Guest guest Posted March 2, 2004 Report Share Posted March 2, 2004 Hello Everyone, just a question for those of you who are also afflicted with Lupus. My rheumy couldn't decide what was wrong with me because I presented positive for lupus, Hepatitis and RA. He consulted with a hemotologist who said I have lupus. Now I will have to go back to rheumy and see what kind of treatment there is available. This seems a very difficult disease to diagnosis but the symptoms are muscular and skeletal pain chronically. Does anyone have any good treatments going on?? Does anyone know if there is a specialist I should see or just the regular rheumy? Thanks for any help! Suzanne -- [ ] Hello I am new and would like to know somethings Hi my name is , I have had Fibromyalgia and sjogrens syndrome for 10 years now and have just started Antibiotic therapy from my Rhuematologist. I was wondering if anyone is on the therapy and the success of the therapy. I am a self employed caterer and find it hard to do my work most of the time especially since I have to do most of the work out in the weather and I live in Upstate New york. Would like to talk to someone and share Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2004 Report Share Posted March 2, 2004 Suzanne, I don¹t have lupus so I can¹t tell you anything from experience. I¹ve collected some links and put them on my site: http://rheumatoid.arthritis.freehosting.net/Lupus.html I hope this helps a > Hello Everyone, just a question for those of you who are also afflicted > with Lupus. My rheumy couldn't decide what was wrong with me because I > presented positive for lupus, Hepatitis and RA. He consulted with a > hemotologist who said I have lupus. Now I will have to go back to rheumy and > see what kind of treatment there is available. This seems a very difficult > disease to diagnosis but the symptoms are muscular and skeletal pain > chronically. Does anyone have any good treatments going on?? Does anyone > know if there is a specialist I should see or just the regular rheumy? > Thanks for any help! > > Suzanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2004 Report Share Posted March 3, 2004 Suzy, I highly recommend Dr. Wallace's " The Lupus Book (2nd edition). " Of all the books I've read for patients with rheumatic diseases, it is the best. Wallace is thorough and writes in a very clear manner. Despite the complexity and wide spectrum of lupus, he has written a very concise and understandable guide for patients and their families. http://www.amazon.com/exec/obidos/tg/detail/-/0195132815/102-4592148-2532168?v=g\ lance This article, 'Management of lupus erythematosus: recent insights, " also by Dr. Wallace, is quite important reading: http://www.rheumatology.org/annual/sessions/Dr%20Wallace.pdf There is much current, reliable information at the Hospital for Special Surgery on lupus: http://rheumatology.hss.edu/phys/diseaseIndex/lupus.asp A rheumatologist is the specialist you need if you have lupus, although you may have others you may consult depending on just what sort of lupus you have and how it has affected you (or might). It would be wise to see a rheumatologist who has a lot of experience treating lupus patients. I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org Re: [ ] Diagnosis > Hello Everyone, just a question for those of you who are also afflicted > with Lupus. My rheumy couldn't decide what was wrong with me because I > presented positive for lupus, Hepatitis and RA. He consulted with a > hemotologist who said I have lupus. Now I will have to go back to rheumy and > see what kind of treatment there is available. This seems a very difficult > disease to diagnosis but the symptoms are muscular and skeletal pain > chronically. Does anyone have any good treatments going on?? Does anyone > know if there is a specialist I should see or just the regular rheumy? > Thanks for any help! > > Suzanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 6, 2005 Report Share Posted September 6, 2005 Dear , When you have dates let me know, I'd love to come up to Denver and visit with you. Things will be a blur for the next month, but you'll be so glad when it's over. Anything I can do let me know! Colorado Springs [ ] Diagnosis Well...hello again. Got my diagnosis. I have failed fusion with flatback. I wasn't surprised about the flatback, but I was about the failed fusion. Anyway...surgery is scheduled for October. They will remove my Harrington rod which is no longer connected at the bottom. It seems L3 & L4 are severely degenerated (causing the numbness in my left leg). L3 and L4 will be fused with a cage replacing the disc, and 2 rods, 4 screws to hold it all together (and some bone from the front of my hip & some BMP). Good news is that since I did not fuse at L3/L4, the doc can create some more natural curve to my spine to minimize flatback. Bad news is he goes in from the front this time and from the back...long recovery. I will find out more details this month...as I have many questions to get answered to get mentally ready for this. I do have a supportive family and husband to get through this which is good. I wanted to also thank you all for your input as I went through this waiting period. God bless. