Guest guest Posted July 2, 2001 Report Share Posted July 2, 2001 In a message dated 7/2/01 3:31:44 AM Eastern Daylight Time, writes: << Also, there was an interesting article in today's Canadian Globe and Mail discussing an alternative treatment for depression involving high doses of vitamins and minerals. See: http://www.globeandmail.com/gam/Health/20010630/FCSCIEY.html >> This is not new therapy.... the field of ortho-molecular medicine focuses on using vitamins and minerals to restore the body. At a recent barn estate sale I found the following book " Mega-Nutrients for your nerves " by H.J. Newbold, MD, psychiatrist, Wyden, 1975. Very good reading with cases of severe mental illness he successfully treated with this nutritional approach. There is also a book entitled " Food and Mood " , can't remember the author. I find the supplement, SAM-e, a naturally occuring substance in our bodies, the single most effective agent in dealing with these issues. I also do take significant amounts of vitamins and minerals. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2001 Report Share Posted December 9, 2001 Hi Kathy, I have AIH, Lupus and Fibromyalgia and I had breast cancer. I know its been a full plate for me for some time now. My friends want to be helpful and they don't know what to say or do, so they say things like, " why don't you try this herb or bee pollen " or any natural approach. They don't understand, that what I have has no cure. It can be control with certain drugs. Right now I have been on Medrol (MethylPrednisolone) for years now. I am on a low dose, but its the only way I can have a life and be able to function. The dose is probably not enough to control the AIH, but I have diabetes so my doctor does not want to raise it right now, unless I have a bad flare of the AIH or the Lupus. They are considering Imuran, but being I had cancer, its a tough choice. Right now I am on Actigall and Medrol as well as medication for the diabetes. I have to be so careful, even what I eat affects me. I will not take anything unless I check it with the doctor. I know my friends mean well. Rose Freeport, NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2001 Report Share Posted December 9, 2001 Hello everyone--- My name is a and was diagnosed with AIH in Nov. 2000. I am not sure if this message is being sent the right way, and would appreciate it if someone could let me know. I would love to be able to share, ask questions and make new friends. You all seem so kind, tender and compassionate. Happy Holiday! [ ] Digest Number 1905 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2001 Report Share Posted December 10, 2001 Rose. You seem to have very good friends that just want to help. I have the same thing. No one understands that there is no cure, but only are we able to control it with medications. You have a good approach on not doing anything without the consent of your doctor. I'm just on Imuran right now and hopefully will be able to cut that down in January. I have to watch what I eat but sometimes it's hard especially with the holidays and all that good baking everyone is doing. Take care. ann Re: [ ] Digest Number 1905 Hi Kathy,I have AIH, Lupus and Fibromyalgia and I had breast cancer. I know its beena full plate for me for some time now. My friends want to be helpful andthey don't know what to say or do, so they say things like, "why don't youtry this herb or bee pollen" or any natural approach. They don't understand,that what I have has no cure. It can be control with certain drugs. Rightnow I have been on Medrol (MethylPrednisolone) for years now. I am on a lowdose, but its the only way I can have a life and be able to function. Thedose is probably not enough to control the AIH, but I have diabetes so mydoctor does not want to raise it right now, unless I have a bad flare of theAIH or the Lupus. They are considering Imuran, but being I had cancer, its atough choice. Right now I am on Actigall and Medrol as well as medicationfor the diabetes. I have to be so careful, even what I eat affects me. Iwill not take anything unless I check it with the doctor. I know my friendsmean well.RoseFreeport, NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2001 Report Share Posted December 10, 2001 Rose, I understand what you mean about your friends not understanding that there is no cure for these things. I heard one friend tonight telling someone else that a mutual friend couldn't be around people because he could catch everything ( he is on chemo for cancer). This is the same friend that exposed to to the flu last week. I wish there was something written up that I could give to him to nicely explain that I am in the same situation as the one with the cancer. I guess because I don't look sick now, he thinks everything is fine and I am in no danger. I also have AIH,cirrhosis and Fibromyalgia. I check out everything the drs prescribe, plus I look them