Short answer · Medically reviewed summary · Last updated: 2026-05-08

There is currently no scientifically proven "natural cure" for Granulomatosis with Polyangiitis (GPA), and it is critical to understand that natural remedies cannot replace conventional immunosuppressive therapy. While lifestyle modifications and mind-body practices can help manage symptoms and improve quality of life, they do not address the underlying autoimmune activity of Granulomatosis with Polyangiitis (GPA). Can natural remedies treat Granulomatosis with Polyangiitis (GPA)? No natural supplement, herbal remedy, or alternative therapy has been shown in clinical trials to induce remission in Granulomatosis with Polyangiitis (GPA).

3 people with Granulomatosis with Polyangiitis (GPA) have shared their first-person experience on this question at DiseaseMaps.

12

Is there any natural treatment for Granulomatosis with Polyangiitis (GPA)?

Natural treatments for Granulomatosis with Polyangiitis (GPA): what patients have tried and reported, with an evidence-based, medically reviewed summary.

Natural treatment of Granulomatosis with Polyangiitis (GPA)

There is currently no scientifically proven "natural cure" for Granulomatosis with Polyangiitis (GPA), and it is critical to understand that natural remedies cannot replace conventional immunosuppressive therapy. While lifestyle modifications and mind-body practices can help manage symptoms and improve quality of life, they do not address the underlying autoimmune activity of Granulomatosis with Polyangiitis (GPA).



Can natural remedies treat Granulomatosis with Polyangiitis (GPA)?


No natural supplement, herbal remedy, or alternative therapy has been shown in clinical trials to induce remission in Granulomatosis with Polyangiitis (GPA). Patients often ask about anti-inflammatory herbs like turmeric or ginger; however, there is no evidence that these modulate the systemic vasculitis characteristic of this disease. Relying on unproven alternatives while delaying conventional treatment, such as corticosteroids or rituximab, poses a severe risk of organ damage or life-threatening complications.



What are the risks of using herbal supplements?


Many herbal supplements carry significant risks for patients with Granulomatosis with Polyangiitis (GPA) due to potential interactions with immunosuppressive medications. For example, St. John’s Wort can alter the metabolism of various drugs, potentially reducing their efficacy. Furthermore, some supplements may stimulate the immune system, which is counterproductive when the goal of GPA treatment is to suppress an overactive immune response.



How can mind-body practices support patients?


While they do not treat the vasculitis itself, integrative therapies can assist with the emotional and physical burden of living with a chronic condition. For our 111 community members on DiseaseMaps.org, the following practices have been reported as helpful for managing stress and pain:



  • Acupuncture: May provide temporary relief for peripheral nerve pain or musculoskeletal discomfort.

  • Yoga and Tai Chi: Gentle movement can help maintain joint mobility and reduce the fatigue associated with Granulomatosis with Polyangiitis (GPA).

  • Mindfulness-Based Stress Reduction (MBSR): Shown to improve psychological well-being and coping mechanisms for those with systemic inflammatory diseases.

  • Physical Therapy: Essential for restoring function if the disease has caused joint stiffness or muscle atrophy.



Next steps



  • Always consult your rheumatologist before starting any new supplement or alternative therapy.

  • Focus on a heart-healthy, anti-inflammatory diet that supports bone health, especially if you are taking corticosteroids.

  • Join our community at DiseaseMaps.org to connect with others managing Granulomatosis with Polyangiitis (GPA).



Medical disclaimer: This content is for informational purposes only and does not constitute medical advice; always consult your healthcare team before making changes to your treatment plan.



References



  • Vasculitis Foundation: vasculitisfoundation.org

  • NIH Genetic and Rare Diseases (GARD) Information Center: rarediseases.info.nih.gov

  • Orphanet: orpha.net

  • American College of Rheumatology: rheumatology.org

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-05-08
Sources cited: Vasculitis Foundation: vasculitisfoundation.org · NIH Genetic and Rare Diseases (GARD) Information Center: rarediseases.info.nih.gov · Orphanet: orpha.net · American College of Rheumatology: rheumatology.org
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
4 answers
Like I have said before, we are all different so something may work on one but not necessarily for another !!!! Some claim hemp oils work for them others say they couldn't tell any different !!!

