Guest guest Posted January 28, 2000 Report Share Posted January 28, 2000 Mark, Congratulations. What a difference a few months make. Not so long ago you were in pretty bad shape. My Reynauds has lessened this year so your may too on the AP. It is bitter cold here to right now and I just go warm up the car, come back in the house and run out and get in when it is warmed up. ps. I hope you carry a cell phone on these treks. :>) Bev > > Well, I must be feeling pretty good - went to town, came back, and > backpacked about 30 Lbs. of groceries up a steep 1/2 mile driveway in the > snow and ice and 11 degree temps and am alive to tell about it! Actually > feel fine - only problem I had was that my fingertips started to get cold - > that's a touch of Reynaud's I have. > > So there is hope! > Mark Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 2000 Report Share Posted January 28, 2000 Mark, Glad you're feeling good. Sounds more like great1 I'm sure the Methotrexate is doing its job and I'm glad you're doing it. Maybe you should keep on the AP anyway since it can't do harm. Have you thought of testing to see if you should perhaps try another antibiotic instead of the mino? Best, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2000 Report Share Posted February 2, 2000 I've also sent this e-mail to the group. What is methrotrex? Sorry I'm not too sure of all the medicines and what they are for. Thanks. Oh, also Mark what kind of results have you seen with Methrotrex? Donna Sapp Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2000 Report Share Posted February 2, 2000 " I've also sent this e-mail to the group. What is methrotrex? Sorry I'm not too sure of all the medicines and what they are for. Thanks. Oh, also Mark what kind of results have you seen with Methrotrex? Donna Sapp Go to www.rxlist.com and look up " methotrexate " . Basically, an immuno-suppressing drug (although at very small dosages, thus some rheumies consider it more anti-inflammatory than immuno-suppressing). It is the " standard " treatment used by rheumies today and has generally been found to work quite well, thus the reason for them prescribing it. It can come with some nasty side effects in certain people but the percentage of people experiencing those side effects is low. If you read the literature and all the possible side effects, it can scare you to death. I felt that way before I took it. However, I have had virtually no problems with it and it has helped me substantially. The question is - how long will it help and does it really control joint damage and can it put you into remission and is it toxic over the long haul? There seems to be considerable debate about all of that. I have to believe that being able to function once again and not being in pain are good indicators - if there is considerable damage going on underneath that process,then I drew an unlucky ticket. You do have to have blood tests every 6 weeks or so to make sure your liver enzymes are not becoming elevated. So far after 7 months, I have not had that problem (knock on wood). Some people have a lot of problems with nausea on the pill - by taking it at night, I don't have that problem. It is also recommended generally to take additional folic acid supplementation with this drug (1mg per day) to prevent some of the side effects, which I do. You will note that on this list you will find people with varying experiences with this drug - some have had very bad experiences, some have had good experiences but quit taking it because they felt like they were putting something " toxic " into their bodies. And some are taking it and finding it helps. It is a very difficult decision to make. You will not find support for it's use in this group because the group considers it to be " toxic " . If I am not wrong, the founders of the group have gone down the road of gold, and other " usual treatments " and found success only here, by using antibiotics. So naturally, you will not find support for the " standard " treatments. If you want to talk to people who actually use it and get their experiences (a wise move, imho), then you can go to the alt.support.arthritis newsgroup. If you are unfamiliar with how those newsgroups operate, then simply go to www.deja.com and do a search for methotrexate - you will find plenty there. I really think you have to think about " your " case and how you feel. There is nothing wrong with reading what every person here in the group feels about it or reading all the posts on other newsgroups. Ultimately, it will come down to you. This disease treats each person differently and what works for one often fails for another. Your rheumie or doctor will be quite familiar with methotrexate - he will be most likely unfamiliar with the antibiotic therapy. I think you should consider how fast the disease is progressing and whether you have given the antibiotics a fair trial. I continue to take antibiotics despite being on methotrexate. My doctors have assured me that there is not a