Guest guest Posted November 17, 1999 Report Share Posted November 17, 1999 Yeah, KayK, I am so happy for you. A day without prednisone is truly a great day!! And normal liver function is reason to celebrate!! Way to go. My day will come, of that I am sure. Ginger AIH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 20, 1999 Report Share Posted November 20, 1999 In a message dated 11/20/99 5:36:34 AM Eastern Standard Time, Carol writes: << Mine has been about half that and I don't know why, but I'm not complaining, and insurance is paying 80%.) >> Hi Carol, Thanks for posting that fascinating post about your visit to Cheney and the discussion about oxygen. I am wondering if the same effect can be had from trying to breathe in a paper bag to get the carbon dioxide? I am thinking of trying it. I also found the book Breathing Free at my library and put a hold on it. Since you are a patient of Cheney's...I was wondering how you manage to see him. Do you live in that area? Also what insurance do you have that will cover him? Thanks, Jane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2000 Report Share Posted March 30, 2000 Barbara, Since there's a May IAQ conference in Texas and there are so many cases of toxic mold cropping up in Texas, I'd like to see if your subscribers would feel any benefit in getting together. Perhaps we can all help one another. Thoughts? Melinda B. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2000 Report Share Posted June 17, 2000 WOW!! Thanks for all the responses to my questions re:school and stroller for Mira!! This is great.. We are working on increasing her endurance for walking and her riding her bike to school. I modified a 12 inch one for her and fit it with straps to help with the peddles and extenders.. She is pretty good on it. The school says that they do not allow kindergarden kids to ride bikes to school but would consider making an exception if I could demonstrate a special need circumstance and if she is " safe " (How do they figure she will be " safe " on the playground anyway??) soooo.. She is quite active and wants to be independent.. Climbs on everything and gets into some amazing spots. I can't believe her upper body strength.. She can press up and pike her hips to get on the kitchen cabinets for a drink using a small stool.. I don't think she thinks of strollers as a baby thing.. she will ask for her blue one (most comfortable).. I knew umbrella ones were bad for baby achons but does that extend up to when they're older too? I do not intend to let them skip her in various areas.. I will put that in the IEP as to helper, line leader ect.. So what if the kids have to go a bit slower from time to time.. They are young and it may help to teach them patience, acceptance, to see things in a different light.. I know for a fact the school makes mega allowances for the deaf kids.. even teaches sign language in the classroom from kindergarden up.. Thanks again for all the respnses and ideas.. Gigi B. ________________________________________________________________________ Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 Date: Tue, 22 Aug 2000 14:41:48 -0000 From: cmontana@... Subject: Water RE:(can help your health improve) " I use a Brita filter. Smoother taste. It has amused me to read the labels on bottled water. Some come from other cities' municipal water supplies. I always think I'm better off drinking our water here than buying somebody else's city water! " I too use a water pitcher filter;(similar to Brita but Shaklee brand); I replace filters about every third month and do have to wash the pitcher often for there is a film left in it from what the filters don't let through. We have well water and have had it tested. . .. it is safe to drink,though it has a smell at times. .. .it also is hard water and has a lot of minerals which leaves residue and makes for hard house cleaning unless you maintain often. The filter has made it much more appealing and my whole family goes through several pitchers a day. Even my kids drink water instead of pop, tea or other sugary drinks.(actually prefer it over other drinks) Cost isn't just an issue initially but over all our health is better. . .water is a very vital part of good health no matter what your condition. It helps us have more oxygen in our system, provides cleansing for toxins and impuritites in the body, and hydrates our muscles to move better. My massage therapist tells me most people go around approx. 