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What is wrong with me?

129 replies

Phantosmia · 02/12/2023 02:27

I've posted about my headache issues before. This post is going to be long and I'll try to be concise but I struggle to form a coherent tought these days.

TL;DR - Icepick headaches, migraines, strange symptoms since June with very few pain free days. GP not listening to me. Feeling worse and more bizarre than ever. Right side of head and body only.

Symptoms have changed/progressed. My GP just isn't hearing me. Each time I go back I just get given a new medication to try and that's it. No discussion, no reasoning, I try to describe new symptoms and I just get told it's a migraine, try this medicine, see ya. Indomethacin, amitriptyline, topirimate. They always have side effects that ruin me and do not do anything for the headache or the other symptoms. I've had no blood tests, nothing. Doesn't even bother taking my bloody pressure (I'm morbidly obese fwiw), I'm in and out of my appointments in 2 minutes.

I feel like a shell of a person. I am always exhausted, mentally and physically, right to my very bones. In fact my bones just ache most of the time. I used to work a very busy/active job - 45 to 60 hours a week, always on my feet, sometimes a 15 hour day with no break, always switched on and just on it. I'd get tired, absolutely, but nothing compared to this. I could still tidy my house and play with my kids and exercise etc. Just function like a person, basically. When the headaches started I thought I was just burnt out so I quit that job, found something a bit easier going, do only 35 hours a week, so much easier. But I will sleep 18 hours on my days off, I get home and I'm too tired to even shower or cook or do anything. My kids, my house, my partner - everything is neglected.

I had never had a single migraine before this. The occasional headache when I had a cold and I think I had a tension headache a couple of times but that's it.

It started in June. I can't remember the exact date but I remember the exact moment it all kicked off. Icepick headache (according to GP) that blinded me in one eye and almost dropped me to my knees it was that painful. Gone in less than a minute. Freaked me out but google told me they happen and I felt absolutely fine for a couple of days.

Then I had icepick headaches happen 1-10 times a day, had 'auras', stabbing and burning pains in my face and eye, I'd feel drunk - wobbly and unbalanced, tired, slurring my words, purple and blue flashes, dark floaters, vision whiteout, weeping eye, dripping nostril. Intense pressure on the top right of my head 24/7. 99% of the time it only affects the right side of my head/body.

August I had a headache every day except 20th & 21st. But still the pressure on those days.

In September I had 7 days (not in a row) without headaches, just the pressure in the top right of my head. Sometmes I would feel it in the back of my neck and it would get so bad I could barely stand and it I would vomit and sweat and get the stabbing pains in my face. It's also when the tingling started. It's like there is a line running down the centre of me, from the top of my head. The tingling, in fact all of my symptoms, is on the right side of my body 99% of the time. I've occasionally felt the tingling and numbness on the left side but only in the top half of my body and only very lightly.
The tingling is unpleasant. It's not pins and needles, it's more like goosebumps, like all of my hair should be standing on end but it's not. Sometimes it's more of a buzzing. I feel it from my scalp to my toes, arm included. I can be standing or sitting. It's completely random.

In October the muscle weakness started. My right hand would suddenly lose grip and I'd drop whatever I was holding. I had half the strength in my hand and arm. My leg would sometimes just give out. The weakness would just be random, come and go, not all the time. My feet would get burning hot or sometimes feel like they've been dipped in ice water. By this point I was no longer having icepick headaches or headaches every day. I was still feeling awful but for new/different reasons.

November the headaches became even less frequent, or at least mild enough I just ignore them now. However the stabbing headache in the top right of my head was still happening, but not icepick levels of pain. No more weepy eye or auras or blindness. Still the burning stabbing pains on the right of my face though but it also moved to the base of my skull with a deep aching pressure. It makes me want to vomit. Still the tingling, the weakness, the numbness, weird aching feeling in my shin. My lips get this icy but burning hot feeling. If you've ever had a strong mint and than drank ice cold water it's that kind of feeling but in my lips only.

My memory is horrible now. I get my words mixed up and use the wrong one entirely. Sometimes I try to say something and it just comes out like huttrhgjgj. Just a nonsense noise. Or I say 'nice have day!' like my brain and mouth are not syncing. Sometimes I get this deja vu feeling but it's intense and I feel sick and scared. Sometimes it's not deja vu but more like a vision of the future? I don't think I'm psychic! But that's what it feels like, as if it's a memory that hasn;t happened yet. It's a very bizarre feeling. When this happens I sometimes feel fuzzy perhaps? Like someone is hugging me too hard but I don't actually feel like I'm being hugged, just that too tight blood rush feeling.

The strangest feeling is that I can feel the shape of the pain in head. I don't think I can sound any crazier after that last paragraph but when I cough or bend down or laugh or get the stabbing headache I can now feel the specific spot in my head. It's mushroom shaped, in the top of my head. Before, the pain was just in that general area, top right of my head, but now it's like I can pinpoint the origin of the pain.

