MSN Home  |  My MSN  |  Hotmail
Sign in to Windows Live ID Web Search:   
go to MSNGroups 
Free Forum Hosting
 
Important Announcement Important Announcement
The MSN Groups service will close in February 2009. You can move your group to Multiply, MSN’s partner for online groups. Learn More
Smiling Fibros[email protected] 
  
What's New
  
  Welcome to the Smiling Fibros Family  
  <  
  Site Disclaimer  
  <  
  Our Mission Statement  
  <  
  Fibro letters  
  Fibro Awareness  
  <  
  Messages  
  General  
  On-Going Posts  
  Chat Schedule CHECK IT OUT  
  CHAT !!!  
  Questions?  
  SFFS Scarf!  
  Member's Mailbox  
  Member Spotlight  
  SF Important Dates :)  
    
  IM id's :)  
  Smiling Memories  
  <>~<>~<>~<>~<>~<>~<>~<>  
  Hotlines & More  
  Smiling's How To  
  <>~<>~<>~<>~<>~<>~<>~<>  
  The Bolds :)  
  The "Bolds", who and what :)  
  <>~<>~<>~<>~<>~<>~<>~<>  
  Check out our Web Site  
  Links  
  If you need to reach someone  
  <>~<>~<>~<>~<>~<>~<>~<>  
  Medical Disclaimer  
  Medical ??'s  
  Medical Info  
  Important Dates!!!!  
  Where are we all from :)  
  Tell us a little about you :)  
  Our Family Tree :)  
  <>~<>~<>~<>~<>~<>~<>~<>  
  Good News Minute  
  PSP help & tips  
  Writing Room  
  Recipes  
  Smiling Recipes  
  SpiritualSmiling  
  Book &Movie Club  
  Books we like :)  
  Tribute Page  
  Games  
  Crafts  
  Jokes &Fun Stuff  
  <>~<>~<>~<>~<>~<>~<>~<>  
  Pictures  
  !!!Members Kennel Pictures!!!  
  Snaggable pics for all  
  <>~<>~<>~<>~<>~<>~<>~<>  
  I QUIT ;) :)  
    
  
  
  Tools  
 
Medical ??'s : Anemia
Choose another message board
 
     
Reply
 Message 1 of 3 in Discussion 
From: Avey_CO  (Original Message)Sent: 5/31/2008 3:49 PM
I have been diagnosed as anemic.  My vit b and iron levels are ok.  The problem seems to be that; i am low on red blood cells and those cells are low on the hemogoblin(sp) that carries oxygen to the cells.  I am on oxygen, 3L 24/7 and my levels test out ok while on oxygen.
 
Doctor doesn't seem to be too concerned since the levels have come up some since my last hopitalization the first of the month.  Didn't even suggest another blood test. 
 
I am being told that I am evidently bleeding internally and my body as of yet has not been able to catch up.  The last stomach scope showed some irritation and inflamation. 
 
Two or three years ago while hospitalized with pneumonia, I was given a transfusion of two units.  Explanation, your blood tests show that you are low on volumn.   A colonoscopy and stomach scope showed normal. 
 
Any comments or insights are welcome...............Avey
 


First  Previous  2-3 of 3  Next  Last 
Reply
 Message 2 of 3 in Discussion 
From: carenSent: 6/2/2008 1:36 AM
don't have any insight, jsut awnted to say hi and I am thinking ofyou

Reply
 Message 3 of 3 in Discussion 
From: MSN Nicknamedini747Sent: 9/4/2008 1:19 AM
Hi Avey,
I just happened to come across this post so thought I would add what I've been through. I was also diagnosed as anemic quite some years ago. The Dr. told me to take iron supplements, which I've tried 3 different kinds of. One is the "green" colored tablet, and another is "red". The "red" colored one is ferrous gluconate, 35 mg. but I forget what you call the green one. LOL! Ferrous Sulphate, maybe? I've also taken "Slow Fe" which is a "slow-release" tablet. I also know that you need vitamin C in order to absorb iron properly. Interestingly, both vitamin C and iron supplements bother my stomach quite a bit so I started to resort to eating foods that are rich in iron, like spinach, beets....I can't remember all of the iron rich foods out there. LOL! I would say getting enough iron in your diet naturally is the best way to go, though. My Dr. had a hard time explaining how I was anemic, as well, and put it this way....I wasn't making enough red blood cells and they did discover that I had an ulcer for which I was also put on medication for which was ranitidine. That seemed to help with my ulcer quite a lot. I was able to stop taking it at some point.
Interestingly, I also discovered that my father had the "thalassemia" trait or gene, so I learned that it was a genetic factor for me, as well. There's no real "cure" for it or anything like that...it's just something that you "have" due to hereditary factors.
It sounds to me like something is irritating the lining of your stomach possibly, so it sounds more like watching what you eat and maybe taking a med for ulcers might help, if your Dr. thinks that might help. Diet really plays a big role in it, I think, and balance is everything so it doesn't irritate your stomach more. Getting iron rich foods is probably the best way to go, but I would ask a nutritionist to suggest a plan that might be beneficial.
Dini