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Pneumonia in CBD
Hi I’ve just found out my mum is in hospital with pneumonia and I’m on holiday in Australia - I’m looking for flights and trying to get home asap. Has anyone had experience of getting this when you already have CBD or has anyone had a loved one who has had pneumonia before? I know it’s not a great thing
Hi I’ve just found out my mum is in hospital with pneumonia and I’m on holiday in Australia - I’m looking for flights and trying to get home asap. Has anyone had experience of getting this when you already have CBD or has anyone had a loved one who has had pneumonia before? I know it’s not a great thing
Chelle1981uk
in
PSP Association
1 year ago
MS exercise issues
Hi my more active friends! I have a question. I need to be more active in hopes that will help me with my insomnia and frankly just need to. I love the pool but frankly it's a lot of work to get to the pool. (even though it's 5 minutes away) Is there any way to avoid triggering the tingling in the legs
Hi my more active friends! I have a question. I need to be more active in hopes that will help me with my insomnia and frankly just need to. I love the pool but frankly it's a lot of work to get to the pool. (even though it's 5 minutes away) Is there any way to avoid triggering the tingling in the legs
AriSmyelin
in
MS Society
1 year ago
In response to Troubleandstrife's request the poem I wrote about my husband no longer being crippled by CBD
Niggly (Nigel B) His wicked sense of humour will have now come to the fore His love of birds and insects will have now returned once more. His ability to answer each and every quiz will once more be in place, and his laughing eyes and lovely smile will now be on his face. He is no longer crippled
Niggly (Nigel B) His wicked sense of humour will have now come to the fore His love of birds and insects will have now returned once more. His ability to answer each and every quiz will once more be in place, and his laughing eyes and lovely smile will now be on his face. He is no longer crippled
AliBee1
in
PSP Association
1 year ago
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Waiting for an ambulance….
My mum is 69, has CBD and as I type we are waiting for an ambulance. The GP has called it and we have been waiting for 3.5 hours already. Mum has been uncontrollably shaking/tremors and is sweating buckets, lying in a pool of sweat after we clean her up. The GP can’t explain as vitals are ok and no temperature
My mum is 69, has CBD and as I type we are waiting for an ambulance. The GP has called it and we have been waiting for 3.5 hours already. Mum has been uncontrollably shaking/tremors and is sweating buckets, lying in a pool of sweat after we clean her up. The GP can’t explain as vitals are ok and no temperature
bichonbear1
in
PSP Association
1 year ago
Cbd and levothyroxine
hello all, After covid last year the relatively mild osteoarthritis in my lower spine became quite inflamed and I began experiencing much more pain in my lower back and what feels like my hip although I know my hips are fine from an mri. I have tried pretty much every supplement out there. I even invested
hello all, After covid last year the relatively mild osteoarthritis in my lower spine became quite inflamed and I began experiencing much more pain in my lower back and what feels like my hip although I know my hips are fine from an mri. I have tried pretty much every supplement out there. I even invested
janiebell
in
Thyroid UK
1 year ago
Final stages of CBD
Hi all My dad is in the final stages of CBD and in fact the Palliative Care Consultant seems to think we have less than 3 months left with him. I am really really struggling with this and can't bear the thought of not having my dad but this illness is the cruellest illness I have ever encountered.
Hi all My dad is in the final stages of CBD and in fact the Palliative Care Consultant seems to think we have less than 3 months left with him. I am really really struggling with this and can't bear the thought of not having my dad but this illness is the cruellest illness I have ever encountered.
Stormtrooper4
in
PSP Association
1 year ago
*update* Sensitive: HCG plateaued and clinic not offering any help
As everyone has been so supportive and helpful a quick but rather sad update: went for a private scan today and they couldn't see anything like a viable pregnancy - just a mass of what they called septations (no idea), possibly a haematoma and fluid. They couldn't see the tubes and only one ovary (with
As everyone has been so supportive and helpful a quick but rather sad update: went for a private scan today and they couldn't see anything like a viable pregnancy - just a mass of what they called septations (no idea), possibly a haematoma and fluid. They couldn't see the tubes and only one ovary (with
MrsOrangejuice
in
Fertility Network UK
1 year ago
Exposure to environmental contaminants and how it relates to increase in Parkinson's disease...
