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Freiberg's disease?
I started with pain in my right foot last December, associated with stiffness and itching about halfway up the foot, all causing me to limp. It feels for all the world as if there's a group of bones all bunched together which I feel like hitting with a hammer to get them back in place- I said this to
I started with pain in my right foot last December, associated with stiffness and itching about halfway up the foot, all causing me to limp. It feels for all the world as if there's a group of bones all bunched together which I feel like hitting with a hammer to get them back in place- I said this to
Toffee1878
in
NRAS
10 months ago
Cotreatment with dichloroacetate and omeprazole exhibits a synergistic antiproliferative effect on malignant tumors
As a follow up to my last post I found this on DCA / Omeprazole. like myself,please treat this as information , not promoting any treatments. For me I find reading and learning about my cancer and possible treatments to be uplifting and gives me hope. To be honest something I never get from my doctor
As a follow up to my last post I found this on DCA / Omeprazole. like myself,please treat this as information , not promoting any treatments. For me I find reading and learning about my cancer and possible treatments to be uplifting and gives me hope. To be honest something I never get from my doctor
85745
in
Advanced Prostate Cancer
5 months ago
Thoughts please
I hope this post is not too long but it's hard to fully explain. I have had severe RLS for 30 years - it started during pregnancy but unfortunately never left and has only worsened over the years. I feel like I have been on every drug with minimal help. I take 0.5 which I went through augmentation
I hope this post is not too long but it's hard to fully explain. I have had severe RLS for 30 years - it started during pregnancy but unfortunately never left and has only worsened over the years. I feel like I have been on every drug with minimal help. I take 0.5 which I went through augmentation
AnnMB
in
Restless Legs Syndrome
10 months ago
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stomach Cancer
hi everyone, I suffer with stomach issues. The usual gastritis/oesophagitis. Long story short. Looking for guidance really. My Mum had stomach cancer and then got another primary in her Oesophagus at the same time. Sadly gone. But I am getting full easy when I eat, pain in stomach, bringing food back
hi everyone, I suffer with stomach issues. The usual gastritis/oesophagitis. Long story short. Looking for guidance really. My Mum had stomach cancer and then got another primary in her Oesophagus at the same time. Sadly gone. But I am getting full easy when I eat, pain in stomach, bringing food back
Crinkles2020
in
Oesophageal & Gastric Cancer
5 months ago
colonoscopy query
I’m scheduled to endure a colonoscopy on 16th January. We are booked on a flight to Thailand on 1st February (14 hours) . Guidelines say two weeks should pass before flight so in theory ok. However this is a trip of a lifetime for us, much delayed and all booked before this cancer worry. I’ve no idea
I’m scheduled to endure a colonoscopy on 16th January. We are booked on a flight to Thailand on 1st February (14 hours) . Guidelines say two weeks should pass before flight so in theory ok. However this is a trip of a lifetime for us, much delayed and all booked before this cancer worry. I’ve no idea
Stills
in
LUPUS UK
5 months ago
restricted urinary flow
Finished IMRT/ SBRT radiation to lymph nodes last week. Since then Ive begun have early AM restricted urinary flow - Very narrow stream. Rad Onc suggested tamsulosin or ibuprophen. MO, tamsulosin. Any work around for the early AM problem that I could take overnight? Ibuprophen has to be taken all
Finished IMRT/ SBRT radiation to lymph nodes last week. Since then Ive begun have early AM restricted urinary flow - Very narrow stream. Rad Onc suggested tamsulosin or ibuprophen. MO, tamsulosin. Any work around for the early AM problem that I could take overnight? Ibuprophen has to be taken all
kainasar
in
Fight Prostate Cancer
5 months ago
Symptoms
HiMy son has been told his symptoms are that of IBS after being tested for Crohns and Colitis three years ago which was negative. His symptoms consist of the following Normal poo then followed by what he has described as Constipation Poo that is wet and soggy and white fluffy mucus which I have also
HiMy son has been told his symptoms are that of IBS after being tested for Crohns and Colitis three years ago which was negative. His symptoms consist of the following Normal poo then followed by what he has described as Constipation Poo that is wet and soggy and white fluffy mucus which I have also
Bowels1
in
IBS Network
5 months ago
TIPS Follow Up Questions
Hi Wonderful community. You truly are wonderful and have helped me reach a dicision to have TIPS done. My follow up questions are the following: 1. Did you get ALL your varices embolized and cemented prior to TIPS? 2. Is your Portal Pressure after TIPS now below 12? I was told that is the goal.
