Guest guest Posted January 1, 2005 Report Share Posted January 1, 2005 I feel isolated for different reasons than you stated. I feel like my family supports me, in fact I think they are very worried. Where I feel isolated is with friends, friends I normally do things with. They call occasionally, but since I cannot do the regular activities , shopping , Eating ( i also recently had gastric bypass), dancing , normal working out...I rarely see anyone anymore... I think they just don't know what to do or say too. I am normally the person arranging the get together, the day with the girls..etc... not so anymore... I feel very lonely for the woman to woman friendship..and frankly it is hard to even relate to people who out and about doing everything a person my age is usually capable of doing. I can no longer do my job, ( used to be around alot of people). Faith N. California -------------- Original message -------------- Does anyone have the same problem I have with family? By that I mean, do you feel isolated? Do you feel like no one in your family beleaves or supports you with your arthritis? I know that I do. I get harrassed by my family members because I use a cane or because I have a service dog. They don't beleave I need it, that if I'd just loose weight I'd be fine. Just need someone who understands what I'm going through and how you handle it. Thanks for your time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2005 Report Share Posted January 1, 2005 I feel isolated for different reasons than you stated. I feel like my family supports me, in fact I think they are very worried. Where I feel isolated is with friends, friends I normally do things with. They call occasionally, but since I cannot do the regular activities , shopping , Eating ( i also recently had gastric bypass), dancing , normal working out...I rarely see anyone anymore... I think they just don't know what to do or say too. I am normally the person arranging the get together, the day with the girls..etc... not so anymore... I feel very lonely for the woman to woman friendship..and frankly it is hard to even relate to people who out and about doing everything a person my age is usually capable of doing. I can no longer do my job, ( used to be around alot of people). Faith N. California -------------- Original message -------------- Does anyone have the same problem I have with family? By that I mean, do you feel isolated? Do you feel like no one in your family beleaves or supports you with your arthritis? I know that I do. I get harrassed by my family members because I use a cane or because I have a service dog. They don't beleave I need it, that if I'd just loose weight I'd be fine. Just need someone who understands what I'm going through and how you handle it. Thanks for your time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2005 Report Share Posted January 2, 2005 , I never gave much thought to what my family is thinking for feeling about my illness. My kids understand most of the time and hubby well he is rather clueless most of the time. I don;t feel isolated. But then again I don't sit in the house or isolate myself from others. I go, do and lead a pretty normal life 95% of the time. The other well I made some modifications. My family knows if I say I do not want to go...then leave me alone about it. As far as believing I have RA, OA and Fibro. Well, I am not sure I even believe it....No admitting disability or defeat here. So why should my family. I think a lot of it is attitude. If you display the poor pitiful me attitude then they grow tired quickly of sick. lame and lazy. (sorry to be so blunt, but I am a ex-Army wife) Its part of human nature. We cast out what we don't understand, accept or is different. I think if you project an attitude, of yes I have this disease that is annoyance to me because it tries to slow me down...but I am not defeated yet. I have my wheelchair, dog, cane, etc.. and I am moving on. People see you differently. I would tell my family this is what I need to go on with my life and it will be with me at this point for the rest of my life. As far as weight is concerned. Your family may have a point is you are overweight to morbid or super morbid obese. For every 10 lbs of weight you loose you take 30 lbs of stress off you back, legs, knees, feet and ankles. There are also benefits such as improvement or resolution of reflux, high BP, diabetes, IBS, cardiac stress, sleep apnea, and respiratory problems. I am a surgical weight loss patient. There are others hear on the list. There are also many here that have lost a ton of weight without surgery. I know loosing weight 40lbs allowed me off all meds. I was on Methotrexate, Enbrel, Bextra, Prednisone, Folic Acid, Leukovorin, calcium/Vit D, mag, ultram, prevacid and a bunch of there meds. I was so drugged I was not really functional!!!! It was horrible. I had to stop meds to have my weight loss surgery. I stopped my meds a month before surgery and I never went back on them!!!! I found I was so crystal clear with my thoughts, my level of pain and frustration went down tremedously, I had NO swelling and slept like a baby. No