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Experiences with
Plaquenil
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Does anyone take fluoxetine for raynauds and does it help at all?
I'm also taking
plaquenil
and ibuprofen 400mg. Thank you :) xxx
I'm also taking
plaquenil
and ibuprofen 400mg. Thank you :) xxx
Belee
in
LUPUS UK
11 years ago
Pain under the fingernails and toenails
I'm on
Plaquenil
and mycophenolate mofetil.
I'm on
Plaquenil
and mycophenolate mofetil.
Purpletop
in
LUPUS UK
11 years ago
A work colleague has just had shingles vaccination which I understand is a live vaccine what, if anything should I do?
I take thyroxin and
plaquenil
and naprosyn. I had alot of pain in my joints but this has improved since taking meds. I was on prednisolone until January.
I take thyroxin and
plaquenil
and naprosyn. I had alot of pain in my joints but this has improved since taking meds. I was on prednisolone until January.
AllyGY2013
in
Vasculitis UK
11 years ago
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Anyone: have you been diagnosed with Achenbach syndrome (paroxysmal haematoma of fingers (& toes)) or Ehlers Danlos?
She says the SLE treatment plan I'm on (
plaquenil
, Amitriptyline, pred tapers & about to start mycophenolate) is appropriate, and no extra treatment for my bleeds is necessary because there is nothing serious underlying these bleeds. Phew!
She says the SLE treatment plan I'm on (
plaquenil
, Amitriptyline, pred tapers & about to start mycophenolate) is appropriate, and no extra treatment for my bleeds is necessary because there is nothing serious underlying these bleeds. Phew!
Barnclown
in
Scleroderma & Raynaud's UK (SRUK)
10 years ago
Anyone: have you been diagnosed with Achenbach syndrome (paroxysmal haematoma of fingers (& toes)) or Ehlers Danlos?
She says the SLE treatment plan I'm on is appropriate (
plaquenil
, Amitriptyline, pred tapers & about to start mycophenolate + all my 'holes' have treatment plans which are more or less effective (eyes, mouth, nose, undercarriage (sorry)) and no extra treatment for my bleeds is necessary because there
She says the SLE treatment plan I'm on is appropriate (
plaquenil
, Amitriptyline, pred tapers & about to start mycophenolate + all my 'holes' have treatment plans which are more or less effective (eyes, mouth, nose, undercarriage (sorry)) and no extra treatment for my bleeds is necessary because there
Barnclown
in
The Australian Sjögren's Syndrome Association
10 years ago
clexane
They also are suggesting
plaquenil
for the pain and for its mild anticogualant effects and also for the lupus type symptoms I have (they are retesting for lupus as I am a weak positive). Still new to all this.
They also are suggesting
plaquenil
for the pain and for its mild anticogualant effects and also for the lupus type symptoms I have (they are retesting for lupus as I am a weak positive). Still new to all this.
stillwaiting
in
Hughes Syndrome APS Forum
11 years ago
Hey ladies and gents,with mild lupus, how often is your rhumetologist suppose to check your blood? I was diagnosed end of June..on plaquenil
(with Rheumetologist)..saw him september..he said nothing...my gp thought it weird no more blood tests...when i go back it will be at 5.5 month mark......Afriend thought i should have had some in 3 month period......Im more tired now, than i was back then............
Plaquenil
cut to 1, funny side effects
(with Rheumetologist)..saw him september..he said nothing...my gp thought it weird no more blood tests...when i go back it will be at 5.5 month mark......Afriend thought i should have had some in 3 month period......Im more tired now, than i was back then............
Plaquenil
cut to 1, funny side effects
dgleds
in
LUPUS UK
11 years ago
Anyone experience muscle spasms all over their body? Also feeling faint and shakey almost like a lack of sugar, but eating doesn't help!
I have recently started taking
Plaquenil
(6 months). I have been experiencing muscle spasms and feeling shakey and faint at times. Wasn't sure if this is a side effect of the new pills? Anyone have the same? I am seeing my consultant next week, but really interested to know peoples experiences?
I have recently started taking
Plaquenil
(6 months). I have been experiencing muscle spasms and feeling shakey and faint at times. Wasn't sure if this is a side effect of the new pills? Anyone have the same? I am seeing my consultant next week, but really interested to know peoples experiences?
JMA_10
in
Hughes Syndrome APS Forum
11 years ago
am 54 had 12 PEs 25 yrs ago.past 2 years hav TIAs , mild stroke ,carotid surgery ,flares joint pain ++ANA and just had 2nd mild pos
- I am on cocktail of drugs inc aspirin,
plaquenil
persantine and amitriptine
- I am on cocktail of drugs inc aspirin,
plaquenil
persantine and amitriptine
Murphy0866
in
Hughes Syndrome APS Forum
11 years ago
Is anyone using low dose naltrexone?
My rheumatologist has asked me to try
Plaquenil
, which I am finding very hard to tolerate and I am interested in the potential promise offered by low dose naltrexone (LDN), as an alternative to steroids, etc.
My rheumatologist has asked me to try
Plaquenil
, which I am finding very hard to tolerate and I am interested in the potential promise offered by low dose naltrexone (LDN), as an alternative to steroids, etc.
MrsMouseSJ
in
LUPUS UK
11 years ago
September's Guest Blog - Brenda Ryder (Member of the Eclipse Support Group)
When I was diagnosed with lupus in 1998 I was prescribed
plaquenil
and advised to wear sunscreen and a hat in summer. Although my other symptoms began to improve, my light sensitivity became increasingly severe to the extent that I was housebound.
