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My Lupus Secret

A safe place to share your lupus secrets. No judgement. No shame. Merely catharsis through honesty.

http://www.mylupussecret.com/

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My Lupus Secret | mylupussecret.com Reviews
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My Lupus Secret | mylupussecret.com Reviews

https://mylupussecret.com

A safe place to share your lupus secrets. No judgement. No shame. Merely catharsis through honesty.

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mylupussecret.com mylupussecret.com
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My Lupus Secret - I’m afraid to tell anyone when I have a cold or...

http://mylupussecret.com/post/155630366907/im-afraid-to-tell-anyone-when-i-have-a-cold-or

I’m afraid to tell anyone when I have a cold or something “ordinary” because I’m afraid it will invalidate the pain associated with my lupus in the eyes of my friends and family. These Resources May Help. January 9, 2017. Anonymous submitted this to mylupussecret. A safe place to share your lupus secrets. No judgement. No shame. Merely catharsis through honesty. My Lupus Secret 2015 2017 Christopher Snider (Moderator), Advisory Team.

2

My Lupus Secret - Posts Tagged -plaquenil’

http://mylupussecret.com/tagged/plaquenil

I am a 24 year old male, diagnosed with SLE 3 years ago. It’s been a roller coaster. I am extremely depressed. I feel very emasculated since Lupus is seen as a women’s disease. My real lupus secret though is that eventhough my lupus is under control - most of the time I wish it would be terminal. These Resources May Help. October 10, 2016. These Resources May Help. September 10, 2016. These Resources May Help. September 7, 2016. These Resources May Help. September 5, 2016. These Resources May Help. Can&r...

3

My Lupus Secret - I have had lupus, Scleroderma, and reynauds for...

http://mylupussecret.com/post/150444372415/i-have-had-lupus-scleroderma-and-reynauds-for

I have had lupus, Scleroderma, and reynauds for more than 13 years. I had a really bad scare two years ago where I almost died and then another one last year. All this brought on a whole new set of problems like a heart condition and stage 3 CKD. I have a husband and two kids who are my life. These Resources May Help. September 15, 2016. Anonymous submitted this to mylupussecret. A safe place to share your lupus secrets. No judgement. No shame. Merely catharsis through honesty.

4

My Lupus Secret - I am a 24 year old male, diagnosed with SLE 3...

http://mylupussecret.com/post/151609393201/i-am-a-24-year-old-male-diagnosed-with-sle-3

I am a 24 year old male, diagnosed with SLE 3 years ago. It’s been a roller coaster. I am extremely depressed. I feel very emasculated since Lupus is seen as a women’s disease. My real lupus secret though is that eventhough my lupus is under control - most of the time I wish it would be terminal. These Resources May Help. October 10, 2016. Anonymous submitted this to mylupussecret. A safe place to share your lupus secrets. No judgement. No shame. Merely catharsis through honesty.

5

My Lupus Secret - Posts Tagged -SLE’

http://mylupussecret.com/tagged/SLE

I’m 17 years old and I can barely walk anymore. I’ve lowered my prednisone dosage to 5 mg and I feel like I’m dying. No matter how many Advils I take the pain in my legs and mostly the bottom of my feet remains. They feel like I’ve ran a marathon with heels on. My chest and heart hurts and I just want to be healthy again. I want to be able to play football or track without having to worry about a flare up in mid sprint. These Resources May Help. December 7, 2016. What’s worse is that sometimes it&r...

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Christopher | A Consequence of Hypoglycemia.

https://tobesugarfree.com/author/iam5partacu5

A Consequence of Hypoglycemia. What good is an incurable disease if you can’t share it with the rest of the world. July 15, 2016. I don’t remember how to do this. Has it really been a year since I tried to look ahead. For months I’ve been battling ideas that seem great on paper, or even within the relatively safe space of a “test the waters” Facebook post. Why have I been thinking about writing this blog post for three weeks but only now have the strength (is it really. And I will try to be more visible.

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I’m afraid to tell anyone when I have a cold or something “ordinary” because I’m afraid it will invalidate the pain associated with my lupus in the eyes of my friends and family. These Resources May Help. January 9, 2017. I’m 17 years old and I can barely walk anymore. I’ve lowered my prednisone dosage to 5 mg and I feel like I’m dying. No matter how many Advils I take the pain in my legs and mostly the bottom of my feet remains. They feel like I’ve ran a marathon with heels on. These Resources May Help.

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Crying Wolf

This is a compilation of some of my memories and experiences that happened during my teenage years. Start. At the begginning of this blog. To hear the beginning of my story. The most recent posts will now be my experiences with Lupus as an adult and mother. Thursday, July 28, 2011. I walked out of my postpartum doctor's appointment the other day and had a mixture of feelings. Good doctors are out there. We sometimes just have to search for them. Pay more for them. They are worth it. I guess the hospital.

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Mitt liv - Min lupus

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