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Simple renal cyst
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What type of scan please?
The first scanner (a doctor) noted a
simple
left
renal
cyst
, mild hydronephrosis in the right kidney and significant post void urinary volume.
The first scanner (a doctor) noted a
simple
left
renal
cyst
, mild hydronephrosis in the right kidney and significant post void urinary volume.
crista1
in
My Ovacome
10 years ago
Tab Nefrosave
I am a Type II diabetic with creatinine 2.0. My doctor has suggested Tab Nefrosave (Morning & Evening) along with other sugar and BP medicines. Can anybody guide me regarding the benefits of Nefrosave.
I am a Type II diabetic with creatinine 2.0. My doctor has suggested Tab Nefrosave (Morning & Evening) along with other sugar and BP medicines. Can anybody guide me regarding the benefits of Nefrosave.
Sunil-gupta
in
Early CKD Support
10 years ago
?Haem or peritoneal dialysis
My eGFR is 12 and I am having a fistula made. Consultant calls it'planned dialysis' although I don't need it right now. I prefer idea of haemodialysis but would really appreciate other peoples' experiences. Look forward to hearing from you. Manon
My eGFR is 12 and I am having a fistula made. Consultant calls it'planned dialysis' although I don't need it right now. I prefer idea of haemodialysis but would really appreciate other peoples' experiences. Look forward to hearing from you. Manon
manon
in
Early CKD Support
10 years ago
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no salt no sugar no potassium help!!!
I have seen my consultant today we have discussed dialysis, I have had a fistula fitted but it hasn't worked so am waiting to have another fitted. he suggested I think about the perennial dialysis which I don't like the idea of. he also suggested I cut out potassium in my diet, I already don't add
I have seen my consultant today we have discussed dialysis, I have had a fistula fitted but it hasn't worked so am waiting to have another fitted. he suggested I think about the perennial dialysis which I don't like the idea of. he also suggested I cut out potassium in my diet, I already don't add
Louise71
in
Early CKD Support
10 years ago
TEST RESULTS @ LANCASTER UNRELIABLE
I just discovered that my results from Lancaster are incorrect. They claimed numerous times that I had an overactive thyroid. I went to Blackpool and got normal results. I had my results from Lancaster reviewed and found out that they are unreliable. This is very worrying for people who are put on medication
I just discovered that my results from Lancaster are incorrect. They claimed numerous times that I had an overactive thyroid. I went to Blackpool and got normal results. I had my results from Lancaster reviewed and found out that they are unreliable. This is very worrying for people who are put on medication
littlemissthyroid
in
Thyroid UK
10 years ago
You've hit a milestone! 300 of you now have joined the Sickle Cell Society HU community
Congratulations for building a true Sickle Cell Disorders health movement in HealthUnlocked! Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Sickle Cell Disorders by spreading the benefit of shared, personal health experiences. And beyond
Congratulations for building a true Sickle Cell Disorders health movement in HealthUnlocked! Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Sickle Cell Disorders by spreading the benefit of shared, personal health experiences. And beyond
HealthUnlocked
HealthUnlocked
in
Sickle Cell Society
10 years ago
What does this test involve?
Hi there, Has anyone had their 'anterior pituitary function' tested? I've got to spend a full morning in hospital on Friday having the test done and it sounds pretty comprehensive! Endo says he will be checking my GnRH, TRH, Short Synacthen. Does anyone know what kind of diagnoses or indications these
Hi there, Has anyone had their 'anterior pituitary function' tested? I've got to spend a full morning in hospital on Friday having the test done and it sounds pretty comprehensive! Endo says he will be checking my GnRH, TRH, Short Synacthen. Does anyone know what kind of diagnoses or indications these
Amalie105
in
Thyroid UK
10 years ago
My kidney function is hovering between 9-7% for the 12 months
Hi everyone it's nice to see all these ppl on here helping each other as least you don't feel alone.... I would just like to share my sidewith you all...I am 30 n unfortubarely am on the final stage of CKD my creatinine I am not sure exactly but it's around 400+... I suffere from high bp n anemia...
Hi everyone it's nice to see all these ppl on here helping each other as least you don't feel alone.... I would just like to share my sidewith you all...I am 30 n unfortubarely am on the final stage of CKD my creatinine I am not sure exactly but it's around 400+... I suffere from high bp n anemia...
Mobeg
in
Early CKD Support
10 years ago
Sickness ...
Hello all. I was diagnosed with good pastures syndrome in March this year. It has left me with chronic renal failure. I started haemodialysis and recently changed to peritoneal dialysis. I feel sick most if the time but it seems to get worse in the evenings. Has anyone else found this? If so what did
Hello all. I was diagnosed with good pastures syndrome in March this year. It has left me with chronic renal failure. I started haemodialysis and recently changed to peritoneal dialysis. I feel sick most if the time but it seems to get worse in the evenings. Has anyone else found this? If so what did
Syreeta
in
Dialysis Support
10 years ago
Dealing with sickle cell anaemia.
ever since I knew I had sickle cell, I've been taking much of folic acid. How does the folic acid help sustain me?
ever since I knew I had sickle cell, I've been taking much of folic acid. How does the folic acid help sustain me?