problem with this. To be honest, I did not try the IV clindy treatments here, nor have I switched from minocycline to doxycycline, etc. Some (perhaps many?) would say that is why the AP isn't working for me anymore. I didn't feel I had the time to try those avenues as I was rapidly progressing, so I went with more conventional treatment combined with the AP which is uncommon, so I am a guinea pig of sorts. Hopefully all this helps. I think you need to look at all the options, try to read as much as you can, discuss with your doctor (whether you get an unbiased view there, depends on your doctor). And then think about what it is that YOU need because in the end, you have to be happy with YOUR choice, not someone elses. Mark http://Mark_Holmes.tripod.com RA 4/98 AP 7/98 Minocycline (Lederle generic) 100mg 2x/day Daily;Methotrexate (9/99)(12.5mg/once weekly); folic acid (1 mg/day); Lodine 400mg 3x/day;Zone Diet;;Fish Oil(9 caps/day);acidopholus;Milk Thistle;Calcium;Multi-Vit ICQ 18123139 AOL IM - ATHiker95 Re: rheumatic feeling good I've also sent this e-mail to the group. What is methrotrex? Sorry I'm not too sure of all the medicines and what they are for. Thanks. Oh, also Mark what kind of results have you seen with Methrotrex? Donna Sapp Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2000 Report Share Posted February 8, 2000 How??? By experimenting for 2 months at a time? That's the one frustrating thing I haven't been able to figure out is how to know if the antibio is working and I'm herxing or just getting worse. That happened for 2 years while trying many antibio to find one that works but unfortunately I was just getting worse until I found Minocin and colloidal silver. (I've been on antibiotics for 8 years and suddenly the combo stopped working--also I was doing better and had skipped dosages..bad mistake!!! But no going back) << Have you thought of testing to see if you should perhaps try another antibiotic instead of the mino? >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2000 Report Share Posted February 9, 2000 , I was feeling the same as you last summer when I was flaring most of the summer and was wondering if I should switch to something else. I stopped all my meds, even the anti inflams and HRT and just took the Mino and my thyroid pills for about two months and was so stiff and sore I had to be helped walk across the street. I decided to start back on my anti inflams and gradually I felt better and better. I could feel the difference each day in more flexibility. This was last fall. I am experimenting with dropping the Minocin on the weekends and it has made a further improvement. I spent all morning at the gym at the rehab centre and I can't believe the difference it is making getting the Kinesiologist to help me with exercises to increase my strength and flexibility even more. I hopped out of the car like my pre RA days. This is how it has been for me. It could change and I could have another flare. I just count my blessings. I hope you get the right combination of meds and anti inflammatories. That was what worked for me. Bev > > How??? By experimenting for 2 months at a time? That's the one frustrating > thing I haven't been able to figure out is how to know if the antibio is > working and I'm herxing or just getting worse. That happened for 2 years > while trying many antibio to find one that works but unfortunately I was just > getting worse until I found Minocin and colloidal silver. (I've been on > antibiotics for 8 years and suddenly the combo stopped working--also I was > doing better and had skipped dosages..bad mistake!!! But no going back) > > > << Have you > thought of testing to see if you should perhaps try another antibiotic > instead of the mino? >> > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2002 Report Share Posted January 21, 2002 -Hi Dean: Glad to hear that you are feeling well. I agree, exercise is a major component to living healthy with PA. I've found that attacking the PA simultaneously from three different fronts works the best for me. First, regular exercise that includes swimming, walking, gardening and yoga. Second, a diet that limits gluten, refined sugar, dairy, red meat, wheat products, alcohol and caffeine. Third, medicine which include antibiotics and celebrex. When I can discipline myself enough to make these three areas a part of my everyday life I usually feel quite good. Unfortunately, being human sometimes I stray from regular exercise and a restricted diet. However, the antibiotics seemed to have kept the arthritis in check even when I am not dieting and exercising on a regular schedule. I had my blood work checked last week and my rheumy was surprised to see that it tested normal after only 5 months on the antibiotic therapy. I wish that the antibiotics were also doing that well with the psoriasis. Any suggestions? Good luck with the new job. Change can be stressful at times but it can also be exciting and challenging. Wishing you the very best. Joe Godfrey -- In @y..., Dean Flory <deanzo@m...