Search
Search
About
Log in
Join
Experiences with
Traumatic macular hole
Posts
Communities
7,195 public posts
Filter results
Is there ANYTHING that does not Ameliorate Rotenone-Induced Parkinson's Disease in Rats?
Idebenone Ameliorates Rotenone-Induced Parkinson's Disease in Rats Through Decreasing Lipid Peroxidation 2021 https://pubmed.ncbi.nlm.nih.gov/33247801/ I have some Idebenone. I bought it because they are trialing it to prevent RBD from turning into PD (or slow it down). I cut it from my stack a while
Idebenone Ameliorates Rotenone-Induced Parkinson's Disease in Rats Through Decreasing Lipid Peroxidation 2021 https://pubmed.ncbi.nlm.nih.gov/33247801/ I have some Idebenone. I bought it because they are trialing it to prevent RBD from turning into PD (or slow it down). I cut it from my stack a while
Bolt_Upright
in
Cure Parkinson's
3 years ago
Zoloft
Finally after years of being afraid of judgment and horrible side effects, I’m allowing myself to seek more help and try medication. I was recently medically retired from the military and my depression and PTSD have been debilitating….I pray to God this helps me because I’ve barely been functioning.
Finally after years of being afraid of judgment and horrible side effects, I’m allowing myself to seek more help and try medication. I was recently medically retired from the military and my depression and PTSD have been debilitating….I pray to God this helps me because I’ve barely been functioning.
AnxietyBucket
in
Anxiety and Depression Support
3 years ago
Blood patches on skin
Has anyone had bleeds into the skin with Apixaban. I have patches of these ln my lower legs. They are starting to fade but it is a bit worrying Dr. Google says it could be a low platelet problem. Should I discuss it with my GP?
Has anyone had bleeds into the skin with Apixaban. I have patches of these ln my lower legs. They are starting to fade but it is a bit worrying Dr. Google says it could be a low platelet problem. Should I discuss it with my GP?
rothwell
in
AF Association
3 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Medication & mental health guidance
Hi, my nearly 11 year old daughter has been treated for impacted bowels since she was 5 by a gastroenterologist. She’s has 3 desimpactations, two of Movicol and one at the hospital with a tube up her nose. She is now only on 10ml of Senna a day. We’ve found when she takes it she gets belly aches, her
Hi, my nearly 11 year old daughter has been treated for impacted bowels since she was 5 by a gastroenterologist. She’s has 3 desimpactations, two of Movicol and one at the hospital with a tube up her nose. She is now only on 10ml of Senna a day. We’ve found when she takes it she gets belly aches, her
Nsin
in
ERIC
3 years ago
Steroid card
Hello all, This might seem a silly question, but I’m in the US and it seems doctors or pharmacies here have never heard of a blue steroid card, something that’s easily visible and universally recognized in an emergency? I know you can buy medic alert bracelets and such, or make a card yourself
Hello all, This might seem a silly question, but I’m in the US and it seems doctors or pharmacies here have never heard of a blue steroid card, something that’s easily visible and universally recognized in an emergency? I know you can buy medic alert bracelets and such, or make a card yourself
Mstiles
in
PMRGCAuk
3 years ago
Vascular Parkinsonism
Hi all After 3 year of doctor visits back and forth ,they have finally concluded to Vascular Parkinsonism due to white matter lesions(hyperintensities)/leukoaraiosis probably linked to several years of uncontrolled High blood pressure. The most obvious symptom is the gait:feet dragging and freezing when
Hi all After 3 year of doctor visits back and forth ,they have finally concluded to Vascular Parkinsonism due to white matter lesions(hyperintensities)/leukoaraiosis probably linked to several years of uncontrolled High blood pressure. The most obvious symptom is the gait:feet dragging and freezing when
Laua
in
Cure Parkinson's
3 years ago
MPN-U
Hi everyone I am a 72 year old female and a new member. I was diagnosed one year ago with ET by my hematologist , but after consulting with an MPN specialist my diagnosis was changed to PV. Now it seems I don't fit exactly into that category so I am MPN-U (unclassified). I've been on Hydroxyurea 500
Hi everyone I am a 72 year old female and a new member. I was diagnosed one year ago with ET by my hematologist , but after consulting with an MPN specialist my diagnosis was changed to PV. Now it seems I don't fit exactly into that category so I am MPN-U (unclassified). I've been on Hydroxyurea 500
