Have any one tryd Herbalife products to manage the symtons????

[Yasmeen]

Just wonderd if any have trayd to use Herbalife products in there every day life?If so wath is your experians with it?

[FionaP]

I tried many diets since having my diagnosis 7 years back all to no benefit and at a cost. Some adverts claims are so wrong and their claims are the same for many conditions. We want to be well so much we can be easy targets.

Try talking through with your doctor and check the web site attached to this one for more info.

If I see a new product I check to see what the Fibro sites have to say and see if it is endorsing one year on now. If there was a real benefit The Fibro sites in USA that are attached to research would know of it and so we all would, very quickly.

[sarah111]

Hi,yes i am on Co-Enzyme Q10....I started myself of on a 100mg a day an im on 300mg a day now.I find it helps with the sweating an the flare-up's and i find the swelling in my hands are not as bad.

Everyone is differant but i find they work for me.Also strong Vitamin.C for the imune system i also take..hope this is of some help to.

[nadine1974]

herbalife is a business, they sell their products for profit and they are very expensive!!! i tried but it didnt help at all,my doctor looked at the products and wasnt impressed either!!!

herbal tablets bought from holland and barratt or similar shops are much better and reliable xx

[pottyness]

and sarah111 mentions Co-Enzine Q10 which you can buy anywhere and i also have found it to work . i had forgotten that Q10 had helped in the past and will get some more. [from somewhere that isnt trying to lighten my purse too much] so thanks for reminding me. fybro fog again.

[LindseyMid]

As I understand it, Herbalife are a brand.

Some supplements (talking generic here!) do help some people. But they are never a cure or all-round treatment.

[Yasmeen]

Hi,thank you for all the answers and tips.

I knowe it is a brand and yes it is exspenve.

It is just that i just wanted to fine out wath people have been traying in the past.

I my self have been traying APESLUTLY EVERY THING,with not a lot off sucsess :((((.But i was werry happy to fine this sithe and knowing i ame not a lone with my acs and pains....So i just wantet to konwe whow to carry on with my life.I have had fm for at lesst 15 years and it was an medical student that sad to my she did not knowe wath my problem was and she referd me to the an spesialist and i was diagnosed last febuary,and i thank that student for beeing anest and listen to me in sted of giving me paracitamol and say that it was just stress and i needed rest.

I ame working full time and fine it incringly hardere and trobbelsom,the iorny is that i work in a hospital and most off my collages don`t have a clue a but fm withc is frustrating and sad.When we have patient with fm on ower ward they allways make funn of how wnciy and that they allways mon a but pain.Wthc make me to not say any thing a but my one problems.I ame not from the UK and don`t knowe wath to do and don`t knowe the systems and so on.So when i found this page my preays was answerd .So thank you a gain for all the tips.

At lest i ame not alone any more....Thank you