I must first lead you to Loretta's journal. On Saturday, January 15, 2005 Loretta wrote about Lupus and Psychological Testing. Did you ever hear a speaker, watch a movie or listen to your Pastor at church and say ....... They are talking directly to me? Well, that is how I felt when I read Loretta's entry.
For the past few months I have been going downhill emotionally. The speed at which I have been going downhill has rapidly increased over the last few weeks. If I had to put my finger on one occurance I couldn't. So many things have changed in my life over the past 18 months. But I did think that I had a handle on those things.
But I was so very wrong. Within the last four months things began to change. I no longer felt sure of myself. I doubted everything in my life. And, as much as I tried to hold on to what I believed was my life I couldn't. You see in my mind I believed I had a purpose. That I was useful. Even after I crashed I felt that I still had a purpose. That I mattered. I was still trying to work. Then there became a time that was no longer possible. My doctors believed that. My family believed that. Friends believed that. My health had deterioriated so that I could no longer do it. My seizure activity had increased to 2 or 3 times a week. My cognitive function was (and is) such that I was making wrong decisions at work. Not to mention the disorientation, pain and fatigue I felt. It was (and still is) a scary time for me. Then one day I woke up and I could not understand and was very confused and my world was never the same. This is where I began to go downhill emotionally.
I have always called May 13, 2003 the day I crashed because it was the day I had my first stroke. I will now call that the day of my medical crash. December 29, 2004 is now the day of my emotional crash. This is the day that I was taken out of my house and brought to the hospital an emotional wreck. A quiet emotional wreck, but one none the less. I was deemed to be a danger to myself. And admitted. My depression was diagnosed to be severe and I was admitted to the psychiatric ward and watched for 6 days. I was assigned a "sitter." Someone to watch me 24 hours a day. The rope was taken from my bathrobe and any string from any item of clothing Gary brought me.
The experience there was harrowing to say the least. I sat there quietly for six days sleeping when I could. Watching others there. I looked around and what I saw around me was what looked like the cast of the video "Thriller." Feeling that I didn't belong there, yet somehow I did. I cried when I could, but sometimes there were no tears. I tried to replay the last months. How did I end up there? I remembered my life before Lupus. Getting up and going to work. Being head strong. Raising my family. Being a wife. Being a woman. Now I felt like nothing. Sleeping in a room with a bed and nothing more. I had a baby sitter. Showering with a baby sitter. Asking for someone to unlock a cabinet so I could get clothing and my hair brush. How horrible my life had become. This is what Lupus had given me. Depression was far more than I could handle. My brain was fighting me now. It was fighting back telling me it could no longer handle everything I was holding in. There were no more smiles. There were no more tears. There was nothing.
Tests are being done and my rheumatologist, neurologist and a psychiatrist all consulted. Some tests are still being done. But, its the Lupus and it has affected my brain. As well as deficits from the strokes. Meds have been changed. My prednisione is being weaned. As prednisone really has no effect on Lupus and APS with CNS involvement. Or just doesn't work for me. My immuno suppressant has been changed. They are working on adjusting my psyc meds. I have another "ologist." A psychiatrist. She's great. Also my health insurance assigned a mental health specialist to call every two weeks to speak to me.
I've decided to write about this now. Only after reading Loretta's journal entry. At the time of this happening to me only family and a few select friends knew. I'm sorry if you were told a different story. I needed time to sort things out. This has been a tumultuous couple of months emotionally. I'm still not healthy emotionally and really not up to the questions and reprove of those un understanding minds.
Lupus is no respector of persons. What we get when we have Lupus is different than another gets. Kidney involvement, Lung involvement, Skin involvement, CNS involvement. It's all horrible. Not one should be taken lightly.
12 comments:
depression comes with many things. one is like mine cancer and bi polar disorder.
loosing someone can be depressing.
so many so much and it is common. but If u need a friend to cry with i will offer my shoulder please email i will pray.
I care and if that helps at all i am pleased to offer.
In respect and friendship
Aaron.
http://journals.aol.com/whisperoangels2/JUSTMEMISERYANDCOMPANY/
Depression is very insidious, before it's recognized for what it is can become very serious.
If I were there I would give you a big hug. To open up and talk about it is so important and you are in the right place. J-Landers are here to support one another.
Talk, talk and talk some more. The more you talk the more you can hear yourself and sometimes that helps us sort through the yucky stuff.
Hang on honey and I'm here if you need to talk.
Deb
I'm so glad you wrote this entry. It helps me understand what Lupus really is and does, and helps me know you better too. There are so many diseases out there, so many people experiecing such horrible things. Sometimes I am at a loss for words. But not when I pray. My heart says what I cannot. Praying for you all the time.Hugs, and love too. *Barb*
http://journals.aol.com/barbpinion/HEYLETSTALK
http://journals.aol.com/barbpinion/BOTHSIDESOFTHECOIN
I checked out Loretta's posting. It was quite interesting. I commend you and I think you are so brave for doing this entry! I have been where you have been with chronic illness and depression. I fight it constantly. We will pray for each other :-)! God bless you, dear friend! xox
ah yes........I understand this. MS is the same way, mine is different than snyone else's. MS causes depression too.