90% dehydrated and don't even know. . . coffee, tea,and sodas, all of those dehydrate or rob the body of fluids. . . I am an ADVOCATE of drinking water! And , those drinks taste better made with the filtered water. . .so I agree its worth it! I can tell a great big difference when I don't drink enough water. . . if I go a day when there isn't quality water available! Less energy, sometimes headaches (oxygen deprived) and aches and pains more. I say we all should drink more water, but it does make a difference the water you drink! Just because you buy bottled water (some brands aren't truly from a spring source or. . .) doesn't mean it's better, so know what you are paying for it may be no better than the tap water you already pay for on your monthly bill! LOL \ / l Bottom's up and enjoy! ________________________________________________________________________ > ________________________________________________________________________ > > Message: 5 > Date: Tue, 22 Aug 2000 11:23:39 EDT > From: KathleenLS@... > Subject: Not CMT - about viruses, hoaxes, and all > that > > Dear friends, > I like to remind you occasionally, and for the sake > of newbies, that if you > receive a message from someone, even a friend or > relative, telling you to > send some warning on to everyone, please send it > privately to me first. I > know how to find out if it is true or just something > designed to worry people > and to clutter the internet. I'll tell you if it's > valid, usually within a > short time. I'll be glad to check it out for you. > kathleenls@... > > Virtually ALL messages of that sort are HOAXES, not > true at all. They > circulate around the internet endlessly because > people are trusting and > assume they are real problem situations. > > FYI: > Things you really should know > > 1) Bill Gates will NOT give you $1,000 for reading > his mail. > > 2) Disney is NOT giving $5,000 to 5,000 people. > > 3) If the subject of an e-mail is: Sorry I missed > you === message truncated === ===== *-* TODAY IS A " GIFT " . . TOMORROW IS NOT A PROMISE. . . MAKE THE MOST OF THE " PRESENT " ! *-* LIBBY FROM ARKANSAS __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2000 Report Share Posted October 10, 2000 To : (I THink)I went on digest to catch up with my e-mail, I have a hard time with digest. a lot of repeats,and I have trouble remembering who wrote what.LOL LOL. I write a column for themestream once a week on chronic illness also, and sometimes when company comes, i get behind in my E-mails. I much prefer the daily mails from this special group.This group has a wholeness that fills every need.Lots of good friends,and very very supportive. Unique and one of a kind. I am in Moosup,Conn. I feel comfortable that you are so nearby.we will have to meet someday, somehow. I have been housebound for 2 years,but on a good day, I've been known to take a JAUNT. for a short time. LOL.If you click on PREV. in the web ring below you can learn more about me.welcome to my part of the world. and I'll be back on daily messages soon. I miss a lot on Digest.Hello to ALL new members,while i'm at it here,and welcome to the best egroup on the net.A GREATER THAN GREAT BUNCH.TRULY A FAMILY WORTH HAVING.Huggs,bev. YOU CAN WRITE ME HERE Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 25, 2001 Report Share Posted April 25, 2001 >It's been brought to my attention that Sara is having low energy in the >afternoon. Because of this we are seeing defiant behaviors, refusing to work >etc... even some aggression but not too much of that lol My son (13, ds) has always been kind of like this also. We have almost always done some sort of snake mid morning and mid afternoon to help him through the day, & had some down time scheduled into his day. He also was diagnosed with sleep apnea, so he sleeps a lot at night, wakes up kind of slow, and is tired by the afternoon. He uses a c-pap machine now, and sleeps better, so he is more willing & able to do his school work, and make it through the day. , mom of (14), (13, ds) & Evan(8) :-) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2001 Report Share Posted November 15, 2001 Please put in the Geek Disease AQ test. I would love to read/take this. Tho I am sure my husband is geekier than me. LOL Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 25, 2001 Report Share Posted November 25, 2001 , I also agree with Sheila's concerns regarding the sign language in the pre-school hand. programs as well as Early Intervention. When my twins were diagnosed we went the EI route as well as the private speech therapy, We were fortunate that we found a SLP that was also fluent in signing and she signed along with her therapy...then she was promoted and of course no other SLPs knew sign language like she did. Also I requested that the EI SLP that came to the house 