CLL Diagnosis:
15 Natural Things to do. When people first find my site, CLLAlternatives.com, it’s generally because either they—or someone they care about—has recently been diagnosed. Of all the gut-punches a person can sustain in their life, this is probably the worst. Even the word leukemia itself strikes terror. A blood cancer. A death sentence.
I get emails and postings from many people who are stunned and trying to figure out what to do. Getting well is possible, but there’s no quick answer as to how. There is no magic bullet; only magic ammunition. The list I’ve compiled here is in no means the entire answer to getting well, but it is certainly a good start.
There is so much to know, and to learn. But every journey starts with the first step, and this list is a very good step in the right direction. With that in mind, here are 16 things you can do to get a jump start on improving your health and either getting totally well – or at least getting well enough to be confident of your future and longevity. The list keeps growing, and I might add to it in a different post from time to time.
There is so much more I could say, but I’m leaving it here at Lucky Sixteen. Please read and consider all these suggestions if you’re just starting out. Please post with your experiences and thoughts, and with your own suggestions. I do answer private emails, but I think we all help each other when we’re willing to post. You can do it anonymously, but do it!
Denise et al:
I was diagnosed in July of 2017. At the time of diagnosis, my level was 43k. Today (Apr’19) unfortunately, I’m around 80k. Still searching for what works for me and my body. I’m in my late 50’s and physically fit. I eat a very clean diet, mostly organic, and have removed “toxins” from my world. Stress level is most likely the biggest contributor to my condition. I’m in a very stressful job, but with the latest WBC levels I’ve received, I’m making headway in changing that too. For the past few weeks, I’ve started on a protocol of green tea supplements (3xday), apricot seeds (30-40/day), and the Budwig regiment. I’m curious if anyone in the group has had success with ESSIAC tea. Thanks for the recommendations and the 16 natural things you can do.
Blessings…
Hi.
I am happy to have found this group.
My sister has been diagnosed with CCL and I am trying to help her.
I am very interested in alternative health and fortunately so far have kept well at 62 with a low carb diet, exercise, lots of vit d and some other supplements. My sister not very good at trying to figure out what to do. She is taking apricot kernels, vit d. I want her to get her levels tested but she wont:((( i test mine yearly. She drinks some green tea but i have heard about the extracts/tablets that ma be better. Has anyone taken Low Dose Naltrexone for this. I have her blood test results but I am not sure what the optimum levels are. I also always have to convert them into the measures that we use here in NZ which can be a bit tricky sometimes. Would love some input from you all. Will buy the book as i have heard about it before. thanks in advance. kindest regards to everyone. cheryl
[…] LuckyVitamins.com, for the best deal.) I have a comprehensive list of what to do in this article: http://www.cllalternatives.com/2017/11/cll-diagnosis-15-natural-things-to-do/. Please read and re-read this. Getting well is a process. It’s good to revisit things you […]
Hello All,
I’m always excited to come to this blog because it always gives me some insight when I’m having an off day. Few months ago I started apricot kernels and in December my Lymph count really took a dive as well as my total WBC. However just today I found out they went back up and I’m not sure if it’s the new brand of kernels that I’ve started (some of them were not that bitter – who knows!) I will go back to the Apricot Power brand and see what the next few weeks bring.
I’ve been on a roller coaster ride and each time I think I may have found something it escapes me. My problem is I don’t keep a log and have no idea what I’ve done. In any case, I’ve started one today and will keep it updated daily. Once thing however that’s been missing each time my count is off is PectoSol-C. It’s made of the rind of citrus fruits I believe. The brand I use is by Ecogenics (or something close to this). I ran out three weeks ago and figured I should be okay with just the apricot seeds. Well, I was wrong. This seems to have happened a couple times already and each time (now that I think of if) I’ve always missed a couple weeks of the PectoSol my count goes up. I don’t know if anyone has heard or even used this product.
Back to the grind and I will report in another month. I hope Jim remembers to visit and give us an update.
Denise, as always, thank you so much for your blog.
Best,
Nathalie
Hi, I love your list and will buy the book. I’m surprised there isn’t more included about green tea extract. My Mayo oncologist recommended it and I’ve been on it. Also, any info on Beta Glucan? Thanks again!
