Acute Myelogenous Leukemia (AML) Support Group
Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. Patients with AML usually present with symptoms such as fatigue, bleeding, infection, prompting medical attention. An abnormal blood test reading will then result in further testing in a hospital with a hematologist to determine AML.
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Let me first say that I am not a doctor, nor an I am giving any medical advice. I am a daughter who loves her father very much and we, as a team, are doing everything we can to help my dad get through this.
Another member here suggested I start this thread as we have been corresponding through email for months and he thought we should share all of our knowledge and experiences so that others may benefit from it if there is any benefit to be had.
First background- then I will tell you want alternative treatments he is trying....
Dad is 70 years old (he just had his 70th birthday :-)
He was diagnosed with AML M0 on April 7, 2011. We brought him to Dana Farber the very next day where we were told the risks, etc. and he began induction within 2 days. At that point he had 88% blasts.
He flew into remission after induction and we were thrilled. Although he had a number of complications during that time, the team was amazing there and he made it through and went home. Unfortunately he became extremely dehydrated from lack of drinking water and was back in the hospital within 5 days in acute kidney failure. They fixed that too, but again he had a number of complications and was almost unable to go through consolidation.
We whipped him into shape and he finally got consolidation. He again ended up with complications: confusion, high fevers, infection, etc., but he again made it through. On our last day in Boston(we were to go home that afternoon) he had blood work and saw the doc. His counts seemed funny. They did a BM biopsy just to check what was going on.
The next week our worst fears were realized. Dad has relapsed. We couldn't believe it. We were devastated. (all this- for 4 months- for nothing we thought). He was 5 weeks out of consolidation.
He was given 4 choices: induction again, palliative care (which is lose-dose chemo for 1 hr. for 5 days on and then 28 days off and repeat, a clinical trial, or nothing in which case we would call hospice and he would die.)
Dad did not want to go through induction again- it was hard on him. He didn't want a trial because that meant months away from home again. He choose the low-dose chemo at home in NY.
The choices were given to him on 7/27/11 and they said he could wait until after his birthday party 8/7 to start the chemo. He was given anywhere from a few weeks to a few months to live.
Here comes the alternative part ......... while we were sitting on the porch on 7/31/11 a neighbor stopped by to see dad. This neighbor has multiple myeloma. He was given 2 years to live. That was 5 years ago. When he was diagnosed, he did not want to do chemo. He went MD Anderson where he was enrolled in a clinical trial. The trial was for 1 year and was given 8000mg of curcumin a day. When the trial was over he was not cured, but his cancer did not progress. He was at 30% when he went to MD Anderson and that is where he is today. He never stopped taking the curcumin. He says he can tired easily because his counts have stayed low, but that in general he feels fine. That was all dad needed to hear. He wanted to try it.
Dad asked for a list of everything the neighbor was doing. He obliged.
He takes:
1.) 8000mg of curcumin a day (4000 in the morning and 4000 a night). Super Curcumin w/Bioperine Time Release 1000mg-60 Tabs
Here is the website:
http://www.agelesscures.com/index.php?main_page=product_info&cPath=3&products_id=1
We bought another brand (1000 mg with bioperine) to get us by at first from a local health food store, but ordered this one since it is the same curcumin he used in his clinical trial at MD Anderson.
2.) Silver : specifically Sovereign Silver (immune system booster)
Here is the website:
http://www.natural-immunogenics.com/
We bought it in a local health food store though
3.) Ojibwa Tea Liquid 16 oz (473 ml) by NOW -
Here is a website: http://www.betterhealthinternational.com/productDetails.asp?prodID=N4855&utm_source=googlebase&utm_medium=comparsionshopping&CAWELAID=556908777&gclid=CNe7q6GwxaoCFQfBKgodBUU8zg
We also got another version from the health food store (Essiac tea concentrate), but we also ordered this version as it is the one our neighbor takes
In addition to what the neighbor has taken for the past 5 years for his multiple myeloma, I have done research and saw some promise for other therapies for AML.
I found that Japan has done a number of clinical trials for AML using high dose vitamin D3 and high doses vitamin K2. There are different kinds of K2 out there, but Japan uses K2 M-4 (Not the K2 M-7 that we see on every vitamin shelf in the USA) It was a tough time to find K2 M-4 for sale in the US, but I finally did.
