Guest guest Posted March 30, 2001 Report Share Posted March 30, 2001 Hi, I have not personally had Multiple Myaloma but have some evidence that may be of interest. The first is a message that was sent to me a year or more ago. Cliff This originally came from a friend of mine. Betsy is a friend of ours, in her 70s I suppose. She has multiple myeloma, a very deadly kind of bone cancer, and is being treated by the same oncologist I go to. We saw Betsy a couple weeks ago. She's bright eyed and bushy tailed...her old self. She mentioned that Dr. had recently told her she was his " miracle patient " . This spring I had heard about Betsy's situation. It was greatly different from what it is today. She was extremely sick and unable to eat. She could only lie in bed and was just wasting away. Her husband, Don, thought she was dying. He may have been right. It had taken a long time for her doctors to diagnose an obviously deteriorating health condition as multiple myeloma, so that it was quite an advanced case before she was referred to Dr.-------, as I understand it. I believe she had recently been started on chemotherapy by -------- a little before I learned what was happening. But no matter how good his treatment might have been, if she couldn't eat she wasn't going to get better. I went down to --------- and bought a pint of Barlean's lignan rich flaxseed oil, some low-fat cottage cheese, a pineapple and some honey, and took it over to Don. Don made Betsy a smoothie, using some of the pineapple to cover the taste of the oil. A little later I learned that Betsy had called the smoothie " delicious food " . She could eat it! Later still, I heard that Betsy likes tuna fish in her flaxseed oil and cottage cheese smoothies, instead of the pineapple. You can use anything in the smoothies to make them taste good to you. In the meantime, Don had ordered some of the oil direct from Barlean's. If you're a cancer patient it's sold to you at wholesale and costs about half as much as at-------------or other health food stores, even with the shipping cost. It wasn't too much longer before Betsy was able to get up and be in a wheelchair. Soon she was able to stand and get around a little with a walker. A month or so ago she went in some cancer event that involved a 3-mile walk. She had intended only to do the first mile but ended up doing the whole thing! She was back. Betsy is an avid gardener and has one of the city plots. She had been able to get the garden planted somehow, with help from Don, and it has been delivering great quantities of produce all summer. Every now and then Don brings some by for us. He thinks I saved Betsy's life. Is Betsy's amazing response to the treatment of this devasting kind of bone cancer because of the combined benefits of the flaxseed oil and chemotherapy? My friend---------- There is contraversy here. I see this as an example of the fact that flaxseed oil will be of real benefit even though chemo is being used. I personally do not know of many , if any,situations where the continuous use of chemo has resulted in real recovery. I do not know the complete details, but I understand that the chemo was continued and eventually won and Betsy passed away. Cliff Let us understand what happens wih chemo. Chemo does kill most cancer cells. It does not kill all of them; maybe up to 98%. That leaves some that are immune to that chemo. It also kills the good cells, including the immune system. When the chemo runs its course and kills all the cancer cells it can, the cancer continues to grow and the body cells keep on being killed. These are the way it looks to me. They are not clinically tested, except that eventually the chemo wins and people die. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2001 Report Share Posted March 31, 2001 Cliff, Thanks for the info. It was MOST appreciated. I, too, have heard that flax seed, ground up or the oil, is beneficial for many cancers. Hey, it's natural, can't hurt me, huh? Cliff Beckwith wrote: > > Hi, > > I have not personally had Multiple Myaloma but have some evidence that > may > be of interest. > > The first is a message that was sent to me a year or more ago. > > Cliff > > This originally came from a friend of mine. > > Betsy is a friend of ours, in her 70s I suppose. She has multiple > myeloma, a > very deadly kind of bone cancer, and is being treated by the same > oncologist I go to. > > We saw Betsy a couple weeks ago. She's bright eyed and bushy > tailed...her > old self. She mentioned that Dr. had recently told her she was his > " miracle patient " . > > This spring I had heard about Betsy's situation. It was greatly > different > from what it is today. She was extremely sick and unable to eat. She > could > only lie in bed and was just wasting away. Her husband, Don, thought > she was > dying. He may have been right. It had taken a long time for her > doctors to > diagnose an obviously deteriorating health condition as multiple > myeloma, so > that it was quite an advanced case before she was referred to > Dr.