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Are you ready to kick neurotoxins to the curb?
You can start by not eating them and clean up your diet. The next step is to remove neurotoxins from your personal care and cleaning products. Edit: Would you be more motivated to change your lifestyle if you understood how Roundup is used and why it's poison? Roundup kills any actively growing plant
You can start by not eating them and clean up your diet. The next step is to remove neurotoxins from your personal care and cleaning products. Edit: Would you be more motivated to change your lifestyle if you understood how Roundup is used and why it's poison? Roundup kills any actively growing plant
SilentEchoes
in
Cure Parkinson's
8 months ago
Could chronic urticaria be related to underactive thyroid?
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
Chestercheese
in
Thyroid UK
5 months ago
Post Cardioversion
In my previous post I explained that my 3rd carioversion did not work even after one hour I was back into afib. However something strange is happening or at least it seems strange to me but may be normal. Five days after my cardio I got up around 2:30-3:00 am to use the loo. I could feel my heart in
In my previous post I explained that my 3rd carioversion did not work even after one hour I was back into afib. However something strange is happening or at least it seems strange to me but may be normal. Five days after my cardio I got up around 2:30-3:00 am to use the loo. I could feel my heart in
dindy
in
Atrial Fibrillation Support
4 months ago
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LUPUS 100 Answers to the most important questions about lupus, verified by world renowned lupus doctors
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 months ago
Car-T cell therapy might cure Systemic Autoimmune Diseases
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy šššš: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy šššš: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Naladog
in
LUPUS UK
5 months ago
Overactive Bladder Syndrome
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Oggy99
in
AF Association
8 months ago
Peginterferon
I'm wondering if anyone else is struggling with poor appetite while being o peginterferon.I have been on it for 4 years diagnosed with MF. The dose has gradually been raised but was then put up again to 135 weekly a few months ago because my spleen was enlarging.im now waiting for another appointment
I'm wondering if anyone else is struggling with poor appetite while being o peginterferon.I have been on it for 4 years diagnosed with MF. The dose has gradually been raised but was then put up again to 135 weekly a few months ago because my spleen was enlarging.im now waiting for another appointment
caroline_284
in
MPN Voice
8 months ago
And again news about clinical trials
Clinical trial tests creatine monohydrate and exercise to preserve muscle mass in prostate cancer
https://www.news-medical.net/news/20231011/Clinical-trial-tests-creatine-monohydrate-and-exercise-to-preserve-muscle-mass-in-prostate-cancer-patients.aspx (hint: been a natural bodybuilder from
Clinical trial tests creatine monohydrate and exercise to preserve muscle mass in prostate cancer
https://www.news-medical.net/news/20231011/Clinical-trial-tests-creatine-monohydrate-and-exercise-to-preserve-muscle-mass-in-prostate-cancer-patients.aspx (hint: been a natural bodybuilder from
Maxone73
in
Advanced Prostate Cancer
8 months ago
Nightly leg cramps
Hi Warriors: I have GCA since June 2023. Down to 35 mg pred from 60 mg. Tapering down by 5mg every 2 weeks til I get to l5mg. Then will go much slower. I am having very painful leg cramps every night that wake me up. after about 3/4 hrs sleep. I have to get up and walk around. Last night I took 2
Hi Warriors: I have GCA since June 2023. Down to 35 mg pred from 60 mg. Tapering down by 5mg every 2 weeks til I get to l5mg. Then will go much slower. I am having very painful leg cramps every night that wake me up. after about 3/4 hrs sleep. I have to get up and walk around. Last night I took 2
Groda
in
PMRGCAuk
8 months ago
amiodarone
Was admitted via A&E to hospital last October with fast AF, 174 bpm., Sob, high bp. Because of other underlying problems with CKD, doc put me on Amiodarone 200mg daily, along with Nebivolol bi-daily, replacing Bisoprolol. Was discharged after 6 days when heart rate was consistently below 80bpm. Now
Was admitted via A&E to hospital last October with fast AF, 174 bpm., Sob, high bp. Because of other underlying problems with CKD, doc put me on Amiodarone 200mg daily, along with Nebivolol bi-daily, replacing Bisoprolol. Was discharged after 6 days when heart rate was consistently below 80bpm. Now
mallet-head
in
Atrial Fibrillation Support
5 months ago
do I need my inhaler ?