Hi Denise,
I found these two points in an article that i read re: mushrooms and thought i’d pass it on. Article linked below
– “Shiitake has been used in medicine for years as a blood balancer”
– “Coriolus Versicolor has been shown to activate T-lymphocyte production” – Here’s a link to the full article:
https://www.canceractive.com/cancer-active-page-link.aspx?n=1488-
Also, a friend whose husband was diagnosed with CLL sent me an email this week saying his platelets went up from 85 to 107. She wrote, ” He started taking 3,000 mg of liposomal vitamin c, 7 tablets of wheatgrass (we use Pines wheat grass tablets, DaVinci Liposomal C – 3 times daily, Papaya leaf extract (smart organics) 2 times daily. We were very concerned about platelets. Had blood work done in Dec. Platelets 107,000. WBC is still high (not out of the woods) but did not go up.â€
Thrivers and strivers keep it going.
Mike
Thanks Mike,
I also feel that mushrooms help though I am not 100% sure because I take so may other herbs. I have tried Bell Supreme Immune support and NewChapter Immune Support.
At present I take 3g of AHCC (Quality of Life) which I feel is helping me.
Regards.
Hi Vin,
I’m so glad we have this site (thanks again to Denise) to share ideas and tonics. I agree, its hard to know what works and what doesn’t. There’s no hard science behind it. So – research, sharing info with others, trying new things, going with our gut & staying with what seems to work is the key for me. Thanks for sharing.
Mike
Yes Mike, please do provide us more info. on your experience. In my case the CD (38) markers in the blood are what they consider to be good. But, does that really mean much?
As yet I am not on any “medication” though I take many herbs etc. And, everything except for the lymphocyte count (about 75% of wbc) everything seems to be normal.
In general, the rate of increase has not been alarming but it varies, sometimes quite high and then other times reasonable slow. But, every preceding blood work has shown increase in lymphocyte cell count without an exception i.e. they have never come down. Hence my question: “But, does that really mean much?”
I wish you good health and an enjoyable life.
Please pardon my carelessness. The post should have been addressed to Jim.
But, yes Mike please do share your experience as well. I find it helpful to share our experiences. That is why I feel so thankful to Dense for providing us this venue, in addition to the direct information she provides us.
Hi Denise,
Thanks so much for your posts, I always learn something new and helpful. Knowledge is key, I appreciate you passing it on.
It would be nice to hear more from Jim. It looks like he has some info that we with a CLL diagnosis could use.
Good health,
Mike
Great post; first time I found this site; I am a First Connections consultant for the upstate NY / Vermont Leukemia and Lymphoma society, specializing in CAM; I am fortunate to have good CD markers, as I am sure you do; I am in a study, not trial, at NIH in Bethesda because I am doing well; backed myself out of full blown CLL to B cell lymphocytosis; I agree with the D3 levels you noted; Also, I take a ton of turmeric , green tea and artimisinin
1 | Karen
June 12, 2020 at 7:48 pm
Hi, I just discovered your site – Very helpful and inspiring. Diagnosed 3 months ago with CLL, asymptomatic with WBC in teens. I am already on a lot of the path you present here. I see that the last posting was a year ago. Are you still on line and available?
Thanks, Karen
Denise
June 15, 2020 at 10:54 am
Hi Karen,
So sorry you were diagnosed, but glad that you’re on the right track, and that you’ve found this site! I don’t post too regularly. But my last post was in March, at the beginning of the pandemic. I am here and very available. I get comments and questions on my old posts all the time from new people, and I always respond, though sometimes it might take me a few days.
I’ve considered going on Facebook, but I’m not sure if Facebook is open to alternatives in the medical arena. When it comes to search engines, Bing, Yahoo, and Duckduckgo are all more likely to bring you to sites with alternative suggestions. To help you be optimistic, I was 46 when diagnosed, and now I’m 65. I’ve never had any conventional treatment. I’ve tried many supplements and alternative treatments like vit C via IV, ultra-violet blood irradiation, and more. These days I’m cruising by with my hybrid keto/low oxalate diet and still a boatload of supplements. I used to wonder when i could stop taking the supplements. Now i know that they keep me healthy. This isn’t a disease you can “cure” and then get on with your life. It’s a condition you learn to live with and live well.
I’m here if you have any questions. So glad you wrote! – Denise