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Three Distinct MS Subtypes Identified
[i]I'm so sorry. I sent a bad link. Hopefully this one will work better.[/i]
MDedge/Neurology 09 Apr 2024
https://www.mdedge.com/neurology/article/268641/multiple-sclerosis/three-distinct-ms-subtypes-identified
[i]I'm so sorry. I sent a bad link. Hopefully this one will work better.[/i]
MDedge/Neurology 09 Apr 2024
https://www.mdedge.com/neurology/article/268641/multiple-sclerosis/three-distinct-ms-subtypes-identified
BettysMom
in
My MSAA Community
4 months ago
My Oligometastatic PCa Journey Continues...coming up on year 9!
It's been a while since I've posted. But wanted to offer a note of
encouragement
for those here that have
oligometastatic prostate cancer
. I was diagnosed in 2015 (227 PSA, Gleason 8, 1 MET in the spine) and still going strong. After years of
hormone therapy
, 6 rounds of
chemo
It's been a while since I've posted. But wanted to offer a note of
encouragement
for those here that have
oligometastatic prostate cancer
. I was diagnosed in 2015 (227 PSA, Gleason 8, 1 MET in the spine) and still going strong. After years of
hormone therapy
, 6 rounds of
chemo
JamesAtlanta
in
Advanced Prostate Cancer
7 months ago
Progression
My mum got diagnosed with PSP just last October,but that took 18 months .She is now in a residential home ,but I fell so guilty I couldn't keep her at home š The PSP has progressed so quickly Her slight is problematic,falling alot,her speech has become very bad over the last month . Thankfully her
My mum got diagnosed with PSP just last October,but that took 18 months .She is now in a residential home ,but I fell so guilty I couldn't keep her at home š The PSP has progressed so quickly Her slight is problematic,falling alot,her speech has become very bad over the last month . Thankfully her
Blitzford72
in
PSP Association
3 months ago
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Detecting undiagnosed AF
I'm a stroke lived-experience person since 2016 and, I've had atrial fibrillation / flutter that started years before that. Intially paroxymal, later becoming permanent. I was the subject of a paper (available on the Internet) on pulmonary toxicity (aka cryptogenic organising pnuemonia) secondary to
I'm a stroke lived-experience person since 2016 and, I've had atrial fibrillation / flutter that started years before that. Intially paroxymal, later becoming permanent. I was the subject of a paper (available on the Internet) on pulmonary toxicity (aka cryptogenic organising pnuemonia) secondary to
john-boy-92
in
Atrial Fibrillation Support
3 months ago
Are Functional Motor Symptoms Influenced by Glutamate and Glutamine Fluctuations?
I was reading an old post and someone commented about this, so naturally I asked the question and found this study: https://www.neurologylive.com/view/functional-motor-symptoms-influenced-glutamate-glutamine-fluctuations Interesting reading and saying that the "functional movements" are down to biology
I was reading an old post and someone commented about this, so naturally I asked the question and found this study: https://www.neurologylive.com/view/functional-motor-symptoms-influenced-glutamate-glutamine-fluctuations Interesting reading and saying that the "functional movements" are down to biology
Lady4
in
Functional Neurological Disorder - FND Hope
7 months ago
Peripheral artery disease, is it associated with cardiac health?
I am going to contact my GP tomorrow, because I think I might have PAD. I get pain in my calves, sometimes but not always, when I walk. I can just leave the house and my legs are aching. I have also found I just cannot rush and walk faster! Also going upstairs. The stairs bit I think I have had for
I am going to contact my GP tomorrow, because I think I might have PAD. I get pain in my calves, sometimes but not always, when I walk. I can just leave the house and my legs are aching. I have also found I just cannot rush and walk faster! Also going upstairs. The stairs bit I think I have had for
Whitecarnation
in
British Heart Foundation
2 years ago
Ablation or Not?
