Last Wednesday saw K & I at the GP to get the results of her blood tests – full blood count, glucose fasting tolerance (diabetes), thyroid, coeliac, liver, kidney, bone. Nothing sinister was found.
You’d think we’d be delirious about that. Well, we’re not! The GP then said that K is depressed and this is causing her symptoms. The reason for this diagnosis? She cried in both consults, she had only been to college twice (for less than 3 hours in total) in the past 9 days, and that she didn’t go out very often.
Let’s break this down a little. If you feel so totally, overwhelmingly tired all the time you tend to lose the ability to smile all the time. Add in to that a new symptom that reared its ugly head between both visits – random, stabbing pains that painkillers don’t touch – and of course she’s going to feel emotional. Then add in that all the blood test that you were pinning your hopes on to show a problem that could be treated (and thereby hoping you’d then start to feel better soon) came back ‘normal’, thus removing that hope, then you’d really be hard pressed to not cry.
She went to college immediately after the successful blood taking – one that had the nurse wiggling the needle around to catch the vein that was hiding in there somewhere (and I should point out that K gave her permission to do this) – but couldn’t concentrate and felt shaky so I had to fetch her home. The next several days were spent in a fog of exhaustion. She did some college work at home – thank goodness for an understanding college and teachers – but often ended up needing a good nap during the afternoon (at least 2 hours). There’s really no point in trying to get to college (2 bus rides and about 10 miles away) when you struggle to walk down the stairs because you are so tired.
As for not going out much in general there’s a long story attached to that, one that the GP didn’t bother to ascertain. Y’see, K doesn’t have many friends within walking distance – even if she had the energy to get there. When we took her out of school one previously good friend in particular decided that K was to be victimised and sent packing at every opportunity. Why? Don’t know. This girl could blow hot and cold all the time with any of her friends. Anyway, K gained some new friends at the home education group. Unfortunately they all pretty much lived at least a bus journey away, and some lived in neighbouring counties. Now K goes to a college that is not on our doorstep and all her friends there live at least one, if not two, bus journeys away. That in and of itself isn’t the problem. No, the problem is that round here the buses finish running at about 7.30ish in the evening! Yes, that’s right! Anyone wanting to use the bus to get back home had better be heading home very early. No chance of a bus back from the nearest town, nothing! I could understand it if we lived in a very rural area but we don’t. Mind you, we don’t live in a big town/city either. So it’s not that K doesn’t WANT to go out, it’s that she can’t get back unless one of us is available to fetch her. We don’t mind here and there but it’s not something we can do several times a week.
I’m not arguing about the depression diagnosis. My daughter quite likely IS depressed at the moment. It’s that the GP thinks that she has been depressed for ages and this is causing her symptoms, whereas both she and I think that the ongoing symptoms and their associated effects are causing the depression. Everyone who has had regular contact with K over the past year or so has said that they wouldn’t have put her down as depressed, yet they can ALL see the change in her in the past couple of months or so.
The GP gave her the contact information for a young person’s service called italk. K has called them and had an initial chat. She will get another call in 2 weeks to discuss possible courses of action for her to try (with them). We talked about it and decided that having somewhere to vent her frustration would be a good thing. Plus, at least the GP can’t say we’re not trying, eh?
Thanks to K’s new pain symptoms she gets a new round of blood tests, this time looking at auto-immune markers. AND she gets to repeat the glucose fasting tolerance test – where you can only drink water in the 12 hours preceding the stick. This test came back normal – the GP showed me the results – and he was happy with that when we saw him at 9am on Wednesday morning. By 11.30 he was on the phone to K asking her to add it to the form he had given her. Harrumph. There were two tests – serum and thyroid – that came back saying abnormal but he said that they were only just outside the limits and wouldn’t be responsible for her symptoms.
Any words of advice gratefully received. However, if you feel compelled to say hurtful stuff – don’t. I have enough to deal with at the moment.