doctor is going to admit this..cerntainly not my bonehead rheummy...but I was GROSSLY OVER MEDICATED!!!! Its been almost 7 months now and I am still 100% med free. I take an occastional tylenol but that is about it. I also had problems with IBS, GERD, sinus and allergies. All of these problems are GONE. My IBS was the first to go, next GERD and last was my sinus and allergies problems...along with the meds to control them. I have also stopped using my two TENS units, as well as a various splints for hands and wrists, Mouth night guard for jaw pain, and my use of shoes with orthodics is less than half the time. Who knows what the future holds I continue to loose weight. I m not near my goal yet. It would be nice if it left and never came back (austoimmune disease). Toni In a message dated 1/2/2005 2:21:43 AM Central Standard Time, writes: Date: Sun, 02 Jan 2005 03:40:37 -0000 From: " " <labsr2kool@...> Subject: Feeling alone Does anyone have the same problem I have with family? By that I mean, do you feel isolated? Do you feel like no one in your family beleaves or supports you with your arthritis? I know that I do. I get harrassed by my family members because I use a cane or because I have a service dog. They don't beleave I need it, that if I'd just loose weight I'd be fine. Just need someone who understands what I'm going through and how you handle it. Thanks for your time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2005 Report Share Posted January 2, 2005 Welcome, ! The problems you are having with your family's lack of understanding of your health status are, unfortunately, not uncommon. Many members of the group have told similar stories. For those in my life who don't " get it, " I try to stay away from the subject. I can't say that anyone is directly negatively critical, but, if someone doesn't understand, for example, that I might need more rest than I did before, I figure that's his or her problem. It used to frustrate me, but not anymore. I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org [ ] Feeling alone > > > > Does anyone have the same problem I have with family? By that I > mean, do you feel isolated? Do you feel like no one in your family > beleaves or supports you with your arthritis? I know that I do. I > get harrassed by my family members because I use a cane or because I > have a service dog. They don't beleave I need it, that if I'd just > loose weight I'd be fine. Just need someone who understands what I'm > going through and how you handle it. > Thanks for your time. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2005 Report Share Posted January 2, 2005 Hi , I'm Noreen, and I usually lurk here, but I had to answer this, because it hit so close to home. I am quite overweight, and my family members had the same opinion when I first started having problems. " you just need to lose weight. " , " you know if you go to the doctor he's just going to tell you to lose weight " I was so frustrated, and felt like it would be a waste of time to go in to see someone. Until my hands swelled up, and I finally saw someone, then a rheumatologist. I'm on methotrexate now and feel so much better, I can't believe it. I know weighing less would help me feel better too, but when family members try to tell you that's all that's wrong, they are missing the point. RA is not a disease of obesity. RA can be worsened by obesity, but thin or fat, the RA is still there. My rheumy, thankfully helped me to see that, and that while losing weight would help me, it isn't what caused my wrists and hands to swell. As far as family, my husband became more sympathetic after a bout of carpal tunnel. My elderly mother I simply had to confront and say tell her she was seriously hurting my feelings. (she was so surprised, like telling me everytime she saw me that I would feel better if I lost weight, would not be hurting my feelings.) Truthfully, I don't think anyone without RA does understand. Not the aching, not the fatigue, not the overall feelings of " blah " . So in truth, the very best support I got, was from this group. I bless the people here every day, because these people understand, and helped me to understand that having RA is not MY FAULT, despite my obesity.Knowing that, makes all the difference in the world, whether family members understand or not. Noreen [ ] Feeling alone Does anyone have the same problem I have with family? By that I mean, do you feel isolated? Do you feel like no one in your family beleaves or supports you with your arthritis? I know that I do. I get harrassed by my family members because I use a cane or because I have a service dog. They don't beleave I need it, that if I'd just loose weight I'd be fine. Just need someone who understands what I'm going through and how you handle it. Thanks for your time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2005 Report Share Posted January 2, 2005 Well said, Noreen! I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org Re: [ ] Feeling alone > > Hi , > I'm Noreen, and I usually lurk here, but I had to answer this, because it hit so close to home. > I am quite overweight, and my family