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MAJOR CANCER CURE! (yeah, I know it's not PD)
Somehow (and i watch, listen, and skim DOZENS of health videos weekly) i missed this one from a YEAR ago! Even though it is a miracle treatment for "cancer" and not "PD" -- the point is that SCIENCE is working VERY HARD to cure, stop, prevent, slow down ... PD! SO DON'T GIVE UP! ------------------
Somehow (and i watch, listen, and skim DOZENS of health videos weekly) i missed this one from a YEAR ago! Even though it is a miracle treatment for "cancer" and not "PD" -- the point is that SCIENCE is working VERY HARD to cure, stop, prevent, slow down ... PD! SO DON'T GIVE UP! ------------------
PDWarrior1900
in
Cure Parkinson's
8 months ago
Update 7.7.5 = Benign
Thanks to all who responded to my last post. The news on the growth removed from my face was good news. It was benign, a Seborrheic Keratosis that suddenly had become inflamed. Due to the coloration, it looked a possible malignant growth, which is why I had it checked out. I would encourage everyone
Thanks to all who responded to my last post. The news on the growth removed from my face was good news. It was benign, a Seborrheic Keratosis that suddenly had become inflamed. Due to the coloration, it looked a possible malignant growth, which is why I had it checked out. I would encourage everyone
hunter5582
in
MPN Voice
5 months ago
Hyperhomocysteinemia or lack of vitamin 12
has anyone suffered from inability to absorb vitamin B12 due to either the Lupus or Methotrexate injections? I’m really struggling with pins and needs and total exhaustion and I’m wondering if this is my problem. It’s impossible getting to speak to dr or rheumy or nurse so could do with advice please
has anyone suffered from inability to absorb vitamin B12 due to either the Lupus or Methotrexate injections? I’m really struggling with pins and needs and total exhaustion and I’m wondering if this is my problem. It’s impossible getting to speak to dr or rheumy or nurse so could do with advice please
BK47
in
LUPUS UK
8 months ago
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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
PiP - Aids being 'prescribed'
This appears to be coming up a few times from reading previous posts regarding PiP claims. People who have bought their own aids to facilitate an easier existence are being told they cannot count as proof of either disability/change in disability, because they have not been 'prescribed' by the GP. Yet
This appears to be coming up a few times from reading previous posts regarding PiP claims. People who have bought their own aids to facilitate an easier existence are being told they cannot count as proof of either disability/change in disability, because they have not been 'prescribed' by the GP. Yet
Alanna012
in
Fibromyalgia Action UK
8 months ago
Cataract removal
I had a cataract removed on Friday last and make the stupid mistake of putting the wrong post op drops in my eye. I had to ring the emergency services and between them and my daughter I managed to get to the emergency room. They sluiced my eye out after administering antiseptic and rang the consultant
I had a cataract removed on Friday last and make the stupid mistake of putting the wrong post op drops in my eye. I had to ring the emergency services and between them and my daughter I managed to get to the emergency room. They sluiced my eye out after administering antiseptic and rang the consultant
Stoneferry8
in
Macular Society
8 months ago
cystitisy like feelings
Hello , I wondered whether anyone has experienced feelings in the bladder and on urination as if they had cystitis , but received a normal urine test ? I have been having this feeling for about a week now , urine sample given at GP’s was normal . I am currently having Avastin 3 weekly and have been
Hello , I wondered whether anyone has experienced feelings in the bladder and on urination as if they had cystitis , but received a normal urine test ? I have been having this feeling for about a week now , urine sample given at GP’s was normal . I am currently having Avastin 3 weekly and have been
Norelo8
in
My Ovacome
8 months ago
Update on Nuclear Scan and where I am at now.
First: thank you all for the kind support I have received since - Much appreciated. To the Nuclear Scan ordered by my GP for suspect spread from bladder cancer to the bones. I got a call from my GP surgery today telling me Dr wanted to let me know, NO bone cancer found. Thant's one worry gone.
First: thank you all for the kind support I have received since - Much appreciated. To the Nuclear Scan ordered by my GP for suspect spread from bladder cancer to the bones. I got a call from my GP surgery today telling me Dr wanted to let me know, NO bone cancer found. Thant's one worry gone.
Ern007
in
Lung Conditions Community Forum
8 months ago
PMR and the effect on mental health.
I consider myself as coping as I am getting to the point of acceptance of this disease after being diagnosed 12 weeks ago as a 57-year-old male but why do I have moments of absolute overwhelming sadness? I have never welled up to this extent and can even feel it coming on, which is very odd indeed.
I consider myself as coping as I am getting to the point of acceptance of this disease after being diagnosed 12 weeks ago as a 57-year-old male but why do I have moments of absolute overwhelming sadness? I have never welled up to this extent and can even feel it coming on, which is very odd indeed.
