Guest guest Posted April 13, 2002 Report Share Posted April 13, 2002 I am also very concerned about someone not wanting to crawl out of the whole. Depression is very seductive. There is almost a thrill at seeing an easy escape, until you realize such a thing can't be reversed. I have been dangerously depressed these past couple weeks, but I also realize this is my one shot and I have got to savor it, however I may do that. I don't want to minimize or dismiss anyone's depression. It is a very real feeling, and it requires medication and therapy. Like anything health related,it will get worse if it's not treated. My boss, with the blessing and butt-covering of his superiors managed to fire me due to illness. I have suffered from undiagnosed fibro for months and months and months. It feels like it's been my whole life now. He pressured me to tell him what my health complaints were and made sure he understood that I needed health insurance, and he let me go. I was pretty humiliated and lost. Now I have to cough up $300 a month for health insurance, along with rent and other basics on a part time job that runs out in two weeks. Work is agony, but I know I have to find a full time job so I don't have to move in with my less than compassionate parents. I don't have a husband, it could take forever to get disability, my doctor seems to think I should try managing this before I go there. Ha. I am a breath away from being out on the street and deep in debt. Sure, I look at the bottles of pills and think, why should I wake up tomorrow. I'll just stress on my job situation, the money, and the pain besides. Somehow I hold onto the glimmer of hope that for god's sakes, something has to get better here. No, maybe I won't have the energy to find a husband, I already can't have kids, I had to give my cat away cause I couldn't afford him or have the energy to take care of him, but maybe I can find some use, some employment I enjoy. I need to find my self respect again, I have a mission. Sometimes breaking out of a hole requires some tough, firm action. Some anger has to be let go. I sit here and say why me a lot, but then I let it go, more and more quickly. Same goes with people who don't understand or aren't supportive. None of us needs the kind of people who make us feel guilty, silly, or uncared for. Even if we feel some attachment to them, they're only hurting us. It's important to surround oneself with good people, like the ones in here, or seek them out. I have been very surprised how many people know someone with fibro once I mention it. My best friend is flying up to Maine from Virgina to take care of me for a while and to try and lift my spirits, as I am in a dark place right now,and have certainly looked at my pill bottles a few time. No one has to be alone in this,whether it's just coming online or seeking out other people who have this in your community. You'd be surprised how many people suffer from this. It's certainly not easy. No post here or one happy moment will change a black mood just like that. It's a fight, but one has to start getting a few positive thoughts going in their head to begin. Baby steps for sure. I am starting small, finding tv shows I like, wesbites and online games to play, losing myself in books, even though I can't physically adventure out myself, short walks on a nice day, a chat with a true friend. Am I gonna go out and run a marathon or play street hockey or party every weekend? No, and sometimes I am bitter about it, but I have got to find a way to accept I cannot be that person anymore, and celebrate life in other ways. Do I want to be the person I've become? heck no. Sometimes I feel ashamed of being borderline agorophobic (afraid to leave the house), crying all the time, wishing I didn't have to get up in the morning, angry at people who used my illness to push me out of a job. But there is nothing to be ashamed of. It's natural, you just can't let it own you. A lot of people here know those mood swings. As for the physical stuff, I never could have imagined that at 26, I would be feeling my entire body cramp up, my joints crack when it rains, falling asleep at work, constant twitching, spasming, clumsiness, needing to rest every hour, or that the photographic memory I prided myself on would fly on the window. I was a dean's list student and now sometimes I don't comprehend the simplest sentence out of a friends mouth. Balance my checkbook? Even with a calculator it's difficult. I love to drive, but now I can hardly drive out of town. Stand up for a long period of time? Sure, if I want tingles, the feeling of my knees giving out, or tight pulling pain. A simple gesture people take for granted is an ordeal for all of us. Even with all that, I know somewhere inside me is