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Living with Sarcoidosis

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June 25

Michael Jackson

Michael Jackson dies today from cardiac arrest. He was just 50 years old and had just passed a battery of physical tests in preparation for his European tour. Now that tell you that you must live each day to the fullest because you never know. This man was of iconic status in the music community. We will definitely miss him. So many immulate him in their performance mannerisms. Usher, Rain (Bi), Chris Brown, Justin Timberlake, etc... I can name so many more. Sadly today is Rain's 28th birthday so I know this is going to hit him hard and affect his whole demeanor on his birthday. I feel for Janet who is the same age as me. I know when I lost my sister a few years ago, how long it took me to get my self back together. My spirit was at a lost. I pray for everyone today. I pray that we all live life to the fullest, because we never know when God is going to call us home. This is something for me to say because I have been feeling down a lot lately wondering what my purpose is. Having each day become a routine can drive a person mad. I say today is a wake up call for me. Lynn Live! Lynn Smile! Lynn Appreciate Life!
 
God is good all the time and all the time God is good!....
 
Peace and blessings everyone,
Lynn
7:16 PM | Add a comment | Permalink | Blog it | Music
June 03

It's my birthday...

I have made it to see another birthday! Happy birthday to me :-p! Still in a lot of pain but I'm here!
5:17 AM | Add a comment | Permalink | Blog it
June 02

not feeling well

Today is the day before my birthday and I am not feeling well. Joints and muscle pain along with dry cough and dizziness. I long for the day when I can wake up with no pain and 100lbs. lighter. I am listening to one of my favorite artist Rain. If I close my eyes I can imagine him performing just for me. Would'nt that be cool ^_^!
4:34 PM | Add a comment | Permalink | Blog it
May 29

Talking about Lynn's World

 

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1:37 PM | Add a comment | Permalink | Blog it

they have returned

the granulomas have returned in my eyes. they are again affecting my vision. dry eyes, excessive floaters and blurred vision.
12:17 AM | Add a comment | Permalink | Blog it
 

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markwrote:
Dear Lynn,
I started to cry when I read about how you fely on your daughters birthday. My youngest girl (#4) will be 9 on October the 2nd. She has already made out a list of what she wants to do that day and who she wants to invite. What kind of party she wants. I have no money for any of it and no energy to do it. I feel so tired all the time I could barely listen to her plans for the special day. I too feel bad about the mother she knows now. I was such a different mother for the other 3 kids. I had so much energy and I never sat down. I now do nothing but sit when I am home. I wish things were different. I grieve the loss of the person I used to be. I tried to tell myself that this is where God wants me to be but it is hard. We are so broke. I don't understand the purpose in any of this.
 
Take care. I will be thinking of you.
Nancy Winningham
Indiana
Sept. 22
Lynn McNeillwrote:

Sarcoidosis Support Groups

sarcoidosis%20awareness%20ribbon

  • American Lung Association of Delaware
    1021 Gilpin Avenue, Suite 202
    Wilmington, DE. 19806
    Contact: Tricia Monnig
    (302) 655-7258  (800) LUNG-USA (586-4872)
     
  • Arthritis Foundation, Delaware Chapter
    222 Philadelphia Pike
    Wilmington, DE.
    (302) 764-8254
    • July 21
    Lynn McNeillwrote:
    Believe it or not, this was my former website when I was with att.net. I received a SOS Golden Lifesaver Award, http://sarcoidosisonlinesites.com/awardgla/awardlibrary.html
    I since, as you can see, have moved and have been pleased with this server because it connects me with more people like me.
    Please sign my guest book and leave your stories in my blogs.  I would love to hear from you and chat with you all.
     
    Marilyn's Sarcoidosis Support
    home.att.net/~twin663/wsb/index.html
    Date launched: November of 2000
    Website Administrator: Marilyn (Lynn)
      My web site addresses all aspects of sarcoidosis. I chat with and e-mail a lot of fellow sufferers. The message board helps me know how my site is doing overall. This is my only outreach since I am confined to my home and cannot attend my local support meetings anymore.
    Nov. 30