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Query re c3 mets plus c3 degenerative arthritis
A little edited update to add a bit more of a positive vibe and lift my doom n gloom post below. Piccy of my beautiful grandson born 2 weeks before lockdown. This is our reunion after 4 months enforced separation. The faces say it all . He recognises me through facetime thank the lord. š Actual post
A little edited update to add a bit more of a positive vibe and lift my doom n gloom post below. Piccy of my beautiful grandson born 2 weeks before lockdown. This is our reunion after 4 months enforced separation. The faces say it all . He recognises me through facetime thank the lord. š Actual post
Mindysooty
in
SHARE Metastatic Breast Cancer
4 years ago
Pain relief
Hi ladies Do any of you take slow release morphine capsules? Iāve been prescribed these but just feel reluctant to take them as I hate side effects although I take codeine (cocodamol) and occasionally ocycodone for worse pain Just wondering if the slow release ones will be more effective...I want to
Hi ladies Do any of you take slow release morphine capsules? Iāve been prescribed these but just feel reluctant to take them as I hate side effects although I take codeine (cocodamol) and occasionally ocycodone for worse pain Just wondering if the slow release ones will be more effective...I want to
Barbteeth
in
SHARE Metastatic Breast Cancer
4 years ago
Rheumy telephone appointment earlier
As most of you know Iāve been struggling despite the steroid injections into the knees and starting Sulfasalazine. I had my follow up with my rheumatologist earlier this afternoon and the upshot is that the steroid injections lasted all of three weeks. The Sulfasalazine she was hoping would have had
As most of you know Iāve been struggling despite the steroid injections into the knees and starting Sulfasalazine. I had my follow up with my rheumatologist earlier this afternoon and the upshot is that the steroid injections lasted all of three weeks. The Sulfasalazine she was hoping would have had
bubblyalex
in
NRAS
4 years ago
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Iodine
Hi does anyone take iodine drops & do they help you?
Hi does anyone take iodine drops & do they help you?
Nessy50
in
Thyroid UK
4 years ago
Medication and general care concerns
Hello to all. I was diagnosed with having a degenerative disease of my lumbar spine back in July 2011. Which has been life changing. When I say I have had all treatments I really have. I have been through and exhausted the pain clinics on two occasions. I have had extensive Physiotherapy, Accupunture
Hello to all. I was diagnosed with having a degenerative disease of my lumbar spine back in July 2011. Which has been life changing. When I say I have had all treatments I really have. I have been through and exhausted the pain clinics on two occasions. I have had extensive Physiotherapy, Accupunture
Daz75
in
Action on Pain
4 years ago
Medication and general care concerns.
Hello to all. I was diagnosed with having a degenerative disease of my lumbar spine back in July 2011. Which has been life changing. When I say I have had all treatments I really have. I have been through and exhausted the pain clinics on two occasions. I have had extensive Physiotherapy, Accupunture
Hello to all. I was diagnosed with having a degenerative disease of my lumbar spine back in July 2011. Which has been life changing. When I say I have had all treatments I really have. I have been through and exhausted the pain clinics on two occasions. I have had extensive Physiotherapy, Accupunture
Daz75
in
Pain Concern
4 years ago
Flare
I think I am having a flare up, am so tired all the time and got a lot off pain in my right shoulder! I take codeine for pain relief. I normally take 2 tablets in the morning 30mg each and that normally does me the whole of the day. But am having to take nearly the maximum to have no pain. I think everything
I think I am having a flare up, am so tired all the time and got a lot off pain in my right shoulder! I take codeine for pain relief. I normally take 2 tablets in the morning 30mg each and that normally does me the whole of the day. But am having to take nearly the maximum to have no pain. I think everything
Carolsos
in
NRAS
4 years ago
Consistent Pain!
Hello! I am in the stages of finally being diagnosed after having excruciating pain and horrendous periods causing me to be on the pill from 11 years old! I was due to have surgery in April however was cancelled due to COVID and I have not heard anything since. Iām finding the pain just keeps getting
Hello! I am in the stages of finally being diagnosed after having excruciating pain and horrendous periods causing me to be on the pill from 11 years old! I was due to have surgery in April however was cancelled due to COVID and I have not heard anything since. Iām finding the pain just keeps getting
GreenQueen-99
in
Endometriosis UK
4 years ago
How much can you take
Iāve been on Fentanyl now Iām on Buprenorphine gabapentin and zapain which is 30mg codeine 500mg paracetamol thatās just the pain and 7 other different medications for other illnesses I have arthritis of the lumbar region right foot left knee left hand which I have steroid injections in every three months
Iāve been on Fentanyl now Iām on Buprenorphine gabapentin and zapain which is 30mg codeine 500mg paracetamol thatās just the pain and 7 other different medications for other illnesses I have arthritis of the lumbar region right foot left knee left hand which I have steroid injections in every three months
Stephend
in
Pain Concern
4 years ago
Radioactive iodine
I have overactive thyroid graves disease doctoers or pushing me to have
Radioactive
iodine
treatment i really dont want it i suffer form health anxiety and really really do not want to have this treatment for so many reasons i have done a lot a research on this treatment.
I have overactive thyroid graves disease doctoers or pushing me to have
Radioactive
iodine
treatment i really dont want it i suffer form health anxiety and really really do not want to have this treatment for so many reasons i have done a lot a research on this treatment.
PeppyPo
in
Thyroid UK
4 years ago
AGRANULOCYTOSIS IN THE MIDST OF COVID-19
[/i] [i]With regards to the risk of cancer following
radioactive
iodine
treatment, it is very easy for anyone who is trying to make sense of the literature to get confused.