intelligence, creativity, cheer, ambition, generosity, and honesty. Nothing can change the essence of who we are, not even a disease, not even a life seeming to fall apart in a matter of months or years can change what's good about you. A disease is not our identity, it's a facet of who we are. I may be trapped inside a body that won't listen to what my brain tells it, but I've got good stuff trapped in here I can use to be happy too. Chellie, you're obviously a good person, people in here care very much about you...think about that! You still can touch people and mean something to people, and to yourself. Please don't sink further into that hole and give in to the temptation not to fight. Fibro is something your body has, not your mind or heart. I hope you're reaching out to all of us cause you want to keep going. We're always here for you, we all understand, and we all want to help. Please hang in....it's going to be worth it. Shandi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 --- I yes I have PSC I am at the end stage on the waiting list, depression seems to come hand and hand with this. I can't work for more then 3 hours at a time, I can't drive because my amonia levels are to high and I even lose where I am at in a store. I am tired and all that stuff this has been going on for a while it has been getting worse recently. Any way I know how you feel. So I spend quiet time with my kids, I read the bible pray alot for a new liver I found a hobby that helps me making a quilt. I also work a little bit I record music for a living but right now its not much of a living. Thank God my husband helps alot, we are financially stressed but hopefully things will get better. This is hard but just get up and walk even if you feel crappy just try it. No pill is going to help just know your limitations and put a smile on your face knowing some day you will be better! I used to ski, hike, workout ect... I miss it painfully but I know I will do those things some day again God willing. Another tip is to walk at least 3 times a week for about 35 min. do it at your own pace but it helps. (don't push yourself) When you feel good take advantage of it if only for a little while. Love PSC 2000 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 >When you are diagnosed there is usually problems such as this have your doctor get this under control with the proper medications. Also the medications that you are on can cause this, ask your doctor about an antidepressant it will keep you level. and just pray to God that he will help you! IT Works Love > I know I am not alone, and this group has helped a lot but I am so depressed right now that all I can do is cry. As I previously mentioned the neighbors brother beat me up in Jan. In the beg. of march I started having seizures and now have had my license revoked. I feel so sad and helpless. I got diagnosed a couple months ago and have had two bile duct infections, this feels like it is too early in the game for that. Does anyone have hopeful news they can share with me. Because I feel so hopeless. > > thank and God Bless you all. > brandi > > > --------------------------------- > Never miss a thing. Make Yahoo your homepage. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 >When you are diagnosed there is usually problems such as this have your doctor get this under control with the proper medications. Also the medications that you are on can cause this, ask your doctor about an antidepressant it will keep you level. and just pray to God that he will help you! IT Works Love > I know I am not alone, and this group has helped a lot but I am so depressed right now that all I can do is cry. As I previously mentioned the neighbors brother beat me up in Jan. In the beg. of march I started having seizures and now have had my license revoked. I feel so sad and helpless. I got diagnosed a couple months ago and have had two bile duct infections, this feels like it is too early in the game for that. Does anyone have hopeful news they can share with me. Because I feel so hopeless. > > thank and God Bless you all. > brandi > > > --------------------------------- > Never miss a thing. Make Yahoo your homepage. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 >When you are diagnosed there is usually problems such as this have your doctor get this under control with the proper medications. Also the medications that you are on can cause this, ask your doctor about an antidepressant it will keep you level. and just pray to God that he will help you! IT Works Love > I know I am not alone, and this group has helped a lot but I am so depressed right now that all I can do is cry. As I previously mentioned the neighbors brother beat me up in Jan. In the beg. of march I started having seizures and now have had my license revoked. I feel so sad and helpless. I got diagnosed a couple months ago and have had two bile duct infections, this feels like it is too early in the game for that. Does anyone have hopeful news they can share with me. Because I feel so hopeless. > > thank and God Bless you all. > brandi > > > --------------------------------- > Never miss a thing. Make Yahoo your homepage. