Ardent Cerebrations: Musings of Lupus Survivors!

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Forum of lupus bloggers & groups express passionate thoughts on disease, body, mind & spirit. Info Hub to share resources, articles & media.

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LupusMCTD.com Courage Award

The Lupus MCTD Foundation of America has nominated you for our Courage Award.
courage award

The Courage Award is being given to you for your public contributions in raising awareness, as well as your demonstration to other's as a fellow patient. Lupus Warriors are people who have overcome many challenges, who have walked through experiences having gained a renewed spirit and determination to thrive. Have gained the spirit of endurance through their difficulties and have in turn help other patients. You exemplify the inner strength of a Lupus Warrior and an empathy that makes your service work to other's rooted in compassion. Sincerely, The Lupus MCTD Foundation Team

 

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Lupus Bloggers

Angie

Family & Friends a part of the Healing Process for The Mind, The Body & The Spirit

I was getting a little depressed Wednesday having the plans I made on the days I felt good being usurped again by my illness. Although I coul
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Posted by Angie on January 29, 2010 at 6:30pm — 3 Comments

cookie

NEEDED GROUP

There should be a group for questions and answers for those who are still searching for answers and don't know where to turn.

Posted by cookie on January 26, 2010 at 4:59pm — 2 Comments

Angie

To Sleep or Not to Sleep? Thats the Question Asked by Lupus & Fibromyalgia Survivors

Most people don’t realize that the inability to sleep is the symptom and the side-effect with the most profound effect on the quality of everyday life for a survivor of lupus an


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Posted by Angie on January 25, 2010 at 12:30pm — 2 Comments

shana ricker

I need help

It's Sunday evening and I'm still trying to recover from the past week. It was one of those weeks where everything went wrong. I know that my stress level plays a big part on my Lupus. The pain becomes almost unbearable. I could deal with everything that has happened expect for losing my medical insurance.

With all of our health problems we need our medical insurance. I look at all of my medications and I wonder what is going to happen when they run out. I can't afford to pay for them and God k… Continue

Posted by shana ricker on January 11, 2010 at 1:35am — 3 Comments

The Salon

shana ricker

A little about me 1 Reply

Hi all, I'm 35 and was diagnosed a couple of years ago with Lupus, Scleraderma, RA, Fibromylgia, and Dermatitis. I take Plaquenil, Methotrexate, Folic Acid, Azulfadine, Protonix, Bentyl, Effexor, Wel…

Started by shana ricker in The Salon. Last reply by Angie Jan 25.

Angie

Fibromyalgia Pain | What's your experience with Cymbalta?

After 2 days of drug resistant fibromyalgia pain. I am looking forward to trying suggestions from my new rheumatologist, such as Cymbalta. I'd like to know what's your experience with Cymbalta? Your…

Tagged: drugs, management, medications, pain, Cymbalta

Started by Angie in The Disease Jan 19.

Amy Domestico

Finding a Cure 1 Reply

Your Lid Matters, with Yoplait and Dr. Funk The Wii Mommies would like to extend their welcome to Dr.Kristi Funk, a board-certified surgical breast specialist and an expert in minimally-invasive diag…

Started by Amy Domestico in The Salon. Last reply by Angie Oct. 26, 2009.

Ruste Jill Vallerie

Confusing Depression and Lupus

I'm new here, so if I stumble a bit, forgive me. I was just diagnosed a couple weeks ago so my head is full of many thoughts. However, for me the biggest suprise is that I just about had to die to ge…

Tagged: depressed, depression

Started by Ruste Jill Vallerie in The Body Oct. 6, 2009.

Latest Activity

Avascular necrosis is very literally the death of bone tissue 'caused by a lack of blood flow to the bone. It's very common in people who have been on steroids for a very long period of time (20 years for me) and people with lupus. It can happen any…
yesterday
Describe the symptoms of avascular necrosis? What area is affected, the hip? How did you find out you had it? How do doctors treat it?
yesterday
Maria :) to all of you!
February 2
January 31
Lea Sapsford updated their profile
January 31
Lea Sapsford updated their profile photo
January 31
January 31
Lea Sapsford is now a member of Ardent Cerebrations: Musings of Lupus Survivors!
January 31
 
 

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