4 hours per week know sign language and of course trained in teaching apraxic children and the " coordinator(?) " did her best to find one trained in both but she had no luck....The SLP was more than willing to learn how to sign, but I was doing that anyway.....When I had the twins evaled for pre-school hand. they said that their teachers knew sign lang, but in fact when I asked they did not. It seems you have everything covered!!!!!!!! Good luck....I'll be thinking of you!!!!!!!! Kathy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2001 Report Share Posted November 30, 2001 Sorry, Have been getting ready for Christmas and this is a late response to your email. All I can say is I understand and know what you are going through. It is a one day at a time deal. I can remember that the first three years,even with therapy were hell and I really try to forget them. I used to cry myself to sleep and wonder what I did to get a child like my son.not only is her apraxic but he also is very high strung and " difficult " which is even harder. I really believe that God gave him to me so that I could learn patience, which I never had and now things don't bother me. Anyway,enjoy the small accomplishments and one day you will look back and see that you have made a lot of progress since earlier in their life. Take care, as you have found this group is great. Gretchen to 6 with apraxia. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 30, 2001 Report Share Posted December 30, 2001 Please visit the Zapper homepage at http://www.ZapLife.org ------------------------------------------------------------------------ There are 25 messages in this issue. Topics in this digest: 1. Re: msg 15 From: " " <rahughes@...> 2. Re: ICD's From: Greenholt <tgreenho@...> 3. Re: Cold/Coughing From: Greenholt <tgreenho@...> 4. My photo From: Greenholt <tgreenho@...> 5. Re: Digest Number 448 From: " Janet " <jifrance@...> 6. RE Medtronic device From: Munson <lmunson@...> 7. Re: Digest Number 448 From: Kathie Lazelle <iggy5519@...> 8. Re: My photo From: rcsejt@... 9. From: J <robertj@...> 10. Re: ICD's From: HANK <kg6ee@...> 11. Re: ICD's From: " BILLANDMARTHAMAHAN " <billandmarthamahan@...> 12. RE: ICD From: HANK <kg6ee@...> 13. Re: ICD's From: " TURK " <goturk1@...> 14. Re: RE: ICD From: coolahm@... 15. Hey Bob From: Munson <lmunson@...> 16. Re: ICD's From: Kathie Lazelle <iggy5519@...> 17. Re: Digest Number 448 From: mw999@... 18. Re: ICD's From: " Dave & Gail Forbes " <charade799@...> 19. Re: ICD's From: HANK <kg6ee@...> 20. Re: To Phyllis, Per your zap and fear From: pschatsky@... 21. Re: ICD's - Hank From: Guin Van Dyke <guin@...> 22. Re: Where in California?? From: Rob Natsch <natschural@...> 23. Re: Re: Where in California?? From: " oplbeach " <oplbeach@...> 24. Re: Re: Where in California?? From: " BILLANDMARTHAMAHAN " <billandmarthamahan@...> 25. Re: ICD's From: HANK <kg6ee@...> ________________________________________________________________________ ________________________________________________________________________ Message: 1 Date: Sat, 29 Dec 2001 09:23:22 -0700 From: " " <rahughes@...> Subject: Re: msg 15 Happy Holidays to all, Re capacitators and battery recharging....I have one of the medtronic jewel II's that they recalled due to charge time increasing disproportionately. While my charge time is increasing, it isn't at the level to be worried at yet. They're not taking this puppy out of me quite yet. When I questioned the pacemaker nurse about it they switched the auto recap to monthly rather than 6 monthly and on my last 3 month check it had not lost any charge time at all, in fact it may have gone down. Of course I have no idea what the auto recap is, but the longer I can put off more surgery the happier I am. Anyone understand enough about electrical systems to explain this one to me? Message: 15 Date: Fri, 28 Dec 2001 19:16:24 -0800 (PST) From: Kathie Lazelle <iggy5519@...> Subject: Re: ICD's HANK <kg6ee@...> wrote: How many of you have kept your old zapper when it was replaced? Mine was taking a bit too long to recharge (or recycle). Isn't it too bad that they can't recycle these with new batteries and give them to 3rd world countries or may be they could use them in some of the larger pets (Like a GREAT DANE). A Vet may know. To those who did keep their old one, I'll bet you couldn't resist passing it around to the group at coffee asking if they could identify what it was. After they had thoroughly examined it, I just love to see the expression on their faces when you tell them what it is and where it had been. See how many reach for a napkin to wipe their hands..... (GRIN) Hank Hank, Did you have your's replaced because the capacitor was taking too long to recharge? How long did you have to stay in the hospital? Was it day surgery? Overnight? Or what? I have to have mine replaced for that reason. I have had mine for almost three years. And I only worried about the batteries running out. Now I hear about the capacitor!!?? 