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Yeah I too get headaches all they can do is give you mild narcotics but I take aleve there is nothing they can do but give you a new liver. All they can do is help alleviate the symptoms. My enzyme levels are between 80 and 100 and that is under control. I have battled this disease for 8 years. My eyes are yellow my skin is dark when I am a fair skined person, I look tannish red now so people think I just got back from vacation until they look at my eyes they are red with yellow tint (i have coyote eyes) Some days are better then others. But I just take it a day at a time and turn to God for He helps me survive its the only way. Yes it is scary to think about a transplant but I have no choice now, so I wait and pray that I will be normal again one day and that all you can do. Also do things that give you moments of happiness too that helps and find a hobby that keeps you busy and your mind off. And by all means you probably anger easily like me these days try to get the stress out of your life. And above all try not to take it out on people around you. Give it to God. Love PSC 2000-- - In , " prazle34 " wrote: > > --- I > yes I have PSC I am at the end stage on the waiting list, depression seems to come hand and > hand with this. I can't work for more then 3 hours at a time, I can't drive because my amonia > levels are to high and I even lose where I am at in a store. I am tired and all that stuff this > has been going on for a while it has been getting worse recently. Any way I know how you > feel. So I spend quiet time with my kids, I read the bible pray alot for a new liver I found a > hobby that helps me making a quilt. I also work a little bit I record music for a living but > right now its not much of a living. Thank God my husband helps alot, we are financially > stressed but hopefully things will get better. This is hard but just get up and walk even if > you feel crappy just try it. No pill is going to help just know your limitations and put a smile > on your face knowing some day you will be better! I used to ski, hike, workout ect... I miss it > painfully but I know I will do those things some day again God willing. Another tip is to walk > at least 3 times a week for about 35 min. do it at your own pace but it helps. (don't push > yourself) When you feel good take advantage of it if only for a little while. > > Love > > PSC 2000 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Yeah I too get headaches all they can do is give you mild narcotics but I take aleve there is nothing they can do but give you a new liver. All they can do is help alleviate the symptoms. My enzyme levels are between 80 and 100 and that is under control. I have battled this disease for 8 years. My eyes are yellow my skin is dark when I am a fair skined person, I look tannish red now so people think I just got back from vacation until they look at my eyes they are red with yellow tint (i have coyote eyes) Some days are better then others. But I just take it a day at a time and turn to God for He helps me survive its the only way. Yes it is scary to think about a transplant but I have no choice now, so I wait and pray that I will be normal again one day and that all you can do. Also do things that give you moments of happiness too that helps and find a hobby that keeps you busy and your mind off. And by all means you probably anger easily like me these days try to get the stress out of your life. And above all try not to take it out on people around you. Give it to God. Love PSC 2000-- - In , " prazle34 " wrote: > > --- I > yes I have PSC I am at the end stage on the waiting list, depression seems to come hand and > hand with this. I can't work for more then 3 hours at a time, I can't drive because my amonia > levels are to high and I even lose where I am at in a store. I am tired and all that stuff this > has been going on for a while it has been getting worse recently. Any way I know how you > feel. So I spend quiet time with my kids, I read the bible pray alot for a new liver I found a > hobby that helps me making a quilt. I also work a little bit I record music for a living but > right now its not much of a living. Thank God my husband helps alot, we are financially > stressed but hopefully things will get better. This is hard but just get up and walk even if > you feel crappy just try it. No pill is