I know that PSP, MSA, and CBD and Parkinsons are not one and the same but this headline caught my eye about the most recent studies involving what effect chemical solvents so many of us are exposed to day to day may have on our brains. My husband, a photographer, farmer, carpenter and sometimes painter
I know that PSP, MSA, and CBD and Parkinsons are not one and the same but this headline caught my eye about the most recent studies involving what effect chemical solvents so many of us are exposed to day to day may have on our brains. My husband, a photographer, farmer, carpenter and sometimes painter
Troubleandstrife
in
PSP Association
1 year ago
CBD oil/gumming Etc
Hello, now I know I'm pretty new to the group as my wife was diagnosed on 12th March but given a PSP diagnosis from 29th Jan but she's had the symptoms for a while now and not seen a Neurologist due to Covid (blah blah blah). But she's been on Co-careldopa and that didn't seem to help, she's now on Pregabilin
Hello, now I know I'm pretty new to the group as my wife was diagnosed on 12th March but given a PSP diagnosis from 29th Jan but she's had the symptoms for a while now and not seen a Neurologist due to Covid (blah blah blah). But she's been on Co-careldopa and that didn't seem to help, she's now on Pregabilin
Derek1uk
in
Multiple System Atrophy Trust
1 year ago
kratom issues
my husband started using kratom about 6 months ago because we can’t get cbd where we live. It was working ok but it’s no longer Easy which has been my problem with it from the Start. We will go back to usa in about 6 weeks. Until then his only option is kratom. he can’t use opiods because he’s bipolar
my husband started using kratom about 6 months ago because we can’t get cbd where we live. It was working ok but it’s no longer Easy which has been my problem with it from the Start. We will go back to usa in about 6 weeks. Until then his only option is kratom. he can’t use opiods because he’s bipolar
RCHD
in
Restless Legs Syndrome
1 year ago
Blood test results for possible adrenal problems and chronic insomnia
I wonder if you’d mind casting an eye over my bloods please? I seem to only be able to post one page, so will also type some results and attach page 2 separately, if I am able. My thyroid results FT4 16.8 (9-19) TSH 0.004 (0.35-4.94) FT3 4.2 (2.9-4.9) I take 125mcg levo and 12.75 T3 daily. I
I wonder if you’d mind casting an eye over my bloods please? I seem to only be able to post one page, so will also type some results and attach page 2 separately, if I am able. My thyroid results FT4 16.8 (9-19) TSH 0.004 (0.35-4.94) FT3 4.2 (2.9-4.9) I take 125mcg levo and 12.75 T3 daily. I
CornishChick
in
Thyroid UK
1 year ago
Trip CBD non alcoholic drink
hi all, Survived my god daughter’s 18th birthday party (and 4 hour’s drive from home) yesterday. Was wondering how the new me on tiny dose of T3 would cope. I always feel awkward with the usual no thank yous to prosecco, non alcoholic prosecco, sugary drinks etc. the whole night on water was a lengthy
hi all, Survived my god daughter’s 18th birthday party (and 4 hour’s drive from home) yesterday. Was wondering how the new me on tiny dose of T3 would cope. I always feel awkward with the usual no thank yous to prosecco, non alcoholic prosecco, sugary drinks etc. the whole night on water was a lengthy
Regenallotment
in
Thyroid UK
1 year ago
CBD OIL FOR SORE KNEES
On two occasions my knees have started to experience pain from over exertion due to exercise and playing golf. Both times I have rubbed on CBD oil and have experienced an almost a miraculous relief from the pain that lasts weeks. Just putting it out there your experience may be different, but for now
On two occasions my knees have started to experience pain from over exertion due to exercise and playing golf. Both times I have rubbed on CBD oil and have experienced an almost a miraculous relief from the pain that lasts weeks. Just putting it out there your experience may be different, but for now
rogerandme
in
Advanced Prostate Cancer
1 year ago
*Sensitive*: hope for the one egg and 3dts
Hi lovely community - if you don't want to see this please scroll on by but I couldn't find a huge amount on 3dts in particular and for those who only get one or a few eggs, maybe this will give a bit of hope. Plus strong support for how important progesterone is for some women. ****** ****** OTD (14dp3dt
