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Thrush from Trimbow worse at the end of inhaler
I’ve been using Trimbow for about 6 months now and it’s changed my life, however, I get horrible dry mouth and oral thrush side effects. Maybe I’m imagining it, but I’ve noticed that it gets much worse towards the end of the inhaler and clears up a bit once I start a new one.? Anyone else? I always
I’ve been using Trimbow for about 6 months now and it’s changed my life, however, I get horrible dry mouth and oral thrush side effects. Maybe I’m imagining it, but I’ve noticed that it gets much worse towards the end of the inhaler and clears up a bit once I start a new one.? Anyone else? I always
GaspingGardener
in
Lung Conditions Community Forum
7 months ago
mid-year covid vaccine
the CDC has recommended we immuno-suppressed get a second covid vaccine this year. i am getting mine tomorrow, six months after the 2023-24 first dose. What has your experience been with a second shot in a year? I have normally only gotten one but with this advisory, I decided to do. Your thoughts
the CDC has recommended we immuno-suppressed get a second covid vaccine this year. i am getting mine tomorrow, six months after the 2023-24 first dose. What has your experience been with a second shot in a year? I have normally only gotten one but with this advisory, I decided to do. Your thoughts
ElMaga
in
CLL Support
5 months ago
Tired Tavern - Discord server for people with CFS/ME and/or Long Covid (PACS)
Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid (PACS). We currently have over 350+ members since starting last December. It's a community where empathy, understanding and shared experiences thrive. We have discussions, support groups as well as community events like
Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid (PACS). We currently have over 350+ members since starting last December. It's a community where empathy, understanding and shared experiences thrive. We have discussions, support groups as well as community events like
TiredTavern
in
Myalgic Encephalomyelitis Community
5 months ago
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Should you take Low Dose Naltrexone (LDN) more than once a day for long Covid?
Should you take Low Dose Naltrexone (LDN) more than once a day for long Covid? Answered by Michelle Kilmer Moser https://youtu.be/HldwdGvCPwA
Should you take Low Dose Naltrexone (LDN) more than once a day for long Covid? Answered by Michelle Kilmer Moser https://youtu.be/HldwdGvCPwA
Shewulf
Administrator
in
LDN Research Trust
5 months ago
COVID
I've had COVID for a few days so have not been in touch. Thank G-D I am not throwing up. Calling my Dr. Monday. I hope everyone is doing well. Leslie
I've had COVID for a few days so have not been in touch. Thank G-D I am not throwing up. Calling my Dr. Monday. I hope everyone is doing well. Leslie
lbenmaor
in
My MSAA Community
5 months ago
h pylori treatment
hello I’d like to hear from anyone who has successfully eradicated helicobacter pylori with either a natural or antibiotic protocol. I’m on low dose NDT with Dr Frey and have thyroid nodules (biopsy tested benign) Tested positive for h pylori via a breath test in October and was offered quadruple
hello I’d like to hear from anyone who has successfully eradicated helicobacter pylori with either a natural or antibiotic protocol. I’m on low dose NDT with Dr Frey and have thyroid nodules (biopsy tested benign) Tested positive for h pylori via a breath test in October and was offered quadruple
Crankyoldbag
in
Thyroid UK
7 months ago
New medication for boosting immunity against covid19
Hello everyone from snowy NY. My spouse received his first kidney transplant 11/2018 and I just told him about this news. Apparently, there is a new IV infusion for people who are very immunocompromised to help improve their health from getting covid19, since the vaccinations were not working as hoped
Hello everyone from snowy NY. My spouse received his first kidney transplant 11/2018 and I just told him about this news. Apparently, there is a new IV infusion for people who are very immunocompromised to help improve their health from getting covid19, since the vaccinations were not working as hoped
Gardner-NY
in
Kidney Transplant
5 months ago
Provera
I've recently been diagnosed with endometriosis. My consultant has issued me with provera tablets as treatment. I was wondering if anyone has had any experience with taking these? Im a little apprehensive of the possible side effects. Many thanks
I've recently been diagnosed with endometriosis. My consultant has issued me with provera tablets as treatment. I was wondering if anyone has had any experience with taking these? Im a little apprehensive of the possible side effects. Many thanks
Dvs24
in
Endometriosis UK
7 months ago
starting again!
hello, I was running around 10 miles in my mid fifties following post surgical PE at 50. Covid in 2022 set off severe flare of Ulcerative Colitis (had since 25) and PE. Spent a year recovering started couch to 5k in January having built up fitness walking and cycling. Doing well then got knocked back
hello, I was running around 10 miles in my mid fifties following post surgical PE at 50. Covid in 2022 set off severe flare of Ulcerative Colitis (had since 25) and PE. Spent a year recovering started couch to 5k in January having built up fitness walking and cycling. Doing well then got knocked back
Aclotintrainers
in
Anticoagulation Support
5 months ago
Cold!