violetta115
in
MPN Voice
3 years ago
Mucoactive natural products
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469994/ Ambroxol is a mucoactive substance, so maybe these natural compounds in article are worth a try if you can’t get or don’t want to use ambroxol. Keywords: Mucins, Inflammation, cancer, natural compounds, Curcumin, Guggulsterone, Apigenin, Glycyrrhizin
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469994/ Ambroxol is a mucoactive substance, so maybe these natural compounds in article are worth a try if you can’t get or don’t want to use ambroxol. Keywords: Mucins, Inflammation, cancer, natural compounds, Curcumin, Guggulsterone, Apigenin, Glycyrrhizin
LAJ12345
in
Cure Parkinson's
3 years ago
Pulmonary embolism Treatment
Hi I’ve been diagnosed with APS as a result of having clots in the lungs (Pulmonary embolism). Current treatment is Apixaban (Eliquis) 5 mg tablet morning and night on going. I have been advised by my specialist that Eliquis may not be as effective as Warfarin. Was wondering if anyone had similar symptoms
Hi I’ve been diagnosed with APS as a result of having clots in the lungs (Pulmonary embolism). Current treatment is Apixaban (Eliquis) 5 mg tablet morning and night on going. I have been advised by my specialist that Eliquis may not be as effective as Warfarin. Was wondering if anyone had similar symptoms
SantaG
in
Hughes Syndrome APS Forum
3 years ago
Lupron Side Effects
I am having Lupron injections. I have been to my doctor- GP complaining about dull headaches and slow thinking. Could this be a side effect of Lupron? From Burnett 1948.
I am having Lupron injections. I have been to my doctor- GP complaining about dull headaches and slow thinking. Could this be a side effect of Lupron? From Burnett 1948.
Burnett1948
in
Advanced Prostate Cancer
3 years ago
Vent
I have PTSD, depression and anxiety. Currently dealing with a infection on my inner leg and a ear infection in my right ear. This Sunday is 1 year since my stepdad died from cancer. I recently turned 28 and have come along way since his passing but it's not been through choice. I suppose it never is
I have PTSD, depression and anxiety. Currently dealing with a infection on my inner leg and a ear infection in my right ear. This Sunday is 1 year since my stepdad died from cancer. I recently turned 28 and have come along way since his passing but it's not been through choice. I suppose it never is
jembella-
in
Mental Health Support
3 years ago
Epidural injection
had an mri 7 weeks ago got results back slipped disc in L4 L5 got to have the epidural injection as the disc in pressing on nurv so worried about geting the epidural due to the side effects ect I have had epidural when I had my 2 children via c section am guessing it’s the same apart from your not numb
had an mri 7 weeks ago got results back slipped disc in L4 L5 got to have the epidural injection as the disc in pressing on nurv so worried about geting the epidural due to the side effects ect I have had epidural when I had my 2 children via c section am guessing it’s the same apart from your not numb
Manchestermum
in
NRAS
3 years ago
Chiropractor / osteopath
Is it advisable to attend chiropractor / Oestopath recently diagnosed vasculitis - Takaysus . On pred 17.5 currently . Dexta is perfect . Have found so helpful in past with spine issues but nervous to attend now . Any thoughts 😊
Is it advisable to attend chiropractor / Oestopath recently diagnosed vasculitis - Takaysus . On pred 17.5 currently . Dexta is perfect . Have found so helpful in past with spine issues but nervous to attend now . Any thoughts 😊
Ballywilliam
in
PMRGCAuk
3 years ago
Removal of tracheostomy after 1 week but advised no further intensive care or ventilation in future?! So confused and scared
Sorry for a lot of posts recently but visited my daughter who has a global anoxic injury yesterday and was taken aside by the consultant afterwards for a discussion regarding their plans going forward and i do not know how to feel and am so worried. The consultant was positive to begin with and said
Sorry for a lot of posts recently but visited my daughter who has a global anoxic injury yesterday and was taken aside by the consultant afterwards for a discussion regarding their plans going forward and i do not know how to feel and am so worried. The consultant was positive to begin with and said
Parapp
in
Headway
3 years ago
Albuterol
Hi, Does albuterol sulfate impact RLS? I was prescribed it for COVID but I am always nervous.