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 6, 2005 Report Share Posted September 6, 2005 , I am trying to remember and didn't locate it on a quick search...Did you see Dr. Kumar? I suspect I am not the only one that cannot remember.It seems there are a few advantages to getting things done so quickly, but as said, the next month will no doubt be a blur. If you haven't already, do check out all of the wonderful tips on preparing for surgery and ask whatever questions you think of...I will be taking notes as well! Best wishes to you. kamala Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 , Wow, that is amazing to think you are going from diagnosis to surgery in just a couple months. You are very brave. I went back to see who your surgeon is...I am confused...did you go to Colorado and is that where you are having the surgery? Is that your second opinion? It sounds like you are getting pretty much the same " treatment " we all get...although I was lucky that only the very botton of my HR had to be removed. I think after all these years having it out would have been a challenge....And of course this all meant the muscles in my upper back didn't get traumatized so it might have been a tad easier recovering. None the less, I still felt like a huge MAC truck had run me over. Will you surgeries be one or two days? Please count on us for anything you need. Take Care, Cam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 In a message dated 9/7/2005 9:40:16 PM Eastern Standard Time, morningsunranch@... writes: I gave up on doctors a long time ago and have never been healtier. , I am with you. Western medicine has only caused more problems for me. I did have a stool test done which told me which bacteria and yeast i have and what to use to kill it. That was very beneficial and i have made great progress. I have been fighting low grade fevers for the last 2 years. Since i started killing my bad bacteria, i haven't had a fever in over a month. I was told that my fevers were from lyme disease and i would have to stay on antibiotics until i was symptom free. Well, if i had followed that advise, i would have destroyed my gut and made my candida even worse than it was. My doctor didn't even mention the fact that yeast could be part of my problem. I strongly feel that because i developed a candida problem, it made my dormant lyme become active. Also, i had surgery for endometriosis which what finally broke " this " camels back. It all adds up. Its not just one thing. So, there is not one thing that will fix the candida. There is not a magic bullet. It is a combination of diet, exercise, supplements, positive thinking amongst other things. Blessings, Jordan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 The doctor that performed my original HR surgery is performing this one. I fly down and meet with him on the 23rd. I have talked to other patients of his and they all were extremely happy with him (I didn't get their names from him either) and the team he uses. He has a team he has worked with for many years and has performs many of these types of surgeries. He mentioned he could leave the rod in and take the end off as you said...but he said the only disadvantage to that is that in the future it could slip again/more. I would rather have it out than go through this again...even if the chance is remote. They said I had a good fusion on the rest of my back which will make the HR easier to remove. It is one long surgery. They will go through the front first to insert the cage and get bone from my hip, then go through the back to finish the fusion with 2 rods, and 4 screws...and take the HR rod out. I have done research and have a list of questions for when I go down to see him. My mother is a nurse and has helped with a lot of what I need to know and ask which has been a blessing. I know this seems fast...but I am noticing more issues with my comfort level each day and I worry I am going to have more nerve damage, pain, etc. if I wait. And...I am getting to where I can't pick up or do a whole lot with my babies. It's bugging me bad. Thank you for your support... > , > > Wow, that is amazing to think you are going from diagnosis to > surgery in just a couple months. You are very brave. > > I went back to see who your surgeon is...I am confused...did you go > to Colorado and is that where you are having the surgery? Is that > your second opinion? It sounds like you are getting pretty much the > same " treatment " we all get...although I was lucky that only the > very botton of my HR had to be removed. I think after all these > years having it out would have been a challenge....And of course > this all meant the