....In our GP’s knowledge about common illnesses.
(As a side note, I’d like to say that I am very dedicated to
making this blog about positive experiences and to help women in the
same/similar situations. But today I’ve pretty much had a blow to the skull, so
you’ll have to excuse this rant.)
I had my GP appointment today. Let the disappointment
commence. First, she looked at my blood results from last month, and told me
that they were borderline. This means that it is POSSIBLE I have an
abnormality. We already established this during my physical examination, but
apparently that can be overlooked.
Dr Mc-Angel-now-Bitch, proceeded to read me the letter from
the ultrasound tech. Ah yes, it would appear that I do have polycystic ovaries.
Shocker. But still, my bloods are “borderline”, she kept saying that over and
over again like the actual cysts on my ovaries didn’t matter.
We had a little chat about where to go from here. She won’t
refer me for another scan because she doesn’t consider the cyst on my left
ovary as “large”, despite concerns made clear by the ultrasound tech. So I just
have to hope that this cyst doesn’t continue to grow and end up bursting inside
me.
I spoke to her about my abdominal pain, but she said that
paracetamol can often help (!!!) and that it is an unfortunate side effect of
my syndrome. Apparently there isn’t much else she can do about that. I got the
same response regarding my weight & excess facial hair. It’s just something
I’m going to have to live with, like we can all take these clearly abnormal
physical issues in our stride. And that doesn’t include what it does to me
mentally.
The next issue is that I don’t ovulate. Her answer was to
put me on a contraceptive pill, which will give me a “bleed” every 4 weeks. I
wasn’t born yesterday, doc. I know that this bleed will not be a result of my
body releasing an egg, which won’t be fertilised and give me a natural period.
This bleed will be a “fake” bleed, brought on by the hormones from the pill. I
feel as though I’ve been completely fobbed off with this pill that will do
nothing except MASK some of the symptoms of the illness, but not actually fix
the problem. Let me be clear, I don’t
expect someone to miraculously cure me of this illness, but I would like a little
bit more help than to be given the Pill. It is a pill with testosterone in it,
and that does not make sense to me. Why would I pile something into my body
that I already have too much of?!
My fertility isn’t really an issue for the doctor because I
already have a child. I can understand this. There are a lot of women that are
desperate for a child and are not yet lucky enough to have one. I am grateful
for my son every single day. HOWEVER, I just want them to acknowledge that
perhaps I’ll require a few months of Clomid if I want to conceive again. To be
disregarded for any future assistance because at 21 I had a child seems ridiculous
to me.
If there is anyone out there that has any ideas about where
I go from here, please help. A little bit lost at the mo... xxx
Lesson we’ve learnt
Unfortunately, I think that GPs are not given enough
information, or enough time to deal with every single patient effectively. The
NHS is a free service, but for me to get some proper help with my illness I’d
have to go private (which we cannot afford!).
The best person to deal with your health is YOU. I’m not in
the position to pay for private healthcare but if you are having the same kind
of problems with hitting dead ends with doctors, PLEASE look into finding a
decent specialist in your area and pay for a private consultation.
My best friend has been through SO many difficulties with
GPs (her problem is thyroid related) and she was forced into going private and
spending so much money just so that she was able to get out of bed in the
morning. I’m going to ask her to guest post on this blog to give you all a bit
more info into her life & story, but if you can give a few minutes please
check out her blog for more details.
Having 'decided' I do not want any more kids I still think most pre-menopausal women would freak at the idea of no longer having the choice to make, no matter how many children they have. It's your right, as a woman (Loretta, Life of Brian) xx
ReplyDeleteIf it is within your financial means - go see a reproductive endocrinologist as soon as possible. GPs have limited knowledge of how to deal with PCOS and far too often focus just on the symptoms. The facial hair, funky periods etc aren't things that you just live with - you can definitely fight to overcome those symptoms.
ReplyDeleteThe first thing will be to get your doc to confirm if you are insulin resistant or not. If not - then your battle may be a bit trickier. Your insulin doesn't have to be way off either - mine is only slightly elevated but it's enough to make my ovaries a mess!
Hang in there - with the right doctor - you can get a handle on this.
unfortunately GPs can be completely rubbish. It took forever to get me diagnosed with PCOS and endo ( I have both...aren't I lucky?!) and in that time I had to go through 3 cysts bursting! yucky. Just stick with it lovely and keep telling them you've done your research so they don't treat you rubbish xoxoox
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