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Life moving too fast..............



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08/15/2008 22:01
Jessykay
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I can't explain how many times I feel like I'm going insane. I used to be successful, working a 40+ hr a week job, going to the gym three times a week and feeling "normal". Now I can barely work 3 days a week and trying to deal with day to day activities gives me a huge amount of anxiety.

Laundry and dish piles up to the ceiling, dirty kitty litter, the floors haven't seen a vacuum in weeks. Not to mention my garden So sad it's gone to nothing but neglected weeds.

Life moves by too fast anymore. Speeding by me as I try and hold on. I moved fromt the booming metropolis on Toronto to rural Alberta Population 500. I thought it was the busy city lifestyle getting to me, but some how I still suffer from the feeling that everything is speeding by me. Changing the scenario doesn't make the problems go away. When will I accept that I have a disease? When will I stop beating myself for feeling like I'm being lazy? How will I learn to cope with this new diagnosis? How do I make others understand that I haven't given up, I'm just sick?

I want my life back, I want my youth back, I'm not ready to feel 90 when I'm only 31.

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08/16/2008 08:32
AndrogynousDream
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I'm 18 years old, and I feel the same way. I am autistic, and have had another chronic illnnes since I was 12, so for that reason, I felt disconnected to others and struggled for various things in various ways, on a day to day basis. Then there were the family problems. So my childhood was a downer. After developing the illness, it was extremely difficult.

Then, when I entered high school, on top of everything else, family and financial problems got out of control. This maded it almost impossible to enjoy my teen years.

Now that I am out of high school, I am finding out that I may have lupus, organ damage and everything, and am having trouble finding a job. I should be enjoying my college years, right? I should be in my prime, right?

Nope. Lupus took that away. I would give so much to shed all my baggage and enjoy my life, but that will never happen. Now I have this weird sense of urgency. My youth is quickly fading, and I cannot savor it. I cannot hold onto any moment long enough. I am terrified of leaving my teen years, knowing that these years are supposed to be part of my prime, and there is so much that I missed and will continue to miss. And I won't even get to enjoy my twenties.

And no one seems to understand. Lupus is enough, and everything else is just too much. Everyone else is all, relax, or the obligatory just get more exercise and eat healthier, pull yourself together crap.

People especially don't understand why I am so terrified of not being a teen anymore. Everyone says, "Oh, you're just afraid to grow up. Everyone goes through that." Shut UP, no they don't all go through this. Sure, those kids will cry when they get out of high school, but in a couple of days, they will be fine. And we are talking about kids that have enjoyed their teen years and are ready to move on.

That's another thing I fear. In high school, everyone is watching you, caring about you, all the time, or at least in most high schools to an extent. They expect you to struggle, and they want to catch you when you fall and comfort you. When you leave, people just expect you to be totally independent, and the stragglers are just lazy, immature, stupid people, not hurting people. Schools expect it, society expects it, families expect it, even you expect it.

You are truly alone.

Anyway, back to your situation, I had to reply to this because I identified so much with it. My adctual advice to you is that, there is no set time at which you can or have to accept that you have an illness. Cry, grieve, rage, an go through that process. Support groups like this one can help. Eventually, you will naturally come to that point where you are ready to move on with life with lupus.

In the meantime, you know you have an illness and none of this is your fault. Seek people that will help you take care of the house. Explain to others your situation, and offer them resources to learn more. And, you have us.

And I sought out this advice when I first came. If people give you a hard time about the lupus, don't talk to them as much or spend as much time with them. You may want to break it off with them completely. Sad, but in the end, it means less stress. Stress is the bane of lupus.

Godd bless.

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08/16/2008 08:48
AndrogynousDream
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Oh, by the way, I'm sorry about your garden and your kitties. I too love plants and cats. I have two Himalayans. Anyway, my father REFUSES to do any work whatsoever around the house, so it all falls on me. Part of adjusting to the illness is being flexible. There will sometimes be dust in the house, dirty dishes in the sink, laudry that needs to be done. Is that the end of the world? It isn't, even though it would be very nice to have a persistently clean house.