muscles in my upper back didn't get traumatized > so it might have been a tad easier recovering. None the less, I > still felt like a huge MAC truck had run me over. > > Will you surgeries be one or two days? > Please count on us for anything you need. > > Take Care, Cam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 , Would you mind giving the name and location (hospital) of your doctor? It could prove helpful to others in the area at some point. Thanks! kam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 If you have to convince your doctor that you are sick, you need another doctor. ALso if friends or family can't understand you are not feeling well, that is their problem. Just start getting well and then you wont have to convince a doctor or have ammo to counter questions with family. I would not waste my money getting tests the treatment will be building your immune system and you can do that on your own. I gave up on doctors a long time ago and have never been healtier. -- Diagnosis Hi everyone, New here and still struggling a bit with accepting (and having others accept) what seems to be wrong with me. I'm just wondering how many of you have been diagnosed by a " proper " brush cytology test and how many, like myself, have suspected candidiasis through consultation with a naturopath or similar. Perhaps there are also those who have self-diagnosed? What does it take to convince your GP to request this test for you? It would be nice to have some orthodox ammo to counter all the questions I get. Thanks to all, Mucusarus Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2005 Report Share Posted September 7, 2005 Hi Jordan, BOth husband and I believe we had lyme also. Never a confirmed Dx. My husband had the chronic fevers also and major joint pain. For me my symptoms were the chronic infections and nuerological stuff. The candida then takes over and has a whole list of symptoms all its own! You are so right that inorder to get well we must have a combination of things. I think so many get stuck on a diagnosis and then try to just treat that particular disease symptom. That just will never work and for some reason the doctors have not quite noticed that year after years their patients just keep coming back sicker and sicker. Glad you are on the right track. I can tell with my experience with lyme, you must keep your immune system strong. I have a good amount of supplements I take everyday, I rest, eat good organic healthy foods and drink only filtered water. Good luck to you. From: jbgoth@... , I am with you. Western medicine has only caused more problems for me. I did have a stool test done which told me which bacteria and yeast i have and what to use to kill it. That was very beneficial and i have made great progress. I have been fighting low grade fevers for the last 2 years. Since i started killing my bad bacteria, i haven't had a fever in over a month. I was told that my fevers were from lyme disease and i would have to stay on antibiotics until i was symptom free. Well, if i had followed that advise, i would have destroyed my gut and made my candida even worse than it was. My doctor didn't even mention the fact that yeast could be part of my problem. I strongly feel that because i developed a candida problem, it made my dormant lyme become active. Also, i had surgery for endometriosis which what finally broke " this " camels back. It all adds up. Its not just one thing. So, there is not one thing that will fix the candida. There is not a magic bullet. It is a combination of diet, exercise, supplements, positive thinking amongst other things. Blessings, Jordan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 8, 2005 Report Share Posted September 8, 2005 Dr. Lowe in Wheatridge Colorado. He performs surgeries at Lutheran Hospital and Denver Childrens Hospital. > , > > Would you mind giving the name and location (hospital) of your doctor? > It could prove helpful to others in the area at some point. > > Thanks! > > kam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2005 Report Share Posted September 9, 2005 ...Thank you. I am scheduled for October 17th at Lutheran Hospital in Wheatridge, provided I don't change my mind after my visit with the doctor in person. One thing I have read that I have questions on is inflamation of the pancreas after back surgery. Do you know anything about this? I didn't have it when I got my HR at 14. I have had a 1/3 of my pancreas removed when I was 11. I gave my doc the op reports so he is aware. I still may get a second opinion from Kumar...I just might have to do it long distance (after my sister in Littleton picks up my xrays and does the transporting for me). > Dear , > > When you have dates let me know, I'd love to come up to Denver and visit with you. Things will be a blur for the next month, but you'll be so glad when it's over. Anything I can do let me know! > > > Colorado Springs > [ ] Diagnosis > > > Well...hello again. Got