Pulmy has dropped me to 3 appts/year now...and today I meet w/rheumy, so there may be a change there too...who knows...it's a crapshoot at best! Sighs, reaches for coffee, spills on lap...sheesh...more drugs to apply! Ha!
Pulmy has dropped me to 3 appts/year now...and today I meet w/rheumy, so there may be a change there too...who knows...it's a crapshoot at best! Sighs, reaches for coffee, spills on lap...sheesh...more drugs to apply! Ha!
Knowing how to think empowers you far beyond those who only know what to think. -NdT
Vdub,that is great to hear about your kids coming home. I hope you have the best Christmas ever. I too think this will take alot of stress and worry off of you and hopefully will make you feel better.
Take Care and MERRY CHRISTMAS !!!!!!!
Life isn't about how you survive the storm, but how to dance in the rain !
Thanks to your daughter for her service, and I hope she is home for good!
Anne, dx'ed April 2011
Enjoy your Christmas and family time. Best to all of you and I thank your daughter for her service.
Cindy
Earth is just a stopover and whatever you achieve there is only a small part of the deal. The Afterlife Of Billy Fingers
So happy to hear that your daughter is home and safe! My son came back from his third tour in September. The stress of the worry was awful! I hope the sigh of relief helps you feel better. Also,my daughter who has been very sick for eighteen years has often worked with her doc's to get off all meds,except the life saving meds. After while it becomes difficult to assess what is causing what and the dr adds more pills and you end up with some kind of toxic soup swishing through your body. Be well and MERRY CHRISTMAS!
I understand the feeling. I seem to be glued to my med drawer and my life evolves around it. However, I know this is what keeps me alive. I also remember what it was like when Weggies was at its height and I was too sick to even complain. Perhaps a short break is okay. I usually talk myself back into the constant tests and meds. My question for anyone is - I have been on cellcept for two years and aranesp injections but still have very low haemoglobin. So low that I am at intervenus level. All my lab tests looked worse this time. The doctor reduced Cellcept a few months ago and Weggies came out of remission. I saw my lab results at family doctor's office but don't see specialist for a week. I think he will change the Cellcept as specialist at Mt. Sinai said it couldn't continue this way. Any ideas?
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