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
Basil73
in
Couch to 5K
11 months ago
Lurgy again!
I had a trip to London on Tuesday to work on a show and that was pretty tiring. I'd run on Monday, hoping for 30 minutes, but surrendering at 23. So the 30 minute run was Wednesday ... but no, just too tired. Thursday? Nah. So today, for sure. I got up early and put my running gear on, did two lots of
I had a trip to London on Tuesday to work on a show and that was pretty tiring. I'd run on Monday, hoping for 30 minutes, but surrendering at 23. So the 30 minute run was Wednesday ... but no, just too tired. Thursday? Nah. So today, for sure. I got up early and put my running gear on, did two lots of
Gthants
in
Bridge to 10K
5 months ago
Flu vaccine
Thank you for your replies and concerns regarding the flu vaccine. However I was querying if people with underactive thyroid/Hashimotos need to be more aware of taking it.
Thank you for your replies and concerns regarding the flu vaccine. However I was querying if people with underactive thyroid/Hashimotos need to be more aware of taking it.
292426
in
Thyroid UK
11 months ago
it’s been a rough six months.
I’m tired of winning the sickness lottery. I swear it’s been one thing after another for five months. Bad cold, chronic inflammation of my eyes (non-ms) which caused sores on my right eye, Covid, extreme vertigo that returned me to the ER, another cold and now shingles. Fortunately the shingles aren
I’m tired of winning the sickness lottery. I swear it’s been one thing after another for five months. Bad cold, chronic inflammation of my eyes (non-ms) which caused sores on my right eye, Covid, extreme vertigo that returned me to the ER, another cold and now shingles. Fortunately the shingles aren
StacyHayward
in
My MSAA Community
7 months ago
Flu and Covid vaccine
I was diagnosed with lupus in March this year. I dont know if I should take the flu and covid vaccine. I am scared it will make my lupus worse. Has anyone here take the vaccine?
I was diagnosed with lupus in March this year. I dont know if I should take the flu and covid vaccine. I am scared it will make my lupus worse. Has anyone here take the vaccine?
kali9
in
LUPUS UK
9 months ago
Chondocalcitis incurable?
At least that's how I think it's spelt. It's a specialised form of RA and I have it in my left knee (along with normal RA in shoulders, elbows, wrists and fingers.It's also called Pseudogout but as the crystals in Chondocalcitis are calcium they can't be dispersed as the uric acid crystals in ordinary
At least that's how I think it's spelt. It's a specialised form of RA and I have it in my left knee (along with normal RA in shoulders, elbows, wrists and fingers.It's also called Pseudogout but as the crystals in Chondocalcitis are calcium they can't be dispersed as the uric acid crystals in ordinary
Jeff1943
in
NRAS
5 months ago
Covid injections
Are the next covid injections due soon
Are the next covid injections due soon
Spacecat1
in
Lung Conditions Community Forum
5 months ago
Flu vaccine
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
292426
in
Thyroid UK
11 months ago
Getting Off of Painkillers
I started seeing a pain management doctor about 4 years ago for severe lower back pain. One of the first things she did was put me on 5 mg Hydrocodone four times a day and gave me a steroid injection. Over the years, I have had several radio frequency ablations and a handful of steroid injections. The
I started seeing a pain management doctor about 4 years ago for severe lower back pain. One of the first things she did was put me on 5 mg Hydrocodone four times a day and gave me a steroid injection. Over the years, I have had several radio frequency ablations and a handful of steroid injections. The
Hidden
in
Pain Concern
5 months ago
Valproate: new safety and educational materials to support regulatory measures in men and women under 55 years of age
I don't think there is any reason to expect many members to be taking any form of Valproate, but this is such an important issue, with such significant consequences, I've decided to post it anyway. Even if you are not taking it, someone you know might be. [i]
Valproate (Belvo, Convulex, Depakote,
I don't think there is any reason to expect many members to be taking any form of Valproate, but this is such an important issue, with such significant consequences, I've decided to post it anyway. Even if you are not taking it, someone you know might be. [i]
Valproate (Belvo, Convulex, Depakote,
helvella
Thyroid UK
in
Thyroid UK
7 months ago
After 10+ years I've been discharged from the Vascular Department
Morning AllI live in London, UK and just before Christmas was discharged from a Vascular Department in a London hospital. I had been under their care for over 10 years, this was the place I went to have the xray where they inject the dye between your toes that will show how and light up how your lymphatic
Morning AllI live in London, UK and just before Christmas was discharged from a Vascular Department in a London hospital. I had been under their care for over 10 years, this was the place I went to have the xray where they inject the dye between your toes that will show how and light up how your lymphatic
Applekenke172
in
LSN
5 months ago
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