my diagnosis. I have failed fusion with > flatback. I wasn't surprised about the flatback, but I was about the > failed fusion. Anyway...surgery is scheduled for October. They will > remove my Harrington rod which is no longer connected at the bottom. It > seems L3 & L4 are severely degenerated (causing the numbness in my left > leg). L3 and L4 will be fused with a cage replacing the disc, and 2 > rods, 4 screws to hold it all together (and some bone from the front of > my hip & some BMP). Good news is that since I did not fuse at L3/L4, > the doc can create some more natural curve to my spine to minimize > flatback. Bad news is he goes in from the front this time and from the > back...long recovery. I will find out more details this month...as I > have many questions to get answered to get mentally ready for this. I > do have a supportive family and husband to get through this which is > good. I wanted to also thank you all for your input as I went through > this waiting period. God bless. > > > > > > > scoliosis veterans * flatback sufferers * revision candidates > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2005 Report Share Posted September 9, 2005 Dear , Anything I can do to help if you want a second opinion just let me know. I'm up in Denver fairly often since my daughter lives up there and I take the Granddaughter everyother weekend. I could run the X-Rays to Kumar if you'd like, just let me know when they are available, no pressure, just trying to help. I know you have prior experience with your doc and feeling comfortable is most important. Just would be good to see if Kumar concurs with your doc on treatment, always good to have options. On the pancreas, I know zero about that complication. Put it out to the other members, maybe they know this one. When is your doc appointment in Wheatridge? My second surgeon Dr. O'Brien was located right next to Lutheran Hospital, been out there tons of times, so if you have surgery there I could come by and visit. You'll do great, and life with your young ones will be much improved when you are in a lot less pain. I'm pulling for you! [ ] Diagnosis> > > Well...hello again. Got my diagnosis. I have failed fusion with > flatback. I wasn't surprised about the flatback, but I was about the > failed fusion. Anyway...surgery is scheduled for October. They will > remove my Harrington rod which is no longer connected at the bottom. It > seems L3 & L4 are severely degenerated (causing the numbness in my left > leg). L3 and L4 will be fused with a cage replacing the disc, and 2 > rods, 4 screws to hold it all together (and some bone from the front of > my hip & some BMP). Good news is that since I did not fuse at L3/L4, > the doc can create some more natural curve to my spine to minimize > flatback. Bad news is he goes in from the front this time and from the > back...long recovery. I will find out more details this month...as I > have many questions to get answered to get mentally ready for this. I > do have a supportive family and husband to get through this which is > good. I wanted to also thank you all for your input as I went through > this waiting period. God bless.> > > > > > > scoliosis veterans * flatback sufferers * revision candidates > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2005 Report Share Posted September 9, 2005 Thank you, , for the info about your doc. It seems mid-October is going to be quite busy around here! I hope all goes well for you, too! kam > ...Thank you. I am scheduled for October 17th at Lutheran > Hospital in Wheatridge, provided I don't change my mind after my > visit with the doctor in person. One thing I have read that I have > questions on is inflamation of the pancreas after back surgery. Do > you know anything about this? I didn't have it when I got my HR at > 14. I have had a 1/3 of my pancreas removed when I was 11. I gave my > doc the op reports so he is aware. I still may get a second opinion > from Kumar...I just might have to do it long distance (after my > sister in Littleton picks up my xrays and does the transporting for > me). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2005 Report Share Posted October 23, 2005 , What are your symptoms??? Also if you and boyfriend have the same thing you would not need to worry about being intimate at this point unless one got well and the other was still sick. GIna -- Diagnosis How does everyone know that they have yeast? I'm experiencing some of the symptoms of cadidiasis, but every culture the doctors take comes back normal and everyone keep stelling me I appear healthy but I don't FEEL well and I would think that it's something autoimmune or something tot hat effect, but my boyfriend has the same symptoms, so I don't know what else to do. We've seen 9 doctors and a dentist between the two of us, including an ENT, various dermatologists and ID. We're afraid to touch each other. How does everyone know how to treat themselves? Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2005 Report Share Posted October 23, 2005 I don't have any of the GI symptoms that everyone is mentioning, but we're both having problems with our mouths. We're worried about touching each other because sometimes I feel good, sometimes he feels good, it varies. It started last winter and then we were ok all summer, we had never been sexually intimate for the 9 months we've been together, but recently I started um... doing things for him and now our problems are resurfacing. I have a vaginal infection, my lips are dry and chapped, I have a disgusting taste in my mouth that I can't describe, I wake up with white cakey mucous in the corners of my mouth and sometimes my tongue burns. He has the same problems and also he feels flushed a lot, like he ahs a fever but he doesnt, pimples near the lips and other various little things that I can't currently remember but that you wouldn't even consider worrying about if it wasn't alll happening at the same time. All the doctors I've seen say my mouth looks normal, I've had the full battery of STD testing and everyting is normal. He's a virgin. I'm at a loss, really. If this ISN'T yeast, which is entirely possible, I have no idea what it could be and I don't know who else to turn to for an answer when everyone keeps telling us we're fine. It's so frustrating. " Kindscher (Charter) " <morningsunranch@...> wrote: , What are your symptoms??? Also if you and boyfriend have the same thing you would not need to worry about being intimate at this point unless one got well and the other was still sick. GIna -- Diagnosis How does everyone know that they have yeast? I'm experiencing some of the symptoms of cadidiasis, but every culture the doctors take comes back normal and everyone keep stelling me I appear healthy but I don't FEEL well and I would think that it's something autoimmune or something tot hat effect, but my boyfriend has the same symptoms, so I don't know what else to do. We've seen 9 doctors and a dentist between the two of us, including an ENT, various dermatologists and ID. We're afraid to touch each other. How does everyone know how to treat themselves? Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2005 Report Share Posted October 23, 2005 Hi , First of all I want to commend you on waiting on the sex with your boyfriend that is a good idea. What you are describing does sound like oral thrush. I don't know why the doctors cannot detect it. Have you done the simple spit test first thing in the morning??? You can look up exactly how to do it online, its very simple and it gives you pictures and everything to compare to . You need to get your immune systems up and running better, balance the bowels even though you have no bowel symptoms The bowels is where everything starts. You need to change your diet to akaline foods, eliminate all sugars, processed foods, high glycemic carbs. Just eat meat, vegies, drink lime juice, coconut oil, and other coconut products, garlic, onions. Its not that hard to get rid of when you change the diet and get the immune system optimal. -- Re: Diagnosis I don't have any of the GI symptoms that everyone is mentioning, but we're both having problems with our mouths. We're worried about touching each other because sometimes I feel good, sometimes he feels good, it varies. It started last winter and then we were ok all summer, we had never been sexually intimate for the 9 months we've been together, but recently I started um... doing things for him and now our problems are resurfacing. I have a vaginal infection, my lips are dry and chapped, I have a disgusting taste in my mouth that I can't describe, I wake up with white cakey mucous in the corners of my mouth and sometimes my tongue burns. He has the same problems and also he feels flushed a lot, like he ahs a fever but he doesnt, pimples near the lips and other various little things that I can't currently remember but that you wouldn't even consider worrying about if it wasn't alll happening at the same time. All the doctors I've seen say my mouth looks normal, I've had the full battery of STD testing and everyting is normal. He's a virgin. I'm at a loss, really. If this ISN'T yeast, which is entirely possible, I have no idea what it could be and I don't know who else to turn to for an answer when everyone keeps telling us we're fine. It's so frustrating. " Kindscher (Charter) " <morningsunranch@...> wrote: , What are your symptoms??? Also if you and boyfriend have the same thing you would not need to worry about being intimate at this point unless one got well and the other was still sick. GIna -------Original Message------- " on the web. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2005 Report Share Posted October 23, 2005 Thanks , I'm definitely going to do the spit test first thing in the morning. The images of thrush that I've seen online don't really appear to match what's going on in my mouth though, I don't have any white patches, neither does he. I just wish there was another way to get a concrete conclusion. It's so weird that between the two of us, no one can come up with a diagnosis. Is that common? > , > > What are your symptoms??? Also if you and boyfriend have the same thing you > would not need to worry about being intimate at this point unless one got > well and the other was still sick. GIna > > -------Original Message------- > > " on the web. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2005 Report Share Posted October 24, 2005 yeast infection back to: health guide | all healthnotes indexes | health concerns index shop related departments . yeast infections . probiotics search for more . see results for 'yeast infection' continue shopping . all drugstore.com departments Also indexed as: Candida vaginitis, Candidiasis (Vaginal), Vaginitis (Candida) See also: Chronic Candidiasis a.. Introduction b.. Checklist c.. Symptoms d.. Treatments e.. Dietary changes f.. Lifestyle changes g.. Supplements h.. Herbs i.. References Vaginal yeast infections are one of the most common reasons that women consult healthcare professionals. Yeast infections result from an overgrowth of a species of fungus called Candida albicans. Checklist for Yeast Infection Rating Nutritional Supplements Herbs Lactobacillus acidophilus Boric acid Cinnamon Echinacea Oregano Tea tree oil See also: Homeopathic Remedies for Yeast Infection Reliable and relatively consistent scientific data showing a substantial health benefit. Contradictory, insufficient, or preliminary studies suggesting a health benefit or minimal health benefit. An herb is primarily supported by traditional use, or the herb or supplement has little scientific support and/or minimal health benefit. What are the symptoms of yeast infection? Yeast infections are a type of vaginitis. The hallmark symptom of a yeast infection is itching of the external and internal genitalia, which is often associated with a white discharge that can be thick and/or curdy (like cottage cheese). Severe infections lead to inflammation of the tissue and subsequent redness, swelling, and even pinpoint bleeding. How is it treated? Yeast infections (vaginal candidiasis) can be treated either with oral antifungal medications (e.g. fluconazole [Diflucan®]) or topical antifungal medications (e.g., miconazole [Monistat®], clotrimazole [Gyne-Lotrimin®]). Doctors often prescribe antifungal medications for insertion into the vagina, either as a cream using a special applicator or as a suppository, for three to seven nights. Antifungal cream may be applied topically to the vulva (external genitalia) to help relieve itching. Dietary changes that may be helpful: Some doctors believe that a well-balanced diet low in fats, sugars, and refined foods is important for preventing vaginal infections caused by Candida. In one preliminary trial, avoidance of sugar, dairy products, and artificial sweeteners resulted in a sharp reduction in the incidence and severity of Candida vaginitis.1 Many doctors advise women who have a yeast infection (or are predisposed to such infections), to limit their intake of sugar, fruit juices, and refined carbohydrates. For persistent or recurrent infections, some doctors recommend that fruit also be avoided. Another trial found that dramatic increases in intake of several sugars in healthy people partially increased stool sample levels of Candida, but only in 12 out of 28 people.2 Lifestyle changes that may be helpful: According to one study, yeast infections are three times more common in women who wear nylon underwear or tights, than in those who wear cotton underwear.3 Additional predisposing factors for Candida infection include the use of antibiotics, oral contraceptives, or adrenal corticosteroids (such as prednisone). Underlying health conditions that may predispose someone to Candida overgrowth include pregnancy, diabetes, and HIV infection. Allergies have also been reported to promote the development of recurrent yeast vaginitis. In a preliminary trial, when the allergens were avoided and the allergies treated, the chronic recurrent yeast infections frequently resolved.4 In most cases, sexual transmission does not play a role in yeast infection. However, in persistent cases, sexual transmission should be considered, and the sexual partner should be examined and treated. Nutritional supplements that may be helpful: Lactobacillus acidophilus is a species of friendly bacteria that is an integral part of normal vaginal flora. Lactobacilli help to maintain the vaginal ecosystem by preventing the overgrowth of unfriendly bacteria and Candida. Lactobacilli produce lactic acid, which acts like a natural antibiotic. Lactobacillus acidophilus can be taken orally in the form of acidophilus yogurt, or in capsules or powder. It can also be administered vaginally. In a controlled trial, women who consumed 8 ounces of Lactobacillus acidophilus-containing