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LDH Question
My typical quarterly checkup with my CLL doctor follows a certain routine - I have the blood draw and then, as soon as CBC results are available, I see the doctor or his nurse practitioner. And then, long after I've left the office, the other blood results are available, including LDH. So, in other
My typical quarterly checkup with my CLL doctor follows a certain routine - I have the blood draw and then, as soon as CBC results are available, I see the doctor or his nurse practitioner. And then, long after I've left the office, the other blood results are available, including LDH. So, in other
hhk50
in
CLL Support
8 months ago
change of meds
Been having a bad year. Ive been unwell since July and was eventually hospitalised with double pneumonia in September. My rheumatologist treated me for a lupus flare as I had been in a similar situation years previous when first diagnosed with lupus. The dose of steroids did the trick and I was sent
Been having a bad year. Ive been unwell since July and was eventually hospitalised with double pneumonia in September. My rheumatologist treated me for a lupus flare as I had been in a similar situation years previous when first diagnosed with lupus. The dose of steroids did the trick and I was sent
mitty
in
LUPUS UK
5 months ago
low dose naltrexone
Having Crohn’s disease I was wondering if anyone has any experience with this drug and if it has proven to be effective or not? my diet is pretty limited at moment but I’m hearing that this will inhibit inflammation to allow me to open up my diet more.
Having Crohn’s disease I was wondering if anyone has any experience with this drug and if it has proven to be effective or not? my diet is pretty limited at moment but I’m hearing that this will inhibit inflammation to allow me to open up my diet more.
Howson123
in
Crohn's and Colitis Support
8 months ago
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PD sucks
PD suspected by GP in November 2022. Confirmed by neurologist in January 2023. Tried different meds - now on rotigotine patches plus after research, I now take mucuna morning and afternoon. Supposed to provide 240mg L-Dopa each day. It helps with constipation. What bothers me most is poor
PD suspected by GP in November 2022. Confirmed by neurologist in January 2023. Tried different meds - now on rotigotine patches plus after research, I now take mucuna morning and afternoon. Supposed to provide 240mg L-Dopa each day. It helps with constipation. What bothers me most is poor
reefeye
in
Cure Parkinson's
8 months ago
angina pain
Hello everyone, I hope you're all doing well and enjoying good health. I have a question regarding angina pain. Earlier this year, in January 2023, I experienced a heart attack. I'm 37 years old, and following the balloon procedure, my doctor prescribed regular medication. However, I have continued to
Hello everyone, I hope you're all doing well and enjoying good health. I have a question regarding angina pain. Earlier this year, in January 2023, I experienced a heart attack. I'm 37 years old, and following the balloon procedure, my doctor prescribed regular medication. However, I have continued to
Madk
in
Weight Loss Support
5 months ago
Ferritin levels
I have collected my blood test results and am looking for information before my g.p. follow up appointment tomorrow.I am under the impression that ferritin levels should be "optimum" in order for my B12 injections to work for pernicious anaemia. Although I've been told all of my blood results are "normal
I have collected my blood test results and am looking for information before my g.p. follow up appointment tomorrow.I am under the impression that ferritin levels should be "optimum" in order for my B12 injections to work for pernicious anaemia. Although I've been told all of my blood results are "normal