Here is the website: http://www.nbihealth.com/p-10-osteo-k.aspx
Dad has asked that we throw everything but the kitchen sink at this (AML). His current chemo doctor told us that he can not condone him taking the supplements, because he has no idea if they will #1. Have any kind of interaction with the chemo and #2. if they will cause the chemo not to work (ie. the supplements and chemo could cancel eachother out).
Dad said he didn't care and that he wants to take it all at the same time. SO- dad has become his own guinea pig.
Here is what dad is taking:
(chemo) - dacogen -- just started 8/8/11 - 1 hr a day for 5 days- then that same regiment is repeated every 28 days)
Supplements:
Totals: (a day) - dad started the supplements on 7/31/11 -
His red and white stayed level at that time, but his platelets went up. He has not needed blood or platelet transfusions since he started the supplements- (blood draws only gave us results from 10 days he had on supplements alone before he started the chemo)- He was getting them (transfusions) every 2 days prior to starting them though.
8000 mg of Super Curcumin w/Bioperine Time Release 1000mg tabs- so 8 pills total for the day
1 teaspoon of Silver
2 tablespoon of Ojibwa Tea Liquid
6 tabs of Osteo-K( 3 with breakfast and 3 with dinner)
4 tabs of 1000mg D3 (so he ends up with 6000mg total for day between straight D3 tabs and what is in the Osteo-K)
How he does it:
Morning: 4000mg of curcumin (IMPORTANT- he can not have food or drink 1 hour before and up to 1 hour after so there is maximum absorption into his blood-according to the neighbor)
-- 1 hour later he takes the rest of his morning pills (other meds for other things- thyroid, etc) and he takes 3 tabs of the osteo-K which has K2 M-4, calcium and D3 in it.
-- He takes an additional 2 tabs of 1000mg of vitamin D3 so we can get higher does of D3(Osteo-K must be taken with food)
Before Lunch:
-- 1 teaspoon of Silver (hold under the tongue for 30 seconds then swallow) - once a day
-- 2 tablespoon of Ojibwa Tea Liquid (swallow once a day)
Dinner: he takes
-- 3 tabs of the osteo-K which has K2 M-4, calcium and D3 in it.
--- He takes an additional 2 1000mg of vitamin D3 (Osteo-K must be taken with food)
--- 1 hour after dinner he has 4000mg of curcumin- he waits an hour- takes his night pills and heads to bed.
SO - he is taking all of these supplements AND the low-dose chemo together at the same time.
I have seen trials with curcumin alone, trials with curcumin with D3, trials with D3 alone, trials with K2 M-4 alone and trials with K2 M-4 and D3 together, but never one with using them all. We have no idea what will happen, but we have high hopes. We have not been able to find a doctor who knows about this or is willing to give the thumbs up as they say they have no knowledge on the subject. MD Anderson has a whole group that deals with supplements and alternative therapies as well as trials, but dad does not want to go to Houston. So here we are trying it ourselves.
I will keep you posted on progress. Dad said if it isn't working - since we will have no way of knowing if chemo or the supplements are not working- we will adjust as we go. If he does well- he will stay on this regiment.
From what I have read- curcumin has killed cancer cells in vitrio and in viro. K2 M-4 and D3 have also done that. They said that they have studies K2 M-4 in vitro and seen some leukemia cells mature into normal cells. Of course these are all trials and the docs here and the FDA will not approve things without tons of research. I welcome people to do their own research and also let me know of there are any other alternatives out there that they have either tried or have heard about. Like I said- we have no way of knowing if this will help, but we will keep you informed on dad's progress.
Another member here suggested I start this thread as we have been corresponding through email for months and he thought we should share all of our knowledge and experiences so that others may benefit from it if there is any benefit to be had.
First background- then I will tell you want alternative treatments he is trying....
Dad is 70 years old (he just had his 70th birthday :-)
He was diagnosed with AML M0 on April 7, 2011. We brought him to Dana Farber the very next day where we were told the risks, etc. and he began induction within 2 days. At that point he had 88% blasts.
He flew into remission after induction and we were thrilled. Although he had a number of complications during that time, the team was amazing there and he made it through and went home. Unfortunately he became extremely dehydrated from lack of drinking water and was back in the hospital within 5 days in acute kidney failure. They fixed that too, but again he had a number of complications and was almost unable to go through consolidation.
