Aspertame/Diet Drinks--Has anyone sto... - LUpus Patients Un...

LUpus Patients Understanding and Support

3,470 members1,290 posts

Aspertame/Diet Drinks--Has anyone stopped drinking them and noticed improvement?

iwantsimple profile image
3 Replies

I just read an article about aspartame/chemical sweeteners and how they (theoretically) relate to Lupus and MS. I'm curious if any of you have tried cutting them out of your diet completely and if you noticed any improvement in symptoms. I've had gastric bypass, so these are the only sweeteners that I can have, and I don't want to give them up if there is no real value in it. Thanks!

Written by
iwantsimple profile image
iwantsimple
To view profiles and participate in discussions please or .
Read more about...
3 Replies
lupus-support1 profile image
lupus-support1Administrator

This misinformation has been circulating the internet for at least 14 years. and I have been sent such emails many times. It angers me because it causes anxiety and is a malicious hoax.

The email message circulating on the Internet warns individuals with lupus about dangers associated with using the artificial sweetener aspartame eg NutraSweet etc. The Lupus Foundation of America consulted with the chair of the LFA Medical Council, Evelyn Hess, MD, MACP, MACR. Dr. Hess is one of the America's leading researchers in the field of lupus specializing in environmental influences. According to Dr. Hess, there is, as of now, no specific proof of an association with aspartame as a cause or worsening of SLE.

People with lupus should always consult with their physician before making any changes in their medical treatment, diet, exercise or other routine based on information received via the Internet or other sources lacking known credentials.

If you have noticed that a food/drink/preparation affects you - people generally can be allergic to foods and drinks, then avoid it and always tell your doctor.

iwantsimple profile image
iwantsimple

I appreciate your answer! I have read that it is a hoax, as well, but when my symptoms are bad, I start looking for anything that could explain it! I guess it is what it is, huh? :) THanks!

lupus-support1 profile image
lupus-support1Administrator

I certainly understand your concerns and of course want to reduce your symptoms. If you want to talk some more to others like yourself, you can register for free at the LuPUS Message Board: lupus-support.org/LuPUSMB

Be well!

Ros

Not what you're looking for?

You may also like...

How can these horrific pains be invisible

I feel like my ankles are broke too they only look different to me.My hands are so shaky I often...

CNS Lupus & Noise Sensitivity

Hi everyone :) I haven't posted in ages, so I hope you're all well, or at least coping! I've been...
Bellaflowe profile image
Volunteer

Nose Sores

Hi all,I'm going through diagnosis at the moment for lupus/multi connective tissue disease and been...
NatalieMai profile image

HYDROXYCHLOROQUINE

Hi, just looking for help from fellow lupus sufferers!! I was diagnosed with Lupus 15 years ago and...
fifi6 profile image

I am new here. :-)

This is my first flare up, resulting in a diagnosis 6 months ago. I have had no remission for 10...
AileenT profile image

Moderation team

lupus-support1 profile image
lupus-support1Administrator
fabwheelie profile image
fabwheelieModerator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.