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Is there any natural treatment for Hereditary Angioedema?

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

Natural treatment of Hereditary Angioedema

Hereditary Angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of swelling in various parts of the body, including the face, hands, feet, and gastrointestinal tract. It is caused by a deficiency or dysfunction of a protein called C1 inhibitor, which leads to the overproduction of another protein called bradykinin. Bradykinin causes blood vessels to become leaky, resulting in swelling and inflammation.



While there is no known cure for HAE, there are several natural treatment options that can help manage the symptoms and reduce the frequency and severity of attacks. It is important to note that these natural treatments should be used in conjunction with medical supervision and prescribed medications.



Dietary Modifications


Dietary modifications can play a significant role in managing HAE symptoms. Some individuals with HAE have reported that avoiding certain trigger foods can help reduce the frequency of attacks. These trigger foods may vary from person to person, but common culprits include processed foods, alcohol, caffeine, and foods high in histamine (such as aged cheese, fermented foods, and cured meats). Maintaining a well-balanced diet rich in fruits, vegetables, whole grains, and lean proteins can also support overall health and immune function.



Stress Management


Stress is known to trigger or worsen HAE attacks in many individuals. Therefore, incorporating stress management techniques into daily life can be beneficial. Practices such as deep breathing exercises, meditation, yoga, and regular physical activity can help reduce stress levels and promote relaxation. It is important to find activities that work best for each individual and make them a regular part of their routine.



Herbal Supplements


While there is limited scientific evidence to support the use of herbal supplements in treating HAE, some individuals have reported positive effects. Quercetin, a natural compound found in fruits and vegetables, has anti-inflammatory properties and may help reduce the severity of HAE attacks. Other herbal supplements such as ginger and curcumin have also shown anti-inflammatory effects and may provide some relief. However, it is crucial to consult with a healthcare professional before starting any herbal supplements to ensure they do not interact with prescribed medications or worsen symptoms.



Acupuncture


Acupuncture is an ancient Chinese practice that involves inserting thin needles into specific points on the body. It is believed to help balance the flow of energy and promote healing. Some individuals with HAE have reported reduced frequency and severity of attacks after incorporating acupuncture into their treatment plan. However, more research is needed to establish its effectiveness in managing HAE symptoms.



Protease Inhibitors


Protease inhibitors are a class of medications that can help prevent the breakdown of proteins, including the C1 inhibitor protein. By inhibiting the activity of certain enzymes, protease inhibitors can increase the levels of functional C1 inhibitor in the body, reducing the frequency and severity of HAE attacks. These medications are available by prescription and should be used under the guidance of a healthcare professional.



It is important to note that while natural treatments can provide some relief for individuals with HAE, they are not a substitute for prescribed medications. The management of HAE should be personalized and tailored to each individual's specific needs. Regular communication with a healthcare professional is essential to ensure the most effective treatment plan is in place.


Diseasemaps
5 answers
Not that I am aware of

Posted May 23, 2017 by Donna 2250
No there is not. You can do things to help like eat healthy and exercise lightly nothing strenuous.
But unfortunately it's in your genes you can't control it. It controls you.

Posted Sep 3, 2017 by Mary Helen 1400
No.. anibolic steroids were the norm until modern preventive meds became available

Posted Nov 29, 2017 by [email protected] 2300
Translated from spanish Improve translation
When I inflamed a limb as the feet or the hands, if I ejercitandolos ( go to work, walk, etc etc ) just before the symptoms and improves the mobility a lot earlier. tested by my. it is hard but at least it lasts less.

Posted Oct 15, 2017 by Juan Salvador Moll Garcia 100

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HEREDITARY ANGIOEDEMA STORIES
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Mine started in 2009 with my first swell, it was my lips and cheek. That is the same time the ucartia started also. It took my Dr. 5 years to find something to help me control and survive my Angioedema. I never knew how bad this could be till I was d...
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Desde niño tuve que soportar los diversos episodios de AEH sin saberlo, pasando de medico en medico con diversidad de diagnosticos y ordenes de cirugias innecesarias, gracias a Dios no acudi a ninguna. Fue hace tres años que optuve el diagnostico r...
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My earliest memory of HAE symptoms was when I was about 6 or 7.  I would occasionally get the abdomen swelling, be sick and sweating all day, then I would finally vomit and then feel better, go to sleep and be better the next morning.  I consider m...
Hereditary Angioedema stories
I was diagnosed accidentally, after seeing a TV show where the host talked about her HAE in 2014. My first attack was at 8, when I was mistakenly hospitalized with appendicitis.  The surgery wasn't done, because I felt better in 3 days.  Next reme...
Hereditary Angioedema stories
i was dx in 2008 with my first fasel swell . im hae type 2 . im co founder of the facebook group ( https://www.facebook.com/groups/156649074393978/ )

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Hereditary Angioedema forum

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Hi All, Is anyone aware of Cinryze experiencing a shortage supply? If so, why and where is this shortage (US or Europe)?   Thanks!
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Hi All, Is anyone aware of Cinryze experiencing a shortage supply? If so, why and where is this shortage (US or Europe)?   Thanks!
Hereditary Angioedema forum
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Hi Everyone, I'm trying to understand what it is like for people with HAE. Therefore, would you ever switch treatment? Why or why not? What happens if you lose insurance coverage? Are you still recieving treatment? Was there a time where you had to ...

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