Question about your experience with aloe vera - CLL Support

CLL Support

22,511 members38,663 posts

Question about your experience with aloe vera

Ankakoza profile image
5 Replies

I have CLL for 5 years, no other symptops but high WBC, 105 000, doctora are about to give me chemo. I also have EDS, and Cusack Protocol reccomends aloe vera, isn't it the risk of increasiing number of leucocyts ? Anyone knows ?

Written by
Ankakoza profile image
Ankakoza
To view profiles and participate in discussions please or .
Read more about...
5 Replies
AussieNeil profile image
AussieNeilAdministrator

The Natural Medicines Comprehensive Database "is a reliable source of information about natural remedies, rating them for safety and effectiveness and providing links to the scientific studies that its ratings are based on. It doesn’t give aloe vera any ratings of “effective” or “likely effective” for any condition."

Also the National Center for Complementary and Integrative Health (NCCIH) says “There’s not enough evidence to show whether aloe vera is helpful for most of the purposes for which people use it.”

sciencebasedmedicine.org/al...

Ehlers Danlos Syndrome is a terrible condition to live with, given it can have such wide ranging impact on your health. I hope you only have it mildly.

Neil

Ankakoza profile image
Ankakoza in reply to AussieNeil

Yes, I do have mildest form, just hipermobility of joints, but during last year I do notice slowly progressing mucsles weakning , without loosing weight. Cusack Protocol seems reasonable complementation to słow the progres Hence my question, thanks

AussieNeil profile image
AussieNeilAdministrator in reply to Ankakoza

Pleased to hear you have the mildest form. When I found out about the connective tissue disorders of EDS and Marfan's syndrome, I did wonder how many contortionists have one of these conditions.

There are the usual claims without much basis for aloe vera and leukaemia, so I suspect it isn't likely to affect your CLL (and I applaud you asking). Here's one reliable evidence based resource regarding the evidence for other claimed medical uses:

mskcc.org/cancer-care/integ...

Just be aware that with the unregulated nature of the supplement industry in most countries, it seems you often don't get what you think you bought, so if you want to try it for your EDS, I strongly recommend you grow your own plants:

healthunlocked.com/cllsuppo...

Neil

Ankakoza profile image
Ankakoza in reply to AussieNeil

If I would take it it would by from my own plant, but I'd rather stick to alternative to aloe- Maitake. This protocol is a synergie of noumeros supplementation , None so controvercial as aloe.

I found it helpful to have a feeling that something depends on me, instead of beeing helpless victim waiting for the moment that blood test will be worse. In my country the newest chemo is not refunded, Car-T doesn't exist, and doctors attitude is - doesn't matter what You eat.

AussieNeil profile image
AussieNeilAdministrator in reply to Ankakoza

Memorial Sloan Kettering Cancer Center on Maitake:

mskcc.org/cancer-care/integ...

You may also like...

No Evidence of Aloe Vera Found in the Aloe Vera at Wal-Mart, CVS

22/no-evidence-of-aloe-vera-found-in-the-aloe-vera-at-wal-mart-cvs How can we know what's in...

Experience about taking ibrutinib

ibrutinib for seven months and his WBC has reached 40,000. Does anyone have experience with using...

Questions about lab results

labs to my CLL doctor prior to my departure and will see him on my return. Have been having recent...

questions about mutated / unmutated

Good morning all, was wondering if anyone had a simple explanation about 13q and mutated versus...

Question about lymph nodes

the time) I know deep down something is not right. Test come back negative. Does anyone have...