Hi lovely community - if you don't want to see this please scroll on by but I couldn't find a huge amount on 3dts in particular and for those who only get one or a few eggs, maybe this will give a bit of hope. Plus strong support for how important progesterone is for some women. ****** ****** OTD (14dp3dt
MrsOrangejuice
in
Fertility Network UK
1 year ago
Hello eyebrows, my old friend
I don’t quite know how to put this, or where this post will end up. I have had super thin/missing eyebrows since iv chemo in 2016. Was on Arimidex follow up for 5 years and noticed that they never returned. Fast forward to my current ibrance/faslodex and xgeva protocol and more of the same. Unit
I don’t quite know how to put this, or where this post will end up. I have had super thin/missing eyebrows since iv chemo in 2016. Was on Arimidex follow up for 5 years and noticed that they never returned. Fast forward to my current ibrance/faslodex and xgeva protocol and more of the same. Unit
Aquamoron
in
SHARE Metastatic Breast Cancer
1 year ago
Fybro & CBD - homemade cream
I have been diagnosed with FM 3 years ago, just before the first COVID-19 lockdown . As almost everyone here - lots of changes in medication, no real GP appointments, uneffective Pain clinic , etc.Had to find alternatives myself. I hate the smell of cannabis, just the smell makes me sick. So I concentrate
I have been diagnosed with FM 3 years ago, just before the first COVID-19 lockdown . As almost everyone here - lots of changes in medication, no real GP appointments, uneffective Pain clinic , etc.Had to find alternatives myself. I hate the smell of cannabis, just the smell makes me sick. So I concentrate
Polly-S
in
Fibromyalgia Action UK
1 year ago
Another anxiety attack 😖
Ugh!!! It is sad when you have been med free and panic free so long that it absolutely turns your world upside down when panic rears it's ugly head.I had a real doozy of a panic attack Friday night. All the old symptoms, but scarier because I had forgotten how scary it really is. I pushed through it,
Ugh!!! It is sad when you have been med free and panic free so long that it absolutely turns your world upside down when panic rears it's ugly head.I had a real doozy of a panic attack Friday night. All the old symptoms, but scarier because I had forgotten how scary it really is. I pushed through it,
Rosiemarie82
in
Anxiety and Depression Support
1 year ago
Hi received from HealthUnlocked the article about CBD & Magnesium cream. I read the trustpilot comments and thought - sounds good to me.
So ordered a tube. Fine - then I thought - that was silly as didn't check whether it interferes with the WARFARIN I have to take. Yes, you've guessed it - its a GREAT BIG NO-NO - can't have CBD if on warfarin. Talk about brain fog took over. Anyway just want to let others know BEFORE they buy (
So ordered a tube. Fine - then I thought - that was silly as didn't check whether it interferes with the WARFARIN I have to take. Yes, you've guessed it - its a GREAT BIG NO-NO - can't have CBD if on warfarin. Talk about brain fog took over. Anyway just want to let others know BEFORE they buy (
fibrojan
in
Fibromyalgia Action UK
1 year ago
Pain control with PLMD
I take 100 mg Lyrica for PLMD, the lowest possible dosage as I never have been able to shake the daytime sedation. Now I have some kind of pinched nerve that has been causing chronic pain. Tylenol is not sufficient (I am going to try a lidocaine patch today for the first time and hope that will help
I take 100 mg Lyrica for PLMD, the lowest possible dosage as I never have been able to shake the daytime sedation. Now I have some kind of pinched nerve that has been causing chronic pain. Tylenol is not sufficient (I am going to try a lidocaine patch today for the first time and hope that will help
wantokporo
in
Restless Legs Syndrome
1 year ago
Continuing Healthcare Farce
We have just been declined for CHC funding for my dad who has advanced stage CBD. Apparently he does not meet the health criteria!! He is on lots of medication which my mum administers. He is at home with carers coming in 4 times a day to do all the personal care and has a visit from the District Nurses
We have just been declined for CHC funding for my dad who has advanced stage CBD. Apparently he does not meet the health criteria!! He is on lots of medication which my mum administers. He is at home with carers coming in 4 times a day to do all the personal care and has a visit from the District Nurses
Stormtrooper4
in
PSP Association
1 year ago
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