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employer moved me
Discovered private nhs employer has moved me from room on my own to room with other staff during my absence from work after emergency hip replacement surgery with no consultation šhave RA and on
anti
tnf
medication and been in room on own since return to work in 2020 and choose to wear face mask still
Discovered private nhs employer has moved me from room on my own to room with other staff during my absence from work after emergency hip replacement surgery with no consultation šhave RA and on
anti
tnf
medication and been in room on own since return to work in 2020 and choose to wear face mask still
1984cockapoo
in
NRAS
3 months ago
CHANGE OF BIOLOGIC TREATMENT
These are all
anti
TNF
drugs as was ENBREL (ETANERCEPT) which has worked well for me in the past. I am seeing the rheumatologist nurse on Tuesday morning so I would greatly appreciate any feedback from anyone who has/is on either of the 3 biologics named drugs above.
These are all
anti
TNF
drugs as was ENBREL (ETANERCEPT) which has worked well for me in the past. I am seeing the rheumatologist nurse on Tuesday morning so I would greatly appreciate any feedback from anyone who has/is on either of the 3 biologics named drugs above.
JGBH
in
Arthritis Action
3 months ago
R A 4 anti tnf on bariticinib 2mg
Severe RA since 1995 has anyone had 2nd total hip replacement ,one keeps dislocating had it 22yrs .
Severe RA since 1995 has anyone had 2nd total hip replacement ,one keeps dislocating had it 22yrs .
Elephant100
in
NRAS
9 months ago
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Flare? Or has biologic stopped working?
I also have melanoma so cannot use
anti
TNF
biologics. What happens now ?
I also have melanoma so cannot use
anti
TNF
biologics. What happens now ?
Gilliancheche
in
NRAS
10 months ago
Reprise for Leflunomide
My rheumy offered me Retuximab but itās
anti
TNF
so the opposite of the cancer treatment, I would rather stick with this or sulfasalazine if it doesnāt work. Any thoughts? xx
My rheumy offered me Retuximab but itās
anti
TNF
so the opposite of the cancer treatment, I would rather stick with this or sulfasalazine if it doesnāt work. Any thoughts? xx
Lyndy
in
NRAS
11 months ago
Cancer messes up RA treatment
I was finally prescribed tocilizumab (you can't take
anti
-
TNF
biologics after cancer) this spring, but it immediately started suppressing my white blood count. All summer I underwent periods of coming off the toci, waiting until my WBC rose, restarting and watching it plummet again.
I was finally prescribed tocilizumab (you can't take
anti
-
TNF
biologics after cancer) this spring, but it immediately started suppressing my white blood count. All summer I underwent periods of coming off the toci, waiting until my WBC rose, restarting and watching it plummet again.
sibilant
in
NRAS
6 months ago
Anaemia and R.Arthritis
Current drugs include, Imraldi injections once a fortnight (
Anti
TNF
), methotrexate once a week, with folic acid and
anti
inflammatories (and blood pressure tablets due to high BP).
Current drugs include, Imraldi injections once a fortnight (
Anti
TNF
), methotrexate once a week, with folic acid and
anti
inflammatories (and blood pressure tablets due to high BP).
Cutes
in
NRAS
8 months ago
RA Bad in Feet - But Feet Not in DAS - So No New Meds
Iāve tried an
anti
-
TNF
inhibitor adalimumab (Humira), and rituximab (Trumira) but to no avail. In both cases the rheumy nurses ensured that the DAS (disease activity score) was over 5.1.
Iāve tried an
anti
-
TNF
inhibitor adalimumab (Humira), and rituximab (Trumira) but to no avail. In both cases the rheumy nurses ensured that the DAS (disease activity score) was over 5.1.
Jimminey
in
NRAS
1 year ago
Vabysmo or Eylea
Hi All, I need an urgent advice from the experts here. My father's dry amd has recently progressed to wet and we have been advised to get an Anti VEGF injection. He has advanced glaucoma as well and this is his only working eye (left). The other eye is already affected by glaucoma (90-95%). We are
Hi All, I need an urgent advice from the experts here. My father's dry amd has recently progressed to wet and we have been advised to get an Anti VEGF injection. He has advanced glaucoma as well and this is his only working eye (left). The other eye is already affected by glaucoma (90-95%). We are
VikPa
in
Macular Society
4 months ago
Update *may be sensitive for some*
Update
I havenāt posted in a while but thought I would give an update. Iām now 24 weeks pregnant and have had a semi-smooth pregnancy so far some of the symptoms Iāve had are;
Symptoms
- light bleed (turned out I am A- (RhD Neg) so needed to get the preventative anti D shot early.
Update
I havenāt posted in a while but thought I would give an update. Iām now 24 weeks pregnant and have had a semi-smooth pregnancy so far some of the symptoms Iāve had are;
Symptoms
- light bleed (turned out I am A- (RhD Neg) so needed to get the preventative anti D shot early.
