New to this: Hi every1, after mths of headaches & b... - Headway

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EVC70 profile image
13 Replies

Hi every1, after mths of headaches & b'in told it was depression, cluster migraines also that I was going through the change I was finally diagnosed with a brain aneurysm. My left side is weak also my left eye only opens a little bit & the sight is damaged.

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EVC70 profile image
EVC70
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13 Replies
MXman profile image
MXman

Hi EVC70,

Welcome to the forum. N

randomphantoms profile image
randomphantoms

Hi EVC70

Welcome to the family of the forum.

Lovenhugs

Xoxo

cat3 profile image
cat3

Hi and welcome. Can you tell us what treatment, if any, has been decided for the aneurism ?

Cat x

EVC70 profile image
EVC70 in reply tocat3

Hi Cat3, I had my opparation on the 3rd Sept they put 6 coils in2 the aneurysm . I've since had another scan becuz of how much pain I am still in I get the results this Tuesday.

cat3 profile image
cat3 in reply toEVC70

I'm not surprised you still have pain Ev ; I only had one coil and I had severe head pain for a couple of months after the op.

Your brain will still be working overtime to heal itself, so try not to be alarmed. Your op was less than two months ago, so very recent.

Please let us know how you get on on Tuesday.........I hope all goes well.

My best wishes, Cat xx

BaronC profile image
BaronC

Hello and welcome along to our wonderful home. Sit back, have a brew, chat away...

Best wishes,

Baron/Andy

Nutkin33 profile image
Nutkin33

Welcome to the sight. Never be shy to talk on here!

☺️😉

Gaia_rising profile image
Gaia_rising

Welcome aboard, EVC70, and welcome to the "I have metal IN my head" club.

I also had years of migraines, spells on-and-off anti-depressants, and one weird phase, in my mid-20's, when they considered putting me on HRT...

In February of this year, I had the mother of all headaches, and then can't remember anything else until I woke up in hospital, post brain-surgery. One of my aneurysms, that hadn't been present on the scans I had as a teenager, had ruptured. I have two more, one of which is viable for surgery, the other isn't, waiting for a date for the surgery to coil the operable one off.

This forum is fantastic, everyone's really supportive, and we can tell it how it was for us/our family members.

razyheath43 profile image
razyheath43

Welcome to this great forum! as a non bi person they have welcomed me,my hubby has bi,and everyone has been lovely,yes please let us know how you get on tuesday

Hello,

Great forum for advice if and whenever you need it.

You can read and reply or just read or just reply..... it all depends on how you feel on a daily basis. I can go months just reading then there's days I will reply..

But, never be worried just ask away and some thoughtful kind person with or without

a B.I. will be here to support you. Take care and the best of luck with your ongoing treatment 😃

steve55 profile image
steve55

welcome evc70

lcd8 profile image
lcd8

Hi EVC70. Your post struck a cord with me. As a teenager I used to get really debilitating headaches that my doctor insisted were migraines. They got increasingly worse and none of the migraine tablets helped. After 2 years it turned out I had recurrent Hydrocephalus and was on the point of brain hemorrhage! Sorry to hear about your left sided weakness etc. But I'm glad you persevered until you got a proper diagnosis. Hopefully things can only get better for you now.

EVC70 profile image
EVC70

Hi Icd8, I am astounded how long it took for u 2 get a diagnosis. I know I am lucky 2 alive but I am angry that I had been 2 my doctors a number of times also had them out 2 my home twice, went 2 Sandwell hospital twice, had been admitted 2 City hospital twice. It was on the 2nd admission at City that I was transferred 2 the Queen Elizebeth, they took a look at the scan City had done and could tell straight away what was wrong. There were times that I was made 2 feel as if I was just attention seeking.

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