World map of Wilsons disease View more
  2. Wilsons disease
  3. Forum
  4. Top questions
  5. Question 12
12

Is there any natural treatment for Wilsons disease?

Are there natural treatment(s) that may improve the quality of life of people with Wilsons disease? Here you can see if there is any natural remedy and/or treatment that can help people with Wilsons disease

Natural treatment of Wilsons disease
2 answers
There is not, however if you very very rarely eat foods that are high in copper there is a chance that you can live your life without medication. However, I do NOT advise this. If you have been diagnosed with Wilson's Disease, please take your medication.
Posted Aug 30, 2017 by Sam 770
well drink lot of water only reverse osmosis
Posted Apr 29, 2020 by kush baroniya 1700

Natural treatment of Wilsons disease

Wilsons disease life expectancy

What is the life expectancy of someone with Wilsons disease?

4 answers
Celebrities with Wilsons disease

Celebrities with Wilsons disease

1 answer
Is Wilsons disease hereditary?

Is Wilsons disease hereditary?

4 answers
Is Wilsons disease contagious?

Is Wilsons disease contagious?

4 answers
ICD9 and ICD10 codes of Wilsons disease

ICD10 code of Wilsons disease and ICD9 code

3 answers
Living with Wilsons disease

Living with Wilsons disease. How to live with Wilsons disease?

3 answers
Wilsons disease diet

Wilsons disease diet. Is there a diet which improves the quality of life of...

3 answers
History of Wilsons disease

What is the history of Wilsons disease?

2 answers

World map of Wilsons disease

Find people with Wilsons disease through the map. Connect with them and share experiences. Join the Wilsons disease community.
View map

Stories of Wilsons disease

WILSONS DISEASE STORIES
Wilsons disease stories
MY BOYS
I am a mom to 5. In 2008, my oldest son complained of a stomach ache for a few days. I figured he had the flu or a bug. Then his eyes turned yellow and just like that, we were thrust into a nightmare. Two weeks in the hospital to figure out what was ...
Wilsons disease stories
HOW WILSON'S DISEASE AFFECTED ME
My name is Samantha Akin. I am 18 years old. I was diagnosed with Wilson’s Disease earlier in January of 2015, and since then have been on Syprine (aka Trientine). Some of my symptoms were: my handwriting had worsened over the years (micrographia),...
Wilsons disease stories
WILSON DISEASE
Wlson Disease 
Wilsons disease stories
CARRIER
my mom had WD I am only a carrying mutation

Tell your story and help others

Tell my story

Wilsons disease forum

WILSONS DISEASE FORUM
Wilsons disease forum
GASTRIC ULCER
i was wondering if anyone else have developed gastric ulcers after taking Galzin for several years? If so, please tell me about your experience and if you continued taking Galzin.

Ask a question and get answers from other users.

Ask a question

Find your symptoms soulmates

From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

Symptoms soulmates

Add your symptoms and discover your soulmates map

Soulmates map