Posted Jul 26, 2018 by Leo 1500
None that I’ve heard of yet

Posted Jul 30, 2018 by Terry 2500
I was diagnosed with GPA at the beginning of 2021. I have been told by my roughly 14 MD's that diet makes no difference and that the necrosis at my fingers and toes was going to lead to amputation; that my lungs and kidneys were permanently damaged and that medications were also to be a permanent part of my life. I have to admit this was not something I was willing to accept and even less for my family. What to do? the only thing that was not recommended...unconventional. I switched my diet over to anti-inflammatory using food as my medicine as you would any other autoimmune disease; added an ND to my team; worked on giving my body what it needed to in essence rebuild what was damaged; ozone MAH infusions and limb bagging, a variety of nutrients that my body was designed to use (ie. glutathione, methyl cobalamin b-12 im injections, unda 2,9,36, PectiSol-C, glutagenics, miraca, EB-N5 and NAC) just to name a few. I've asked myself, does along with as much exercise as I can get, this make a difference? I can't honestly say. I do know that my lungs are clear, my kidneys have gotten progressively better every month, my ANCA numbers have reduced by 50+% each month since leaving the hospital and I am hoping to see 0 or less this month and a filtration rate within acceptable limits if my progress continues, I have yet to have any amputations (1 finger and 3 toes still healing out of 6 fingers and 5 toes but intact because I refused to give them up without an unconventional fight. I was told that none of this was going to happen so if it worked/works than awesome, nothing lost but a few bucks. If you or a loved one have this disease I would suggest you add a Naturopathic Physician (ND) to your team; their focus is to deal with the root while using what God has provided to rebuild us into the strong trees we are meant to be.

Posted Jul 31, 2021 by HearyBeary 200

Natural treatment of Granulomatosis with Polyangiitis (GPA)

Granulomatosis with Polyangiitis (GPA) life expectancy

What is the life expectancy of someone with Granulomatosis with Polyangiiti...

5 answers
Celebrities with Granulomatosis with Polyangiitis (GPA)

Celebrities with Granulomatosis with Polyangiitis (GPA)

2 answers
Is Granulomatosis with Polyangiitis (GPA) hereditary?

Is Granulomatosis with Polyangiitis (GPA) hereditary?

3 answers
Is Granulomatosis with Polyangiitis (GPA) contagious?

Is Granulomatosis with Polyangiitis (GPA) contagious?

3 answers
ICD9 and ICD10 codes of Granulomatosis with Polyangiitis (GPA)

ICD10 code of Granulomatosis with Polyangiitis (GPA) and ICD9 code

2 answers
Living with Granulomatosis with Polyangiitis (GPA)

Living with Granulomatosis with Polyangiitis (GPA). How to live with Granul...

3 answers
Granulomatosis with Polyangiitis (GPA) diet

Granulomatosis with Polyangiitis (GPA) diet. Is there a diet which improves...

5 answers
History of Granulomatosis with Polyangiitis (GPA)

What is the history of Granulomatosis with Polyangiitis (GPA)?

2 answers

World map of Granulomatosis with Polyangiitis (GPA)

Find people with Granulomatosis with Polyangiitis (GPA) through the map. Connect with them and share experiences. Join the Granulomatosis with Polyangiitis (GPA) community.

Stories of Granulomatosis with Polyangiitis (GPA)

GRANULOMATOSIS WITH POLYANGIITIS (GPA) STORIES
Granulomatosis with Polyangiitis (GPA) stories
My journey with this monster of a disease started out in March 2018 with ear problems and quickly persisted into all of my joints rendering me disabled and having to leave work after a month of hobbling around campus like an old woman. I finally tapp...
Granulomatosis with Polyangiitis (GPA) stories
For about a week I was having a dry cough/asthma flare up that I first went to our local urgent care(my regular GP was out the country for the next month) on June 28th, and they diagnosed me w. cough and acute bronchitis which they treated with a bre...
Granulomatosis with Polyangiitis (GPA) stories
Had sever fatigue and joint pains. Began coughing up blood. Went to hospital. Admitted right away. Lung and Kidney biopsy. 60mgs Pred w/ 1 year taper. 4x Rituxan. 150mgs Imuran orally. Feel better. In Remission.

Tell your story and help others

Tell my story

Granulomatosis with Polyangiitis (GPA) forum

GRANULOMATOSIS WITH POLYANGIITIS (GPA) FORUM

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