1-520-626-7088 Science Education Liaison Molecular and Cellular Biology University of Arizona Life Sciences South, Rm 444 1007 E. Lowell Street P.O. Box 210106 Tucson, AZ 85721-0106 rahughes@... ________________________________________________________________________ ________________________________________________________________________ Message: 2 Date: Sat, 29 Dec 2001 11:59:39 -0500 From: Greenholt <tgreenho@...> Subject: Re: ICD's At 04:23 PM 12/28/01 -0800, you wrote: >How many of you have kept your old zapper when it was replaced? Hank, I had my ICD replaced for the first time on September 10 (the day before the terrorist tragedies). Before they started the procedure I asked if I could have the old one. The Guidant representative who was present in the operating room said I could but that they would have to sterilize it first. The replacement was no big deal and I was home by afternoon with just a little soreness. I did eventually receive my old ICD in the mail with a label on it that said that it was sterilized, etc. I keep it in a drawer. Most people I show it to kind of stand back like it may be dangerous to be near....and I suspect it is kind of gross to them to know that it was inside my body......Yuck! Anyway, wouldn't it be good if they were willing to buy one back from you for some future use. As expensive as they are, it would be nice to have that money to use for a new one. Like trading in a car. But alas, as long as there are insurance companies out there to pay, I doubt that this will happen. Thank God for insurance. Take care, Tom in PA > >Please visit the Zapper homepage at >http://www.ZapLife.org > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 19, 2002 Report Share Posted February 19, 2002 When I say yogurt cream, I mean cream that has been cultured with yogurt. It makes cream fraiche, otherwise known as yogurt cream. It is no longer just plain cream. So when we make a frozen dessert from it, we think of it as ice cream, but it is really high-fat frozen yogurt. There is much less lactose in cream than in yogurt, but there is still a little bit. To remove it all, you need to culture it for 48 hours. I think it takes longer to culture cream than milk because of the high fat content of cream. If you are tolerant of the lactose in cream, then you probably don't have to culture it to make ice cream - unless you want to. People who are intolerant of dairy can be sensitive to the lactose in it or to the milk protein. If you can eat hard cheese, then you can have the milk protein. I'm not sure about butter; I think it carries the milk protein also. Best wishes, > Date: Mon, 18 Feb 2002 11:22:17 -0600 > From: " Dennis " <nancydancy@...> > Subject: Re: ice cream recipe > > , you wrote: > > <snip>make yogurt cream (creme fraiche), incubating for 48 hours to remove all > lactose. > > I'm wondering why you call it " yogurt " cream. The NT recipe for Creme > Fraiche starts with cream. Are you using cream for this? And if so, does > this mean that cream contains lactose? I am trying to understand the > nature of my own intolerance for dairy. I seem to have no problem with > butter and butter is made from cream. I have thought that butter IS cream > minus the buttermilk. Is the lactose in the buttermilk? > > Thanks, > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2003 Report Share Posted May 27, 2003 Thanks for the suggestions LeighAnn and . I got back a biopsy result of the rashes on my arm and leg said it could be a drug sensitivity. My GP won't give me anything but Lortab for the hep/fibro pain. I have tried to tell her that the tylenol is killing my liver and giving me extreme itching that gets worse in the sun, but then the age old bull--- about addiction rears it's ugly head. when i talked to my gastro about it he doesn't believe in fibro and suggested a shrink. Now I'm not saying that i'm too good to talk to a shrink, done it many times before. But for pain? Oh well, I am going to buy me one of those big hats and cover my arms and legs while out in the sun, but it really pisses me off to have to do that in the boat! but if that is the hardest thing i ever had to do life would be a breeze, right? I wonder if i replaced my trazadone with benedryl at night if that might take care of the sleeping problem and the