going to help just know your limitations and put a smile > on your face knowing some day you will be better! I used to ski, hike, workout ect... I miss it > painfully but I know I will do those things some day again God willing. Another tip is to walk > at least 3 times a week for about 35 min. do it at your own pace but it helps. (don't push > yourself) When you feel good take advantage of it if only for a little while. > > Love > > PSC 2000 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Depression seems to be fairly common for those of us with PSC. And when my UC flares up, I tend to get even more fatigued and more depressed. As other's have suggested, exercise, like walking (assuming you're not too debilitated to get out and walk) seems to help somewhat. For depression I've been taking SAM-e for over a month now. It's OTC, a bit expensive, but various studies indicate that it helps in eliminating depression. Additionally, it's supposedly good for the liver, although I don't know that there's conclusive evidence indicating that it necessarily helps PSC all that much; but it certainly doesn't seem to be harmful for those of us with PSC. (Additionally, oddly and unexpectedly, the SAM-e seems to have helped in getting over my recent UC flare-up . . . go figure.) I take 800 mg (two 400mg enteric coated tabs), on an empty stomach, twice a day (1600 mg total a day). I've been using Nature Made SAM- e which seems to be the gold standard for SAM-e, but I've recently purchased NSI SAM-e (at a better price), which I think is probably (hopefully) a good brand too, and will see if it is as effective as the Nature Made product. It seems to take two weeks to a month b/f you'll notice a difference, although for some it may be sooner. If you're going to try it, be sure to buy a good brand. Shop the Internet for SAM-e and best prices that seem to change frequently. My local Wal-Mart is selling Nature Made 400 mg (36 tabs) for around $35, but I was able to find better prices on the net (drugstore.com had a sale for a few weeks --$22 plus shipping; and recently the NSI product-----30 400 mg tabs for $19 plus shipping from vitacost.com). Now that I'm convinced the SAM-e works, I'll buy larger quantities whenever I find a good price. Fred > > Hi everyone, > > I've been concerned for some time that I am depressed, and it seems > to be getting worse.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Depression seems to be fairly common for those of us with PSC. And when my UC flares up, I tend to get even more fatigued and more depressed. As other's have suggested, exercise, like walking (assuming you're not too debilitated to get out and walk) seems to help somewhat. For depression I've been taking SAM-e for over a month now. It's OTC, a bit expensive, but various studies indicate that it helps in eliminating depression. Additionally, it's supposedly good for the liver, although I don't know that there's conclusive evidence indicating that it necessarily helps PSC all that much; but it certainly doesn't seem to be harmful for those of us with PSC. (Additionally, oddly and unexpectedly, the SAM-e seems to have helped in getting over my recent UC flare-up . . . go figure.) I take 800 mg (two 400mg enteric coated tabs), on an empty stomach, twice a day (1600 mg total a day). I've been using Nature Made SAM- e which seems to be the gold standard for SAM-e, but I've recently purchased NSI SAM-e (at a better price), which I think is probably (hopefully) a good brand too, and will see if it is as effective as the Nature Made product. It seems to take two weeks to a month b/f you'll notice a difference, although for some it may be sooner. If you're going to try it, be sure to buy a good brand. Shop the Internet for SAM-e and best prices that seem to change frequently. My local Wal-Mart is selling Nature Made 400 mg (36 tabs) for around $35, but I was able to find better prices on the net (drugstore.com had a sale for a few weeks --$22 plus shipping; and recently the NSI product-----30 400 mg tabs for $19 plus shipping from vitacost.com). Now that I'm convinced the SAM-e works, I'll buy larger quantities whenever I find a good price. Fred > > Hi everyone, > > I've been concerned for some time that I am depressed, and it seems > to be getting worse.