We whipped him into shape and he finally got consolidation. He again ended up with complications: confusion, high fevers, infection, etc., but he again made it through. On our last day in Boston(we were to go home that afternoon) he had blood work and saw the doc. His counts seemed funny. They did a BM biopsy just to check what was going on.
The next week our worst fears were realized. Dad has relapsed. We couldn't believe it. We were devastated. (all this- for 4 months- for nothing we thought). He was 5 weeks out of consolidation.
He was given 4 choices: induction again, palliative care (which is lose-dose chemo for 1 hr. for 5 days on and then 28 days off and repeat, a clinical trial, or nothing in which case we would call hospice and he would die.)
Dad did not want to go through induction again- it was hard on him. He didn't want a trial because that meant months away from home again. He choose the low-dose chemo at home in NY.
The choices were given to him on 7/27/11 and they said he could wait until after his birthday party 8/7 to start the chemo. He was given anywhere from a few weeks to a few months to live.
Here comes the alternative part ......... while we were sitting on the porch on 7/31/11 a neighbor stopped by to see dad. This neighbor has multiple myeloma. He was given 2 years to live. That was 5 years ago. When he was diagnosed, he did not want to do chemo. He went MD Anderson where he was enrolled in a clinical trial. The trial was for 1 year and was given 8000mg of curcumin a day. When the trial was over he was not cured, but his cancer did not progress. He was at 30% when he went to MD Anderson and that is where he is today. He never stopped taking the curcumin. He says he can tired easily because his counts have stayed low, but that in general he feels fine. That was all dad needed to hear. He wanted to try it.
Dad asked for a list of everything the neighbor was doing. He obliged.
He takes:
1.) 8000mg of curcumin a day (4000 in the morning and 4000 a night). Super Curcumin w/Bioperine Time Release 1000mg-60 Tabs
Here is the website:
http://www.agelesscures.com/index.php?main_page=product_info&cPath=3&products_id=1
We bought another brand (1000 mg with bioperine) to get us by at first from a local health food store, but ordered this one since it is the same curcumin he used in his clinical trial at MD Anderson.
2.) Silver : specifically Sovereign Silver (immune system booster)
Here is the website:
http://www.natural-immunogenics.com/
We bought it in a local health food store though
3.) Ojibwa Tea Liquid 16 oz (473 ml) by NOW -
Here is a website: http://www.betterhealthinternational.com/productDetails.asp?prodID=N4855&utm_source=googlebase&utm_medium=comparsionshopping&CAWELAID=556908777&gclid=CNe7q6GwxaoCFQfBKgodBUU8zg
We also got another version from the health food store (Essiac tea concentrate), but we also ordered this version as it is the one our neighbor takes
In addition to what the neighbor has taken for the past 5 years for his multiple myeloma, I have done research and saw some promise for other therapies for AML.
I found that Japan has done a number of clinical trials for AML using high dose vitamin D3 and high doses vitamin K2. There are different kinds of K2 out there, but Japan uses K2 M-4 (Not the K2 M-7 that we see on every vitamin shelf in the USA) It was a tough time to find K2 M-4 for sale in the US, but I finally did.
Here is the website: http://www.nbihealth.com/p-10-osteo-k.aspx
Dad has asked that we throw everything but the kitchen sink at this (AML). His current chemo doctor told us that he can not condone him taking the supplements, because he has no idea if they will #1. Have any kind of interaction with the chemo and #2. if they will cause the chemo not to work (ie. the supplements and chemo could cancel eachother out).
Dad said he didn't care and that he wants to take it all at the same time. SO- dad has become his own guinea pig.
Here is what dad is taking:
(chemo) - dacogen -- just started 8/8/11 - 1 hr a day for 5 days- then that same regiment is repeated every 28 days)
Supplements:
Totals: (a day) - dad started the supplements on 7/31/11 -
His red and white stayed level at that time, but his platelets went up. He has not needed blood or platelet transfusions since he started the supplements- (blood draws only gave us results from 10 days he had on supplements alone before he started the chemo)- He was getting them (transfusions) every 2 days prior to starting them though.
