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my day took a dive.
My brother was diagnosed with pancreatic cancer. His surgery early this morning revealed the cancer had spread undetected. They ended the procedure and sent him home giving him 6 months to live. Life seems random and impersonal. My son’s dog Roxie understands.
My brother was diagnosed with pancreatic cancer. His surgery early this morning revealed the cancer had spread undetected. They ended the procedure and sent him home giving him 6 months to live. Life seems random and impersonal. My son’s dog Roxie understands.
Gobbsofjoy
in
Cure Parkinson's
15 days ago
Pain in lower left abdomen for 5 years and now a very little bright red blood in stool once in a while
Hi All,When I was 24 (10 years ago)years old I consulted a gastroenterologist with stomach discomfort and bloating. He did an colonoscopy and an endoscopy..One polyp was found and was benign on biopsy.I was diagnosed with IBS..Time passed stomach problems were a daily concern for me.5 years ago suddenly
Hi All,When I was 24 (10 years ago)years old I consulted a gastroenterologist with stomach discomfort and bloating. He did an colonoscopy and an endoscopy..One polyp was found and was benign on biopsy.I was diagnosed with IBS..Time passed stomach problems were a daily concern for me.5 years ago suddenly
S_searching
in
Colon Cancer Connected
8 months ago
Advice after possible Covid
Hi all, I've been horribly ill with what is probably Covid (no positive LFT test but typical weird breathlessness, fluid lungs, fatigue, dizziness and all the rest). However, three weeks later and a course of antibiotics, and I'm still feeling rotten - massive fatigue, pains everywhere, dizziness
Hi all, I've been horribly ill with what is probably Covid (no positive LFT test but typical weird breathlessness, fluid lungs, fatigue, dizziness and all the rest). However, three weeks later and a course of antibiotics, and I'm still feeling rotten - massive fatigue, pains everywhere, dizziness
Treetop33
in
LUPUS UK
8 months ago
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Questions about experience with rinvoq
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
gnstric66
in
NRAS
10 months ago
immune system
I am on immune suppressants, Is it advisable to take vitamins to help immune system fight against Cold and flu therefore also general Feeling crappy. Thank you for advice in advanc
I am on immune suppressants, Is it advisable to take vitamins to help immune system fight against Cold and flu therefore also general Feeling crappy. Thank you for advice in advanc
Toiletseat
in
NRAS
5 months ago
advice
Hello! I havnt posted before but was looking on the lupus Uk website and wanted some advice if possible. I have been struggling with weird symptoms for a while since my son was born 4 years ago- ( then cot covid and was really unwell so was all put down to long covid) I have positive APS antibodies
Hello! I havnt posted before but was looking on the lupus Uk website and wanted some advice if possible. I have been struggling with weird symptoms for a while since my son was born 4 years ago- ( then cot covid and was really unwell so was all put down to long covid) I have positive APS antibodies
Ell5
in
LUPUS UK
8 months ago
Advice needed please
I've had GPA for 25 years with 2 relapses. I last had Rituximab in June 21, I then in November had Covid with 2 hospital admissions. I now have long Covid. I cannot have RTmab because my Immune system is so low, Igg 3.4IgA 0.48 IgM 0.42p Yesterday I was walking around and felt extreme fatigue,
I've had GPA for 25 years with 2 relapses. I last had Rituximab in June 21, I then in November had Covid with 2 hospital admissions. I now have long Covid. I cannot have RTmab because my Immune system is so low, Igg 3.4IgA 0.48 IgM 0.42p Yesterday I was walking around and felt extreme fatigue,
Fleen
in
Vasculitis UK
8 months ago
Shocking story about women dying of CRF/ME
Did anyone read about the women who died from CFS/ME? https://news.sky.com/story/woman-with-me-died-after-begging-gp-for-help-inquest-told-13183530 Why didn't anyone try B12 and see if it could help her? If you look online there is masses of information about how B12 can help CFS/ME. For example
Did anyone read about the women who died from CFS/ME? https://news.sky.com/story/woman-with-me-died-after-begging-gp-for-help-inquest-told-13183530 Why didn't anyone try B12 and see if it could help her? If you look online there is masses of information about how B12 can help CFS/ME. For example
charks
in
Pernicious Anaemia Society
25 days ago
overlapping symptoms
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
TheRedOnes
in
LUPUS UK
9 months ago
Long covid
Im struggling to get over covid and im on day 13. I have symptoms of long covidfever, diarrhea, loss of smell and taste. I have hashimotos and taking levothyroxine 100mcg alongside t3 15mcg. Any advice on how to deal with this will be very welcome
Im struggling to get over covid and im on day 13. I have symptoms of long covidfever, diarrhea, loss of smell and taste. I have hashimotos and taking levothyroxine 100mcg alongside t3 15mcg. Any advice on how to deal with this will be very welcome
Geegee777
in
Thyroid UK
8 months ago
EMED A200 Piston Nebuliser.
Just back home from Hospital with pneumonia Good morning all COPD Warriors, thankfully I am back home from now after a stay in hospital with pneumonia. whilst I was in hospital my Respiratory Nurses noticed that it was time for my nebuliser to be serviced as it had been 12 months since last done.