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Depression seems to be fairly common for those of us with PSC. And when my UC flares up, I tend to get even more fatigued and more depressed. As other's have suggested, exercise, like walking (assuming you're not too debilitated to get out and walk) seems to help somewhat. For depression I've been taking SAM-e for over a month now. It's OTC, a bit expensive, but various studies indicate that it helps in eliminating depression. Additionally, it's supposedly good for the liver, although I don't know that there's conclusive evidence indicating that it necessarily helps PSC all that much; but it certainly doesn't seem to be harmful for those of us with PSC. (Additionally, oddly and unexpectedly, the SAM-e seems to have helped in getting over my recent UC flare-up . . . go figure.) I take 800 mg (two 400mg enteric coated tabs), on an empty stomach, twice a day (1600 mg total a day). I've been using Nature Made SAM- e which seems to be the gold standard for SAM-e, but I've recently purchased NSI SAM-e (at a better price), which I think is probably (hopefully) a good brand too, and will see if it is as effective as the Nature Made product. It seems to take two weeks to a month b/f you'll notice a difference, although for some it may be sooner. If you're going to try it, be sure to buy a good brand. Shop the Internet for SAM-e and best prices that seem to change frequently. My local Wal-Mart is selling Nature Made 400 mg (36 tabs) for around $35, but I was able to find better prices on the net (drugstore.com had a sale for a few weeks --$22 plus shipping; and recently the NSI product-----30 400 mg tabs for $19 plus shipping from vitacost.com). Now that I'm convinced the SAM-e works, I'll buy larger quantities whenever I find a good price. Fred > > Hi everyone, > > I've been concerned for some time that I am depressed, and it seems > to be getting worse.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 I have low calcium and bone loss due to psc. Last year I felt the same as you were describing in which it took everything out of me to walk a few steps. I felt sad and like crying for no reason. I began taking Viactiv plus calcium without vitamin k and my endocrinologist prescribed prescription medication. I work full time and have felt the best that I have in years. Without question my bone loss due to the advancement of my disease affected my emotions. As a clinical social worker also get an evaluation but talk to your doctor. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 I have low calcium and bone loss due to psc. Last year I felt the same as you were describing in which it took everything out of me to walk a few steps. I felt sad and like crying for no reason. I began taking Viactiv plus calcium without vitamin k and my endocrinologist prescribed prescription medication. I work full time and have felt the best that I have in years. Without question my bone loss due to the advancement of my disease affected my emotions. As a clinical social worker also get an evaluation but talk to your doctor. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 I have low calcium and bone loss due to psc. Last year I felt the same as you were describing in which it took everything out of me to walk a few steps. I felt sad and like crying for no reason. I began taking Viactiv plus calcium without vitamin k and my endocrinologist prescribed prescription medication. I work full time and have felt the best that I have in years. Without question my bone loss due to the advancement of my disease affected my emotions. As a clinical social worker also get an evaluation but talk to your doctor. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 I feel like I could have written that myself. That is, if I could get focused and get my thoughts together and describe it. I am suffering from depression. My PCP gave me some antidepressents and I see a couselor. Nothing helps much but just wanted you to know you're not alone. I just try to be gratefull for what I do have and know that someday it will get better. PSC, PBC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 I feel like I could have written that myself. That is, if I could get focused and get my thoughts together and describe it. I am suffering from depression. My PCP gave me some antidepressents and I see a couselor. Nothing helps much but just wanted you to know you're not alone. I just try to be gratefull for what I do have and know that someday it will get better. PSC, PBC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Hi Fred; Glad to hear that SAM-e seems to be helping your depression. I don't want to put a damper on your enthusiasm, but would like to add a word of caution from: S-Adenosyl Methionine as a food supplement: Pros' and Cons' Winston Wicomb, Ph.D. at The Stone Clinic http://www.stoneclinic.com/sam_e.htm The greatest potential risk from taking SAM-e is if you are vitamin B12, or folic acid deficient, and don't have an adequate dietary intake of betaine (betaine is found at high levels in some vegetables such as spinach leaves). The reason is that in these conditions homocysteine conversion to methionine is impaired, resulting in hyperhomocysteinemia. When SAM-e is metabolized in the body, it