Markandevie
in
PMRGCAuk
5 months ago
Neurological processing disorder from bacterial meningitis
morning, I was just wondering if anyone has had any experience with neurological processing disorders please? I went to the hospital recently for an auditory processing disorder but it’s now thought that this is wider neurological processing disorder that I need to be referred to a brain trauma specialist
morning, I was just wondering if anyone has had any experience with neurological processing disorders please? I went to the hospital recently for an auditory processing disorder but it’s now thought that this is wider neurological processing disorder that I need to be referred to a brain trauma specialist
ElephantLover2023
in
Meningitis Now
8 months ago
IBS and wind
I have had IBS for years and I am really suffering at the moment not only with the unpredictability of BMs but also terrible bloating and wind. It seems to be worse as soon as I go out shopping or to social events. I wonder if anxiety is partly to blame. I keep a food diary and am really careful
I have had IBS for years and I am really suffering at the moment not only with the unpredictability of BMs but also terrible bloating and wind. It seems to be worse as soon as I go out shopping or to social events. I wonder if anxiety is partly to blame. I keep a food diary and am really careful
Starry56
in
IBS Network
5 months ago
Pregabalin and Intestinal Cramps
I came off of carbamazepine (due to fixed drug eruptions) and after a while the trigeminal pain reappeared. I started Pregabalin (Lyrica), taking 50mg (two 25mg pills hours apart) for two days and woke with very bad intestinal cramping. Bad enough for me to search and see that some have this and it remits
I came off of carbamazepine (due to fixed drug eruptions) and after a while the trigeminal pain reappeared. I started Pregabalin (Lyrica), taking 50mg (two 25mg pills hours apart) for two days and woke with very bad intestinal cramping. Bad enough for me to search and see that some have this and it remits
coldfeet7
in
Restless Legs Syndrome
8 months ago
just diagnosed
Hi, I’m a 69 yr old retired nurse. For the past nine years I have been experiencing all the common symptoms of PV and have had three embolitic events, a DVT, Pulmonary embolism and a cerebral venous thrombosis. I was treated for other things and no specific blood tests were ever done. Things got so bad
Hi, I’m a 69 yr old retired nurse. For the past nine years I have been experiencing all the common symptoms of PV and have had three embolitic events, a DVT, Pulmonary embolism and a cerebral venous thrombosis. I was treated for other things and no specific blood tests were ever done. Things got so bad
Janbu
in
MPN Voice
8 months ago
colonoscope
Just wondering if anybody had deep sedation with this procedure and how was it thanks Sue. Just anxious about it all with Emphysema.
Just wondering if anybody had deep sedation with this procedure and how was it thanks Sue. Just anxious about it all with Emphysema.
soul-123
in
Lung Conditions Community Forum
5 months ago
Paleontology Diet – By Dr Barry Durrant-Peatfield
Excerpt from the transcript of a talk given by the late Dr Barry Durrant-Peatfield at one of TPA's Annual Conferences several years ago.
I'm posting this here because we've recently had a few questions/posts about extreme diets such as the carnivor diet. Personally, I think what Dr Peatfield
Excerpt from the transcript of a talk given by the late Dr Barry Durrant-Peatfield at one of TPA's Annual Conferences several years ago.
I'm posting this here because we've recently had a few questions/posts about extreme diets such as the carnivor diet. Personally, I think what Dr Peatfield
RedApple
Administrator
in
Thyroid UK
8 months ago
Dry eyes
Hi I have RA for years on lefluminide celebrex thyroxine b12 ,I have suffered terrible head and face sweating for a few years getting worse,just had cataracts done sight is fine but my dry eyes are causing me so much discomfort,I have hi lo tears and ikervis at night it's 5 weeks since cataracts done
Hi I have RA for years on lefluminide celebrex thyroxine b12 ,I have suffered terrible head and face sweating for a few years getting worse,just had cataracts done sight is fine but my dry eyes are causing me so much discomfort,I have hi lo tears and ikervis at night it's 5 weeks since cataracts done
Pansy78
in
NRAS
8 months ago
Twisted ankle and foot
HiDoes anyone know if injuring your foot and ankle by twisting it takes longer to heal when you have lupus? On the 24th I slipped on the narrow step trying to get into my sister's car. My left foot slipped off the step, 1st going over on my ankle and then twisted making a horrible snapping noise. My
HiDoes anyone know if injuring your foot and ankle by twisting it takes longer to heal when you have lupus? On the 24th I slipped on the narrow step trying to get into my sister's car. My left foot slipped off the step, 1st going over on my ankle and then twisted making a horrible snapping noise. My
Cal66
in
LUPUS UK
8 months ago
BPPV ADVICE
Just wanted to ask how you cope living with bppv ? I have had it a long time but only mildly had episodes of balance and dizziness just today I had sudden dizzy spell just by taking washing out of the dryer turning my head I came really dizzy I managed to hold on to the kitchen work surface till it passed
Just wanted to ask how you cope living with bppv ? I have had it a long time but only mildly had episodes of balance and dizziness just today I had sudden dizzy spell just by taking washing out of the dryer turning my head I came really dizzy I managed to hold on to the kitchen work surface till it passed
Glenkerry40
in
Tinnitus UK
8 months ago
new med
Just Brad my first 3 doses of Hydroxyurea. 2nd time I’ve had high platelets, first time about 3 years after the6 were stable had a TIA! As you can imagine, feeling very concerned. Anyone had any similar experience?
Just Brad my first 3 doses of Hydroxyurea. 2nd time I’ve had high platelets, first time about 3 years after the6 were stable had a TIA! As you can imagine, feeling very concerned. Anyone had any similar experience?
Livingwithpup
in
MPN Voice
8 months ago
three weeks of ear infection now at breaking point
hi, I’ve not written on this site for a long time so long I don’t remember the last post but I’ve had tinnitus in my left ear for years now and learnt to live with it but I’m hitting 3 weeks of an ear infection and I’m reaching the end of my rope. I’ve had medication her feels like it’s doing the
hi, I’ve not written on this site for a long time so long I don’t remember the last post but I’ve had tinnitus in my left ear for years now and learnt to live with it but I’m hitting 3 weeks of an ear infection and I’m reaching the end of my rope. I’ve had medication her feels like it’s doing the
djv1985
in
Tinnitus UK
8 months ago
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