Never take the blues lightly.....the can be very dark indeed sweet lady.
Yes, Lu... I had you in mind along with some of our other lupie pals...and...synchronicity...I had just gotten the final results from my neuropsych testing last week.
Thanks for linking!
Loads of Love,
Loretta
Lu dear, I congratulate you with all my heart for choosing to write about this trying and frightening experience! I am praying that as you write, share and read responses that the Lord will bless your heart, your body and your life as you see how you help and inspire others!
loving you
karyl
The Lord be with you..........You are in my prayers.
Eileen
LuAnne Honey, It is really good to know when there is something going on with yourself. Because when you discover this, you can get help. And it is also good to talk about it and write about it. When I came out in my journal I was so glad I did, it was such a freeing thing. Now I can discuss the depression and other emotional problems whenever I want and people do seem to understand. And still really care. I am so glad you are really dealing with everything and getting the help you need. If you ever need ANYTHING, email or IM me. I am here to listen. -Krissy
http://journals.aol.com/fisherkristina/SometimesIThink
First of all, LuAnne...I owe you a huge apology.
I had not read the journal entry in full. I have no idea what happened and I make no excuses. I am so very very sorry and hope you can forgive me for this.
I believe that God had us cross paths for a reason. I am learning much from you...and consider you to be a blessing in my life.
Your suffering carries my tears with yours.
You have shown an incredible amount of courage in sharing this part of your life, simply, clearly, honestly... you are helping those who are afraid to seek help for themselves.
Depression and lupus can hit anyone.
Anyone.
Thank you for being brave.
Thank you for going to the hospital.
Thank you God that LuAnne is home again, and Lu, many special prayers for you tonight. Once again, I am so sorry that I did not comprehend this entry the first time I was here.
With all of my love,
Loretta
Hello Luanne & Happy Anniversary.
I just found this site last night (Wednesday, January 19th, 2005)
I woke up yesterday recognizing for the first time that there is a difference between feeling sad or blue and suffering from depression. I have systemic lupus but because of everything that's occurred in the last few years, severe Agoraphobia is the one single symptom I can say has honestly brought me to my knees. I hae meds for this, pain killers for that, a Rheumotologist, great psycho "ologist", and a pleasant but not so good therapist. We have long distance phone sessions. BUT before I get into any details about myself, my physical health, and my emotional status I wanted to address a rather bizarre coincidence.
I haven't figured out how to find Lorretta's journal but I'm very interested in reading about Lupus and Pshychological Testing. Aside from discussions about fatigue, pain, and not feeling well on any given day, no one has ever addressed or linked Lupus with my various emotional and psychological symptoms. Privately I've always wondered - Hmmm.
Anyway, I don't know how to follow up on this entry but I must tell you that
May 13, 2003 is also the day for me when life as I knew it stopped and nothing will ever be the same again. Somehow I've managed to keep myself out of a hopital psychiatric wards but I'd love to share a story with you about what happened to me when I had a panic attack and went to an emergency room in July of 2002. Yes, we must always keep a sense of humor. I'd forgotten that until I found you.
God Bless and I'll check in regularly. Please advise how I best to communicate after today.
To everyone else who's reading this: See you soon and am wishing you all the best.
Carol (My screen name's Miss Colman)
Hello Luanne & Happy Anniversary.
I just found this site last night (Wednesday, January 19th, 2005)
I woke up yesterday recognizing for the first time that there is a difference between feeling sad or blue and suffering from depression. I have systemic lupus but because of everything that's occurred in the last few years, severe Agoraphobia is the one single symptom I can say has honestly brought me to my knees. I have meds for this, pain killers for that, a Rheumotologist, great psycho "ologist", and a pleasant but not so good therapist. We have long distance phone sessions. BUT before I get into any details about myself, my physical health, and my emotional status I wanted to address a rather bizarre coincidence.
I haven't figured out how to find Lorretta's journal but I'm very interested in reading about Lupus and Pshychological Testing. Aside from discussions about fatigue, pain, and not feeling well on any given day, no one has ever addressed or linked Lupus with my various emotional and psychological symptoms. Privately I've always wondered - Hmmm.
Anyway, I don't know how to follow up on this entry but I must tell you that
May 13, 2003 is also the day for me when life as I knew it stopped and nothing will ever be the same again. Somehow I've managed to keep myself out of a hospital psychiatric wards but I'd love to share a story with you about what happened to me when I had a panic attack and went to an emergency room in July of 2002. Yes, we must always keep a sense of humor. I'd forgotten that until I found you.
God Bless and I'll check in regularly. Please advise how to communicate after today.
To everyone else who's reading this: See you soon and am wishing you all the best.
Carol (My screen name's Miss Colman)
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