Hi, Does albuterol sulfate impact RLS? I was prescribed it for COVID but I am always nervous.
Megamania
in
Restless Legs Syndrome
3 years ago
Update on my GCA/Large vessel vasculitis journey: off pred and back to normal (with TCZ)
I have been diagnosed with GCA/LVV in February of this year. My main symptoms were fever and fatigue and I had CRP values of up to 80 and an ESR of 100. I am living in Germany and here it is a standard scheme to start with pred (40 mg in my case) and Actemra (Tocilizumab) weekly injections. I feel that
I have been diagnosed with GCA/LVV in February of this year. My main symptoms were fever and fatigue and I had CRP values of up to 80 and an ESR of 100. I am living in Germany and here it is a standard scheme to start with pred (40 mg in my case) and Actemra (Tocilizumab) weekly injections. I feel that
DeepThought2
in
PMRGCAuk
3 years ago
Is it advisable to stay at ...say 8mg pred?
I have had PMR & GCA since Feb 2017. It has been a rocky ride with all sorts of complications including Pulmonary Embolism & Pneumonia. Have got down to 6mg last year (summer 2020) but at 5.5mg troubles with pains every where. Had knees Xrayed but although nothing showed to warrant the pain. With
I have had PMR & GCA since Feb 2017. It has been a rocky ride with all sorts of complications including Pulmonary Embolism & Pneumonia. Have got down to 6mg last year (summer 2020) but at 5.5mg troubles with pains every where. Had knees Xrayed but although nothing showed to warrant the pain. With
Gypdyp45
in
PMRGCAuk
3 years ago
Akkermansia bacteria in gut health
https://drhyman.com/blog/2021/07/26/akkermansia-muciniphila/?_kx=apfgrmgyRq8RXiW5XnHAO8jNq_ApimWvMVEweegI0qHS-vQsTB77BJsRj8ahxigO.HKMsXE “Lactobacillus and bifidobacterium are considered the superstars (or should I say, “superbugs”?) of gut microbiome research because their abundance is linked to better
https://drhyman.com/blog/2021/07/26/akkermansia-muciniphila/?_kx=apfgrmgyRq8RXiW5XnHAO8jNq_ApimWvMVEweegI0qHS-vQsTB77BJsRj8ahxigO.HKMsXE “Lactobacillus and bifidobacterium are considered the superstars (or should I say, “superbugs”?) of gut microbiome research because their abundance is linked to better
LAJ12345
in
Cure Parkinson's
3 years ago
Probiotic supplementation may confer advantageous therapeutic potential for people with PD (lowers inflammation)
Found this in an old post of Art's and thought it deserved its own topic https://healthunlocked.com/cure-parkinsons/posts/142240155/il-8-the-inflammatory-mediator-that-is-220-higher-in-pwp-cerebrospinal-fluid-than-in-control-subjects-and-possible-ways-to-deal-with-it The Effects of Probiotic Supplementation
Found this in an old post of Art's and thought it deserved its own topic https://healthunlocked.com/cure-parkinsons/posts/142240155/il-8-the-inflammatory-mediator-that-is-220-higher-in-pwp-cerebrospinal-fluid-than-in-control-subjects-and-possible-ways-to-deal-with-it The Effects of Probiotic Supplementation
Bolt_Upright
in
Cure Parkinson's
3 years ago
How did you manage your initial diagnosis?
Hi, everyone. I’ve just had an official IBS diagnosis last Thursday. I had a call from a GP who just wanted to get me off the phone ASAP - I’ll be calling back tomorrow and asking for a f2f appt with my preferred and trusted GP. Because right now, I know very little. I don’t know what type of IBS
Hi, everyone. I’ve just had an official IBS diagnosis last Thursday. I had a call from a GP who just wanted to get me off the phone ASAP - I’ll be calling back tomorrow and asking for a f2f appt with my preferred and trusted GP. Because right now, I know very little. I don’t know what type of IBS
Zedi39
in
IBS Network
3 years ago
1
...
61
62
63
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Atrial Fibrillation Support
923 results
Hughes Syndrome APS Forum
631 results
Anxiety and Depression Support
451 results
View top 10 communities
Sort by
Most Relevant
Newest