What is wrong with me? 30+ years with only a handful of headaches and never had a migraine before. Now I am broken and exhausted with a constant barrage of head pain.

I tried seeing 2 other GPs but they just tell me I need to go back to the one that doesn't listen to me because he's the migraine expert and they can't help me.

If anyone manages to read even a little bit of this post - Thank you. If anyone has felt like these and had a doctor that has heard them and fixed them please share your experience with me.

I feel lost and alone.

OP posts:
Thread gallery
5
Cornettoninja · 08/01/2024 19:29

You’re not a time waster, you’re also not a doctor and it’s incredibly disheartening to not be taken seriously by the people with the knowledge, skills and access to investigations. You aren’t an attention seeker either - your symptoms are real. Even if it does turn out to be migraines (which I’m pretty sure should really be a diagnosis after everything else has been ruled out) then your symptoms are still real and intolerable with your day to day life.

on the bright side, in most cases those symptoms aren’t always caused by anything sinister which is probably why the hcp’s you’ve seen so far are happy hedging their bets because the odds are it isn’t. The other side of that is you really do have to keep pushing, if you give up and go away it just confirms to the dr they were right to deter you from intrusive/expensive investigations iyswim.

It really shouldn’t have to be this hard but we are where we are and we all have to play the game to some extent. You’re not time wasting or demanding more attention than you deserve, you’re just trying to live your life and need a particular profession to help you do that.

bsfgham · 08/01/2024 20:15

Is there any history of antiphosphlipid syndrome in your family OP? Have you had a blood test for this ?

Brava · 08/01/2024 20:36

I am so sorry you’re experiencing this & not getting the help you need. I haven’t read all the replies here but I would go to A&E - they will carry out tests and probably do an MRI scan. I would never normally advocate A&E as they are overwhelmed at the moment - but this is now an emergency. Good luck xx

DaisyCat33 · 08/01/2024 21:07

Phantosmia · 08/01/2024 15:36

I tried to advocate for myself using advice given earlier in the thread but no one has taken me seriously. I saw another gp at the same surgery and they said they didn't feel comfortable recommending any sort of treatment or med changes and I need to go back to the original gp. So that was very... I can't think of the word. Made me feel even worse.

I see a neurologist at the end of February. It was the earliest appointment I could get.

I have had a private gp appointment and they said an MRI is probably the best next step but they are not sure what else to do for me because my symptoms are all over the place and come and go. They think it's just migraines as well.
I've paid for blood tests and everything tested for was within normal levels. I've taken my blood pressure multiple times and it's always normal range, even during an attack. I've had an eye test, the in depth one, and my eyes are fine.

I feel like I've just been labelled as attention seeking or dramatic.

I'm so sorry you've had such poor treatment from your GP surgery. Its absolutely not the way they should be treating you. You're not an attention seeker or being dramatic - you're just unwell.

I agree with a previous poster who said next step is A&E. If you have another really bad attack, that's probably the place to go. They can do a CT scan and check that things really are ok with your brain. I have a friend suffering with persistent migraines the past few months, and she was recommended to go to A&E by her GP to check for more concerning things if she had a severe attack.

If it were me I'd be really worried about what could be going on, but then I'm prone to anxiety. You don't seem too worried which is a good thing, but can you manage to wait until the end of February? If not, don't be afraid to go to A&E. I think at this point its warranted.

tass1960 · 08/01/2024 21:30

Can I suggest that you keep phoning either the appointments team or the neurology secretary at the hospital you are booked into in Feb to check for cancellations. I actually work as a neurology secretary and people do this all the time - it also saves last minute cancelled slots going to waste.

Notsure94 · 09/01/2024 04:40

My partner is having persistent headaches and started to get pins and needles and he was advised to go to A&E by his GP. He had a long wait but was given full bloods including the extra thyroid ones and a CT scan which came back clear but he has a referral to neurology. This is within a week of him seeking help Your GP sounds rubbish. I'm pleased youre going to get your scans but if you're in pain perhaps go to A &E during an episode. It sounds awful.

HowNice23 · 09/01/2024 04:51

Incidentally the feeling of anger/sadness/despair can have a chemical/hormonal trigger. It's called dysphoria and is a powerful physical thing. I had it with DMER which is a totally different medical condition but just to say I recognised the feeling you describe and in my case like I said it was linked to a physical thing in my case hormone drop. Definitely mention it as one of your symptoms x

Phantosmia · 11/01/2024 02:02

I'm really nervous about tomorrow.

How long will I have to wait for the results if they find something? Will I have to wait until I see the neuro at the end of February?

OP posts:
NYName · 11/01/2024 02:38

Usually about 3 weeks to get mri results.

Have you consulted your dentist?
I know someone who had 2 years of headaches, frequently missing work. Tried loads of medication for migraines, saw neurology, lots of tests.
Eventually it was sorted by a device from her dentist. Turned out she was clenching her jaw in her sleep and causing a headache. Now wears the device every night andi doesn't have headaches

Good luck tomorrow

DaisyCat33 · 11/01/2024 10:13

Phantosmia · 11/01/2024 02:02

I'm really nervous about tomorrow.