Suesue246
in
Pernicious Anaemia Society
5 months ago
Pvcs and pacs following acute afib episode and Apple watch ecg/ekg
Following my first (confirmed) afib attack a month ago(with rvr) I seem to have an occasional flip flop or thud and flutter from my heart. Cardiologist and EP discontinued my beta blocker after 10 days because my HR is already low and the flip flopping came a few days later. Yesterday I discovered
Following my first (confirmed) afib attack a month ago(with rvr) I seem to have an occasional flip flop or thud and flutter from my heart. Cardiologist and EP discontinued my beta blocker after 10 days because my HR is already low and the flip flopping came a few days later. Yesterday I discovered
Iamfuzzyduck
in
AF Association
5 months ago
New PAS blog posts
Hi, I noticed that there were recent blog posts on PAS (Pernicious Anaemia Society) website. From 8th Nov 2023 is "The Patient Experience in Diagnosis and Treatment of Autoimmune Gastritis and Pernicious Anaemia" https://pernicious-anaemia-society.org/blog/the-patient-experience-in-diagnosis-and-treatment-of-autoimmune-gastritis-and-pernicious-anaemia
Hi, I noticed that there were recent blog posts on PAS (Pernicious Anaemia Society) website. From 8th Nov 2023 is "The Patient Experience in Diagnosis and Treatment of Autoimmune Gastritis and Pernicious Anaemia" https://pernicious-anaemia-society.org/blog/the-patient-experience-in-diagnosis-and-treatment-of-autoimmune-gastritis-and-pernicious-anaemia
Sleepybunny
in
Pernicious Anaemia Society
5 months ago
Sources and experiences of LDN
Hi again, Just one more sourcing question - does anyone have any recommendations of UK sources of low dose naltrexone? I would also love to hear of anyone's experiences of taking LDN. I have hashimoto's underactive thyroid and am also trying to conceive and have read that it could be v beneficial
Hi again, Just one more sourcing question - does anyone have any recommendations of UK sources of low dose naltrexone? I would also love to hear of anyone's experiences of taking LDN. I have hashimoto's underactive thyroid and am also trying to conceive and have read that it could be v beneficial
Becsf
in
Thyroid UK
5 months ago
Liver and Digestion
How has your liver disease affected your digestive system? My digestion has been unpredictable for years, sometimes constipation and sometimes diarrhea (sorry TMI). Dr always said it was IBS since nothing was seen on colonoscopies etc. I’m wondering if my digestive issues have been from my liver all
How has your liver disease affected your digestive system? My digestion has been unpredictable for years, sometimes constipation and sometimes diarrhea (sorry TMI). Dr always said it was IBS since nothing was seen on colonoscopies etc. I’m wondering if my digestive issues have been from my liver all
FlippinOut
in
British Liver Trust
8 months ago
Can anyone Assist?
A couple of weeks ago, I partially read a lengthy and extremely interesting post explaining many aspects of PCa..., also the link between PSA and PCa and many other facts. I flagged the post to read later but for some reason the post has been deleted. Can anyone point me to this post as from what
A couple of weeks ago, I partially read a lengthy and extremely interesting post explaining many aspects of PCa..., also the link between PSA and PCa and many other facts. I flagged the post to read later but for some reason the post has been deleted. Can anyone point me to this post as from what
StuartS
in
Advanced Prostate Cancer
8 months ago
Laxido and acid reflux
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
Spaceboy_60
in
IBS Network
5 months ago
Recompensated Liver. Safe to travel.