[/i] [i]With regards to the risk of cancer following
radioactive
iodine
treatment, it is very easy for anyone who is trying to make sense of the literature to get confused.
lynmynott
Thyroid UK
in
Thyroid UK
4 years ago
Starting on thyroxine tomorrow
I had my tft bloods done on Friday and on Monday morning (very early) had a text to contact my GP with ref to them. I had a telephone appointment with her and she said that my tsh was 14.9, my previous level in November was 9.78, so she was prescribing me 25 mg thyroxine to start on and would like retests
I had my tft bloods done on Friday and on Monday morning (very early) had a text to contact my GP with ref to them. I had a telephone appointment with her and she said that my tsh was 14.9, my previous level in November was 9.78, so she was prescribing me 25 mg thyroxine to start on and would like retests
Kimkat
in
Thyroid UK
4 years ago
Urgent help needed please
Hello. Writing from acute medical ward after admission Saturday afternoon following a severe reaction to taking codeine (a single 30mg dose). It's a big ask, but if anyone reading this could reach out with any ideas as to why I have now reacted so badly to this drug when years ago I could take it, I
Hello. Writing from acute medical ward after admission Saturday afternoon following a severe reaction to taking codeine (a single 30mg dose). It's a big ask, but if anyone reading this could reach out with any ideas as to why I have now reacted so badly to this drug when years ago I could take it, I
Hoofprints
in
LUPUS UK
4 years ago
Saved by Methadone
After years on Pramipexole 0.75 mg long acting , the inevitable augmentation occurred and I got off it with great difficulty. Since that time, August 2019, I have had very little sleep. I have tried tramadol, codeine, oxycodone, lyrica, Gabapentin, clonazepam, MSContin and various combinations. I have
After years on Pramipexole 0.75 mg long acting , the inevitable augmentation occurred and I got off it with great difficulty. Since that time, August 2019, I have had very little sleep. I have tried tramadol, codeine, oxycodone, lyrica, Gabapentin, clonazepam, MSContin and various combinations. I have
wairoa36
in
Restless Legs Syndrome
4 years ago
Back pain - anyone got anything similar?
Ok, so hereās the story... 23rd June - woke up with pain in my left SI joint. Could literally pinpoint it to that spot. Iāve had a sore back before, but it was just muscle pain from overuse and was never over the SI joint. Standing and walking were both painful, and the pain disappeared when I sat or
Ok, so hereās the story... 23rd June - woke up with pain in my left SI joint. Could literally pinpoint it to that spot. Iāve had a sore back before, but it was just muscle pain from overuse and was never over the SI joint. Standing and walking were both painful, and the pain disappeared when I sat or
Chukkin
in
Pain Concern
4 years ago
Headaches
Hi everyone Iāve been having headaches almost daily for a few weeks now and Iāve been prescribed beta blockers and Sumatriptan which didnāt work at all so I contacted my GP again and was prescribed Naproxen and Omeprazole which also did not work Last week I took a trip to A&E and they took blood tests
Hi everyone Iāve been having headaches almost daily for a few weeks now and Iāve been prescribed beta blockers and Sumatriptan which didnāt work at all so I contacted my GP again and was prescribed Naproxen and Omeprazole which also did not work Last week I took a trip to A&E and they took blood tests
jaxie28
in
Thyroid UK
4 years ago
Graves
I was diagnosed in November with Gravesā disease, on Carbimazole and doing ok. Have just been told that this is not a long term drug and will have to think about RAI as the way going forward. Anyone been through the same situation?
I was diagnosed in November with Gravesā disease, on Carbimazole and doing ok. Have just been told that this is not a long term drug and will have to think about RAI as the way going forward. Anyone been through the same situation?
Boaby
in
Thyroid UK
4 years ago
Reintroduction of gluten into my diet and possible iodine deficiency
Hi everyone, Following on from my post about 4 months ago and suggestions made in reply by SlowDragon and Greygoose, I reintroduced gluten into my diet as an experiment after more than two years of being gluten-free. The plan was to see if I felt any different and if my antibodies would go up again -
Hi everyone, Following on from my post about 4 months ago and suggestions made in reply by SlowDragon and Greygoose, I reintroduced gluten into my diet as an experiment after more than two years of being gluten-free. The plan was to see if I felt any different and if my antibodies would go up again -
Caroline888
in
Thyroid UK
4 years ago
Update - starting treatment 50mcg Levothyroxine, thank you for your previous advice
Hey guys, Posting an update from may last post, and now seeking more advice from you clever lot! latest results for my follow up blood test: tsh was 16.14 (0.3 - 4.2) free t4 15.8 (12.00-22.00) So the doctor has decided to start me on 50mcg Levothyroxine and take it from there. I have a test again
Hey guys, Posting an update from may last post, and now seeking more advice from you clever lot! latest results for my follow up blood test: tsh was 16.14 (0.3 - 4.2) free t4 15.8 (12.00-22.00) So the doctor has decided to start me on 50mcg Levothyroxine and take it from there. I have a test again
Iris16257
in
Thyroid UK
4 years ago
Stage 5 Endo at age 27.
I've had stage 5 endometriosis for 5 years now, I first got diagnosed after 3 years of constant visits to the doctor who would just send me off with even more painkillers to try until 2017 when they sent me for my first laproscopy. It was successful for the first 5 months until I went for a check up
I've had stage 5 endometriosis for 5 years now, I first got diagnosed after 3 years of constant visits to the doctor who would just send me off with even more painkillers to try until 2017 when they sent me for my first laproscopy. It was successful for the first 5 months until I went for a check up
MellMelly
in
Endometriosis UK
4 years ago
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