Just back home from Hospital with pneumonia Good morning all COPD Warriors, thankfully I am back home from now after a stay in hospital with pneumonia. whilst I was in hospital my Respiratory Nurses noticed that it was time for my nebuliser to be serviced as it had been 12 months since last done.
Joseph260268
in
Lung Conditions Community Forum
5 months ago
Covid question
I’ve avoided Covid up until now. My partner and I picked it up in Cuba. Started with what we thought was food poisoning, the dreaded diarrhea. It’s now been 14 days. We’ve had chills, fevers, fatigue and daily diarrhea. I’m at the final three months of V treatment so was advised to start the antiviral
I’ve avoided Covid up until now. My partner and I picked it up in Cuba. Started with what we thought was food poisoning, the dreaded diarrhea. It’s now been 14 days. We’ve had chills, fevers, fatigue and daily diarrhea. I’m at the final three months of V treatment so was advised to start the antiviral
Cottager1989
in
CLL Support
8 months ago
Hi all I'm newbie. Anyone here have lung damage due to Amiodarone treatment?
Rather than going into too much detail I will keep it brief. Was prescribed Amiodarone for AFib and took it for a total of four months six days. After being on it for 3 months I started coughing mostly while asleep. Also started to get really bad pain in left lung lobe that was much worse if I lay on
Rather than going into too much detail I will keep it brief. Was prescribed Amiodarone for AFib and took it for a total of four months six days. After being on it for 3 months I started coughing mostly while asleep. Also started to get really bad pain in left lung lobe that was much worse if I lay on
DizzyD
in
Lung Conditions Community Forum
8 months ago
Erythromelalgia?
I was diagnosed with cellulitis 5 or 6 weeks ago, I’ve had 2 lots of antibiotics, 2 scans to make sure no blood clots, this redness has spread around my leg and is now starting in the other one. My left leg and foot are quite swollen. I’ve seen various nurses and GP’s - never the same one twice - the
I was diagnosed with cellulitis 5 or 6 weeks ago, I’ve had 2 lots of antibiotics, 2 scans to make sure no blood clots, this redness has spread around my leg and is now starting in the other one. My left leg and foot are quite swollen. I’ve seen various nurses and GP’s - never the same one twice - the
lizzziep
in
MPN Voice
1 year ago
Flu won’t go away.
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
Rkdevo
in
Lung Conditions Community Forum
5 months ago
Another day another other saga!!You couldn’t make it up!
Thanks everyone for your advice yesterday. It’s been a learning curve & I will be able to navigate better next time. I went to A & E first thing & in triage the nurse said it’s sounds like you have flu. So she did a nasal swab. She asked me to wear a mask & I said oh I’ve done a Covid test. She said
Thanks everyone for your advice yesterday. It’s been a learning curve & I will be able to navigate better next time. I went to A & E first thing & in triage the nurse said it’s sounds like you have flu. So she did a nasal swab. She asked me to wear a mask & I said oh I’ve done a Covid test. She said
Otto11
in
Lung Conditions Community Forum
5 months ago
Diagnosis
This is my 4th week in hospital. I’ve had 3 chest x-rays, ct scans and mris of all the bony bits of my body to try and find the source of infection that was showing with spikes in temperature, they told me I’ve got pneumonia!
This is my 4th week in hospital. I’ve had 3 chest x-rays, ct scans and mris of all the bony bits of my body to try and find the source of infection that was showing with spikes in temperature, they told me I’ve got pneumonia!
helenlw7
in
Lung Conditions Community Forum
5 months ago
walking aids???
has any used a walking aid to improve balance as I walk looking at the ground and I can’t look to the side without stopping first .. flat ground is the best and uneven or incline causes pain in my old hamstring injury and the new hip pain I have developed .. I also still walk slightly to one side
has any used a walking aid to improve balance as I walk looking at the ground and I can’t look to the side without stopping first .. flat ground is the best and uneven or incline causes pain in my old hamstring injury and the new hip pain I have developed .. I also still walk slightly to one side
Teazymaid
in
Headway
1 month ago
BFP last week but now ill with suspected COVID.
Tested positive after my FET but ever since I’ve been feeling poorly with covid symptoms. Persistent cough, fever, headaches etc. I’m worried that this will impact the pregnancy because it’s so early on - any advice? My viability scan isn’t until 22/12 and I feel like I’m going to be an absolute mess
Tested positive after my FET but ever since I’ve been feeling poorly with covid symptoms. Persistent cough, fever, headaches etc. I’m worried that this will impact the pregnancy because it’s so early on - any advice? My viability scan isn’t until 22/12 and I feel like I’m going to be an absolute mess
RedFox23
in
Fertility Network UK
8 months ago
Finally got flu vax!
After 4+ months of waiting told 'on the list' many times, nurse from gp surgery came. Says don't know what district nurses are doing lately. 🤷♀️ Also gave me pneumonia vax- never had or been offered before🤔 No Covid as run out. Can I sue if I contract Covid or is it all forgotten about now? Yet I
After 4+ months of waiting told 'on the list' many times, nurse from gp surgery came. Says don't know what district nurses are doing lately. 🤷♀️ Also gave me pneumonia vax- never had or been offered before🤔 No Covid as run out. Can I sue if I contract Covid or is it all forgotten about now? Yet I
fraid
in
Asthma Community Forum
7 months ago
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