yogurt per day had a threefold decrease in the incidence of vaginal yeast infections and a reduction in the frequency of Candida colonization in the vagina.5 In another trial, women who were predisposed to vaginal Candida infection because they were HIV-positive received either Lactobacillus acidophilus vaginal suppositories, the antifungal drug, clotrimazole (e.g., Gyne-Lotrimin®), or placebo weekly for 21 months.6 Compared to those receiving placebo, women receiving Lactobacillus acidophilus suppositories had only half the risk of experiencing an episode of Candida vaginitis-a result almost as good as that achieved with clotrimazole. Many women find relief using an acidophilus-containing yogurt douche daily for a few days or weeks, depending on the severity of the infection.7 Three capsules of acidophilus or one-quarter teaspoon of powder can be taken orally one to three times daily. Acidophilus can also be taken preventively during antibiotic use to reduce the risk of Candida vaginitis.8 9 Boric acid capsules inserted in the vagina have been used successfully as a treatment for vaginal yeast infections. One study demonstrated that 85% of women who used boric acid vaginal suppositories were cured of chronic recurring yeast vaginitis.10 These women had all previously failed to respond to treatment with conventional antifungal medicines. The suppositories, which contained 600 mg of boric acid, were inserted vaginally twice a day for two weeks, then continued for an additional two weeks if necessary. Boric acid should never be swallowed. Are there any side effects or interactions? Refer to the individual supplement for information about any side effects or interactions. Herbs that may be helpful: A small, preliminary trial found that a mouthwash with diluted tea tree oil was effective in decreasing the growth of Candida albicans and in improving symptoms in AIDS patients with oral Candida infections (thrush) that had not responded to drug therapy.11 People in the study took 15 ml of the oral solution (dilution of tea tree oil was not given) four times per day and were instructed to swish it in their mouth for 30 to 60 seconds and then spit it out. For use of tea tree oil as a mouthwash, one should not exceed a 5% dilution and should be extremely careful not to swallow the solution. Many doctors recommend that people with recurrent yeast infections take measures to support their immune system. Echinacea, which has the capacity to enhance immune function, is often used by people who suffer from recurrent infections. In one study, women who took echinacea experienced a 43% decline in the recurrence rate of yeast infections.12 The essential oil of cinnamon contains various chemicals that are believed to be responsible for cinnamon's medicinal effects. Important among these compounds are eugenol and cinnamaldehyde. Cinnamaldehyde and cinnamon oil vapors exhibit extremely potent antifungal properties in test tubes.13 In a preliminary study in people with AIDS, topical application of cinnamon oil was effective against oral thrush.14 A test tube study demonstrated that oil of oregano, and an extract in the oil called carvacrol in particular, inhibited the growth of Candida albicans far more effectively than a commonly employed antifungal agent called calcium magnesium caprylate.15 However, clinical studies are needed to confirm these actions in humans. Love and Light Blessings too! -Blakeslee Http://www.loveandlight.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2005 Report Share Posted October 24, 2005 Re: Diagnosis > , > > What are your symptoms??? Also if you and boyfriend have the same thing you > would not need to worry about being intimate at this point unless one got > well and the other was still sick. GIna > On the other hand there are many strains of fungus and bacteria. It's possible one has more potent strains that could be spread to the other making the other worse. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2005 Report Share Posted October 24, 2005 Both husband and I went for years without diagnosis of our illnesses. It turns out we had late stage lyme disease. Having Candida was just one of the many symptoms that went with that. There are just too many illnesses and not very good diagnostics. That is why I believe that supporting the bodies immune system and getting the bowels healthy will make a huge difference no matter what you have. -- Re: Diagnosis Thanks , I'm definitely going to do the spit test first thing in the morning. The images of thrush that I've seen online don't really appear to match what's going on in my mouth though, I don't have any white patches, neither does he. I just wish there was another way to get a concrete conclusion. It's so weird that between the two of us, no one can come up with a diagnosis. Is that common? --- In candidiasis , " Kindscher (Charter) " < Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2005 Report Share