hives? i only take 25mg of trazadone. Love ya all, Joalle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2003 Report Share Posted May 27, 2003 Hi Joalle, My therapist once gave me an antidepressant that is suppose to control pain, by controling the pain sensations. It might work, but any doctor can give you that. I took Trazadone for a while to help me sleep, but my system got used to it and it doesn't work any more, or takes me 3 hours to get to sleep. So I got off of it. You have to get off of it gradually. Take 1/2 dose for awhile. I take Tylenol PM at night, just one, and sometimes that helps me get to sleep. It helps with the fever and aches and contains the meds in Benadryl. Good luck with finding something that works for your pain. Marie in Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2003 Report Share Posted May 27, 2003 US FILTHY DIRTY DRUG ADDICTS DONT DESERVE PAIN RELIEF!!!! I have put up with that crap for so long now, even though I KNOW it's in my best interests to be honest with my doctors.....I LIE about my past drug use. I get a half good tooth ripped out of my mouth cause I can't afford a root canal, take that back, I get a half good tooth surgicaly removed from my mouth, and the bas---- can't even give me tylenol #3s for the pain. Ya I did a lot of dope in my life and I enjoyed the hell out of it. What's up with that? And I don't even want to hear about the doctor putting himself at legal risk. The same hospital had no problem giving me morphine and Vicadin when I had my gall bladder removed. Joalle go back and ask that a-- hole if he or she's a doctor or a cop??!! Sorry for the rant....one of my pet peeves. > Thanks for the suggestions LeighAnn and . I got back a biopsy result of the rashes on my arm and leg said it could be a drug sensitivity. My GP won't give me anything but Lortab for the hep/fibro pain. I have tried to tell her that the tylenol is killing my liver and giving me extreme itching that gets worse in the sun, but then the age old bull--- about addiction rears it's ugly head. when i talked to my gastro about it he doesn't believe in fibro and suggested a shrink. Now I'm not saying that i'm too good to talk to a shrink, done it many times before. But for pain? > Oh well, I am going to buy me one of those big hats and cover my arms and legs while out in the sun, but it really pisses me off to have to do that in the boat! but if that is the hardest thing i ever had to do life would be a breeze, right? > I wonder if i replaced my trazadone with benedryl at night if that might take care of the sleeping problem and the hives? i only take 25mg of trazadone. > Love ya all, > Joalle > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2003 Report Share Posted May 27, 2003 Right on Man --- overdehump <payton323@...> wrote: > US FILTHY DIRTY DRUG ADDICTS DONT DESERVE PAIN > RELIEF!!!! I have put > up with that crap for so long now, even though I > KNOW it's in my > best interests to be honest with my doctors.....I > LIE about my past > drug use. I get a half good tooth ripped out of my > mouth cause I > can't afford a root canal, take that back, I get a > half good tooth > surgicaly removed from my mouth, and the bas---- > can't even give me > tylenol #3s for the pain. Ya I did a lot of dope in > my life and I > enjoyed the hell out of it. What's up with that? And > I don't even > want to hear about the doctor putting himself at > legal risk. The > same hospital had no problem giving me morphine and > Vicadin when I > had my gall bladder removed. Joalle go back and ask > that a-- hole if > he or she's a doctor or a cop??!! Sorry for the > rant....one of my > pet peeves. > > > > Thanks for the suggestions LeighAnn and . > I got back a > biopsy result of the rashes on my arm and leg said > it could be a > drug sensitivity. My GP won't give me anything but > Lortab for the > hep/fibro pain. I have tried to tell her that the > tylenol is killing > my liver and giving me extreme itching that gets > worse in the sun, > but then the age old bull--- about addiction rears > it's ugly head. > when i talked to my gastro about it he doesn't > believe in fibro and > suggested a shrink. Now I'm not saying that i'm too > good to talk to > a shrink, done it many times before. But for pain? > > Oh well, I am going to buy me one of those big > hats and cover my > arms and legs while out in the sun, but it really > pisses me off to > have to do that in the boat! but if that is the > hardest thing i ever > had to do life would be a breeze, right? > > I wonder if i replaced my trazadone with benedryl > at night if that > might take care of the sleeping problem and the > hives? i only take > 25mg of trazadone. > > Love ya all, > > Joalle > > > > > > [Non-text portions of this message have been > removed] > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 28, 2003 Report Share Posted May 28, 2003 I'm a drug addict in recovery, not filthy, certainly not dirty. As one addict to another what are you whinin' about? Two years ago I had ALL my teeth pulled and never took anything stronger than Motrin. I'm no saint, I just didn't need it. Why do dope fiends always think they need to take something? It's not for pain, it's just to forget where they are...And why would I want to put more crap in my body that only taxes my liver more, anyhow? Jesus, I have enough problems these days without adding to it all. Some things are necessary, a great deal are not. My problem is Doctors always trying to give me something that I don't want. Kelli -- Re: Digest Number 449 Right on Man --- overdehump <payton323@...> wrote: > US FILTHY DIRTY DRUG ADDICTS DONT DESERVE PAIN > RELIEF!!!! I have put > up with that crap for so long now, even though I > KNOW it's in my > best interests to be honest with my doctors.....I > LIE about my past > drug use. I get a half good tooth ripped out of my > mouth cause I > can't afford a root canal, take that back, I get a > half good tooth > surgicaly removed from my mouth, and the bas---- > can't even give me > tylenol #3s for the pain. Ya I did a lot of dope in > my life and I > enjoyed the hell out of it. What's up with that? And > I don't even > want to hear about the doctor putting himself at > legal risk. The > same hospital had no problem giving me morphine and > Vicadin when I > had my gall bladder removed. Joalle go back and ask > that a-- hole if > he or she's a doctor or a cop??!! Sorry for the > rant....one of my > pet peeves. > > > > Thanks for the suggestions LeighAnn and . > I got back a > biopsy result of the rashes on my arm and leg said > it could be a > drug sensitivity. My GP won't give me anything but > Lortab for the > hep/fibro pain. I have tried to tell her that the > tylenol is killing > my liver and giving me extreme itching that gets > worse in the sun, > but then the age old bull--- about addiction rears > it's ugly head. > when i talked to my gastro about it he doesn't > believe in fibro and > suggested a shrink. Now I'm not saying that i'm too > good to talk to > a shrink, done it many times before. But for pain? > > Oh well, I am going to buy me one of those big > hats and cover my > arms and legs while out in the sun, but it really > pisses me off to > have to do that in the boat! but if that is the > hardest thing i ever > had to do life would be a breeze, right? > > I wonder if i replaced my trazadone with benedryl > at night if that > might take care of the sleeping problem and the > hives? i only take > 25mg of trazadone. > > Love ya all, > > Joalle > > > > > > [Non-text portions of this message have been > removed] > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 28, 2003 Report Share Posted May 28, 2003 If you want to play macho toughy go for it!My 1st wife had fillings put in and would never use novacane. I got stabbed in the stomach with an ice pick, and had to wait in the E.R. for 4 hours (5 gunshots ahead of me). I have had teeth pulled too. No big deal. Ever had one cut out with a scalpel, and then had your gums stitched up and offered tylenol? I'm glad you are in recovery but dont get all huffed over the dirty filthy stuff you know! I'm just being facetious. I used to go through a box of 100 syringes every 3 to 4 days. I REALLY like doing drugs, even though i'm over 3 years clean. But back to the point here. Different people have different pain thresholds, just like they have different reactions to the TX. Some can tolerate it, some can't. Those that can't shouldn't be denied the relief from their pain thats available through modern drugs, because of their past. If you don't want pain drugs because you think you are too weak to resist the urge to go back on them, then I would say just go ahead and suffer then. But don't get in my face because I'm angered over what I see as mistreatment of these people by the doctors. That wasn't my last " whine " and this won't be my last rant!!!! " Moral indignation is jealousy with a halo " H.G. Wells > > > Thanks for the suggestions LeighAnn and . > > I got back a > > biopsy result of the rashes on my arm and leg said > > it could be a > > drug sensitivity. My GP won't give me anything but > > Lortab for the > > hep/fibro pain. I have tried to tell her that the > > tylenol is killing > > my liver and giving me extreme itching that gets > > worse