Allow yourself to share your experience with this invisible illness and help yourself and others too. Share your tools, how you deal with everyday life, and gain access to information on Chronic Fatigue and Immune Dysfunction Syndrome and Fibromyalgia (CFIDS/FMS). My mission is to empower patients to take control of their health by providing my own story and experience with treatment information, quality health products, community, and advocacy.
Wednesday, July 14, 2010
What did I do?
Hi Everyone!
Oh boy, I did it! What I messed up my blog template and do not know how to fix it. I have no idea what I am doing except for loosing all of my data. Scary. Wish me luck. I don't even know where to start
I hope you are doing well these days. I have been trying to update my site slowly. Jerry is finally out of the hospital, so I was able to sleep last night.
Glad to hear your husband is out of the hospital. All the best for his recovery.
I have just a comment on fibro. My rheumatologist suggested to have me tested for sleep apnea, and after being on the machine for 4 months, I think it's making a difference. Just a suggestion for the readers. Thanks.
When I went to visit a Rheumy specialist years ago, he told me to loose weight and assumed I ate tortillas and Mexican food all of the time! He was not only rude, he was uneducated on how to listen and talk to patients. Never again.
I know there are some good specialist out there, I am just not willing to place myself in that situation again. My PCP wanted me to complete a sleep study when I was unemployed and had no insurance. No luck. Perhaps I will consider it someday. However, for now my husband has been diagnosed with Sleep Apnea...so one person at a time:(
8 comments:
Viv! Been there done that! You have my prayers!
Hi Dominique,
I hope you are doing well these days. I have been trying to update my site slowly. Jerry is finally out of the hospital, so I was able to sleep last night.
Will visit your site soon. Soft hugs your way!
I hope for your recovery from illness.
work from home
Hello Stela,
Thanks for your well wishes and for stopping by by blog site.
Glad to hear your husband is out of the hospital. All the best for his recovery.
I have just a comment on fibro. My rheumatologist suggested to have me tested for sleep apnea, and after being on the machine for 4 months, I think it's making a difference. Just a suggestion for the readers. Thanks.
Glad to hear your husband is out of the hospital, and I hope for a good and quick recovery.
Just a suggestion for fibro readers: my rheumatologist had me get a sleep apnea test and after 4 months I think it makes a difference. Thanks.
Thank you for visiting my blog site. I pray that God's Grace will carry you beyond your best desires.
When I went to visit a Rheumy specialist years ago, he told me to loose weight and assumed I ate tortillas and Mexican food all of the time! He was not only rude, he was uneducated on how to listen and talk to patients. Never again.
I know there are some good specialist out there, I am just not willing to place myself in that situation again. My PCP wanted me to complete a sleep study when I was unemployed and had no insurance. No luck. Perhaps I will consider it someday. However, for now my husband has been diagnosed with Sleep Apnea...so one person at a time:(
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