8000 mg of Super Curcumin w/Bioperine Time Release 1000mg tabs- so 8 pills total for the day
1 teaspoon of Silver
2 tablespoon of Ojibwa Tea Liquid
6 tabs of Osteo-K( 3 with breakfast and 3 with dinner)
4 tabs of 1000mg D3 (so he ends up with 6000mg total for day between straight D3 tabs and what is in the Osteo-K)
How he does it:
Morning: 4000mg of curcumin (IMPORTANT- he can not have food or drink 1 hour before and up to 1 hour after so there is maximum absorption into his blood-according to the neighbor)
-- 1 hour later he takes the rest of his morning pills (other meds for other things- thyroid, etc) and he takes 3 tabs of the osteo-K which has K2 M-4, calcium and D3 in it.
-- He takes an additional 2 tabs of 1000mg of vitamin D3 so we can get higher does of D3(Osteo-K must be taken with food)
Before Lunch:
-- 1 teaspoon of Silver (hold under the tongue for 30 seconds then swallow) - once a day
-- 2 tablespoon of Ojibwa Tea Liquid (swallow once a day)
Dinner: he takes
-- 3 tabs of the osteo-K which has K2 M-4, calcium and D3 in it.
--- He takes an additional 2 1000mg of vitamin D3 (Osteo-K must be taken with food)
--- 1 hour after dinner he has 4000mg of curcumin- he waits an hour- takes his night pills and heads to bed.
SO - he is taking all of these supplements AND the low-dose chemo together at the same time.
I have seen trials with curcumin alone, trials with curcumin with D3, trials with D3 alone, trials with K2 M-4 alone and trials with K2 M-4 and D3 together, but never one with using them all. We have no idea what will happen, but we have high hopes. We have not been able to find a doctor who knows about this or is willing to give the thumbs up as they say they have no knowledge on the subject. MD Anderson has a whole group that deals with supplements and alternative therapies as well as trials, but dad does not want to go to Houston. So here we are trying it ourselves.
I will keep you posted on progress. Dad said if it isn't working - since we will have no way of knowing if chemo or the supplements are not working- we will adjust as we go. If he does well- he will stay on this regiment.
From what I have read- curcumin has killed cancer cells in vitrio and in viro. K2 M-4 and D3 have also done that. They said that they have studies K2 M-4 in vitro and seen some leukemia cells mature into normal cells. Of course these are all trials and the docs here and the FDA will not approve things without tons of research. I welcome people to do their own research and also let me know of there are any other alternatives out there that they have either tried or have heard about. Like I said- we have no way of knowing if this will help, but we will keep you informed on dad's progress.
Thanks -- dave
We are first of all trying to alkalize his body with Ph balancing water, nutrients, minerals and diet- cleansing, detoxing, purifying with right now. He is also on a small electromedicene machine(Photon Genie) and hopes to be in the larger machine(Photon Genius) in a month. Also in a month we will hope to start him on the Celect Budwig Protocol as well. My friend of course is so knowledgeable in the cancer area traveling nationally with top "natural" cancer doctors, so she has been the one to lead us. We are so thankful for her expertise in this area. A very reknown cancer site in which to find the information on what we are trying is www.cancertutor.com. Dad continues to feel good. I am reminded that even with Heathers dad, the doctors told him six weeks if he didn't do anything and he is still here and many others were like him. I know man may say what they want but ultimately God is the one with the final word.
You may want to look to see if the TIGECYCLINE trial is still going on. Canada started it in late 2011 and it was supposed to come to the states in 2012. It is an FDA approved drug so any MD can prescribe it without having to be in a trial. Canada was seeing good results in it fighting AML....at least the last time I researched it. May be worth seeing if there is still info on it if other options are limited. I wish your dad all the best.
Tigecycline is an antibiotic...you are right about that. But studies in Canada show that it can bring the blasts down. They believe it might be another alternative to fight AML in addition to being an anitbiotic for other things. I know Heather has researched and watched Tigecycline as well. If nothing else is working...it may be worth at least researching. Anything that gives hope or possibilities in fighting this monster of a disease is worth the time to look into. Just my two cents...
No problem -- I said it might have other effects in addition to the reason that it is typically administered. Thanks for telling us about the studies in Canada, and I appreciate all of the people on this thread who are trying various things and reporting them to us. I feel that at some point someone will pull all of these things together in a table or something. I really encourage everyone to report anything that has shown even the possibility of being effective, especially if you know and have tried it first hand. Thanks again -- I really appreciate your participation and comments -- dave
WBC- 9.3
RBC- 3.27
Hemo - 11.3
Platelets - 180
This is the best his red has been since his relapse in July of 2011.
