Dealing With This Life
#1
Posted 15 June 2011 - 04:42 PM
#2
Posted 15 June 2011 - 04:55 PM
I deal with the bowl & bladder 2 & of course there are bad day some worst than others just try keep the spirits up!
Ask youself would all the people walking be able to deal with what u have been through..?Hardly that makes u a VERY strong person draw strenght from that!
Edited by Ted 303, 15 June 2011 - 05:07 PM.
#4
Posted 15 June 2011 - 05:32 PM
after saying that, i love life...and the people in my life.Theres still so much joy to be had. I try to find the positives all the time especially when my mind wanders to that dark place.
i guess we all cope very differently and our injuries levels differ on here, even though we all have SCI's in common.
Keep strong...i listen to music i like, often quite loud and it takes you away for a little while, takes your mind off things a little.
Keep talking and sharing your feelings as you are doing now
#5
Posted 15 June 2011 - 06:13 PM
Its true that all of us on this forum are sci -- but there are so many varying abilities. I guess it is ok to be grateful for whatever we do have; and that definitely this situation is one of the most challenging that most of us will face, just getting through it on a day by day basis, staying positive, trying to be independent, learning, looking for some ways to still be productive, feeling love and giving love and caring to others.
cheer up my friend. Know that others here are feeling the same and try to think of something else. direct your thoughts to the positive even tho the negative will keep coming back.
I know that I never really thought very much about disability and what it would mean to me until it happened to me. Now I know and I am much more interested in others who are disabled and admire so much the way that each individual handles these challenges.
#6
Posted 15 June 2011 - 07:40 PM
#7
Posted 15 June 2011 - 08:29 PM
Get on Youtube and look up the word paraplegic. Then, spend hours watching people who are even higher injured than you are get on with there life. There are two ways to live, looking at others and wishing you had more, or....live in such a way (especially with a disability)that others will think you are awesome and will look up to you as an inspiration. Personally, I think there have been people on here (who I love dearly) who have struggled and literally fought with every ounce just to take the next breathe. We have it easy my friend. Bowel and bladder are a nuisance but they are not life and death. Come on, figure out what you would like to do and do it! Anything can be done (especially for us paras) - it just has to be done differently. It can be fun just trying to figure it out! When you feel frustrated, try to find the humor. It is there (and in plenty) if you look for it.
www.aliciareagan.com
#8
Posted 15 June 2011 - 08:46 PM
Ferguson Clan Motto: Dulcius Ex Asperis (Sweeter after difficulties)
#9
Posted 15 June 2011 - 08:47 PM
#10
Posted 16 June 2011 - 12:16 PM
I went through rehab with some brain injury patients and it really helped me put things in perspective. You still have a lot of life to live...the trick is figuring out how to appreciate what you have. Good luck! I know you can do it.
#12
Posted 16 June 2011 - 06:04 PM
#13
Posted 22 June 2011 - 11:38 AM
airart1, on 16 June 2011 - 06:04 PM, said:
#14
Posted 08 July 2011 - 12:04 AM
#15
Posted 08 July 2011 - 05:04 AM
Astack23, on 16 June 2011 - 02:10 PM, said:
Anthony
#16
Posted 30 August 2011 - 03:43 PM
Yeap, i spent many a day sulking..hoping that that day was when the power of me sulk would shuuu sci away
We go thorough each day in agony....what was the point of going thorough all that hard work..for yet another boring day? i know that thought well.....
i kept pushing meself into situations were i thought 'i will do this like before' - but it just is not the same anymore so quite quickly got fed up of trying to do these things, ending up in agony and just wanting to be home comfortable and relaxed.
because no matter where we go..sci comes with us....its like wanting to go to 18 year old nightcubs when we are 30..with a nagging, grumpy, boring horrid relative in tow with us...getting there, realising its sooo not the same anymore.
No point living life from the outside looking in...this with sci is our normal world now...and the more we enjoy living in the now..the better memories we are going to be able to look back on tomorrow..For if we live a life full of depression..no wonder we skip all the memories we have had with sci and just remember pre-sci life.
Sorry not a great answer but the only one that works for me so far.....
Edited by pinkcloud, 30 August 2011 - 03:45 PM.
#17
Posted 30 August 2011 - 06:17 PM
#18
Posted 30 August 2011 - 06:31 PM
I have been having one those days today where all i want to do (and have) is cry.....and still am as i write.
My day has just been a bad one from the start..nothing major has happened..ive just been downright peed off with it all...and i can normally be so very positive but not today.