-------, > as I understand it. I believe she had recently been started on > chemotherapy > by -------- a little before I learned what was happening. But no > matter how > good > his treatment might have been, if she couldn't eat she wasn't going to > get > better. > > I went down to --------- and bought a pint of Barlean's lignan rich > flaxseed > oil, some low-fat cottage cheese, a pineapple and some honey, and took > it > over to Don. > > Don made Betsy a smoothie, using some of the pineapple to cover the > taste of > the oil. A little later I learned that Betsy had called the smoothie > " delicious food " . She could eat it! Later still, I heard that Betsy > likes > tuna fish in her flaxseed oil and cottage cheese smoothies, instead of > the > pineapple. You can use anything in the smoothies to make them taste > good to > you. In the meantime, Don had ordered some of the oil direct from > Barlean's. > If you're a cancer patient it's sold to you at wholesale and costs > about > half as much as at-------------or other health food stores, even with > the > shipping cost. > > It wasn't too much longer before Betsy was able to get up and be in a > wheelchair. Soon she was able to stand and get around a little with a > walker. A month or so ago she went in some cancer event that involved > a > 3-mile walk. She had intended only to do the first mile but ended up > doing > the whole thing! She was back. > > Betsy is an avid gardener and has one of the city plots. She had been > able > to get the garden planted somehow, with help from Don, and it has been > delivering great quantities of produce all summer. Every now and then > Don > brings some by for us. He thinks I saved Betsy's life. > > Is Betsy's amazing response to the treatment of this devasting kind of > bone > cancer because of the combined benefits of the flaxseed oil and > chemotherapy? > > My friend---------- > > There is contraversy here. I see this as an example of the fact that > flaxseed oil will be of real benefit even though chemo is being used. > I > personally do not know of many , if any,situations where the > continuous use > of chemo has resulted in real recovery. > > I do not know the complete details, but I understand that the chemo > was > continued and eventually won and Betsy passed away. > > Cliff > > Let us understand what happens wih chemo. Chemo does kill most cancer > cells. It does not kill all of them; maybe up to 98%. That leaves > some > that are immune to that chemo. It also kills the good cells, > including the > immune system. > > When the chemo runs its course and kills all the cancer cells it can, > the > cancer continues to grow and the body cells keep on being killed. > These are > the way it looks to me. They are not clinically tested, except that > eventually the chemo wins and people die. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2002 Report Share Posted June 16, 2002 Hi Dawna, I am new also in the preband stage and doing a lot of research. I live in Tacoma, Wa. and went to Dr. Fox's Informational meeting. I am currently waiting to find out if my insurance will pay. In the mean time i have been looking into mexico just in case. I found if you go up to search archives and type in tijauna or just mexico it will give you hours of posts giving you any info you probably could think of needing. I read for an hour yesterday and got a real education. hope that helps some. take care, and good luck. > Hello All, > > My name is Dawna. I have been lurking here for a week or two, and > decided it was time to introduce myself and ask a few questions. > I am still in the research phase of my weight loss journey. I am soo > ready for a change. I will most likey be a private pay patient, if I > decide to go with a band. My Insurance still considers LapBand > experimental/investigational. I could get the Bypass and they might > cover it, but I feel that route is not for me. I really like the > thought that the band is reversable, if need be. I have looked into > the UWMC and have heard that they have up to a two year wait, and I > believe that is for the bypass surgery. I have learned a lot about > various doctors who perform lapband surgeries from you all, and I > aprreciate your knowledge. You are a great group of people, and I am > soo glad to have found this group! ) > > A few questions, how does one begin this process? It seems that a > lot of you have had your surgeries done in Mexico. How did you start > the ball rolling, so to speak? How long did you have to wait before > you were able to have your surgeries? Have you heard of, or is there > any reasons a person would not be allowed to have this surgery? > > Sorry to ask so many questions, but I have been obsessed with finding > out as much as I can since hearing of this. I really think this is > for me, but I am also a bit scared as well. Knowledge is the key! > > Thanks for any advise/information you can share! > -Dawna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2002 Report Share Posted June 16, 2002 I started the actual process by calling Dr. Ortiz in Mexico. He gave me details about his costs and pretty much let me pick a date when I would be ready. I scheduled for about 3 weeks from that original phone call. He has a website: www.obesitycontrolcenter.com which has his phone number on it. Elise Dr. Ortiz, TJ 2/1/02 200/165/120 _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2002 Report Share Posted June 16, 2002 i am going thru the process..private pay, dr fox, 240lbs, 51 yrs, 5 " 2 1/2 " . at my statistics can anyone give me an idea if i will need/want a tummy tuck? i figure i am 100lbs overweight, maybe a little more. thanks! Sandy Landry Landco@... Lynnwood, Wa. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2005 Report Share Posted September 21, 2005 In a message dated 9/21/2005 8:50:36 P.M. Pacific Daylight Time, lil_nora77@... writes: I'm trying to decide whether to go with behind the ear or the box (it's about the size of the pager i hope)? I'm leaning toward the box because the BTE looks humongous than the current hearing aid i'm wearing now. With the box, i can hide the cord under my shirt. I would like to hear from people why they choose BTE or the box? Does the box interfere with your lifestyle? I'm also concerned about clothing. If I wear an evening gown or a dress with no pockets, how the heck am i going to clip the box to my dress? (I need input from women out there). hello Nora (if this is your name),, welcome to the board. Did you look at the 3 BTE processors? I thought one of them is about the same size as Oticon hearing aid. I was dead set against body (box) processor for one obvious reason. I grew up with body aid until I was 19 and I hated it. I have lost count how many times my hearing aid fell off because the cord got in the way. I find that the BTE processor is very comfortable to wear, in fact, I don't even notice it when I am wearing it, something I would notice with BTE hearing aid. All in all, it is the cord that I did not want to deal with. This is only my opinion. Lee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2005 Report Share Posted September 22, 2005 Lil, I choose the BTE for the " freedom " it provides me. No cords, no hassles and it is a very self contained business. I don't particularily like the cord business getting in the way. It reminds too much of my early days back in the '60s using the body worn HA. But that is just my preference. If the BWP works for you, go for it! Dale lil_nora77 <lil_nora77@...> wrote: Hi this is my first time here. Since I was four, I have profound hearing loss in my left ear and it is not aided. I had severe hearing loss on my right (70 DB loss) and with the help of an hearing aid, I was able to understand speech with lipreading. I could also hear on the phone too. But something happened in mid june. It started with a running nose then somehow I was diagnosed with bronchitis. I was so sick with bronchitis for just over a month with persistent coughing. After two days of fever (I took 4 tylenol to help keeping my temp down), I woke up hearing everything sounded plugged up. I thought i had an ear infection so I went to the doctor about it. He said no infection but gave me antibiotics just in case. In one week it got even progressively worse. Everything sounded so muffled then within a few days, i went profoundly deaf. Then in 1 or 2 weeks my hearing came back a little. But it hasn't come back any more since mid July. I just met the audiologist with the cochlear implant program on tuesday. She said I'm eligible for the CI and that she will schedule a balance test and appt with the doctor. She gave me 3 companies to choose from, advanced bionics (clarion), cochlear (nucleus) and med-el. THis is a really tough decision. I read your advices to to join each companies' website to get unbiased info from each group. I will certainly do that. I hope y'all won't mind me asking questions on here too. THe audiologist at the hospital said all 3 companies are the same and cost wise (for batteries) they are the same too. It's a matter of preferences who I want to go with and what is my wearing option. I'm trying to decide whether to go with behind the ear or the box (it's about the size of the pager i hope)? I'm leaning toward the box because the BTE looks humongous than the current hearing aid i'm wearing now. With the box, i can hide the cord under my shirt. I would like to hear from people why they choose BTE or the box? Does the box interfere with your lifestyle? I'm also concerned about clothing. If I wear an evening gown or a dress with no pockets, how the heck am i going to clip the box to my dress? (I need input from women out there). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2005 Report Share Posted September 23, 2005 Hello Nora, Welcome to and congrats on your decision to be implanted. I just want to say that the bte processor isn't heavy at all and fits my ear well. I forget I have it on sometimes Have even come close to getting it a bit wet by stepping into the shower with it on, but realizing just in time it was there because I could hear water running. LOL One good thing about the newest Freedom processor from Cochlear is that it is water resistant meaning it can withstand a dunking under the shower with no damage! I wore a body processor (bwp) for the first 6 months after my activation and while I was thrilled at being able to hear, the cord did tend to get in my way at times and would make noise every time it rubbed against my clothing, skin, or anywhere. I love the freedom of having no cords to worry about. It is a personal choice though so just decide on which one best fits your life style and go from there. I come from a family of several deaf members and there are 4 implant users to this date with more to come in the future. we all wear the bte processors and have all worn a body processor at one time or another. I wish you well in your quest to have better hearing. Where abouts are you from and what center are you using for your ci journey? Please feel free to email me either here on the forum or privately if you have any questions at all. Hugs, Silly MI In , " lil_nora77 " <lil_nora77@y...