I'm currently waiting for an ablation and have been for over 6 months. When I first developed AF I was quite badly affected by it. I would: Get out of breath just walking a short distance Keep falling asleep Found climbing stairs and carrying 'heavy' things more difficult than they should Occasionally
I'm currently waiting for an ablation and have been for over 6 months. When I first developed AF I was quite badly affected by it. I would: Get out of breath just walking a short distance Keep falling asleep Found climbing stairs and carrying 'heavy' things more difficult than they should Occasionally
Peakoverload
in
Atrial Fibrillation Support
3 months ago
Leg Problems after CABG / Saphenous Vein Harvested
Hi, I had a CABG x 3 about 18 months back (June 2022). During the ops my left saphenous vein was harvested. I had a stroke in the recovery room, however my question is to other folk that have had CABG and vein removal. Do you have any complications with your leg, loss of feeling, feeling heavy,
Hi, I had a CABG x 3 about 18 months back (June 2022). During the ops my left saphenous vein was harvested. I had a stroke in the recovery room, however my question is to other folk that have had CABG and vein removal. Do you have any complications with your leg, loss of feeling, feeling heavy,
BlueberryBob
in
British Heart Foundation
10 months ago
Suspect I have Addison's
I had a blood test yesterday and my serum cortisol was 330 nm/l.I have some hyperpigmentation & vitaligo. I think my GP was checking for Addison's. Hopefully now I can see an endocrinologist
I had a blood test yesterday and my serum cortisol was 330 nm/l.I have some hyperpigmentation & vitaligo. I think my GP was checking for Addison's. Hopefully now I can see an endocrinologist
antiloquax
in
Thyroid UK
4 months ago
MTHFR and Lupus
I noticed that some members have both of these diagnosis as well as Sjogrens. No one ever checked my homocysteine level until after I had Complete Heart Block and was implanted with a Pacemaker/defibulator. I have always felt that if the MTHFR was diagnosed before all the other autoimmune diseases, I
I noticed that some members have both of these diagnosis as well as Sjogrens. No one ever checked my homocysteine level until after I had Complete Heart Block and was implanted with a Pacemaker/defibulator. I have always felt that if the MTHFR was diagnosed before all the other autoimmune diseases, I
DogHospiceMom
in
LUPUS UK
3 months ago
Stomach issues
Morning all, So I am just about at my wits end with chronic gastric reflux and chronic wind up and down without much smell. Sometimes I vomit with it, and now I can only eat jasmine rice and even struggle to get water down at the moment. My stomach feels like I have been beat up from the inside
Morning all, So I am just about at my wits end with chronic gastric reflux and chronic wind up and down without much smell. Sometimes I vomit with it, and now I can only eat jasmine rice and even struggle to get water down at the moment. My stomach feels like I have been beat up from the inside
M0wnt
in
LUPUS UK
4 months ago
Arrhythmia Checklist
Do you or a family member experience unexplained chest pain, a rapid or irregular pulse, breathlessness, or light-headedness, these are all symptoms that should not be ignored and could be the early warning signs of an underlying heart rhythm disorder/ For further guidance, download the Arrhythmia
Do you or a family member experience unexplained chest pain, a rapid or irregular pulse, breathlessness, or light-headedness, these are all symptoms that should not be ignored and could be the early warning signs of an underlying heart rhythm disorder/ For further guidance, download the Arrhythmia
TracyAdmin
Partner
in
Sudden Cardiac Arrest & Heart Attack
3 months ago
We could tell in advance if enzalutamide works on a patient: computational biology
hopefully it will be clinically tested soon āFor the study in Nature Communications, Mitrofanova's team developed computational algorithms to discover why the prostate cancer drug enzalutamide (sold under the brand name Xtandi) never works for some patients and why it eventually stops working in others
hopefully it will be clinically tested soon āFor the study in Nature Communications, Mitrofanova's team developed computational algorithms to discover why the prostate cancer drug enzalutamide (sold under the brand name Xtandi) never works for some patients and why it eventually stops working in others
Maxone73
in
Advanced Prostate Cancer
7 months ago
Nebivolol 2.5mg
I started Nebivolol for my AFIB about one month ago for my heart rate! I like the drug but seem to have a lot of gas on my stomach! Has anyone else had this problem?