members had the same opinion when I first started having problems. " you just need to lose weight. " , " you know if you go to the doctor he's just going to tell you to lose weight " > I was so frustrated, and felt like it would be a waste of time to go in to see someone. Until my hands swelled up, and I finally saw someone, then a rheumatologist. I'm on methotrexate now and feel so much better, I can't believe it. > > I know weighing less would help me feel better too, but when family members try to tell you that's all that's wrong, they are missing the point. RA is not a disease of obesity. RA can be worsened by obesity, but thin or fat, the RA is still there. > My rheumy, thankfully helped me to see that, and that while losing weight would help me, it isn't what caused my wrists and hands to swell. > As far as family, my husband became more sympathetic after a bout of carpal tunnel. My elderly mother I simply had to confront and say tell her she was seriously hurting my feelings. (she was so surprised, like telling me everytime she saw me that I would feel better if I lost weight, would not be hurting my feelings.) > Truthfully, I don't think anyone without RA does understand. Not the aching, not the fatigue, not the overall feelings of " blah " . > So in truth, the very best support I got, was from this group. > I bless the people here every day, because these people understand, and helped me to understand that having RA is not MY FAULT, despite my obesity.Knowing that, makes all the difference in the world, whether family members understand or not. > > Noreen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2005 Report Share Posted January 2, 2005 Faith, I don't understand why you are nt participating in any of your old activities. Hmm...I have RA, OA and Fibro and I had lapband weight loss surgery. I still shop, eat out, exercise( slower and not as much). I would go back to planning some activities when you feel well. Plan them in places where there is food you can eat or eat at home and have drinks when you are out. I do not know where you are in your food progression post-op gastric bypass but even on liquids or soft food you can find food to eat at many popular eateries. Most places will puree food on request and are more than happy to provide carry out containers for what is left uneaten. I can give you plenty of tips from others that are very successful, working fulltime and travel a lot, hence eating out almost every day. Do you attend any of your weightloss support groups, autoimmune support group, PACE(people with arthritis can exercise) or have tried some counseling sessions for those with chronic illness? I don't understand when you say its hard to relate. Because I know longer work and I am more busy now than when I was when I was working!!! I have my kids high school which I volunteer with, numerous friends that eat out, shop with, hangout in general, my animals which I care for and a husband and two children that keep me REAL busy. I would get back into the swing of things. Branch out make new friends. I know there are only a few people that I still socialize with from work. Most of those we were good friends for a very long time and still are even after I left my job. The other friends were basicly work related people I knew and once I left my job we had nothing in common anymore. Do some real soul searching about those friends from work. Are they truly your friends and what do you have in common to sustain a life long friendship. You may find that they are not so much your good friends as you think. I think one is only as limited as they allow themselves to be. Start thinking and getting creative to maintain as normal a life as possible. Toni In a message dated 1/2/2005 6:41:35 PM Central Standard Time, writes: Date: Sun, 02 Jan 2005 06:58:34 +0000 From: fmt2002@... Subject: Re: Feeling alone I feel isolated for different reasons than you stated. I feel like my family supports me, in fact I think they are very worried. Where I feel isolated is with friends, friends I normally do things with. They call occasionally, but since I cannot do the regular activities , shopping , Eating ( i also recently had gastric bypass), dancing , normal working out...I rarely see anyone anymore... I think they just don't know what to do or say too. I am normally the person arranging the get together, the day with the girls..etc... not so anymore... I feel very lonely for the woman to woman friendship..and frankly it is hard to even relate to people who out and about doing everything a person my age is usually capable of doing. I can no longer do my job, ( used to be around alot of people). Faith N. California Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2005 Report Share Posted January 3, 2005 I have never posted, in fact I just joined this morning for support with chronic, fms, oa, ra and lupus. After reading Toni's message to Faith I was concerned. Faith, I want you to know that I understand and a lot of other folks do as well. I got on anti-depressants and that has helped me. Also support groups have been a big help. One of my biggest problems was with folks who