> wrote: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2002 Report Share Posted January 22, 2002 Hi Joe: Thanks for the encouragement. This change is a very good one and the stress is actually leaving versus starting. I found during this past summer that when I went on a very restrictive diet by Dr. Mercola my psoriasis started to clear up. However, I was also outside every day getting a lot of sun, so it could have been the sun at work. With the onset of winter here in Minnesota I noticed the psoriasis coming back. In addition to the thing you mentioned as key, I've found the following help too: proper supplements (as PAers tend to be deficient in several key vitamins, minerals and enzymes like B complex as our bodies don't absorb them well. Also C and E if you are on antibiotics to help offset their affects on your liver and kidneys) and hydration (I live with a bottle of water attached to my hand!). Another tidbit if you are on AP... I've seen several people personally report that doxycycline has shown to be as effective (if not more in my case) than minocycline for PAers. And you don't have to worry about being in the sun on doxy which is a big bonus for me. Thanks again! deano On Monday, January 21, 2002, at 04:23 PM, sierra4733 wrote: > -Hi Dean: > > Glad to hear that you are feeling well. I agree, exercise is a major > component to living healthy with PA. I've found that attacking the PA > simultaneously from three different fronts works the best for me. > First, regular exercise that includes swimming, walking, gardening > and yoga. Second, a diet that limits gluten, refined sugar, dairy, > red meat, wheat products, alcohol and caffeine. Third, medicine which > include antibiotics and celebrex. > > When I can discipline myself enough to make these three areas a part > of my everyday life I usually feel quite good. Unfortunately, being > human sometimes I stray from regular exercise and a restricted diet. > However, the antibiotics seemed to have kept the arthritis in check > even when I am not dieting and exercising on a regular schedule. I > had my blood work checked last week and my rheumy was surprised to > see that it tested normal after only 5 months on the antibiotic > therapy. I wish that the antibiotics were also doing that well with > the psoriasis. Any suggestions? > > Good luck with the new job. Change can be stressful at times but it > can also be exciting and challenging. Wishing you the very best. > > Joe Godfrey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2002 Report Share Posted August 19, 2002 Think about them one at a time BEFORE going on to the next one...... ..IT DOES MAKE YOU FEEL GOOD - especially the thought at the end. 1. Falling in love. 2. Laughing so hard your face hurts. 3. A hot shower. 4. No lines at the supermarket 5. A special glance. 6. Getting mail. 7. Taking a drive on a pretty road. 8. Hearing your favorite song on the radio. 9. Lying in bed listening to the rain outside. 10. Hot towels fresh out of the dryer. 11. Finding the sweater you want is on sale for half price. 12. Chocolate milkshake. (or vanilla!) (or strawberry) 13. A long distance phone call. 14. A bubble bath. 15. Giggling. 16. A good conversation. 17. The beach. 18. Finding a 20 note in your coat from last winter. 19. Laughing at yourself. 20. Midnight phone calls that last for hours. 21. Running through sprinklers. 22. Laughing for absolutely no reason at all. 23. Having someone tell you that you're beautiful. 24. Laughing at an inside joke. 25. Friends. 26. Accidentally overhearing someone say something > nice about you. 27. Waking up and realizing you still have a few hours left to sleep. 28. Your first kiss (either the very first or with a new partner). 29. Making new friends or spending time with old ones. 30. Playing with a new puppy. 31. Having someone play with your hair. 32. Sweet dreams. 33. Hot chocolate. 34. Road trips with friends. 35. Swinging on swings. 36. Wrapping presents under the Christmas tree while eating cookies and drinking your favorite tipple. 37. Song lyrics printed inside your new CD so you can sing along without feeling stupid. 38. Going to a really good concert. 39. Making eye contact with a cute stranger. 40. Winning a really competitive game. 41. Making chocolate chip cookies. 42. Having your friends send you home-made cookies. 43. Spending time with close friends. 44. Seeing smiles and hearing laughter from your friends. 45. Holding hands with someone you care about. 46. Running into an old friend and realizing that some things (good or bad) never change. 47. Riding the best roller coasters over and over. 48. Watching the _expression on someone's face as they open a much desired present from you. 49. Watching the sunrise. 50. Getting out of bed every morning and thanking God for another beautiful day. --------------------------------- Quote Link to comment Share on other sites More sharing options...
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