up on the internet for interactions and to see if they are liver toxic. My sister, who works for a poison control center, also checks them out for me. Right now I am having a fibro flare and have been very uncomfortable for the last few days. The muscle spasms are the worst I have had in a long time. Hang in there, Joanna in Wa state AIH 8/01 Fibromyalgia 99 > Hi Kathy, > I have AIH, Lupus and Fibromyalgia and I had breast cancer. I know its been > a full plate for me for some time now. My friends want to be helpful and > they don't know what to say or do, so they say things like, " why don't you > try this herb or bee pollen " or any natural approach. They don't understand, > that what I have has no cure. It can be control with certain drugs. Right > now I have been on Medrol (MethylPrednisolone) for years now. I am on a low > dose, but its the only way I can have a life and be able to function. The > dose is probably not enough to control the AIH, but I have diabetes so my > doctor does not want to raise it right now, unless I have a bad flare of the > AIH or the Lupus. They are considering Imuran, but being I had cancer, its a > tough choice. Right now I am on Actigall and Medrol as well as medication > for the diabetes. I have to be so careful, even what I eat affects me. I > will not take anything unless I check it with the doctor. I know my friends > mean well. > > Rose > Freeport, NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2001 Report Share Posted December 11, 2001 Your message made it and your questions and friendship are very welcome. We all need it!! I was just recently diagnosed and they have been tremendous!!! Bethanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2001 Report Share Posted December 11, 2001 Joanna, I hope they get your flare up under control. That sounds like it could be pretty miserable. Just wanted you to know your in my thoughts. Take care!! Bethanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2001 Report Share Posted December 16, 2001 Hi Harper, I just wanted to thank you for responding & sharing with me about anemia. I appreciate your wisdom! And not once did I think you were going on about yourself. It is just nice to share with someone who truly understands the full effects of the disease. I would have responded earlier, however, have been out of it. I have a severe ear infection and have been in bed taking Cipro and Loratab. The doctor wanted me to be in the hospital on IV antibiotics, but I asked that we try the oral procedure first. My daughter is getting married this Friday and there is so much to do. I did make a promise to myself and the doctor that if I didn't feel as if I am any better by Monday, I will go back and try his way. He said I basically have NO immune system left and must take all of this very serious. Again, I just wanted to say thank you and I look forward to getting to know you, as well as everyone else. This is a great group! Happy Holidays to all! a [ ] Digest Number 1918 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2001 Report Share Posted December 16, 2001 I do hope you start feeling better and congratulations on your daughters wedding. Don't overdo it!!! Easier said than done though I know. Good luck with everything and keep us updated. Bethanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2001 Report Share Posted December 16, 2001 Oh what fun! A wedding! With any luck, I am going to get to have a wedding next year....IF my daughter gets her act together! She and her boyfriend want to date a little longer before getting married. They will have gone together 1 year on Valentine's Day! What romantics the two of them are! Have a wonderful week a...and have a great wedding!!!!!debby RE: [ ] Digest Number 1905 Hi Harper,I just wanted to thank you for responding & sharing with me aboutanemia. I appreciate your wisdom! And not once did I think you weregoing on about yourself. It is just nice to share with someone whotruly understands the full effects of the disease. I would haveresponded earlier, however, have been out of it. I have a severe earinfection and have been in bed taking Cipro and Loratab. The doctorwanted me to be in the hospital on IV antibiotics, but I asked that wetry the oral procedure first. My daughter is getting married thisFriday and there is so much to do. I did make a promise to myself andthe doctor that if I didn't feel as if I am any better by Monday, I willgo back and try his way. He said I basically have NO immune system leftand must take all of this very serious.Again, I just wanted to say thank you and I look forward to getting toknow you, as well as everyone else. This is a great group!Happy Holidays to all!a-----Original Message-----From: [mailto: ] Sent: Friday, December 14, 2001 10:48 PM Subject: [ ] Digest Number 1918 Quote Link to comment Share on other sites More sharing options...
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