He continues to feel well and be very active. Yesterday marked the 2 year anniversary of our arrival in Boston for initial treatment of dad's AML. At that time he was given 9 days to live if no treatment was sought. We did 1 round of induction and 1 round of consolidation but as you all know- dad relapsed in July of 2011. He was sent home with few options. We then did 2 rounds of dacogen before we quit chemo altogether in favor of his treatment using supplements - (MK4, D3 and curcumin). He has been AML free since October of 2011 with this treatment. We are proud to report it has been 18 1/2 months now of dad on supplements alone!!! No transfusions in 17 months and he is doing great! It is hard to believe it was 2 years ago yesterday that we rushed him to Boston in literally a race against the clock to try and save his life. It was such an intense and horrific time for all of us. It some ways it feels like yesterday and in more ways it feels like a hundred years ago.
Thank you so much for everyone on this board. Your constant support has meant the world to us. I wanted to take a moment again to thank you all from the bottom of our hearts and to share this milestone with all of you.
Our thoughts and prayers continue to be with everyone here.
Our best to each and every one of you. And of course we are remaining as always open to anyone who needs a shoulder or information or any help we can give at all.
Best,
Heather
I have been remiss in reporting on my status as a subject in the unofficial DS trial using Osteo-K (MK-4) etc. in the treatment of AML.
First, let me say how pleased I am for Heather and her parents to read of her Dads most recent blood results. You have been greatly blessed as a family. Please continue to keep us all posted.
Everyone in my family knows about Heather and Heathers Dad and seems to be pulling as much for him and for me.
By way of background and so you do not have to search through earlier posts, I was diagnosed in January 2012 at age 75. I went through 7:3 Induction and two rounds of Consolidation which ended in early July. There was a longer than usual break between the Consolidation rounds so I could attend the wedding of a son in NY and visit other family and friends on the East Coast. I was in remission and got stronger and stronger and was exercising almost as much as before my dx, although not with as much vigor. I never made it to the level of Dave and his chain saw, but I was doing pretty well.
In about October or November, I decided to start taking MK-4, etc. as a preventative against a possible relapse. (Daves position- understandable and reasonable-was then, and I assume is now, that he will take MK-4 in the event he relapses.) I started with 30 mgs, one-third of the 90 mgs Heathers dad is taking. I thought that if I did relapse, I could increase to 90 mgs.
In December, I experienced some slight decline in my endurance. The results of a cbc on January 2 caused ny onc to do a BMB. It showed 10-20% blasts. He gave me three options: in-patient chemotherapy in the Vasoroxin trial; out-patient chemotherapy with Dacogen five days out of every 28; and do nothing (palliative care). I said I wanted to give MK-4 a try for awhile to see if it would work for me as it had for others I had read about. He agreed.
I telephone the people at MK-4 and was told: (i) that I should increase my dosage of MK-4 to 135 mgs, 50% more than Heather's dad takes; (ii) that there was a 25-50% chance it would work; and (iii) that the average time it takes to work is eight weeks and I should take it for ten weeks.
I took the 135 mgs for twelve weeks, not just the suggested ten. At that point, I cut back to 90 mgs.
About the middle of March, my blood counts seemed to go bananas. White count, which had been in the range of 1.09 to 2.7, went from 10, to 42, to 65, to 25, and back to 54. The dr has prescribed 500 mg of Hydrea twice a day. Yesterday his nurse practitioner in his absence said to increase to three times a day.
Platelets, which had been between 70 and the low hundreds, went from 46, to 23, to 20, to 9, and most recently to 7. Hgb has ranged between 10 and 8.1. I have had two units of blood five times
in 2013 and platelets twice. I doubt that such tinkering with my blood can go on forever, and I am approaching a decision about further chemotherapy. I anticipate I will eventually opt for Dacogen, but I want to coordinate the infusions with a trip east to attend a class reunion and visit family on the east coast. I will ask my doctor about the possibility of getting transfusions or even Dacogen in a facility on the east coast. Rihgt now he is in DC and has told me about professional trips to NYC so he may have some connections. I would like to visit Londan where a son, daughter-in-law, and their three children live. They have an extra bedroom; however, I am reuctant to go outside the US and be subject to National Health Care. Has anyone had experience with this issue?
