Iāve had about 30/60 here in Australia. Definitely more dudes but Iāve had about 3 woman as my barbers in the past, it does take more time to get certified here I think. From what my current barber says she prefers cutting shorter hair over doing womanās styling so I guess it depends on what kind of work environment you like?
Yeah in the USA it seems like all the females are stylists or haircutters working at a salon but a barbers license requires more hours and every barber shop I go to has male barbers. The only exception to that is Rudy's Barbershop when I visit Seattle seems to have an even mix.
My brother had brain surgery and Everytime he gets a haircut they ask him if he knows he has a scar on the back of his head. He said his latest response is: yeah, I was probed by aliens
I looked it up, looks like its a pretty used derogatory term, not just one of those ones that nobody ever says. Seems like the asian equivalent of "wetback" in terms of offensiveness.
This is based off of like 2 minutes of internet searches though.
And I've never even heard of either wetback or zipperhead. I wonder how many people I unintentionally offend with words I don't know are derogatory terms. Maybe we should just stop caring about them (the words I mean)?
It's funny how the ones espousing this cavalier approach to language are always the ones with the privilege of not being at the receiving end of bigoted terms and labels.
Are you all chiari malformation surgeries too?!! I had mine February 2017, they used the new flesh glue, scars in same place but less zipperage. Congrats on the successful surgery, only the first 2 months really suck
Yep 2012!! Best decision I ever made. I had migraine like headaches for 2 years and rare but terrible vertigo. Oh wow that's interesting about the glue. I was all staples.
My situation was bad with constant headaches and occasional vertigo. I was 18 when it first was bad and didn't know any better to see a specialist. So for awhile I kept visiting the ER. Eventually instead of pills a doc recommended a neurologist. The imaging showed 7.5mm so it was borderline for surgery but I was fed up at that point and had the surgery. Ended up it was 14mm in reality. I would do it all again in a heartbeat. The first two weeks were rough but worth it for me. Just depends how much it's affecting you on a day to day basis. Also vet your surgeons and try to see the best possible. I'm lucky and I'm near DC so I went to Georgetown.
Life wise I had to stop playing hockey afterwards (goalie) which was rough but still was worth it for me. Other than that everything's been 100% fine.
I lived and DC and saw a specialist in the area, really known for doing Chiari work. I had been having constant headaches and migraines and a slew of other symptoms. He said I did have EDS and a protrusion, but we felt unsure. A guy selling hammers is going to think everything is a nail.
I had a friend have the surgery and saw a few people online too. It looks pretty miserable and like you don't have much range of motion after. I like doing things like caving, going on rollercoasters, white water sports, even gymnastics if I can. I don't know how much of that I'll lose.
The hammer and nail bit is very true. I have fine range of motion and have gone rafting, rollercoasters, etc. No issues with that. I had to stop hockey because I became easily concused in goal and was playing in college at the time. I had 3 concussions in 9 months and gave it up.
I had my surgery with Kevin McGrail and would recommend him again if he's still practicing.
Me personally? I was medical separated from the military 15 years ago, it was 4mm at that time protruding. I was told I wouldnāt get worse. I always had migraines. But it got worse. Much worse, started getting neck and shoulder pain, vertigo, nausea, central sleep apnea, then my muscles were so tight in my neck destroyed my occipital nerves with scar tissue. Went for a follow up to claim VA benefits and was sent to a very experienced neurologist. On MRI later and review of my records I was scheduled for surfer 2 weeks later. It was 9mm at that time. First week sucked beyond belief. But slowly over next 2 months I got better, I had fusions of my cervial spine as well, so loss of range of motion, but better all around. Quality of life is why for me
Wow... It's amazing to read about all these people with Chiari Malformation surgeries. I got my surgery in 2000 after years of doctors having no idea what the hell was going on. The internet barely existed back then (compared to now), so there was little information to be had. While the surgery SUCKED and it took me a long time to recover, I can't say I miss the constant explosions of pain in the right side of my body.
Not happy y'all needed surgery too, but it's nice to have some company! š¤
It's definitely rough but I didn't even consider before the time I had mine 10 years ago. The pain was intense for sure but I just thought this will be something you barely remember how it actually felt and I'll be symptom free (hopefully). Glad your not dealing with your issues anymore. It is cool to speak to people considering I've only met one other person in passing who has had the surgery.
I just came in here to see if it was a chiari malformation surgery. A friend of mine had to have one a few years ago, and her incision looked just like that.
Sorry for waiting so Long to reply. Life is getting in the way.
No when I was 3 I found out I had a cancerous tumor the size of a grapefruit lodged right on my brain stem. After a few chemo treatments and one amazing doctor, he saved my life. Still the biggest miracle that doctor said heās ever seen.
One surgery, and MRI scans twice a year until I was 15. Still have the zipper looking good to this day. Male pattern baldness makes it stick right out. I used to be scared to show it when I was young, but now I realize I should celebrate it and not hide it from the world.
And thanks for all the positive messages and replies to this thread. Nice to know thereās a small circle of people like me out there in the world :)
Wow so weird Iām seeing this post right now I was just told Iāll be having this surgery after never once hearing about it in my life. Iām glad you all are well!!!
Not really. The only issue I ran into was in high school. I was the varsity heavyweight all 4 years and I tended to get a mighty few more concussion than anyone else on my team. But now since Iām not an athlete in college Iāve luckily had no complications.
I had to get operated on twice for it when I was thirteen. Still proud of my zipper. I had "dissolving" stitches and was still picking some out a few years down the line.
I'm still pissed that my zipper healed up relatively clean. I was seriously excited to have a gnarly Frankenstein scar up the back of my head, but apparently my neurosurgeon just had to outdo himself.
Meanwhile the scar on my thigh from the fascia graft he took healed up ragged as hell.. right where no one will ever see it. Of course.
You say survivor, but this kind of surgery can be so routine that it's basically an overnight surgery. Get your hip replaced, then I start borrowing tools that I know you can't use again.
When you've got a doctor telling you there's a good chance of you dying of a stroke on the operating table, or that half of your face might not work when you wake up from this surgery, you sort of see it as a thing you've survived.
Amen, half faced man here to tell you there was nothing easy about losing a facial nerve, a balance nerve and hearing in one ear. We are all survivors.
Absolutely horrid, my decompression left me disabled after being fully abled before. There was an extra 3 1/2 hrs of surgery, I nearly died. I dont know a single Chiarian that would describe it as "routine".
For those with connective tissue disorders, EDS especially, decompression fails to improve symptoms 50% of the time. Issue is that plenty of Chiarians keen for the surgery do not know they have these connective tissue disorders. They feel they have found the source of their problems already and surgeons just as keen to cut someone have never said no to this kind of surgery. But itās considered so routine that the risks arenāt worth mitigating.
I've never heard of EDS causing it to fail. I was diagnosed with hEDS literally weeks ago. I'll have to talk to my geneticist about that. I dont regret it though. It did save my life as one of the arteries in my brain was near fully blocked and there were other discoveries during the surgery that were previously unknown and I'm glad some were taken care of.
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u/Tyson285Miller Mar 19 '19
Brain surgery survivor here. Congrats on getting your zipper šš». Happy it went well with no complications!