in the sun, > > but then the age old bull--- about addiction rears > > it's ugly head. > > when i talked to my gastro about it he doesn't > > believe in fibro and > > suggested a shrink. Now I'm not saying that i'm too > > good to talk to > > a shrink, done it many times before. But for pain? > > > Oh well, I am going to buy me one of those big > > hats and cover my > > arms and legs while out in the sun, but it really > > pisses me off to > > have to do that in the boat! but if that is the > > hardest thing i ever > > had to do life would be a breeze, right? > > > I wonder if i replaced my trazadone with benedryl > > at night if that > > might take care of the sleeping problem and the > > hives? i only take > > 25mg of trazadone. > > > Love ya all, > > > Joalle > > > > > > > > > [Non-text portions of this message have been > > removed] > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2003 Report Share Posted May 29, 2003 this was not meant as a personal attack on you, it was meant as a question to us all....do we really need to take something or many times is it that we want to take something? After many years of recovery I have found that it just isn't always necessary.....and people need to hear that too......... - Re: Digest Number 449 If you want to play macho toughy go for it!My 1st wife had fillings put in and would never use novacane. I got stabbed in the stomach with an ice pick, and had to wait in the E.R. for 4 hours (5 gunshots ahead of me). I have had teeth pulled too. No big deal. Ever had one cut out with a scalpel, and then had your gums stitched up and offered tylenol? I'm glad you are in recovery but dont get all huffed over the dirty filthy stuff you know! I'm just being facetious. I used to go through a box of 100 syringes every 3 to 4 days. I REALLY like doing drugs, even though i'm over 3 years clean. But back to the point here. Different people have different pain thresholds, just like they have different reactions to the TX. Some can tolerate it, some can't. Those that can't shouldn't be denied the relief from their pain thats available through modern drugs, because of their past. If you don't want pain drugs because you think you are too weak to resist the urge to go back on them, then I would say just go ahead and suffer then. But don't get in my face because I'm angered over what I see as mistreatment of these people by the doctors. That wasn't my last " whine " and this won't be my last rant!!!! " Moral indignation is jealousy with a halo " H.G. Wells > > > Thanks for the suggestions LeighAnn and . > > I got back a > > biopsy result of the rashes on my arm and leg said > > it could be a > > drug sensitivity. My GP won't give me anything but > > Lortab for the > > hep/fibro pain. I have tried to tell her that the > > tylenol is killing > > my liver and giving me extreme itching that gets > > worse in the sun, > > but then the age old bull--- about addiction rears > > it's ugly head. > > when i talked to my gastro about it he doesn't > > believe in fibro and > > suggested a shrink. Now I'm not saying that i'm too > > good to talk to > > a shrink, done it many times before. But for pain? > > > Oh well, I am going to buy me one of those big > > hats and cover my > > arms and legs while out in the sun, but it really > > pisses me off to > > have to do that in the boat! but if that is the > > hardest thing i ever > > had to do life would be a breeze, right? > > > I wonder if i replaced my trazadone with benedryl > > at night if that > > might take care of the sleeping problem and the > > hives? i only take > > 25mg of trazadone. > > > Love ya all, > > > Joalle > > > > > > > > > [Non-text portions of this message have been > > removed] > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 The Prednisone is not working on me & my hands are swollen and my joint are damage, My right hand fingers are going to right side and it look weird. I hate to show my hand. Thank you. Lucy For those suffering from joint-swelling, let me quote my doctor again "Swelling is very dangerous for a joint and it can cause permanent damage. If oral Prednisone is not working and swelling remains there after some weeks, do consider taking it through infusion. This is costly but its more effective and quick in action" Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 For those suffering from joint-swelling, let me quote my doctor again " Swelling is very dangerous for a joint and it can cause permanent damage. If oral Prednisone is not working and swelling remains there after some weeks, do consider taking it through infusion. This is costly but its more effective and quick