Discussion on intro-to-my-crazy-ness-debimaddox
kennedy...@yahoo.com
if mine has gotten better, I have been taking Embrel or Inbrel or
whatever its called injections and they are making all the difference,
still have pain but don't have the swelling so much and my hands and
feet and shoulders and elbows actually work as long as I stick myself
once a week every week and don't get behind...... I havn't heard from
you in so long. I don't know what all you have tried, I know like
myself they started you out on methotrexshit! I hated that crap, made
me sick..... Deb you need to keep me posted, I will check your sight,
you have my e-mail address.... let me know whats up I'm at work and
don't wanna get in trouble for misuse of the companies crappy
computers but I'll check on you periodically
debra maddox
debraBmaddox
out everyone,, loves contoll too,,hehehehee(just thinkin bout the
goodol days)
On Sep 12, 9:24 am, "debra maddox" <debrabmad...@gmail.com> wrote:
> hi aaron u'd be surprised to know that we do think of U Alot INFACT- i
> even told kelly just the other day,
> ,"funny how Cavalry placed <UNKNOWINGLY> 2 ppl with RHEUMATOID
> side-by-side desks and ..thats JUST FREAKY to me, isnt it to u?
> I menan 1 percent of the population,,and im just suprised Im in that 1% and
> U TOO!!!!!!!!!!
> ok -im just trippin on that fact and you should TOO! because it is a weird
> thing,,i HAVE TO BLOG that today on my site where i try to keep a diary of
> RA and how i am doing on a daily basis ,,im either crying OR laughing,,its
> all so "dramatic" w/me u know,,,LOLhttp://ihatera.blogspot.com/
> dunno if u have internet,but heres a link to that blog and i am really just
> so glad 2 hear that u r OK an doing goodi have NOT tried ENBRIL,,it is the
> OLNY thing i have NOT tried,,otherwise "been there-done that-didnt work-
> results are always the same = IT only make RA mad and come back harder
> everytime"
> i would love to try Embril but for now i do not have a rheumatolojust ..i
> was with Dr McKay over here right around the corner from my friggen house,,
> they still have my files and thats OK for now,,i have a copy here @ home if
> i need them,,for any emergengy or new Dr.-blablabla=\
> im stable but sleep alllll the time,, i mean i will not see more then 5
> hours a day then rewst is sleeping,i have to sleep,,it makes me sick to
> styay awake,,i get swollen then inflammed and hot and go down hard,,
> so i just give up..and sleep,,
> kelly is struggling to keep us going here ..shes wrking downtown at Tulsa
> Abstract Tile-doing a legal type job.
> We barely r making it,,the meds i take are so expensive (im talking about
> the pain meds) IM ALSO still
> HOOKED ON PREDNISONE and cant survive with any less then 20 miligrams a
> day,,
> Ive gotten myself down to 15 mg BUT OMG i flared up at any sign of stress-
> i should increase to 25 mg a day BUT I REFUSE TO because it plays mental
> tricks on me -plus, its just not a good thing,
> * I see you entered the *HELL OF METHOTREXATE*- im just glad to see
> that someone else testify that shit is not a friendly drug*,,its what sent
> me to the hospitial ,i had serous isssues and became toxic liver
> or ??whatever they called it,,*but i got pulled off of the INJECTIONS of
> metho & as time went by i felt better, i begged NOT to go back to metho-and
> have stayed away from it altogether now,whew,,i better get offfa here and
> go do housethings for now-DO keeep writting *,,just thow ideas here on this
> blog/group,,and any type of RA hate ,,ahh feelings and anyhting,,man throw
> it ionhere* and ill keep getting more to sign up here k>??your friend,
> debi maddox