Novbby
in
Fertility Network UK
8 months ago
At my wits end
After suffering with stomach issues for an absolutely years (getting progressively worse each year) I was eventually given a test from the GP, the stool sample flagged something so was sent off to gastro. They did the usual colonoscopy which came back with ulcers in the colon. They took samples, which
After suffering with stomach issues for an absolutely years (getting progressively worse each year) I was eventually given a test from the GP, the stool sample flagged something so was sent off to gastro. They did the usual colonoscopy which came back with ulcers in the colon. They took samples, which
FedupwithIBS1
in
IBS Network
8 months ago
ITP, Need your help
In May 2016, some purpura and Petechia was observed in my legs, to know about it I did CBC. CBC report showed that Platelets of my blood had reached about 47,000 and by passage of 20 days it decreased and reached to 10,000. Beside this I had heavy bleeding and Epistaxis along with purpura. I stated
In May 2016, some purpura and Petechia was observed in my legs, to know about it I did CBC. CBC report showed that Platelets of my blood had reached about 47,000 and by passage of 20 days it decreased and reached to 10,000. Beside this I had heavy bleeding and Epistaxis along with purpura. I stated
Homayoon
in
ITP Support Association
8 months ago
Unable to take NSAID's due to blood thinners...
I suffer from chronic glute/back pain due to lumbar spinal stenosis, but am unable to take NSAID's due to taking Rivaroxaban blood thinners. Is there any effective pain killer that I can take?...
I suffer from chronic glute/back pain due to lumbar spinal stenosis, but am unable to take NSAID's due to taking Rivaroxaban blood thinners. Is there any effective pain killer that I can take?...
geoffpuma
in
Pain Concern
2 days ago
day6 embryos
hi everyone, I have a day 6 embryo that has been frozen. I have heard that day 5 embryos are better than day6 and success rate is higher for day5. Although my day5 euploid didnāt implant. Can anyone share their experiences with day 6 embryo and what was done to improve the chances of pregnancies.
hi everyone, I have a day 6 embryo that has been frozen. I have heard that day 5 embryos are better than day6 and success rate is higher for day5. Although my day5 euploid didnāt implant. Can anyone share their experiences with day 6 embryo and what was done to improve the chances of pregnancies.
Shwet_16
in
Fertility Network UK
3 days ago
broken bones and MPN
Iāve never broken any bone in my body but last week I broke my ankle. Iāve been told itās a stable fracture and have been given a boot and crutches. I do normally have bone pain anyway but my lower leg is extremely painful and hot to touch. Iām taking zapain full daily dose but itās only barely touching
Iāve never broken any bone in my body but last week I broke my ankle. Iāve been told itās a stable fracture and have been given a boot and crutches. I do normally have bone pain anyway but my lower leg is extremely painful and hot to touch. Iām taking zapain full daily dose but itās only barely touching
Val_P
in
MPN Voice
4 days ago
menopur only protocol? Pcos ivf
hello! Has anyone been on a menopur only protocol? How was your success? i am due to start a menopur only protocol , 300 iu for 2 days then 150 iu on wards didnt respond too well to gonal f 112 iu on the first round I was 25 and good amh and normal bmi - i have pcos
hello! Has anyone been on a menopur only protocol? How was your success? i am due to start a menopur only protocol , 300 iu for 2 days then 150 iu on wards didnt respond too well to gonal f 112 iu on the first round I was 25 and good amh and normal bmi - i have pcos
Hidden
in
Fertility Network UK
4 days ago
Stage 3 A chronic kidney disease
One year ago I had a GFR of 60+ . I had a bad fall that tore a foot tendon in half and is inoperable so I was using heavy doses of ibuprofen for pain. after a few months of this my GFR started deteriorating and is now 25 . yesterday a lab result showed Parathyroid Hormone Intact Molecule 125 pg
One year ago I had a GFR of 60+ . I had a bad fall that tore a foot tendon in half and is inoperable so I was using heavy doses of ibuprofen for pain. after a few months of this my GFR started deteriorating and is now 25 . yesterday a lab result showed Parathyroid Hormone Intact Molecule 125 pg
mendobear53
in
Kidney Disease
5 days ago
Where to go next? Please help!
Hi all Firstly, sorry for the length post. Iām desperate for adviceā¦ Weāve just had a failed cycle at ARGC. 3 blasts sent for PGT-A testing, all come back abnormal. The follow-up consultation was extremely thorough. Weāve had karyotype tests (normal), hysteroscopy (normal), at beginning of cycle: FSH
Hi all Firstly, sorry for the length post. Iām desperate for adviceā¦ Weāve just had a failed cycle at ARGC. 3 blasts sent for PGT-A testing, all come back abnormal. The follow-up consultation was extremely thorough. Weāve had karyotype tests (normal), hysteroscopy (normal), at beginning of cycle: FSH
Vivkim
in
Fertility Network UK
6 days ago
New to group
Good morning, I just found this group online while looking for a support group for my husbandās demyelinating syndrome. I have been through the wringer with chronic back pain due to degenerative disc disease since 1989. I try not to let my pain define me, though. My new pain specialist recommended
Good morning, I just found this group online while looking for a support group for my husbandās demyelinating syndrome. I have been through the wringer with chronic back pain due to degenerative disc disease since 1989. I try not to let my pain define me, though. My new pain specialist recommended
TrueBlue1212
in
Pain Concern
12 days ago
Private care?
Hi everyone, I'm in a desperate situation which I am sure a lot of you can relate to. Quickly, my story: At 24 years old, I have had severe period pains since I started menstruating 12 years ago. Cramps in lower tummy, back, and most painfully, all down my legs, front and back. The leg pains have
Hi everyone, I'm in a desperate situation which I am sure a lot of you can relate to. Quickly, my story: At 24 years old, I have had severe period pains since I started menstruating 12 years ago. Cramps in lower tummy, back, and most painfully, all down my legs, front and back. The leg pains have
mousemeb
in
Endometriosis UK
14 days ago
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