> wrote: > Hi this is my first time here. > > Since I was four, I have profound hearing loss in my left ear and it > is not aided. I had severe hearing loss on my right (70 DB loss) and > with the help of an hearing aid, I was able to understand speech > with lipreading. I could also hear on the phone too. But something > happened in mid june. It started with a running nose then somehow I > was diagnosed with bronchitis. I was so sick with bronchitis for > just over a month with persistent coughing. After two days of fever > (I took 4 tylenol to help keeping my temp down), I woke up hearing > everything sounded plugged up. I thought i had an ear infection so I > went to the doctor about it. He said no infection but gave me > antibiotics just in case. In one week it got even progressively > worse. Everything sounded so muffled then within a few days, i went > profoundly deaf. Then in 1 or 2 weeks my hearing came back a little. > But it hasn't come back any more since mid July. I just met the > audiologist with the cochlear implant program on tuesday. She said > I'm eligible for the CI and that she will schedule a balance test > and appt with the doctor. She gave me 3 companies to choose from, > advanced bionics (clarion), cochlear (nucleus) and med-el. > > THis is a really tough decision. I read your advices to to join > each companies' website to get unbiased info from each group. I will > certainly do that. I hope y'all won't mind me asking questions on > here too. > > THe audiologist at the hospital said all 3 companies are the same > and cost wise (for batteries) they are the same too. It's a matter > of preferences who I want to go with and what is my wearing option. > > I'm trying to decide whether to go with behind the ear or the box > (it's about the size of the pager i hope)? I'm leaning toward the > box because the BTE looks humongous than the current hearing aid i'm > wearing now. With the box, i can hide the cord under my shirt. I > would like to hear from people why they choose BTE or the box? Does > the box interfere with your lifestyle? I'm also concerned about > clothing. If I wear an evening gown or a dress with no pockets, how > the heck am i going to clip the box to my dress? (I need input from > women out there). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2005 Report Share Posted September 24, 2005 Hi , Thanks for the we.lcome mat. I'm lucky that I live 15-20 minutes away from the Sunnybrook Hospital. They're the only hospital in toronto that has the Cochlear Implant program. > I wish you well in your quest to have better hearing. > Where abouts are you from and what center are you using for your ci > journey? > > Please feel free to email me either here on the forum or privately > if you have any questions at all. > > Hugs, > Silly MI > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 3, 2008 Report Share Posted April 3, 2008 Dennis, Welcom aboard!!!!! If you have any questions or concverns about anything just ask...Someone will be able to give you some friendly advice... It is really nice to beable to get some first hand information about your concerns.. I was diagnosed back in June of last year.. I have decided if I want to take tx yet or not... There is alot of things I am still unsure of when it comes to the whole tx thing... But, again welcome aboard... We are always here for someone to vent to and ask questions to... Dennis <lvjanet@...> wrote: My wife of 37 yrs was diagnosed with HCV yesterday. The world suddenly seems entiely different and even more complicated. I joined this forum to help answer some of her many questions. She is not at the point of being able to discuss them so I will just be reading you posts and learning as we go. She had the HCV RNA test today and now we have another week to wait and hope. I have been reading article after article the past two days to try and familiarize us with this virus and it's effects. I look forward to reading your posts. Tammy R. Ehrlich --------------------------------- You rock. That's why Blockbuster's offering you one month of Blockbuster Total Access, No Cost. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 Welcome to the group...sorry you find yourself in these circumstances. There is a lot of good information available, and certainly plenty of experienced folk in this group! If you don't mind my asking...how old is your wife, and how did she find out that she has HCV? **************Planning your summer road trip? Check out AOL Travel Guides. (http://travel.aol.com/travel-guide/united-states?ncid=aoltrv00030000000016) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 Hello again, I'm new in this group, actually i'm a wife and the one who has HCV is my husband. He is 53 now, very active person and he found out that he had hep-C in 1997-1998. Before he knew, he used to give blood for children who has thalasemia's. How did he had? We didn't know exactly, but I thought from the dentist because view months before, he went to the dentist for 2-3 months and they didn't have a special hepatitis sterilization. He had a HCV genotype 1, already try with interveron or combination with ribavirin on 1999-2000 but the virus became increase, so we stopped the treatment. Until now he takes only vitamin and food supplement (vit C, B complex, Hp pro, Milk Thystle) and traditional herb (curcuma). For the last 2 years, he has problem with skin rash, itching, joint or muscle aches, diarrhea. We know that there is not therapeutic / medicine solution yet, so we need to know more information about HCV Thank you Aprilcupcake@... wrote: Welcome to the group...sorry you find yourself in these circumstances. There