Hi Wonderful community. You truly are wonderful and have helped me reach a dicision to have TIPS done. My follow up questions are the following: 1. Did you get ALL your varices embolized and cemented prior to TIPS? 2. Is your Portal Pressure after TIPS now below 12? I was told that is the goal.
Livmar
in
British Liver Trust
10 months ago
Hello all I've had crohns and stomas since 1976 I now have short bowel and an Ileostomy
I've had crohns since 1976 and my first resection june 1977 colostomy formed I spent six weeks in hospital because I couldn't accept mt colostomy at first I wouldn't touch it or change the bag, then after five weeks I thought I've got to accept it and get on with my life, after 46 years I've had five
I've had crohns since 1976 and my first resection june 1977 colostomy formed I spent six weeks in hospital because I couldn't accept mt colostomy at first I wouldn't touch it or change the bag, then after five weeks I thought I've got to accept it and get on with my life, after 46 years I've had five
SoFedUp2023
in
Crohn's and Colitis Support
5 months ago
Venetoclax and blood sugar
hi everyone, I have been on “V” since the end of last August. In the last five months, I’ve been experiencing severe hypoglycemic attacks: however, my blood sugar is in dropping below 70. my doctor (endocrinologist, who im not happy with) put a blood sugar monitor on me for a week and said no worries
hi everyone, I have been on “V” since the end of last August. In the last five months, I’ve been experiencing severe hypoglycemic attacks: however, my blood sugar is in dropping below 70. my doctor (endocrinologist, who im not happy with) put a blood sugar monitor on me for a week and said no worries
WittyApricot
in
CLL Support
10 months ago
Case report: Rhabdomyolysis and kidney injury in a statin-treated hypothyroid patient-kill two birds with one stone
This case report has a good side: the patient did get diagnosed and treated. But that only follows the dreadful treatment - missing cause of high cholesterol, took statins, rhabdomyolysis, kidney injury. Claims to have been reversed. (I'd like to see the patient's opinion!) But questionable whether
This case report has a good side: the patient did get diagnosed and treated. But that only follows the dreadful treatment - missing cause of high cholesterol, took statins, rhabdomyolysis, kidney injury. Claims to have been reversed. (I'd like to see the patient's opinion!) But questionable whether
helvella
Thyroid UK
in
Thyroid UK
10 months ago
All clear now for two years
Just sending a positive story. Diagnosed 2b HG clear cell, endometrioid 2020. Big op, chemo, diagnosed my own recurrence after 6 months. Another op, then RT. 2021. Last couple of scans have been clear. They are still going to check me every 6 months. I am taking alternative supplements and vitamins
Just sending a positive story. Diagnosed 2b HG clear cell, endometrioid 2020. Big op, chemo, diagnosed my own recurrence after 6 months. Another op, then RT. 2021. Last couple of scans have been clear. They are still going to check me every 6 months. I am taking alternative supplements and vitamins
candyapplegrey
in
My Ovacome
9 months ago
SI Help and Info
Hi All My preps continue...not buying anything yet though...just getting ready.. A few questions on SI if you dont mind. The advice / experience on using hypo needles that I have gleaned from some of our wise friends in here - for subcutaneous injection - is to use G30 1/2 (half inch) needles (
Hi All My preps continue...not buying anything yet though...just getting ready.. A few questions on SI if you dont mind. The advice / experience on using hypo needles that I have gleaned from some of our wise friends in here - for subcutaneous injection - is to use G30 1/2 (half inch) needles (
Treesong2023
in
Pernicious Anaemia Society
1 year ago
Central vision 'scarring' following wet AMD injection course
I currently still have quite blurred vision in my left eye following a sequence of 10 Lucentis injections during 2021. I am now in a stable / 'watching brief' phase of 6 week visits to the eye clinic. (My wet AMD has significantly reduced / disappeared). When I finished my sequence of injections, my
I currently still have quite blurred vision in my left eye following a sequence of 10 Lucentis injections during 2021. I am now in a stable / 'watching brief' phase of 6 week visits to the eye clinic. (My wet AMD has significantly reduced / disappeared). When I finished my sequence of injections, my
Fuzzbox100
in
Macular Society
1 year ago
My 6 Month Lupron cost
No comment!!! 08/07/2023 Leuprolide Acetate injection Total charge $33,685.45 Discount $31,927.45 Plan rate $1,758.00 Other insurance $0.00 KP paid $0.00 Not covered $0.00 Deductible $0.00 Copay / Coinsurance $351.60 Your share $351.60
No comment!!! 08/07/2023 Leuprolide Acetate injection Total charge $33,685.45 Discount $31,927.45 Plan rate $1,758.00 Other insurance $0.00 KP paid $0.00 Not covered $0.00 Deductible $0.00 Copay / Coinsurance $351.60 Your share $351.60
Hidden
in
Advanced Prostate Cancer
10 months ago
Nearly 14 years on - time has flown.
