Butterfly Flare |
このアプリは現在ストアで閲覧することができません。 | ||||
価格 | 120円 | ダウンロード |
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ジャンル | ヘルスケア/フィットネス | |||
サイズ | 29.3MB | |||
開発者 | The Lupus Liar LLC | |||
順位 |
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リリース日 | 2017-10-17 11:50:44 | 評価 | 評価が取得できませんでした。 | |
互換性 | iOS 8.0以降が必要です。 iPhone、iPad および iPod touch 対応。 | |||
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****** Lupus App ******
Having a chronic illness sucks! If you are one the millions of people who have Lupus , also known as Systemic Lupus Erythromatosus, or any other related chronic immune illness, you’ll love the fun you can have with tracking your good and bad days with Butterfly Flare! This app is designed to put the smile in not feeling well. Butterfly Flare, with the tap of the screen and stroke of a text, will allow you to share your lupus pain, fatigue, and symptom patterns through the use of Emoji expressions.
Using visual learning prompts like Emojis helps you feel better, and take control of how to track your symptoms. A quick look back at your day or communication can help show you how you were feeling on any given day to your friends, family, and others you communicate with.
At least 1.5 million Americans have lupus, and it's believed that 5 million people worldwide are living with the disease, which is a chronic, autoimmune disease that can damage any part of the body. More than 16,000 new cases are reported annually across the country, and lupus occurs nine times more often in women than in men and is more common in those of non-European descent.
The unpredictable changing nature of Lupus makes it a challenge to triumph over. There are many resources that can help you take charge in taking care of your lupus. This app can help you smile while doing so!
The Butterfly Flare App is the world's 1st of its kind iOs app, providing fun Emojis to place a creative spin on living and coping with Lupus.
Features:
Using The Butterfly Flare Lupus App you can
* Track your Lupus symptoms with visual expression
* Share how you feel with family and friends or even your physicians
* Create a picture diary of how you feel
* Check in on others who are not feeling well
*Note: This is app is not a substitution for medical advice. Please contact your physician for medical care, advice, and maintenance.
Find the full terms and conditions, and our privacy policy, at http://www.thelupusliar.com/privacypolicy and http://www.thelupusliar.com/termsofservice respectively.
Support URL -
Find the full terms and conditions, and our privacy policy, at http://www.thelupusliar.com/privacypolicy and http://www.thelupusliar.com/termsofservice respectively.
Having a chronic illness sucks! If you are one the millions of people who have Lupus , also known as Systemic Lupus Erythromatosus, or any other related chronic immune illness, you’ll love the fun you can have with tracking your good and bad days with Butterfly Flare! This app is designed to put the smile in not feeling well. Butterfly Flare, with the tap of the screen and stroke of a text, will allow you to share your lupus pain, fatigue, and symptom patterns through the use of Emoji expressions.
Using visual learning prompts like Emojis helps you feel better, and take control of how to track your symptoms. A quick look back at your day or communication can help show you how you were feeling on any given day to your friends, family, and others you communicate with.
At least 1.5 million Americans have lupus, and it's believed that 5 million people worldwide are living with the disease, which is a chronic, autoimmune disease that can damage any part of the body. More than 16,000 new cases are reported annually across the country, and lupus occurs nine times more often in women than in men and is more common in those of non-European descent.
The unpredictable changing nature of Lupus makes it a challenge to triumph over. There are many resources that can help you take charge in taking care of your lupus. This app can help you smile while doing so!
The Butterfly Flare App is the world's 1st of its kind iOs app, providing fun Emojis to place a creative spin on living and coping with Lupus.
Features:
Using The Butterfly Flare Lupus App you can
* Track your Lupus symptoms with visual expression
* Share how you feel with family and friends or even your physicians
* Create a picture diary of how you feel
* Check in on others who are not feeling well
*Note: This is app is not a substitution for medical advice. Please contact your physician for medical care, advice, and maintenance.
Find the full terms and conditions, and our privacy policy, at http://www.thelupusliar.com/privacypolicy and http://www.thelupusliar.com/termsofservice respectively.
Support URL -
Find the full terms and conditions, and our privacy policy, at http://www.thelupusliar.com/privacypolicy and http://www.thelupusliar.com/termsofservice respectively.
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