I do not feel good. As you all know until recently I have handled my disabilities really well. That was when it didn't really get in the way that much. Now it is really beginning to bite.
Our desire to visits Stockholm has gone out the window because there is no way I can drive there. I used to be able to drive to my friends in Copenhagen in one day.
It has always been the case that dog shows exhaust me the following day. Now it is taking me longer to recover than the one day it used to. I got up at 1 PM and of course I have taken my drugs.
I said to John that my friend Gail who took me to the show yesterday has gone to the cinema and my other friends Wendy and Drew are going back to Crufts. What I was really trying to tell him was that this upsets me and brings home the fact of my disease to me. I would love to be able to go out today. It is a beautiful sunny day. John did not react to what I said in the way that I expected and it felt to me like he didn't understand at all what I meant by what I said.
I know there is nothing I can do about my condition but I really do wish that people would take into consideration more than they do. Of course when it makes people laugh they do not notice it is only when what I do could be construed as being rude to they seem to notice.
I had forgotten that veterans are shown first at Crufts. I suddenly heard clapping so I turned around and I saw that dogs had been placed. I panicked thinking it was the puppy class and that Alexander should be in the ring ready to be judged in the junior class so I ran in with him, well hobbled as quickly as I could, only to the steward to tell me that I didn't have my ring number on so I rushed back and my friend passed it to me and put it on. So I went back. Only for the steward to tell me that I wasn't in this class. I said yes I am and I have the tickets to prove it and I showed him that I had entered the junior class he said this is not the junior class this as the puppy class. Of course people found that very funny and I wasn't embarrassed at all I've got used to that part of my disease.
But other people have not got used to that part of my disease. I felt embarrassed to tell John how I felt and so got upset with him for not realising what I was saying about my friends being out today.
Yesterday didn't start off well. I didn't feel well at all. And it wasn't until after I had taken my second lot of drugs that I began to feel glad to be there. For the first few hours I just sat and knitted. It took all my strength not to tell people who came up to me to talk about my knitting to fuck off. It would have been very unkind of me to do so because I do understand that people come up and talk to me about it because they are surprised to see a man knitting and they are surprised to see that I'm knitting a very complicated Aaron or what they see as very complicated and many of the people who ask are genuine knitters themselves so that is why they are talking to me about it.
Yesterday, when I did start to feel better it was because I had taken a double dose of tramadol. I'm going to talk to my doctor about this because I discovered that tramadol is available in 50 mg 100 milligram and 200 mg tablets so I felt it would be safer me to take another hundred milligrams. it made all the difference it even made a great deal of difference to the pain I was in.
I also made the mistake of not taking my drugs until I arrived at Crufts. I did this because I didn't want to take a lot more than my allotted dose. I am allowed to take more morphine but yesterday would have been meant taking quite a lot more over my allotted dose. It was a stupid thing to have done because I am not a good driver if I am not medicated and it possibly contributed me to feeling crap even after I had taken my drugs.
On a positive note, people were very complimentary about my outfit and I have lost count of the amount of people that are asked to photograph me some of which I think were professional but most were using their phones. I was very surprised at the amount of men who complimented me on my dress sense. I enjoy that. And I think that these men who come up and tell me how classy look to have a lot of courage doing that. All of these men are straight as far as I can tell and as far as I can tell no gay men have ever done so! Life is strange.
So I feel not brilliant today, a bit down, and more than a little upset that even my nearest and dearest have to have it spelt out to them how I feel.
None of you know her but my friend Gail was of such enormous help to me yesterday and I would have found the day extremely difficult without her. In fact I wonder if I could do Crufts at all without a helper.
Another long stretch, but hoping to be more regular
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9 comments:
Sometimes you just have to spell it out in black-and-white...my DH never gets my 'message' if I am subtle, he takes what I say at face-value and it infuriates me but, after almost 40-years, I have learned to deal with it and just tell him outright. I agree, we shouldn't have to and I keep thinking if he really cared he would understand the nuances - but he doesn't and never will. And remember you do more even with your disease than most people do without having this disease...so you are the winner and one of the most remarkable people I know!
hi Colin,
I wish you that you feel better next week.
All the best, Christa
P.S.
It would be great to see your outfits again on the blog too....
Even your nearest and dearest aren't psychic! So go easy on him! My blokey only gets it if I'm sarcastic... Hugs!
I hear you and I think you are "doing" life to your fullest at the moment. Big Hug! Not only go easy on John, but go easy on yourself. Please try to find a cd called Feel Better Fast by Daniel G. Amen, MD. through A.C.I. Clinical audio series, if you like. It can help you focus on your thoughts thus feel better and not your disease.
About knitting, Thank you for moderating the for sale group on Ravelry. I've had superior results. Blessings of Gratitude to you. D
Hi Colin! :) I have to say you looked super as always at Crufts and although you made a mistake by going in the ring at the wrong time, something I've done myself, to my embarrassment, you did really well with Alexander(?). Sorry I'm not good remembering which dog is which LOL. Still trying to place people! LOL. Please never be embarrassed by your disability, it's part of who you are, for better or worse. I also understand how you feel when John doesn't 'get it'. My oldest daughter doesn't either but I don't think she wants to, the truth be known. I still think you're brilliant xxx
Thank you all and Midnight velvet you got Alexander's name right!
I have basixcallly been ignoeing my ill nesss. Alright, peopl could see I had trouble walking hence the chair ans sticks. But they sdidn';t know the 'blank episodes' when I would start into space and disappear for a whilel. A close frind of mione it for the first time 2 years ago whrn I was at her house and she was talking toi me =but I wanst there. It is this neurological pro=blems I have not tol anyone about. No one like s a moaner. But I guess irt is is importnat hey do know..
I think sometimes, Colin, we need to tell people at least some of it so that they don't think we're being rude. We'd prefer not to but it's in our best interest that we do I suppose.
xxxxx
Do you think there might be a nice strong, young fellow in your area who is out of a job right now and might be delighted to earn a little bit by going on vacation with you and John and acting as driver, lifter of heavy suitcases, generally as an attendant? You nd John could sit back and enjoy the trip without worrying about anything.
Julie in San Diego
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