Indahi-keith
in
MPN Voice
10 years ago
Believe it, or not!
It is now over a year since I had a kidney transplant. I have just been referred back to Ipswich Hospital, for all things relating to the actual transplant. I am however, for the present anyway, remaining under Addenbrooke's Hospital for vasculitis. The new doctor that I'm under , DR Ande (Andy) IS
It is now over a year since I had a kidney transplant. I have just been referred back to Ipswich Hospital, for all things relating to the actual transplant. I am however, for the present anyway, remaining under Addenbrooke's Hospital for vasculitis. The new doctor that I'm under , DR Ande (Andy) IS
AndrewT
in
Vasculitis UK
10 years ago
Calcichew
I have been taking calcichew for several years and have had no problems with them [ I take one a day ] I had a bone scan recently which revealed my bone density had improved since my last one 2 years ago, so no treatment required, however I continued to take them. My question is can too much calcium
I have been taking calcichew for several years and have had no problems with them [ I take one a day ] I had a bone scan recently which revealed my bone density had improved since my last one 2 years ago, so no treatment required, however I continued to take them. My question is can too much calcium
bowler
in
PMRGCAuk
10 years ago
Who do you talk to when you feel very down?
I feel like I haven't been allowed to be honest to anyone about how very down I feel. Being ambivolent about accepting renal replacement therapy has led to wild accusations from doctors - that I am begging for money, manipulative. They don't seem to get it - some of us have been so bullied by bad partners
I feel like I haven't been allowed to be honest to anyone about how very down I feel. Being ambivolent about accepting renal replacement therapy has led to wild accusations from doctors - that I am begging for money, manipulative. They don't seem to get it - some of us have been so bullied by bad partners
lizzy50
in
Dialysis Support
10 years ago
Is Galvus met 50/500 harmful
I am insulin dependent diabities patient my doctor has advised to take Galvus met 50/500 is it safe drug a k sachan
I am insulin dependent diabities patient my doctor has advised to take Galvus met 50/500 is it safe drug a k sachan
sachanak
in
Diabetes India
10 years ago
Renal Transplant Optimisation Trial - Positive T-Antibody
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the APS, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks,
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the APS, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks,
Hidden
in
Kidney Transplant Patient Support
10 years ago
Transplant Optimisation Trial - the fall out
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the Lupus, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the Lupus, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks
Hidden
in
LUPUS UK
10 years ago
Transplant Optimisation Trial - fall out
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the APS, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks,
Hi - just thought I'd share this, I wrote it to explain to a relative what was happening. I know it is more about my transplant than the APS, but someone might have some thoughts so I thought it might be worth sharing.... Tx I guess it started a few weeks back; my relationship was on the rocks,
Hidden
in
Hughes Syndrome APS Forum
10 years ago
Constipation and Kidney Failure. Does anyone have any advice, or ideas about the management of chronic constipation in Peritoneal Dialysis.
I am a PD patient on four daily fluid exchanges. Since my last PD catheter was fitted in Feb14, I have been diagnosed with gastro-paresis. Constipation is chronic and my Bowel has slowed down to hardly function at all, only going every four days, even with lactulose, docusate, movicol, senna! I am getting
I am a PD patient on four daily fluid exchanges. Since my last PD catheter was fitted in Feb14, I have been diagnosed with gastro-paresis. Constipation is chronic and my Bowel has slowed down to hardly function at all, only going every four days, even with lactulose, docusate, movicol, senna! I am getting
Quintillius
in
Dialysis Support
10 years ago
i m 39 yrs old, dibetic 2, my hba1c was 8.3 (first test) on 17 jan 14, i had janumet 50/500 twice a day, simultaneous i did regular walk of
mins. & control my diet. now i done my hba1c which is 4.3, now dr given me kombiglyze 5/500 in a day. my quetions are - dr reduce my medicine dose ?? - can i control it without medicine only with diet & excercise?? - i am taking meganeuron od a day since last three months, is it safe drug & can
mins. & control my diet. now i done my hba1c which is 4.3, now dr given me kombiglyze 5/500 in a day. my quetions are - dr reduce my medicine dose ?? - can i control it without medicine only with diet & excercise?? - i am taking meganeuron od a day since last three months, is it safe drug & can
kshanky
in
Diabetes India
10 years ago
Peritoneal dialysis. I am struggling badly to adjust to the routine. It is making me quite depressed. Are there any help groups or support?
I am new to peritoneal night time dialysis. The machine keeps alarming, makes a frightful noise. My catheter is positional and I have problems with constipation, night sweats and weight loss. I am very depressed about this as I recently lost use of a Kidney transplant after twenty five years. Can anyone
I am new to peritoneal night time dialysis. The machine keeps alarming, makes a frightful noise. My catheter is positional and I have problems with constipation, night sweats and weight loss. I am very depressed about this as I recently lost use of a Kidney transplant after twenty five years. Can anyone
Quintillius
in
Dialysis Support
10 years ago
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