And I don't know if you would WANT to follow this advice, but when I have people over for any reason and they don't like how I keep it, I tell them what my problem is.

And, that if they don't like how I maintain my house, they're more than welcome to maintain it for me. I coul use the help.



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08/17/2008 16:49
amymollman
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I know what you mean, I worried people see me as lazy when I can't help out at my kids school or church.

But I also know I am a good (not perfect) mommy to my two kids and good (not perfect)wife. Laundry is not always done and dinner is not always homemade, but they know I love them. Try to look forthe things you do well and be proud of those

amy

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08/18/2008 09:47
momwife26
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I ran into those same problems the teachers at my kids school just assumed I was a lazy parent b/c I could not be at everything they had or b/c I forgot to sign a paper. I have three children work a full time job and my husband refuses to do house work, and I am in college online. I often feel overwhelmed and tired and unfortunately at the end of the day my house takes the hit. It is way mare dusty and there are a lot of unreached crevices and it drives me crazy because I am a neat freak as is my husband and i am just too tired or takes too much from me to do it all. My kids help out as much as they can and I often feel bad for them having to do that because they shouldn't have to worry about certain things all the time. I do the best I can though in my current situation. My family really do not get it either they are a bunch of religious people who believe that if I wanted to be healed that I could I just don't believe enough and I like the attention so they are often nonsupporting as well. Which leaves everything on me, I have so much anxiety feeling as though one day I will not be able to do what I do now anymore, then what? I am only 26 years old now and feel like I am 50 what will happen to me in the next 10 to 15 years and will my family come around and help in that time.... I completely get you and wish you the best I have the same struggle coping with it all but I think the guilt is the worst for me. Everyone has always depended on me to do everything but in the last four years I have gotten worse and worse.

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08/18/2008 19:16
amymollman
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momwife26.

I try to focus on my accomplishments and when it gets tough I focus on day to day. You sound busier then me. My godsend was a friend I found through my sons school who also has a chronic illness that's symptoms are invisible. I call her my "sick" friend. Guilt and worrying about what bad could happen have often upset me. Not may people understand that. You are ten years younger then me. There is no knowing if you will have more difficult times, but try not to worry about what you can't do anything about.

take care

I will begin grad school online in Sept.

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08/18/2008 19:18
AndrogynousDream
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I am going to college soon to get my undergrad. It's a difficult transition, and it's during transitions like this that we need connections more than ever.

Together we can.



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08/19/2008 05:35
momwife26
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Thanks for the support I need it. Good luck with school! Keep me posted on how things are going for you all.

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09/01/2008 11:09
temeraire
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I was so moved by your post - I just cried, because I could have been writing it. I was just diagnosed in May and I really did think I was going crazy. My family kept telling me I was in so much pain because I was fat. They don't say things like that to me anymore, luckily. I used to be the BEST at my job and everyone came to me for advice. This last year with all the problems, I was lucky to still have my job. Top to the muddy bottom in one year. My poor husband is so awesome, but I feel so guilty, because he has to take up for what I can't do anymore. I am only 37. Is this going to be the rest of my life? I have a 9 year old that has to "take care of me". I should be taking care of her! I just have to keep thinking back to my psych classes. Chronic illnesses have the same cycle of grieving, just like when someone dies. There are days when it consumes you and others you have acceptance. You have to take each day at a time and focus on the positives, no matter how small. Just the fact that several people cared enough to reply to your post and to tell you that we are here to support you - add that to your happy list! Hugs!
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09/01/2008 14:26
amymollman
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It is always nice to know there are others thinking and feel the same thing. Yes chronic illness does have a griefing process. At it all pops back up when you have bad days. I always remind myself that there are others worse off then myself. Recently I had a friend loss her husband to a stroke leaving her with two young daughters. I'll take lupus to that any day.

Bonus to our having gone through all of this is that we can help others. My husband has been sick for a while now and the doctors can't figure it out. Alot of the symptoms are like lupus so he is getting frustrated. I think he may finally understand what I have dealt with for years.

Your daughter may be helping to take care of you but I'm sure she will learn a lot from the situation. Just make sure to let her know you appreciate her and give her time to be the kid that she is.

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