When I was diagnosed with lupus in 1998 I was prescribed
plaquenil
and advised to wear sunscreen and a hat in summer. Although my other symptoms began to improve, my light sensitivity became increasingly severe to the extent that I was housebound.
Paul_Howard
LUPUS UK
in
LUPUS UK
11 years ago
Does anyone take LDN(low dose naltrexone) and plaquenil?
It doesn't seem that they are incompatible together as the LDN supposedly increases endorphin levels and
plaquenil
,well,as I understand it the jury is still out there, but it does seem to work differently.I'd be interested in any feedback.
It doesn't seem that they are incompatible together as the LDN supposedly increases endorphin levels and
plaquenil
,well,as I understand it the jury is still out there, but it does seem to work differently.I'd be interested in any feedback.
StevePT
in
Hughes Syndrome APS Forum
11 years ago
Bio-Injections??
and have been controlling it with Mxt,
Plaquenil
, sulfasalazine and mobic but at my last appointment with my rheumatologist she suggested that we might have to start looking at bio-injections. Needless to say freaked me out a little!
and have been controlling it with Mxt,
Plaquenil
, sulfasalazine and mobic but at my last appointment with my rheumatologist she suggested that we might have to start looking at bio-injections. Needless to say freaked me out a little!
JessieW82
in
NRAS
11 years ago
Methotrexate or azathioprine?
Hi All, I was diagnosed with sle in february & started on
plaquenil
, prednisone & tramadol for knee pain. When I last saw my rhuemy he said I have arthritis too & need to go on either methotrexate or azathioprine as
plaquenil
alone isn't working. Researched both & don't want to go on either.
Hi All, I was diagnosed with sle in february & started on
plaquenil
, prednisone & tramadol for knee pain. When I last saw my rhuemy he said I have arthritis too & need to go on either methotrexate or azathioprine as
plaquenil
alone isn't working. Researched both & don't want to go on either.
sezzie
in
LUPUS UK
11 years ago
Warfarin withdrawal, now I am worried
I am really scared I think I have had TIAs, but if I am put back to aspirin or plavix ( which did not work) or
plaquenil
which I reacted badly too twice. My life will end, I can't function, in fact I can't even see properly if my INR goes below 3. Gosh this is so scary.
I am really scared I think I have had TIAs, but if I am put back to aspirin or plavix ( which did not work) or
plaquenil
which I reacted badly too twice. My life will end, I can't function, in fact I can't even see properly if my INR goes below 3. Gosh this is so scary.
Jade
in
Hughes Syndrome APS Forum
11 years ago
How to transfer from one Consultant at St. Thos, to another within the Lupus unit.
I also take
Plaquenil
, which after about 4 months improved me tremendously, however that improvement has vanished and the Cognitive Impairment is very bad and I feel concerned about my ability to function with daily paperwork etc.
I also take
Plaquenil
, which after about 4 months improved me tremendously, however that improvement has vanished and the Cognitive Impairment is very bad and I feel concerned about my ability to function with daily paperwork etc.
Zamalek
in
Hughes Syndrome APS Forum
11 years ago
On clopidogrel, going on a 4.5 hour flight - do I need more?
I'm on 75mg clopidogrel (and
plaquenil
). I've read the stuff about flying on the HSF website. The flight is 4.5 hours. Should I be asking my GP about whether I need any additional blood thinner or should I try to contact prof K? Do I even need to bother seeing as I've never had any clots?
I'm on 75mg clopidogrel (and
plaquenil
). I've read the stuff about flying on the HSF website. The flight is 4.5 hours. Should I be asking my GP about whether I need any additional blood thinner or should I try to contact prof K? Do I even need to bother seeing as I've never had any clots?
Paleosooze
in
Hughes Syndrome APS Forum
11 years ago
Possible Plaquenil side effects?
My latest being: I started on 200mg/day
Plaquenil
12 days ago and am experiencing what would seem to be very unpleasant side effects.
My latest being: I started on 200mg/day
Plaquenil
12 days ago and am experiencing what would seem to be very unpleasant side effects.
MrsMouseSJ
in
Hughes Syndrome APS Forum
11 years ago
"Tissue bleeds" anyone?
I'm on daily 40mg
plaquenil
+ nightly 20mg Amitriptyline + 3x 4week 10mg pred tapers per year + various topical steroids on maintenance regimes including high strength dermovate. Am having a series of steroid injections in my feet for mortons neuromas + bursitis.
I'm on daily 40mg
plaquenil
+ nightly 20mg Amitriptyline + 3x 4week 10mg pred tapers per year + various topical steroids on maintenance regimes including high strength dermovate. Am having a series of steroid injections in my feet for mortons neuromas + bursitis.
Barnclown
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Info please: wondering about my "tissue bleeds"
I'm on daily 40mg
plaquenil
+ nightly 20mg Amitriptyline + 3x 4week 10mg pred tapers per year + various topical steroids on maintenance regimes including high strength dermovate. Am having a series of steroid injections in my feet for mortons neuromas + bursitis.
I'm on daily 40mg
plaquenil
+ nightly 20mg Amitriptyline + 3x 4week 10mg pred tapers per year + various topical steroids on maintenance regimes including high strength dermovate. Am having a series of steroid injections in my feet for mortons neuromas + bursitis.
Barnclown
in
Vasculitis UK
11 years ago
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