yes me to high levels after tea,good levels all day then bang up they go after tea6.3 this morn at 8.30, its my high levels after tea time that annoy me
Some call it migraine babble (there's a few different official names for it) and I never knew it was even a thing until I had it and was trying to google the symptoms.OMG... and it's migraine?
I phoned GP about fluid retention and about 80% of the callback was a lecture on still vaping a little bit after quitting a 20 cigs a day habbit and staying off them for 2-3 years.and started lecturing me on eating low fat according to the NHS "eatwell plate".
I get this with anxiety, proper medical consultants will insist I’m hypo and assume I have the hypo confusion when I say I’m not, until I test in front of them and show them the results.It probably doesn't help that I have some other conditions that when then flair up can cause simpler symptoms of a hypo. Like yesterday I was almost sure I was having on because I got sundellu hot and dizey. e and I checked I wass 11.3(which I'm still bit confused about)
I did learn this week that migraines are often genetic. To be honest that made me doubt mine are migraines since I don’t really fit the typical migraine symptoms and have no genetic history of them at all!OMG... and it's migraine? I have had those exact symptoms 3 times and the two last times (in 2019 and 2020) hubby has called an ambulance because I was struggling to speak coherently. I was rushed to A&E where they did CT scans and could find nothing wrong, no evidence of a stroke or TIA. Eventually 2 days after the last hospital incident this horrible woman doctor who had never met me in person rang to say that in her opinion I had had a TIA (which is now on my medical records) and started lecturing me on eating low fat according to the NHS "eatwell plate". I politely said I ate "lowish carb" being a diabetic. She then launched into a rant about how unhealthy my diet was and how I didn't eat fruit or veg, without ever asking what I do eat. I filed a complaint about her through PALS as she upset me so much. I got an official apology. I digress... my father was a martyr to migraines, he got them twice a week on his days off and had to lie in a darkened room. Nausea, vomiting the lot. I had some infrequent aural migraines in my late 20s, but not since then. I feel rather relieved to see your post!
Well... better get on... we have lunch guests today.
6.2 on waking at 8 am.
CONGRATULATIONS to @Sitosea, @harbottle and @goodybags on your HS... Stars of the firmament known as "the forum".
Not everyone has the same symptoms (as with a lot of medical stuff).I did learn this week that migraines are often genetic. To be honest that made me doubt mine are migraines since I don’t really fit the typical migraine symptoms and have no genetic history of them at all!
I think my frustration is more that I’ve been given a pile of migraine medication (which has stopped the cycle) and not told anything about whether this is a temporary or permanent issue, if i need the medications long term or just to break this cycle, if it’s normal to have had a virus for more than a month etc. Just keep being told to take another week off work. Have made a GP appointment for Friday to ask some of these questions before hopefully going back to work next week. It’s been a month of feeling rubbish and being unable to work so I think my frustration has just been building up!Not everyone has the same symptoms (as with a lot of medical stuff).
If anything just ask whoever diagnosed you how they came to that diagnosis if it will put your mid at ease.
Opps i posted this in wrong thread it was suppose to in my test strips thread.I get this with anxiety, proper medical consultants will insist I’m hypo and assume I have the hypo confusion when I say I’m not, until I test in front of them and show them the results.