normally gets converted to S-adenosylhomocysteine, and then to homocysteine. The enzyme methionine synthase will convert the homocysteine to methionine, which can then be processed back to SAM-e again. The enzyme methionine synthase is vitamin B12-dependent, and uses a substance called methyl-tetrahydrofolate (derived from folic acid) to convert homocysteine to methionine. When B12 or folic acid is low, then homocysteine will tend to build up. This build-up of homocysteine can be overcome, in part, by a 'back- up' enzyme system in the body which allows betaine to be used as an alternative methyl donor to convert homocysteine to methionine. Obviously, when betaine intake is low, then this back-up system can't function. So low B12, low folic acid, and low betaine intake could potentially result in large accumulation of homocysteine when SAM-e is taken in large amounts? High homocysteine is linked to heart disease and thrombosis. It might be good to be checked for hyperhomocysteinemia (high serum homocysteine) before taking SAM-e as there is concern that taking SAM- e might worsen the hyperhomocysteinemia? A trial on this very subject is underway at Baylor: http://www.baylorhealth.edu/Research/Grants/bloodhomocysteine.htm But, it may turn out that this concern is unfounded, and that SAM-e itself promotes homocysteine metabolism and conversion into glutathionie, thereby lowering homocysteine levels! The answer is not yet in ... I don't think the study (above) will be completed until 2009. Best regards, Dave (father of (22); PSC 07/03; UC 08/03) > For depression I've been taking SAM-e for over a month now. It's > OTC, a bit expensive, but various studies indicate that it helps in > eliminating depression. Additionally, it's supposedly good for the > liver, although I don't know that there's conclusive evidence > indicating that it necessarily helps PSC all that much; but it > certainly doesn't seem to be harmful for those of us with PSC. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 Hi Fred; Glad to hear that SAM-e seems to be helping your depression. I don't want to put a damper on your enthusiasm, but would like to add a word of caution from: S-Adenosyl Methionine as a food supplement: Pros' and Cons' Winston Wicomb, Ph.D. at The Stone Clinic http://www.stoneclinic.com/sam_e.htm The greatest potential risk from taking SAM-e is if you are vitamin B12, or folic acid deficient, and don't have an adequate dietary intake of betaine (betaine is found at high levels in some vegetables such as spinach leaves). The reason is that in these conditions homocysteine conversion to methionine is impaired, resulting in hyperhomocysteinemia. When SAM-e is metabolized in the body, it normally gets converted to S-adenosylhomocysteine, and then to homocysteine. The enzyme methionine synthase will convert the homocysteine to methionine, which can then be processed back to SAM-e again. The enzyme methionine synthase is vitamin B12-dependent, and uses a substance called methyl-tetrahydrofolate (derived from folic acid) to convert homocysteine to methionine. When B12 or folic acid is low, then homocysteine will tend to build up. This build-up of homocysteine can be overcome, in part, by a 'back- up' enzyme system in the body which allows betaine to be used as an alternative methyl donor to convert homocysteine to methionine. Obviously, when betaine intake is low, then this back-up system can't function. So low B12, low folic acid, and low betaine intake could potentially result in large accumulation of homocysteine when SAM-e is taken in large amounts? High homocysteine is linked to heart disease and thrombosis. It might be good to be checked for hyperhomocysteinemia (high serum homocysteine) before taking SAM-e as there is concern that taking SAM- e might worsen the hyperhomocysteinemia? A trial on this very subject is underway at Baylor: http://www.baylorhealth.edu/Research/Grants/bloodhomocysteine.htm But, it may turn out that this concern is unfounded, and that SAM-e itself promotes homocysteine metabolism and conversion into glutathionie, thereby lowering homocysteine levels! The answer is not yet in ... I don't think the study (above) will be completed until 2009. Best regards, Dave (father of (22); PSC 07/03; UC 08/03) > For depression I've been taking SAM-e for over a month now. It's > OTC, a bit expensive, but various studies indicate that it helps in > eliminating depression. Additionally, it's supposedly good for the > liver, although I don't know that there's conclusive evidence > indicating that it necessarily helps PSC all that much; but it > certainly doesn't seem to be harmful for those of us with PSC. Quote Link to comment Share on other sites More sharing options...
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