In the meantime, things are going well. I am still driving, shopping, visiting friends, doing some work, and exercising with light weights, stretching, and walking in the neighborhood at least a mile on most days. Last week my oldest son, his wife, and their four youngest sons visited us from Salt Lake City for five days. Great to have them with us. Today I pickup at the airport the wife of one of my sons who lives in the NYC area. Although she is traveling here on business
and will be here about five days, she is bringing their son with her. Tomorrow, I pick up my youngest son, who also lives in SLC, his wife and their young son. They will be staying with us for a week. Busy but happy time around here.
In connection with this condition, I have seen family members in a new light and meet some other fine people. My wife has been marvelous care provider to degree I feel I could not duplicate if the roles were reversed. I have met interesting medical professional who have been caring beyond their normal duties. In the tranfusion clinic, I have met patients and their family or pofessional care providers. Sometimes it is hard to tell who is the patient and who is the careprovider. All are pleasant and cheerful.
Recently, two days before a transfusion of red, I was walking back to my home on an uphill slope. I had stopped and was leaning against an empy trach contianer to catch my breath. A man in a Jeep-like Ford vehicle stopped and asked if I was alright. Judging from the color of the license plates, he or a member of his family must have owned it since at leat the early sixties. I thanked him and said yes. He then asked if I would like a ride. "No thanks, but thanks for asking." "Are you sure?" "No I am not. Could you give me a ride home: I live two blocks from here?" On the way to my house, he said he too got dzzzy sometime since he sustained a concussion when he was hit in the head several times in an attempted car-jacking while he was driving that very vehicle about four years ago. A very nice man. People can be wonderul when they "love one another as I have loved you."
One last thought. I occasionally visit some friends, very good people, who have limiting illnesses. Although they will likely outlive me, I would not trade my condition for theirs, although I do acknowledge I have not yet traveled the entire road.
I read of the challenges and success of you all. Your stories are very uplifting. Keep on posting. I will reply when I feel I can be helpful
Cheers to all.
Jonathan
PS. Dave, thanks for the link to your music site. Is there a G-rated song about a chain saw? One would go well with your bass voice.
J
Thanks so much for taking the time to give us that update, and also I really appreciate your kind of going back to day one. There are so many on these various threads now that those of us with chemo brain (and perhaps some others as well) have a hard time keeping up with everyones' histories. What has me concerned most is the blasts. You said in December you had 10-20% blasts. Have you had a recent BMB to check this? The other numbers should be watched carefully, especially if you get neutropenic; and for sure get a transfusion if that is in order. But the real bottom line in my mind is whether those blasts are increasing or decreasing. My onc told me at last visit that if my blood numbers remained stable that would be sufficient evidence of no problem; but that if my numbers changed dramatically that would be an indication that the blasts were crowding out the good cells and they would follow up on that (I would expect with a BMB). I am think it would be good for you to get a BMB before too long. You still have a lot of options. You need all of the facts so that you can evaluate them and take the best ones.
Please don't let things go too long between giving us updates -- we are really interested in your progress. We will be praying for you and for Heather's dad as well. But most of all to everyone -- just enjoy each day that we have as a gift from God ... it will sure make you feel a whole lot better. -- dave
WBC - 9.8
RBC - 3.25
Platelets - 180
The doc said he is doing amazingly well. :-)
I want to encourage others who are trying this regiment or any variation of it to please write your stories here and update as frequent as possible. I am in contact through email, texts and phone calls with people all over the United States as well as several foreign countries.
I will certainly continue to speak with you and offer any help that I can but I also want others to be able to benefit from your stories as well. I encourage you all to post anything that is happening during treatment both good and bad. It would be a wonderful gift for others looking for answers too.
All my best to everyone,
Heather
My husband often looks at this site in case I need to go in a different direction. He has allowed himself to be quite educated.
I cannot add anything in terms of alternative treatments since I am still in the thick of things, but I do look at this post.
Be well. Very happy about your day's counts!!
Peace, love and hope,
Andrea
A dear, well meaning friend is encouraging me to go on an all vegetable diet with a little protein powder. Not sure of this one. He insists it has turned around his diabetes.
But, as we all know, diabetes is a bit different than AML.
lily