would say, " I can, I don't understand why you cant " , Just to let you know I have had that pet peeve following me for some time too. Mostly by people who did not have the same illness. We can't because we are sick, sickness sometimes causes depression, depression needs treatrment, and support. Toni, I am glad to hear your life is back in order and that you are now active and your life is full. Some of us are not that fortunate, please do not support them in there isolation by affirming how " abnormal " they are. If you can't try to understand and support, why are you here? > > > Faith, > I don't understand why you are nt participating in any of your old > activities. Hmm...I have RA, OA and Fibro and I had lapband weight loss surgery. I > still shop, eat out, exercise( slower and not as much). I would go back to > planning some activities when you feel well. > I don't understand when you say its hard to relate. Because I know longer > work and I am more busy now than when I was when I was working!!! I have my > kids high school which I volunteer with, numerous friends that eat out, shop > with, hangout in general, my animals which I care for and a husband and two > > Do some real soul searching about those friends from work. Are they truly > your friends and what do you have in common to sustain a life long friendship. > You may find that they are not so much your good friends as you think. > > I think one is only as limited as they allow themselves to be. Start > thinking and getting creative to maintain as normal a life as possible. > > Toni > > In a message dated 1/2/2005 6:41:35 PM Central Standard Time, > writes: > > Date: Sun, 02 Jan 2005 06:58:34 +0000 > From: fmt2002@c... > Subject: Re: Feeling alone > > > > I feel isolated for different reasons than you stated. I feel like my family > supports me, in fact I think they are very worried. Where I feel isolated is > with friends, friends I normally do things with. They call occasionally, but > since I cannot do the regular activities , shopping , Eating ( i also > recently had gastric bypass), dancing , normal working out...I rarely see anyone > anymore... I think they just don't know what to do or say too. I am normally > the person arranging the get together, the day with the girls..etc... not so > anymore... I feel very lonely for the woman to woman friendship..and frankly it > is hard to even relate to people who out and about doing everything a person > my age is usually capable of doing. I can no longer do my job, ( used to be > around alot of people). > > Faith > N. California > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2010 Report Share Posted August 3, 2010 Traci, You are so not alone. I sometimes want to wear a T-shirt that explains things! I truly hate it when I hear, " but you look fine! " (I actually did make one T-shirt that said " I don't take naps, naps take me! " ) There's just no way to explain to the public that it hurts to move. It's taken along time for the people around me to adjust to the 'new' me. (I was diagnosed 8 years ago) My husband took the longest, but now he can take one look at me and tell that I need my nap! Once the family and friends adjusted fairly well, I stopped worrying about what strangers think. When the fatigue gets bad, I schedule the nap into my day, usually really starts hitting me in the afternoon, so that way, at least I can kind of work around it. Are you having a lot of pain lately? Pain always makes me depressed and pain really makes me tired more than normal. I thank you for asking this question and can't wait to see what others reply! Life may not be the party we hoped for, but while we're here we might as well dance. From: lucydes29@... Date: Wed, 4 Aug 2010 00:04:21 +0000 Subject: [ ] Feeling Alone Hi there everyone. My name is Traci and I was wondering if anyone else ever feels like no one understands what we go thru? I have been feeling that way and It is an awful feeling. I cant manage to fight the fatigue that goes along with RA. If anyone can help, please let me know Sincerely Traci Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2010 Report Share Posted August 4, 2010 Hi Traci - We all understand what you are feeling. It is such a horrible thing to feel like no one understands. I lost a good friend unfortunately because I didn't feel up to going down town overnight for her birthday - this was shortly after I was initially diagnosed. She hasn't talked to me since. Very sad! Then there are people who will start to understand. I usually don't even talk about it to friends any more! The fatigue is so hard, but all we can do is rest when we can (easier said than done ) I hope you start to feel better - we all understand Traci! Donna > > Hi there everyone. My name is Traci and I was wondering if anyone else ever feels like no one understands what we go thru? I have been feeling that way and It is an awful feeling. I cant manage to fight the fatigue that goes along with RA. If anyone can help, please let me know > Sincerely > Traci > Quote Link to comment Share on other sites More sharing options...
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