is a lot of good information available, and certainly plenty of experienced folk in this group! If you don't mind my asking...how old is your wife, and how did she find out that she has HCV? **************Planning your summer road trip? Check out AOL Travel Guides. (http://travel.aol.com/travel-guide/united-states?ncid=aoltrv00030000000016) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 Hello to all, expecially the newbies! Well I survived the night after my first dose of PEG- yuck . Was not so bad until 1am and the fever and shaking like a leaf for 2 hours my husband could not find enough blankets to keep me warm. I had a little nausea but nothing extreme. I dont feel like I am going to burst into tears at least not yet lol. My baby is 4 months I did enough of that the first 2 months after he was born. The headache sucks a little but actually it is not as bad as I was told. But I think I could sleep allday if I had the chance lol but no such luck with a 4 year old and 3 year old lol. They keep me going and they are why I decided to begin treatment and I pray this helps and does not make things worse. In the end of this if I get that SVR I was hoping for it will all be worth it. Well I did realize how much my husband loves me last night when I am sick as a dog he tells me I dont think I can bare to lose you. I told him I am to mean to die lol. Anyways God bless all on this interesting journey and I wish all good health and happiness! Re: a newbie Welcome to the group...sorry you find yourself in these circumstances. There is a lot of good information available, and certainly plenty of experienced folk in this group! If you don't mind my asking...how old is your wife, and how did she find out that she has HCV? **************Planning your summer road trip? Check out AOL Travel Guides. (http://travel.aol.com/travel-guide/united-states?ncid=aoltrv00030000000016) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 hey there, wtg,the 1st few ain't bad ,or at least they where not for me.but sounds like you got a great partner and kids to motivate you you will do great. http://www.drhepper.com Re: a newbie Welcome to the group...sorry you find yourself in these circumstances. There is a lot of good information available, and certainly plenty of experienced folk in this group! If you don't mind my asking...how old is your wife, and how did she find out that she has HCV? ************ **Planning your summer road trip? Check out AOL Travel Guides. (http://travel. aol.com/travel- guide/united- states?ncid= aoltrv0003000000 0016) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 non-responder? i'd keep up the C, B-complex, turmeric (curcumin), & add in E (with mixed tocopherols), and for sure try: ***ALA (alpha lipoic acid - 300mg twice/day) along with un-denatured whey or NAC (n-acetyl cystiene -works with the ALA- the whey might be better from recommendations) ***milk thistle (lots- grind seeds immediately before use, or at least a standardized extract... or both) ***selenium (not TOO much, but supps of 200mcg and a few brazil nuts do fine for me) ***and lots of home-made colloidal silver ... you'll know in a coule days if it's working for you. i recently talked to someone whose husband cleared HCV and stayed SVR for 3 years so far by drinking a quart/day of home-made CS for 4 months... i'm trying that now, after having much success managing symptoms for the last couple years with much lower amounts. ***green tea/dandelion blend > Re: a newbie > > > Hello again, > > I'm new in this group, actually i'm a wife and the one who has > HCV is my husband. > He is 53 now, very active person and he found out that he had > hep-C in 1997-1998. > Before he knew, he used to give blood for children who has > thalasemia's. > How did he had? We didn't know exactly, but I thought from the > dentist because view months before, he went to the dentist for > 2-3 months and they didn't have a special hepatitis sterilization. > > He had a HCV genotype 1, already try with interveron or > combination with ribavirin on 1999-2000 but the virus became > increase, so we stopped the treatment. > > Until now he takes only vitamin and food supplement (vit C, B > complex, Hp pro, Milk Thystle) and traditional herb (curcuma). > > For the last 2 years, he has problem with skin rash, itching, > joint or muscle aches, diarrhea. > > We know that there is not therapeutic / medicine solution yet, > so we need to know more information about HCV > > Thank you > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 9, 2009 Report Share Posted July 9, 2009 Hi, I have a 21 year old daughter with autism spectrum disorder and am trying Zyme Prime enzymes. Steph has awful medication reactions so I've learned to introduce medications reactions very slowly. To get an idea of what would happen I started it too. Her reactions have been okay on only 1/4 of a ta b with eqch meal. she was very active and very vocal, a little agitated, wet her bed constantly. My reactions are the question, I felt awful, almost like a mild migraine every day, and dizzy! The reactions only kicked in after I had been on the enzymes for a few days. I stopped them yesterday and the dizziness has gone away, and I feel better. It sounds silly but they were definitely affecting me neurologically. Is this common? Any ideas would be greatly appreciated. Quote Link to comment Share on other sites More sharing options...
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