Posted November 1, 2005 Sorry to hear you have to make these decisions alone and that your hubby is in Iraq! Hopefully we can make you feel not so alone in this since we've all been there! I'm not sure why your doc would write that as the diagnosis instead of just plagio, but that is the characteristics of plagio. Where do you live? Is there a helmet provider in your area? Check out our Database section, there is a helmet/band locator in there, you just type in your state at the top and it will bring up all the providers near you. Lacy Waydon 1 year DOCgrad www.waydonsnoodle.com > > My 5.5 month old son saw the pediatric plastic surgeon today about the > flat spot on the side of his head. The doctor said it was cause from > laying too much on that one side. His diagnosis was moderate and > about a 6 on a scale of 1-10. The doctor said that he needs a > helmet. On the paperwork that the doctor gave me to send to the > insurance he had checked that the condition was " anomilies of the face > and skull bones " instead of " plagiocephaly " . What is the difference? > > Also, the insurace we have is Tricare. Does anyone have any > experience with getting them to pay? > > All of this is new to me and my husband is in Iraq. It is difficult > not having him here to help me make decisions. I would appreciate any > advice you can give me. > > Thanks in advance! > Missy > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2005 Report Share Posted November 1, 2005 Sorry to hear you have to make these decisions alone and that your hubby is in Iraq! Hopefully we can make you feel not so alone in this since we've all been there! I'm not sure why your doc would write that as the diagnosis instead of just plagio, but that is the characteristics of plagio. Where do you live? Is there a helmet provider in your area? Check out our Database section, there is a helmet/band locator in there, you just type in your state at the top and it will bring up all the providers near you. Lacy Waydon 1 year DOCgrad www.waydonsnoodle.com > > My 5.5 month old son saw the pediatric plastic surgeon today about the > flat spot on the side of his head. The doctor said it was cause from > laying too much on that one side. His diagnosis was moderate and > about a 6 on a scale of 1-10. The doctor said that he needs a > helmet. On the paperwork that the doctor gave me to send to the > insurance he had checked that the condition was " anomilies of the face > and skull bones " instead of " plagiocephaly " . What is the difference? > > Also, the insurace we have is Tricare. Does anyone have any > experience with getting them to pay? > > All of this is new to me and my husband is in Iraq. It is difficult > not having him here to help me make decisions. I would appreciate any > advice you can give me. > > Thanks in advance! > Missy > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2005 Report Share Posted November 1, 2005 Missy,Welcome. I know this hard and I feel for you not having hubby with you to help. God Bless him, and tell him I said Thank You. The diagnosis is the same as plagiocephaly, just worded different. Maybe that will help with insurance,LOL. Have you found a provider for the helemt or band yet? I cannot help much on the Tricare issue, but we have a couple people right now working on the same issue, so maybe you can all work together. There is an insurance database here where you can look up who got Tricare to pay and how.Please know that you are doing the right thing by seeking treatment for your son. I am not sure who you will be using, my son wore the Doc Bnad by Cranial Technologies and I made him a website to help others. You can take a look at it, to get an idea of how the treatment process works and what kind of results you can expect. I have lots of pictures and talk about the associated risks, and the ups and downs of the journey you are about to embark on. It's called My Banded Baby and I hope it helps. You stay with us here and we will try our best to provide the support you want and need during this time. CAROLG >> My 5.5 month old son saw the pediatric plastic surgeon today about the > flat spot on the side of his head. The doctor said it was cause from > laying too much on that one side. His diagnosis was moderate and > about a 6 on a scale of 1-10. The doctor said that he needs a > helmet. On the paperwork that the doctor gave me to send to the > insurance he had checked that the condition was "anomilies of the face > and skull bones" instead of "plagiocephaly". What is the difference?> > Also, the insurace we have is Tricare. Does anyone have any > experience with getting them to pay? > > All of this is new to me and my husband is in Iraq. It is difficult > not having him here to help me make decisions. I would appreciate any > advice you can give me.> > Thanks in advance!> Missy> Quote Link to comment Share on other sites More sharing options...
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