in action " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 You probably need to increase the Prednisone. In a recent flare I upped mine from 10 mg to 50 mg and then dropped off 5 to 10 mg daily until I reached a minimum level. this was done on doctor's advice. Good luck, Jay > The Prednisone is not working on me & my hands are swollen and my joint > are damage, > My right hand fingers are going to right side and it look weird. I hate to > show my hand. > Thank you. > Lucy > > > For those suffering from joint-swelling, let me quote my doctor again > > " Swelling is very dangerous for a joint and it can cause permanent damage. If oral > > Prednisone is not working and swelling remains there after some weeks, do > > consider taking it through infusion. This is costly but its more effective and > > quick in action " > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 what happens when you can't take Prednisone because of high blood sugar? I am on glucophage to keep that in line. -----Original Message-----From: Jay Bishop [mailto:jbirdak@...]Sent: Tuesday, August 26, 2003 1:38 PMRheumatoid Arthritis Subject: Re: Digest Number 449You probably need to increase the Prednisone. In a recent flare I upped mine from 10 mg to 50 mg and then dropped off 5 to 10 mg daily until I reached a minimum level. this was done on doctor's advice.Good luck,Jay> The Prednisone is not working on me & my hands are swollen and my joint > are damage,> My right hand fingers are going to right side and it look weird. I hate to > show my hand.> Thank you.> Lucy> > > For those suffering from joint-swelling, let me quote my doctor again > > "Swelling is very dangerous for a joint and it can cause permanent damage. If oral > > Prednisone is not working and swelling remains there after some weeks, do > > consider taking it through infusion. This is costly but its more effective and > > quick in action"> > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 Lucy, That is a problem beyond my scope of knowledge. I would suggest you call your rheumy or doctor and discuss it whith one of them. It maybe possible to increase your Glucophage to manage your diabetes if you take or increase your Prednisone, I don't know. I'm only an EMT and can't help much, Sorry. Best of luck, Jay > > The Prednisone is not working on me & my hands are swollen and > my joint > > are damage, > > My right hand fingers are going to right side and it look weird. I > hate to > > show my hand. > > Thank you. > > Lucy > > > > > For those suffering from joint-swelling, let me quote my doctor > again > > > " Swelling is very dangerous for a joint and it can cause > permanent damage. If oral > > > Prednisone is not working and swelling remains there after some > weeks, do > > > consider taking it through infusion. This is costly but its more > effective and > > > quick in action " > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 I know what you mean! I took a prednisone night before last and my blood sugar went bonkers on me!!!! I have been able to control my diabetes with diet so far. But the inflammation and pain are so bad right now (raining pretty much ALL of the time!), I am not sure what to do. I get my mtx shot on Thurs. I will mention it to my doc and see what he says! Carla -----Original Message----- From: SportsFanHome [mailto:rivals@...] Sent: Tuesday, August 26, 2003 2:21 PM To: Rheumatoid Arthritis Subject: RE: Re: Digest Number 449 what happens when you can't take Prednisone because of high blood sugar? I am on glucophage to keep that in line. -----Original Message----- From: Jay Bishop [mailto:jbirdak@...] Sent: Tuesday, August 26, 2003 1:38 PM Rheumatoid Arthritis Subject: Re: Digest Number 449 You probably need to increase the Prednisone. In a recent flare I upped mine from 10 mg to 50 mg and then dropped off 5 to 10 mg daily until I reached a minimum level. this was done on doctor's advice. Good luck, Jay > The Prednisone is not working on me & my hands are swollen and my joint > are damage, > My right hand fingers are going to right side and it look weird. I hate to > show my hand. > Thank you. > Lucy > > > For those suffering from joint-swelling, let me quote my doctor again > > " Swelling is very dangerous for a joint and it can cause permanent damage. If oral > > Prednisone is not working and swelling remains there after some weeks, do > > consider taking it through infusion. This is costly but its more effective and > > quick in action " > > > > > > Your use of is subject to the Terms of Service. Quote Link to comment Share on other sites More sharing options...
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