is the first time i have to consciously realise and accept that a part of my body that was working just fine not too long ago is now defunct. Dead. No more. And with it, my body has lost one more tool available to it to fine tune and regulate my metabolism and maintain homeostasis. And so, even though i can just take eltroxin and carry on and this doesn't really affect much else, on the other hand, in a myriad of small ways, this affects everything. And that makes me a little sad.

Perhaps the bigger over-riding reaction to this, that has simmered down since april but remains always lurking in the background, is a loss of faith in my immune system. No, make that the gain of a deep sense of suspicion of my immune system. For this, perhaps a bit of background information may be useful. 

I am the only person in my family with diabetes. Among all the aunts and uncles and cousins and grandparents, parents and siblings (ok, i only have one sibling, but that's besides the point), i'm the only one. There's not type two diabetes in my family either. Nothing. It's just me. This may strike people as unusual, but there's another clear pattern in my family which makes perfect sense. Autoimmune diseases. Almost exclusively from my father's side of the family, there is a very strong pattern of autoimmune disorders, big and small. Besides my diabetes, there's addison's, lupus, hypothyroidism, hyperthyroidism, hypoparathyroidism, otosclerosis, scleroderma, vitiligo, dermatitis and rheumatoid arthritis- all autoimmune linked. And that's just the stuff i know about. My point is, we do autoimmune diseases. You may as well make us t-shirts. 

Up until this year, i had mostly just accepted diabetes as my portion of these lovely (<-- sarcasm) genes. I figured my immune system had chosen to pick on my pancreas, it got that genetic aggression out of its, uh, system, and now we can all move on with life. Not so much apparently.

With a hashimoto's diagnosis, it's not longer just diabetes. I now have diabetes AND ---. l'm now more complicated, more high maintenance. And more at risk of more autoimmune crap. A lot of people get no more than the diabetes-hyothyroid combo. But some others go on to get a third disease, usually addisons. Its common enough to have a name: poly-glandular autoimmune syndrome. Knowing this, and knowing my genetic background makes me nervous. I had some extra tests done when my hashimoto's was diagnosed, and nothing looks unusual so far. But i know i need more extensive tests done. And most probably semi-regularly from now on. 

In the mean time, it feels like there's always a constant worry in the back of my mind. i no longer trust my immune system to stay at bay. I don't trust it to keep me healthy. I supplement my diet with a whole bunch of stuff, including high quality, high dose omega-3 FAs (EPA and DHA). I'm trying to exercise more. I'm trying to reduce my carbohydrate in take (although i'm not completely sure i buy the whole low-carb thing- more research into that is on my to-do list). I'm trying, really really trying to minimise any levels of inflammation in my body. I've tried to not be too stressed about my thesis and up-coming exam (way easier said than done).

And everytime i don't feel that great, feel a little more run-down or emotional than usual, a little more drained and tired, every time i get a joint or muscle injury that resurfaces or just won't clear up; a little bit of that worry resurfaces. Just for a moment.  But it's there.

I'm still here..

I'm still here. I'm around, I promise...
I finished my thesis/dissertation/monster... Submitted end of August.. Phew!
Since then, i took a too short but much needed holiday in durban, visiting two of my favourite peoples, my brother and TUE (I would insert some photos from the trip. Except this is unnecessarily complicated to do from my iPad, and I'm lazy. I admit it.), and have been oscillating between catching up on much needed sleep and frantically preparing for my oral exam/defense.. Which was potentially going to be this week. Seeing as I found out yesterday that its in the beginning of november I can breathe a bit, maybe write some blog posts (?) and keep studying, because i'm so not ready yet... But i'm nearly there. I'm nearly finished. this bumpy three-year ride is nearly over. The end is in sight.

This is a familar feeling for this time of year. We have the most beautiful weather, with spring rapidly merging into summer, jacaranda trees bursting purple blooms all over the place, jasmine bushes and syringa trees more subtly perfuming the evenings, and the most fantastic high-veld storms cooling the evenings and lighting up the sky. And the only thing getting in the way of you just sitting back and soaking in the beauty is the last stretch of school work, matric, or university exams. Strangely enough its actually enough to incite some melancholy, it brings back so many memories from childhood through to student days, plus the remembered sense that you just have to get through this last stretch, and then its full blown summer, december holidays, and everything that comes with it...

Today has been a stormy, gloomy, rainy day. I love such weather, its the perfect punctuation to our mostly bright and sunny heat. And with it all comes some of the familiar and not unwelcome melancholy as well. I've been looping the Jars or Clay Furthermore double album all day. This is some of my favourite music, heavy with emotions and memories for me- and perfect for this weather, and this time of year- there are just so many memories to link the two, good and bad.

So hopefully more posts will follow with some D-related stuff that needs to be written and told. For today, i leave you with a particulary beautiful live version of a track from the Furthermore album- enjoy :)