I read your reply pinkcloud and you described exactly how i feel about the old granny in tow...:-)
Im fed up of the hospital/docs/clinic/pyhsio appointments.....lugging this fat ass around and feelin like ive run a marathon when all ive done is have a shower..im fed up of wondering if my b & b programme is effective...is there somethin i need to mention to the doc still, is my blood pressure still high?..did i dream again last night that i was 'cured' and was walking home again to tell everyone my good news? (yes i did dream it).....its poo poo and more poo!
Yes this IS the new normal...and im still so lucky and thankful that im here to tolerate the poo side of SCI and enjoy the good days to be had however shite it is...lol
Thankfully us SCI peeps are made of strong stuff!!
#19
Posted 30 August 2011 - 07:10 PM
When I see abled-bodied people out and about, I get a little jealous, but I'm just glad their not flopped down in front of a TV and not doing something but napping and wasting what they've been blessed with.
Find something that you enjoy doing that motivates you, and do it. You have a winning lottery ticket, cash that thing in.
Again, I hate to be harsh, but I'm reading this at a time when I'm pissed that I can't get the door open enough for my dog to get out an hour ago, and last night I coulda swore I heard a prowler on my porch and the only defense I had was to yell out and pretend to call the police.
#20
Posted 31 August 2011 - 02:43 AM
Joining Apparelyzed was the best thing I could have done, as reading the inspirational stories of people who have done so much with their lives, gives me the hope that I will one day be able to get back out there and live life to the fullest.
So my advice is to give yourself time, there is no deadline on when you start to feel like things are going to be ok and your life is still going to be a good one, wheelchair or not. Don't be too hard on yourself, everyone is different when it comes to how long it takes to come to grips with your injury.
Take care.
Edited by scaldedcat, 31 August 2011 - 02:55 AM.
#21
Posted 31 August 2011 - 11:04 AM
scaldedcat, on 31 August 2011 - 02:43 AM, said:
Joining Apparelyzed was the best thing I could have done, as reading the inspirational stories of people who have done so much with their lives, gives me the hope that I will one day be able to get back out there and live life to the fullest.
So my advice is to give yourself time, there is no deadline on when you start to feel like things are going to be ok and your life is still going to be a good one, wheelchair or not. Don't be too hard on yourself, everyone is different when it comes to how long it takes to come to grips with your injury.
Take care.
I know we all have differeing views about medication but I also had bouts of depression pre sci and afterwards. My GP was pretty clear that I was "blaming" the SCI for my depression when he felt it was just the old black dog returning. It wasnt my fault that I was depressed because I wasnt coping but the other way around. I have found short courses of medication when things are really bad to be very helpful.
Take care.
Tin
Never grow old, never die young.
#22
Posted 04 December 2011 - 09:49 PM
Astack23, on 15 June 2011 - 04:42 PM, said:
#23
Posted 13 December 2011 - 02:08 PM
Rdunn6469, on 08 July 2011 - 12:04 AM, said:
Sounds like your nephew could really use a mentor. I see your in Lake Havaseu...I'm the peer mentor coordinator here in Phoenix. If he'd like, I can check if there is anyone out his way who could visit with him. Sometimes having someone to talk to who is in a similar situation helps. Feel free to give us a call- Karen @ Az Spinal Cord Injury Association 602-507-4209 He can also call the Reeves Foundation and request a mentor in his area- they can be reached here- http://www.christoph...J2LaMQKpK2LiO2H or If you have questions about the Peer & Family Support Program, please contact the Paralysis Resource Center at 800-539-7309 ext. 7226.
Everyone deals with SCI differently, of course. How long has he been injured? Some deal with it ok, others don't,sadly...it's a HUGE life change. It can either swallow you up or you learn to go on and live again. It's not a life sentence...we just have to learn what works for us. I'm also a T-12 incomplete. I was 44 when I was injured. I can't transfer due to no upper body strength as well as I had broken my arm and torn rotator. It sucks, yeah, but I adapt. He'll have to find what works for him, then get out there and enjoy life...yeah it does suck to be in a chair but life does go on...and there are others who have it worse,sadly...Hopefully your nephew is doing better...
The Reeves Foundation has a HUGE resource center that you can check information out. They'll send any info out to you for free...http://www.christopherreeve.org/site/c.mtKZKgMWKwG/b.4486101/k.A2E9/Paralysis_Resource_Guide_Request_Form/apps/ka/ct/contactus.asp?c=mtKZKgMWKwG&b=4486101&en=juKOL1PMJiKRL2OPJcIMK9OWKrLZKbOTKeLXLjN1LuJbE
They also have an AWESOME resource book you can request for free- THE PARALYSIS RESOURCE GUIDE is a FREE 336-page book, a comprehensive information tool for people affected by paralysis and for those who care for them. You may request multiple copies. The book comes in English or Spanish (you may request some of both languages). http://www.christoph...OTKeLXLjN1LuJbE
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