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perrycornish

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About perrycornish

  • Birthday 10/10/1940

Converted

  • Biography
    Ex Management Consultant and Counsellor
  • Location
    North Antrim, N.Ireland
  • Interests
    The environment, photography, my animals ( Mainly dogs and cats but not exclusively
  • Occupation
    Retired and happy! Was a Social worker and then Management Consultant.
  • SAH/Stroke Date
    March 2008 coiled

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  1. Sorry to come in on this discussion so late, I have not logged in,until yesterday, for ages for various reasons and I won't bore you with those! As I understand it an SAH is indeed a type of stroke, indeed a haemhorragic one. My own feelings are that people tend to expect you to conform to the 'person who has had a stroke pattern' and if you don't then they think that it was only a mild stroke, if there is such a thing I'm not sure that stroke and mild go together at all! For any of us who have had a 'mild stroke' it's a darned significant thing! I tend to tell folk that I had a brain haemmorhage which produces shock, horror but not much understanding;-) I asked Alison ( my partner) what she was told and she said that when I was admitted to the local A&E they told her it was a type of stroke, as they did not have adequate technology to be sure of a proper diagnosis. I was transferred that same day to Belfast's Royal Victoria Hospital where she was told I had an SAH, she then Googled it when she got home:) Where would we be without the net! I didn't have vasospasm but did have seizures whilst in hospital, several I believe but I don't remember, for which I am grateful. I have, since I had the SAH had two TIA's the docs think because of the original SAH and the subsequent mini bleeds when I came uncoiled:oops: Since my re-coil I have had no more neuro symptoms although there is still a sign or three! All my knowledge about this is from being told or doing research as I'm one of the one's with only fleeting memories of random bits of the eight weeks I was in hospital, but I do, like Karen, like to know what is going on and what caused things etc etc. My brain, my body, explain you medics;-) Agree with the statements that ignorance in the community and in many cases the medical world is rife.
  2. Hello Lynz, me too with the symptoms you describe, I'm two years on but still things ain't wot they used to be;-) My GP decided yesterday that he thought my neuro team should do more and he has rattled their cage, we'll see if anything happens! Sorry not to have reacted before but I haven't been on the board as much as usual for one reson or another but as always I see plenty of folk have said it's OK you are as normal as the rest of us! It's great not to be alone isn't it? All the best
  3. Here you go John, I'm another one who can't remember, I have asked questions of those who knew me, especially my partner. I felt guilty as she obviously had to face the whole thing without my support as I was 'absent to say the least' I still don't actually remember much, just tiny realisations. In many ways I feel lucky, I only heard of the horrors and have no memory of them. It is I think quite common, especially in those of us who had a sort of sudden onset.....Bang! just like that, one minute fine next time for me anyway ( two weeks later and in a high dependency bed. Very puzzling. I have not as yet written my story (two years later) as I feel I am still gathering information. So don't fret, you are not alone and if you think about it, maybe it's a really good thing not to remember, it doesn't sound much like fun does it? The aftermath is enough for me I reckon:-D
  4. Well this shows me that is has been ages since I logged in to BTG:oops: I love Marmite and will eat it at any time:-D For thirty years, Alison my partner had Marmite sandwiches for her packed lunches at work, so I reckon she likes it too;-) What a bonus to find it's good for me too! Sorry about my abscence, life has been a tad chaotic and may well be still, but I'll pop in when I can! love to all:-D
  5. Hello Zoe, I'm so glad that you found us. Of course you are worried, anyone who cares would be, it sounds as though your husband is in the best hands. As others have said, these are very early days and his poor injured brain needs a rest which it is getting now, I'm sure that you will be amazed at the progress he will make and with your support I bet he does well. It's a long and tough road but the support here will help you both. Just ask if you want to know anything at all, no matter how trivial it may seem. If it's worrying then it isn't trivial. We will all be thinking of you both and looking forward to hearing about the progress:-D
  6. Sorry not to say Hello before now, but I have for various reasons not been on site for about a week. Welcome though and do just let yourself be spoilt ( if it's on offer) and try to give in but not give up:)
  7. Saffy , hi and I agree with the others! Let yourself be pampered and i bet it was all of those things including the lowering of your BP. That certainly was the case for me and still is sometimes even two years down the line. Let yourself be pampered
  8. Oops, I have been absent without leave for a week but now that I'm back I am so pleased that your time with your mum went well and that the book arrived in good time ( I keep referring to my copy) so pleased for you and I do hope that things continue to progress
  9. Momo, I can't find a silver bullet anywhere, but this site and sharing comes very close to being the greatest help there is, your referrals will help too, and don't worry about making others feel down, you probably won't and it may help you. I do hope that the NHS soon comes up with your support network. Don't bottle it up, let rip and keep cuddling the cat, mine are nearly all cuddled flat and so is my dog:) The best I can offer right now is hope and the promise that it will improve. I'm two years down the road now and even getting to quite like the new me
  10. Just a quick message for you and your Mum, miss griff! You sound as though you are pretty special, and obviously so is your Mum, Have a wonderful time together for your first proper Mother's day with your 'New Mum'
  11. Hello! There is no doubt at all, the smoker has to want to stop. I had been smoking for fifty years when I had my SAH and knew it would be a good idea to stop but never quite made it. I was in hospital, and confined to bed for seven weeks, so when I came out I was over the worst of the cravings and it seemed daft to start again, so here I am wealthier, healthier and two years on. But I was obviously ready to stop! That I am sure is the only way, don't push, it used to make me more determined not to stop:crazy:
  12. Hi Saffy and a big apology from me, I had not seen this thread ( I think that I must have been coming online in my sleep! I'm sure that you have done the right thing, I am another of those who did have an SAH and later was told that I needed a recoil, as mine had misbehaved. It is a tough decison to make and you have obviously got courage and made the decision to go ahead. A wise one, we will all be thinking of you when you go in, and I promise that the coiling is no problem at all, an SAH is quite another matter. I have a second anuerysm which is being monitored but believe me when the experts say to me 'time to coil, Perry......I will be there like a shot:) My thoughts are with you
  13. Hi again, I'm so sorry that you are another victim of today's work full time and without expectation of co-operation and understanding from us school of employment:shocked: Sorry but I think there is steam coming out of my ears and it is clouding my normal equanimity! You have already been given some excellent advice, go to your professional association or to your union whichever is appropriate and also I think someone said your GP. I would go back to him and say that you need some support over this. He should be able to help, I would also suggest that you revisit your HR Dept armed with some literature about SAH, or at the very least a request that they look at this site or put SAH into Google and chew on that, oops I think that steam is coming out again. You do so much need all the support you can get, all I can do is say yep the advice you have been given so far is good and tell you I will think of you, do let us know how it all goes. I'm off to take a pop at something I can't hurt:roll: Good Luck
  14. Welcome Aakki, I'm sure that you will find much info and support on this site:) I am one of the luckier ones at least I had an anuerysm and so did know the reason for the headache and passing out! There are others on here who will I'm sure be able to answer your questions. I can at least think about you and hope that your recovery goes well:)
  15. Hi Kel, Sounds to me as though you 'have it sussed' Good Luck, I do hope that it proves not too hard and that you go from strength to strength:)
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