hi all, Iām new to this forum and new to my illness which I havenāt really been informed of in much detail. I had a collapsed lung in September last year and they did a cat scan 3 weeks later. The results letter that they sent my doctor was also sent to me. Iāve gathered that I have emphysema and bronchial
hi all, Iām new to this forum and new to my illness which I havenāt really been informed of in much detail. I had a collapsed lung in September last year and they did a cat scan 3 weeks later. The results letter that they sent my doctor was also sent to me. Iāve gathered that I have emphysema and bronchial
50shadesofgrey
in
Lung Conditions Community Forum
5 months ago
High gamma gt
Hi. My husband has cirrhosis and at the moment is compensated. He is worried because his latest gamma gt blood test was over 600. Should we be worried. He has no hospital appointment till after Christmas
Hi. My husband has cirrhosis and at the moment is compensated. He is worried because his latest gamma gt blood test was over 600. Should we be worried. He has no hospital appointment till after Christmas
trekmum
in
British Liver Trust
8 months ago
Some key differences found in lupus symptoms in men vs. women: Study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 months ago
QoL Please, always
Friends, please remember to include the letters "QoL" in front of your title whenever you post about quality of life things that are not directly related to prostate cancer
Friends, please remember to include the letters "QoL" in front of your title whenever you post about quality of life things that are not directly related to prostate cancer
Darryl
Partner
in
Advanced Prostate Cancer
8 months ago
Straw therapy for low speech volume
Hubby has low volume speech. He is currently doing work with the Parkinsonās Voice Project (PVP) with some success ā IF he keeps up with it. We recently saw exercises for help projecting with volume using a straw (you blow into a glass of water), supposedly this helps with increasing the muscle tone
Hubby has low volume speech. He is currently doing work with the Parkinsonās Voice Project (PVP) with some success ā IF he keeps up with it. We recently saw exercises for help projecting with volume using a straw (you blow into a glass of water), supposedly this helps with increasing the muscle tone
1rocketman
in
Cure Parkinson's
8 months ago
Is it possible for me to get back to skateboard with autoimmune disease ever?Or do I need to give it up forever?
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Crow9
in
LUPUS UK
5 months ago
Help For Pernicious Anaemia Injections Effect
I was diagnosed with Pernicious Anemia, B12 Deficiency and vitamin D Deficiency. I started B12 Injections in October 2/3 a week until a full course of ten injections were given now I'm down to one every three months. My doctor allowed me an injection between the now every three months dosages as I feel
I was diagnosed with Pernicious Anemia, B12 Deficiency and vitamin D Deficiency. I started B12 Injections in October 2/3 a week until a full course of ten injections were given now I'm down to one every three months. My doctor allowed me an injection between the now every three months dosages as I feel
So_Drained
in
Pernicious Anaemia Society
4 months ago
One litre of fluids
After having pneumonia with fluid on the lung I have now developed heart failure.My recent x-ray was showing I still have fluid on my lung. I don't have any shortness of breath at the moment. I was surprised to hear this. Apparently it's worse than it was. A consultant from the hospital rang me to ask
After having pneumonia with fluid on the lung I have now developed heart failure.My recent x-ray was showing I still have fluid on my lung. I don't have any shortness of breath at the moment. I was surprised to hear this. Apparently it's worse than it was. A consultant from the hospital rang me to ask
Cosychair
in
Asthma Community Forum
5 months ago
Psa doubled in less than a month
I had 10 infusions of Doxytaxel. I started reading about the consequences of CDK12 and was concerned that since I have this mutation doxy was not a treatment of choice. After giving time for the PSA to settle I had a test which showed that it doubled in close to 3 months. In preparation for a CT and
I had 10 infusions of Doxytaxel. I started reading about the consequences of CDK12 and was concerned that since I have this mutation doxy was not a treatment of choice. After giving time for the PSA to settle I had a test which showed that it doubled in close to 3 months. In preparation for a CT and
spencoid2
in
Advanced Prostate Cancer
8 months ago
GFR question
Hi everyone, I'm a 59 year old male. I have high blood pressure and diabetes. A few years ago my GP said that I was dehydrated and need to drink more water. Didn't look at my test results other than to keep taking my meds for high blood pressure and diabetes. Fast forward to around 6 months ago I
Hi everyone, I'm a 59 year old male. I have high blood pressure and diabetes. A few years ago my GP said that I was dehydrated and need to drink more water. Didn't look at my test results other than to keep taking my meds for high blood pressure and diabetes. Fast forward to around 6 months ago I
tatarsalad
in
Early CKD Support
8 months ago
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