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Medical Forum / Diseases and Disorders / Lupus / August 2008

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Doing Good!!!!!!!!

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Steveo - 30 Jul 2008 21:02 GMT
Well, it has been a very long time since I posted here but I
wanted to let everyone know that Finally after 5yrs of treatment My
lupus is completely undercrontrol.  Not only that but the Kidney
desease that came along with it is finally stopped.  I guess the 8
rounds of Retuxin and all the Cellcept finally did what it was suppose
to.  Althought my Kidneys are down to 45% they are currently clean and
there is no desease activity.  So I am starting to taper off the
cellcept and all the other meds.  I have been off steroids since Feb.
so I am flippin happy.  18months of treatment that went to 5
years..........  Man, I just need to tell some people that can
understand.

-Steve
George Parton - 30 Jul 2008 21:41 GMT
Steve,
I am so happy for you!
Good news is always refreshing.
Thanks for the bright spot in my day.....
George

>      Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve
Shelagh - 31 Jul 2008 01:19 GMT
Congratulations Steveo!!
I completely 'feel' you about the steroid thing....
Now THAT is just too cool!!
And so now after 5 years you have made it!

Just keep on walkin that walk....talking that talk cause
it sounds so darn good coming from a new and healthier you!

And good luck with the tapering on the other meds...
I know you'll have no problems cause you've already
beat the 'mother' of all meds lol!!
If you can beat steroids? .... well, enough said!
hugs,
Shelagh
http://members.shaw.ca/tiderington - Lupus ~ Invisible in Plain Sight

>     Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve
Sherry - 31 Jul 2008 03:13 GMT
Great news Steve!

Sherry

>     Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve
Mair - 02 Aug 2008 17:22 GMT
Happy to hear it, Steve!

Way to go, and just keep on!

Mair

>     Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve
notamythologist@gmail.com - 19 Aug 2008 20:29 GMT
>      Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve

Rah, rah!
Steveo - 20 Aug 2008 22:44 GMT
Thanks everyone, I appriciate.  I love the fact that I can post on
this board and everyone here can relate.  When I tell my wife or my
friends they look at me like "Big Deal, you look fine".  It is
frustrating sometimes but I am very happy and already my celllcept is
cut in half.  So everyone have faith it can be fought, but it takes a
lot of work.  :)
Andy - 21 Aug 2008 11:25 GMT
In message
<08fd1694-f538-48c1-bc54-21c97b5be838@e39g2000hsf.googlegroups.com>,
>Thanks everyone, I appriciate.  I love the fact that I can post on
>this board and everyone here can relate.  When I tell my wife or my
>friends they look at me like "Big Deal, you look fine".

It's one of the symptoms ;)
Signature

Andy Taylor [Chair, N E Lupus Group].
<URL:http://www.northeastlupus.org.uk>

Shelagh - 21 Aug 2008 16:47 GMT
> In message
> <08fd1694-f538-48c1-bc54-21c97b5be838@e39g2000hsf.googlegroups.com>,
[quoted text clipped - 3 lines]
>
> It's one of the symptoms ;)

Oh yes it is  *!* ....  and the real fun starts when it becomes
the symptom you probably already know as: 'hypochondria' *?*,
which you will be labeled with for a fair period of time by doctors
and friends and family until
they finally come to realize that 'the looking so well, while feeling like
utter shyte'
is just all part and parcel of the same diagnosis:
Lupus! / the great imitator!  / disease of 1000 faces!

(hateful really when you consider all that we try to do daily, regardless of
the aches and pains and inflammation that seemingly never ends .. so that we
are seen as normal or as typical as our peers ...
and still get hung with that mouthful anyhow !!)

'Lupus / Invisible in Plain Sight' @  http://members.shaw.ca/tiderington
hugs,
Shelagh
KCat - 22 Aug 2008 02:41 GMT
Well done, Steve.

So very pleased for you.

yes, having someone who "gets it" helps a great deal.  I've got
supportive family but it wasn't always that way.  Makes a world of
difference.

>      Well, it has been a very long time since I posted here but I
> wanted to let everyone know that Finally after 5yrs of treatment My
[quoted text clipped - 9 lines]
>
> -Steve
 
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