I had my telephone consultation yesterday with my liver nurse and had some reassuring news. I asked her if I was safe to travel abroad and she said that my liver had recompensated and was functioning normal and that my bloods and scans are normal range and they have no features of concern. It will be
I had my telephone consultation yesterday with my liver nurse and had some reassuring news. I asked her if I was safe to travel abroad and she said that my liver had recompensated and was functioning normal and that my bloods and scans are normal range and they have no features of concern. It will be
Nip1
in
British Liver Trust
8 months ago
Swollen knees
I have inflammatory arthritis, Osteo arthritis, Sjogrens and now have been diagnosed with FND . I also have/ had Polymyalgia . I had a hip replacement in 2017 and at that time I was suffering with painful knees. I have been on various medications and am on Imraldi and Methotrexate. I
I have inflammatory arthritis, Osteo arthritis, Sjogrens and now have been diagnosed with FND . I also have/ had Polymyalgia . I had a hip replacement in 2017 and at that time I was suffering with painful knees. I have been on various medications and am on Imraldi and Methotrexate. I
Bailybiscuit
in
NRAS
5 months ago
York Lupus Group Coffee and Chat meeting - 9th December at 11.30
Come join the York Lupus Group for our next Coffee and Chat meeting on the 9th December, 11.30 until 1.30 at Sledmere House Cafe, Sledmere, Driffield, Yorkshire, YO25 3XG. This is a great opportunity to meet others with lupus or associated conditions, friends and family also welcome! For more information
Come join the York Lupus Group for our next Coffee and Chat meeting on the 9th December, 11.30 until 1.30 at Sledmere House Cafe, Sledmere, Driffield, Yorkshire, YO25 3XG. This is a great opportunity to meet others with lupus or associated conditions, friends and family also welcome! For more information
michaellasmith
Administrator
in
LUPUS UK
5 months ago
Polymyalgia and Rheumatoid arthritis
I was diagnosed with PMR in June 2014. Over a period of about 7 years I managed to come off prednisone but after a time the PMR returned. Since 2022 I have managed to get down to 7mg daily and then have a flare. Back to 10 down to 8 and another flare. I live in France and it seems PMR is not as common
I was diagnosed with PMR in June 2014. Over a period of about 7 years I managed to come off prednisone but after a time the PMR returned. Since 2022 I have managed to get down to 7mg daily and then have a flare. Back to 10 down to 8 and another flare. I live in France and it seems PMR is not as common
Deemar
in
PMRGCAuk
5 months ago
PMR Heavy Legs / Lead Legs / Low Energy
Hello, I haven't posted in a long time. I've read many articles. I didn't know what DSNS was until I went to the FAQ's and then tapering plans page. Both PMRpro and DorsetLady, and others have tapering plans (thank you PMRpro & DorsetLady). I have bounced around 15 to 5 MG for the past year. I'm currently
Hello, I haven't posted in a long time. I've read many articles. I didn't know what DSNS was until I went to the FAQ's and then tapering plans page. Both PMRpro and DorsetLady, and others have tapering plans (thank you PMRpro & DorsetLady). I have bounced around 15 to 5 MG for the past year. I'm currently
Me_2
in
PMRGCAuk
8 months ago
Update on Dipyridamole
Talked to my Doctor and he felt that taking Dipyridamole as needed was OK. In two months I have had three bad nights. To me a bad night is going to bed and getting back up in 10 minutes, when ya know ya know. So that is the good news. I am also going for a blood test next week, that should be
Talked to my Doctor and he felt that taking Dipyridamole as needed was OK. In two months I have had three bad nights. To me a bad night is going to bed and getting back up in 10 minutes, when ya know ya know. So that is the good news. I am also going for a blood test next week, that should be
WideBody
in
Restless Legs Syndrome
8 months ago
How high must the PSA levels be before cancer can be seen in a CT scan?
Following the end of my treatment (radiation, lupron, Zytiga, prednisone) with curative intent back in May, my PSA has risen from undetectable to 0.09. As discussed on another thread this is not alarming at this stage since I still have a prostate as I never had surgery to remove it. However I am
Following the end of my treatment (radiation, lupron, Zytiga, prednisone) with curative intent back in May, my PSA has risen from undetectable to 0.09. As discussed on another thread this is not alarming at this stage since I still have a prostate as I never had surgery to remove it. However I am
Mascouche
in
Advanced Prostate Cancer
8 months ago
Creatinine and LDH
I have hashimoto's and I have been seeing a functional medicine doctor because my endocrinologist was not helping. He recently ran a bunch of labs. Both my creatinine and LDH were lab low. Does anyone know what that would mean and if is connected with my thyroid in any way?
I have hashimoto's and I have been seeing a functional medicine doctor because my endocrinologist was not helping. He recently ran a bunch of labs. Both my creatinine and LDH were lab low. Does anyone know what that would mean and if is connected with my thyroid in any way?
CraftyGamer19
in
Thyroid UK
8 months ago
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