Still not able to get a straight sleep of at least 6 hours. Still wakes up in the middle of the night and awake for at least 2 or 3 hours after. Still waking up at the same time though. I think it is because I took a nap or something in the middle of the day. I am thinking of trying this, sleep if you can thing.
I don't exactly know what it is called, but one of my classmate some semesters ago is doing it. He sleeps anywhere, anytime, if he can. Like you I saw him sleeping for a good 10 minutes in class. But in total, he would only sleep like 3 hours a day. it's like he has a power nap all the time that keeps he alert and awake. But I don't think I would be that intense. I still try to go back to sleep every time i wake up. But then sometimes I would think of something to do that I forgot or would like to see. I blame Facebook for being sleep deprived! LOL
I would try to discuss it my doctor when I see her again.
Also, I took 25mg of Prednisone today, some of my joints, which don't hurt even when I have my Lupus flare up, are hurting. And I think it's because I went from a 30 to 25 mg in 2 weeks, and 25 to 20 in a week. I don't know for sure, but I am hurting. And since my doctor told me that if I am not feeling well about I just raise it back to what it was. So, i only have been drinking 20mg for 3 or 4 days. Sucks. I would really like to be out of the steroid pill. It's a bit hard to be weaned down from it. But then that is the only thing that's actually controlling my skin rashes and joint pain. Noticed too, that I have been eating a lot, so I am trying to control that... hehehe
So far, and as far as I am concerned. I think I am getting good health. :) so thank God!!
I will write till the world knows more about me, and about Lupus. Forgive me, I am a bit of a scatterbrain, so this will be random, unorganized, unedited and plain casual. :) I do hope you will read about me soon...
Showing posts with label sickness. Show all posts
Showing posts with label sickness. Show all posts
Sunday, October 16, 2011
Sleep Deprived. Part 2
Labels:
Arthritis,
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immunodeficiency,
Joint,
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SLE,
Sleep,
sleep disorder
Tuesday, September 27, 2011
Lupus and Me... yes me...
Hi, I am Joan Paula Ocol-Abella. I am 27 years old. I have been divorced for 3 to 4 years now. And I have Lupus.
I think I should write that every time, what do you think? I should I should own it. Remember that I do have it and it will be a long way and struggle to be better. I have lupus, lupus doesn't have me. OK, I might have gotten that from some cancer survival thing from long time ago, but whatever keeps me going right? Support guys. :)
First, this is what you need to know about Lupus. It is an autoimmune disease which no one knows why it happens to certain people, and how to end it.
Second, there are different kinds of Lupus, some minor or mild, some very aggressive and makes a lot of people very sick. I unfortunately, have the most common kind but if not followed up or treated right could make me end up in a very bad state. I have, wait for it, Systemic Lupus Erthematosus (SLE).
So, who does actually have Lupus? I know no one in my family having it. As I have researched before, here are the most common people who could have Lupus:
Unlike other people, I have only been recently diagnosed with Lupus. Some people who had suffered great pain as they were growing up because of this disease have been living a normal life now, most probably. You see, Lupus is and will always be there, I was just diagnosed later or my "Flare ups" came in a little late. Maybe its the stress, maybe its the change of conditions in my surroundings. For the past year, there has been a lot of changes in my life, some good, some bad but it's a change. I think Lupus was my body's response to this change that this change is wrong for me.
I am Joan Paula Ocol-Abella, I am 27 years old. I have Lupus at the peak of my life.
Links/References:
I think I should write that every time, what do you think? I should I should own it. Remember that I do have it and it will be a long way and struggle to be better. I have lupus, lupus doesn't have me. OK, I might have gotten that from some cancer survival thing from long time ago, but whatever keeps me going right? Support guys. :)
First, this is what you need to know about Lupus. It is an autoimmune disease which no one knows why it happens to certain people, and how to end it.
Second, there are different kinds of Lupus, some minor or mild, some very aggressive and makes a lot of people very sick. I unfortunately, have the most common kind but if not followed up or treated right could make me end up in a very bad state. I have, wait for it, Systemic Lupus Erthematosus (SLE).
So, who does actually have Lupus? I know no one in my family having it. As I have researched before, here are the most common people who could have Lupus:
- women
- ages 25 - 40
- asian, hispanic, african american
this is what it said according to womenshealth.gov
Anyone can get lupus. About 9 out of 10 adults with lupus are women ages 15 to 45. African-American women are three times more likely to get lupus than white women. Lupus is also more common in Latina, Asian, and Native American women. Men are at a higher risk before puberty and after age 50. Despite an increase in lupus in men in these age groups, two-thirds of the people who have lupus before puberty and after age 50 are women.So dear women of the world, be careful. You may think you are very healthy but is not.
Unlike other people, I have only been recently diagnosed with Lupus. Some people who had suffered great pain as they were growing up because of this disease have been living a normal life now, most probably. You see, Lupus is and will always be there, I was just diagnosed later or my "Flare ups" came in a little late. Maybe its the stress, maybe its the change of conditions in my surroundings. For the past year, there has been a lot of changes in my life, some good, some bad but it's a change. I think Lupus was my body's response to this change that this change is wrong for me.
I am Joan Paula Ocol-Abella, I am 27 years old. I have Lupus at the peak of my life.
Links/References:
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