How long will I have to wait for the results if they find something? Will I have to wait until I see the neuro at the end of February?

Good luck, you'll be okay.

If they find something urgent, you won't have to wait. They'll let you know very quickly.

Also I was told 3 weeks for my MRI results recently (in December), but my GP had them back after 4 days. So it might be quick even if there's nothing found.

SpottyCrumpet · 11/01/2024 14:57

Good luck OP. MRIs are daunting but you’ll be absolutely fine. Not sure how long results are on the NHS but the person looking after you during your scan should be able to tell you

Cornettoninja · 11/01/2024 15:39

Good luck at @Phantosmia. I could choose a million better things to do with my time over having an MRI but it’s really not that bad. Just lie there and try and day dream good stuff

Phantosmia · 11/01/2024 21:02

Thanks all. I appreciate your kindness and reassurance.

Not as bad as I was expecting, the time passed quickly.

Now to wait for the results.

OP posts:
Phantosmia · 15/01/2024 13:16

MRI results are in - brain is all clear! Everything is normal, no signs of anything out of the ordinary!

I am so relieved. Pleased to have an answer to some questions.

I also saw a new GP who has ordered more blood tests (getting that done today) and will form a plan with me when we get those results back on Thursday.

OP posts:
DaisyCat33 · 15/01/2024 13:35

Phantosmia · 15/01/2024 13:16

MRI results are in - brain is all clear! Everything is normal, no signs of anything out of the ordinary!

I am so relieved. Pleased to have an answer to some questions.

I also saw a new GP who has ordered more blood tests (getting that done today) and will form a plan with me when we get those results back on Thursday.

Oh that's good news, I'm relieved for you that your brain is all clear.

Finger's crossed for you that the bloods help figure out what's going on 🤞

Phantosmia · 15/01/2024 14:53

Thank you, Daisy!

I feel like a huge weight has been lifted.

But I still don't feel like migraines are the answer. Currently sitting in the Dr surgery with intense pressure on the right side of.my skull and the whole right side of my body tingling away. Not really in pain, just feel a bit sick.

OP posts:
Nearlythere80 · 15/01/2024 14:55

Are you taking painkillers op?

Phantosmia · 15/01/2024 15:12

No, they've never made a difference to the pain and GP advised I stop taking them to avoid rebound headaches. Currently on no meds at all.

OP posts:
Castellanos · 15/01/2024 15:30

Obviously really good news the scan was clear but really feeling for you still having to find a way to live with this - sounds awful and debilitating. Hope you find something that helps.

SpottyCrumpet · 15/01/2024 17:21

Fantastic news it’s nothing structural. I hope they get to the bottom of what’s wrong and find treatment for you.

Nearlythere80 · 15/01/2024 18:54

OP worth looking up about complex migraine or atypical migraine to help you understand the range of symptoms possible

DaisyCat33 · 16/01/2024 12:54

Phantosmia · 15/01/2024 14:53

Thank you, Daisy!

I feel like a huge weight has been lifted.

But I still don't feel like migraines are the answer. Currently sitting in the Dr surgery with intense pressure on the right side of.my skull and the whole right side of my body tingling away. Not really in pain, just feel a bit sick.

If it is migraines, its strange that you suddenly started having them so frequently and out of nowhere.

What did the GP say are the next steps?

Taciturn · 16/01/2024 13:08

Iron deficient anemia can causes headaches, goosebumps and some of your other symptoms. So can some B Vit deficiencies.

Obviously it would be better to get blood tests, but you could try (high-dose) supplements and see if symptoms improve.

Taciturn · 16/01/2024 13:13

Sorry, I didn’t read the whole thread. I see you're getting blood tests. That's good news!

HipHop63 · 16/01/2024 13:21

Sorry to hear of your issues. I used to get migraines really badly, for four years, one or two a week. Sickness, hot flushes, nausea and a thumping over my right eye. I tried coming off the oral contraception pill in case it was that, drank more fluids (to this day fizzy orange makes me heave as I associate it with migraines and feeling very nauseous) and got my bite pattern checked at the dentist in case i was grinding my teeth. I'd had a whiplash injury falling off my horse and my arm was paralysed for four days as I'd damaged the nerves. When I stuck my fingers into my neck (jugular vein maybe) the migraine would stop in its tracks, soon as I took my fingers away it would come thumping back. I had no quality of life, we'd organise trips away or I'd go miles to a venue with my horse and go down with a migraine when I was there, day totally spoilt, the sickness was unreal, one time I crawled through the front door on my hands and my knees and actually threw up, the first and last time I was ever physically sick with them.

In the end I visited the doctors for what felt like the 100th time and saw a lovely locum doctor who put me on betablockers. I took them for 3 months, I never had another migraine. I don't know why they worked or how and I don't care. Proprananol and Doctor Liley literally saved my life.