Well, today is 2/2/08. I havn't gotten many replies to my requests to make friends. I need people to talk to about this diagnosis. I am scared and feel very alone. I sure hope this site is not a joke to people.
We are here Kate trust me and this site has basically saved my life. Lots of people here use computer at work and dont have one at home. You will be a friend for everyone and just give em time. Many get on at night also. You will be just fine,,,we love you.
Nice to meet you.
Sorry, I\'ve been sick with the flu and just been off and on this past week.
No, this site isn\'t a joke. It\'s serious business with alot of fun at the same time.
You always have to remember to smile. Belly laughs are best medicine.
Also, my day\'s start rather early when my father wakes up and I\'m really not able to get on the computer until his bedtime.
I would love to hear from you.
I know all too well the fear, frustration, confusion and feeling of helplessness.
Message me anytime and we can talk.
Just know for sure...you are not alone. You are with the best people in the world.
Again, nice to meet you and hope to hear from you soon.
Tasmoe
Hey there,Sweety.You\'ve come to a sweet and caring lot of people.I\'m recently diagnosed too.You are not alone.We are all here.:)
I\'m afraid too.But...i figure you just keep on going.I know i got it...not sure how(maybe fun in my youth...maybe a transfusion...maybe a tattoo on my ass in my midlife crises!)LOL
The important thing is to do what you can to get medical attention to it,support ,try to get it the hell out of our bodies.
No...you are definetly not alone.You are among friends.Let me know if you\'d like to talk...we can wonder about this thing together:)
I\'ve just signed up and am so glad there are now people to talk to. I\'ve been on combo treatment for 5 months now - I\'ve been exhausted - extremely dry skin and scalp (using all kinds of creams) - losing my hair now in the last 3 weeks about 50% gone - I know it will grow back but damn! Not the hair! How are you doing?
Good news for me so keep your chin up! I\'ve been on the treatment since September 07 and they have not been able to detect the virus in my blood system since November 07 - so there is lots of hope!
Replies
We are here Kate trust me and this site has basically saved my life. Lots of people here use computer at work and dont have one at home. You will be a friend for everyone and just give em time. Many get on at night also. You will be just fine,,,we love you.
Nice to meet you.
Sorry, I\'ve been sick with the flu and just been off and on this past week.
No, this site isn\'t a joke. It\'s serious business with alot of fun at the same time.
You always have to remember to smile. Belly laughs are best medicine.
Also, my day\'s start rather early when my father wakes up and I\'m really not able to get on the computer until his bedtime.
I would love to hear from you.
I know all too well the fear, frustration, confusion and feeling of helplessness.
Message me anytime and we can talk.
Just know for sure...you are not alone. You are with the best people in the world.
Again, nice to meet you and hope to hear from you soon.
Tasmoe
Hey there,Sweety.You\'ve come to a sweet and caring lot of people.I\'m recently diagnosed too.You are not alone.We are all here.:)
I\'m afraid too.But...i figure you just keep on going.I know i got it...not sure how(maybe fun in my youth...maybe a transfusion...maybe a tattoo on my ass in my midlife crises!)LOL
The important thing is to do what you can to get medical attention to it,support ,try to get it the hell out of our bodies.
No...you are definetly not alone.You are among friends.Let me know if you\'d like to talk...we can wonder about this thing together:)
I\'ve just signed up and am so glad there are now people to talk to. I\'ve been on combo treatment for 5 months now - I\'ve been exhausted - extremely dry skin and scalp (using all kinds of creams) - losing my hair now in the last 3 weeks about 50% gone - I know it will grow back but damn! Not the hair! How are you doing?
Good news for me so keep your chin up! I\'ve been on the treatment since September 07 and they have not been able to detect the virus in my blood system since November 07 - so there is lots of hope!