On Friday 16th April 2010 I joined the Pernicious Anaemia Society and posted the following: “I was diagnosed with PA back in 1972 consequent upon having had surgery for a peptic ulcer in April 1959 at the tender age of 17. In those days I was not many years from having to be put on a diet of raw liver
On Friday 16th April 2010 I joined the Pernicious Anaemia Society and posted the following: “I was diagnosed with PA back in 1972 consequent upon having had surgery for a peptic ulcer in April 1959 at the tender age of 17. In those days I was not many years from having to be put on a diet of raw liver
clivealive
Forum Support
in
Pernicious Anaemia Society
5 months ago
Jardiance side effects? Off Metformin for diabetes 2, but high blood sugar 88, overweight, aged 67, scared reactions due other conditions?
Am terminally ill, irreparable brain damage, epilepsy, so can't do much exercise! Was on metformin from start of diabetes 2 in 2020, found my blood sugar level was 88, have been dieting lost 2 half stone, cholesterol not too bad, so they have put me on just Jardiance 10mg a day! Am taking medication
Am terminally ill, irreparable brain damage, epilepsy, so can't do much exercise! Was on metformin from start of diabetes 2 in 2020, found my blood sugar level was 88, have been dieting lost 2 half stone, cholesterol not too bad, so they have put me on just Jardiance 10mg a day! Am taking medication
Adlon57
in
Healthy Evidence
10 months ago
Apixaban (Eliquis) and Omega 3 supplements
Hey All!! Question...Are others who take Apixaban (Eliquis) also taking Omega 3 supplements (that include DHA)? I've read that it could be problematic...increase length of time for bleeding, etc. Any feedback would be much appreciated. Thanks!
Hey All!! Question...Are others who take Apixaban (Eliquis) also taking Omega 3 supplements (that include DHA)? I've read that it could be problematic...increase length of time for bleeding, etc. Any feedback would be much appreciated. Thanks!
ktf2022
in
AF Association
10 months ago
Ablation trade off?
I’ve had continuous AF for about 5 years. I’m on pradaxa and had a cardioversion last year that didn’t help. I haven’t been on any AF meds but am scheduled for a catheter ablation in two weeks. I’m still very active and don’t notice the AF much except for some general tiredness. Since ablation destroys
I’ve had continuous AF for about 5 years. I’m on pradaxa and had a cardioversion last year that didn’t help. I haven’t been on any AF meds but am scheduled for a catheter ablation in two weeks. I’m still very active and don’t notice the AF much except for some general tiredness. Since ablation destroys
Monomono1234
in
AF Association
10 months ago
hello
I have recently been diagnosed as suffering ( and I’m really suffering) from Tinnitus. The constant high pitch is unbearable at time. I am due to go on holiday next Monty and I am getting very anxious about spending 5 hours on a plane with the noise levels possibly making the “ ringing” a lot worse.
I have recently been diagnosed as suffering ( and I’m really suffering) from Tinnitus. The constant high pitch is unbearable at time. I am due to go on holiday next Monty and I am getting very anxious about spending 5 hours on a plane with the noise levels possibly making the “ ringing” a lot worse.
PMJ01
in
Tinnitus UK
10 months ago
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