I started Nebivolol for my AFIB about one month ago for my heart rate! I like the drug but seem to have a lot of gas on my stomach! Has anyone else had this problem?
BaileyC57
in
Atrial Fibrillation Support
3 months ago
Low Testosterone and value of continuing Hormone Therapy
83 year old male with a question: My understanding is that the role of hormone therapy is to lower oneās testosterone level. Does hormone therapy provide additional benefits in fighting prostate cancer beyond lowering testosterone levels? I was diagnosed with high grade prostate cancer (Gleason 10
83 year old male with a question: My understanding is that the role of hormone therapy is to lower oneās testosterone level. Does hormone therapy provide additional benefits in fighting prostate cancer beyond lowering testosterone levels? I was diagnosed with high grade prostate cancer (Gleason 10
saniku
in
Advanced Prostate Cancer
7 months ago
need some guidance, feeling desperate..
My husband has advanced, Stage IV castration resistant prostate cancer. When he was diagnosed in May 2022 his PSA was 4700, he has widespread bone metastases. He stopped responding to Docetaxel, Pluvicto and is now not responding to Cabazitaxel, his PSA is now over 700. He is feeling good, no pain
My husband has advanced, Stage IV castration resistant prostate cancer. When he was diagnosed in May 2022 his PSA was 4700, he has widespread bone metastases. He stopped responding to Docetaxel, Pluvicto and is now not responding to Cabazitaxel, his PSA is now over 700. He is feeling good, no pain
Kiki27
in
Advanced Prostate Cancer
7 months ago
Extra steroids?
Having had my first cold since before the pandemic after Christmas, I went off the to the doctors about 10 days ago because although I felt I'd recovered I was deaf in one ear and had sticky eyes. One ear hadn't 'popped' on the flight out or back to the UK and once the cold kicked in it got worse. Currently
Having had my first cold since before the pandemic after Christmas, I went off the to the doctors about 10 days ago because although I felt I'd recovered I was deaf in one ear and had sticky eyes. One ear hadn't 'popped' on the flight out or back to the UK and once the cold kicked in it got worse. Currently
ladygigger
in
PMRGCAuk
7 months ago
Three Distinct MS Subtypes Identified
From MDedge/neurology 09April 2024
https://www.mdedge.com/neurology/article/268641/multiple-sclerosis/three-distinct-ms-subtypes-identified?ecd=WNL_EVE_240411_mdedge&icd=login_success_email_match_norm&print=1
From MDedge/neurology 09April 2024
https://www.mdedge.com/neurology/article/268641/multiple-sclerosis/three-distinct-ms-subtypes-identified?ecd=WNL_EVE_240411_mdedge&icd=login_success_email_match_norm&print=1
BettysMom
in
My MSAA Community
4 months ago
Lipid results
Since my last post regarding elevated finger prick sample for cholesterol, I am now in receipt of my formal blood test results for lipid profile which are borderline and need to speak to Doctor. I do have a GP follow up next week to discuss these but wondered if anyone on here can interpret them and
Since my last post regarding elevated finger prick sample for cholesterol, I am now in receipt of my formal blood test results for lipid profile which are borderline and need to speak to Doctor. I do have a GP follow up next week to discuss these but wondered if anyone on here can interpret them and
Maynan17
in
Thyroid UK
3 months ago
My folate deficiency merry-go-round.
Hi all,I have joined here in hope of learning more about why l keep getting folate decifiency. It is currently 2.1. I become deficient usually every 7/8 months and it has been this way for about 3 years. Each time it happens, l complain to my GP that l feel exhausted, he runs blood tests and it is
Hi all,I have joined here in hope of learning more about why l keep getting folate decifiency. It is currently 2.1. I become deficient usually every 7/8 months and it has been this way for about 3 years. Each time it happens, l complain to my GP that l feel exhausted, he runs blood tests and it is
Blue_feather
in
Pernicious Anaemia Society
4 months ago
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