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April 9, 2009 at 3:01 pm #302109DARParticipant
I am having trouble with my right hand swelling and hurting all the time this started about 2 weeks after my iv predisone treatment, I use to take these treatments every week and now my dr has changed them to every 3 weeks is this from the change in the predisone treatments or is it a sign that the scleroderma is flaring?:angry:
April 9, 2009 at 9:12 pm #328735MazKeymaster[user=387]DAR[/user] wrote:
I am having trouble with my right hand swelling and hurting all the time this started about 2 weeks after my iv predisone treatment, I use to take these treatments every week and now my dr has changed them to every 3 weeks is this from the change in the predisone treatments or is it a sign that the scleroderma is flaring?:angry:
Hi DAR,
I'm not an expert on this, but I would think that the reduction of your prednisone from weekly IVs to 3-weekly IVs is quite a big drop and you are likely suffering some rebound flaring. So probably both…change of dosing and flaring, as a result.
I haven't heard of many here having IV prednisone, but if you're suffering it might not be a bad idea to speak with your prescribing physician and ask if you can lower your doses a little more slowly. I don't know much about IV predinsone (its half life, doses, reasons for its use, etc)…are you using it for a particular reason as opposed to taking oral prednisone? Just wonder if orals might be easier to to wean from over time?
Peace, Maz
April 10, 2009 at 2:14 pm #328736DARParticipantThanks for the replay, I think that the dr put me on the iv's because it is easier on my stomach, right now I take prilosec 2x every day to keep the acid down, but with my hand hurting the way it does I think I would rather put up with more stomach acid than this,
Thanks Darlene
April 10, 2009 at 7:13 pm #328737superperroRAParticipantI recently learned that Voltaren is available as suppositories. This might be an option for people like you in danger of GI bleeding. Better than prednisone, in my opinion
April 11, 2009 at 5:50 am #328738Rockin AnnieParticipantHi Dar,
I don't know if this will help at all, but I am weaning off pred, I was on 5mg and wean 1/4 of a mg every 2 weeks and even that small amount I go through hell with my wrists. I am only down to 3 1/2 but will keep on till I am off it completely.
Just wanted to let you know just how even small amounts of weaning can effect you.
Hope you can get to the bottom of your pain…………..Annie
Diagnosed with RA in 2004, after trying many conventional meds I changed to mino.
2015 changed to doxy 50mgs
2016 went off doxy, after getting double pneumonia and massive flare put myself on 250 mgs Zith & 50 mgs doxy, which I will increase slowly.
Supps, magnesium, NAC, vit c, krill oil, oregano oil, thisylin, turmeric, olive leaf extract, vit B, multi vit.April 11, 2009 at 7:14 am #328739RandyParticipantHi DAR,
Sounds like you are getting some decent advice here. I might add that Dr. F. told me that Prednisone is VERY BAD for SD. Forgive me, but I don't know any more than this. You may want to research this, or maybe someone will chime in who can speak more knowledgeably.
Randy
Diffuse SD since Apr '07
AP since Feb '08
100mg Mino twice daily
Stopped Clindamycin IVs Aug 2019
"No one should profit over someone else's illness" -
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