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To Big Tow Arthritis
I have mild arthritis in my foot. I use Wiley's Wild Alaskan Fish oil 2300 MG, half a teaspoon daily and have no foot pain. If I forget it for a few days the pain returns. It's good for the heart and brain as high Omega 3. Apparently its stronger than other fish oils. Hope it helps.
I have mild arthritis in my foot. I use Wiley's Wild Alaskan Fish oil 2300 MG, half a teaspoon daily and have no foot pain. If I forget it for a few days the pain returns. It's good for the heart and brain as high Omega 3. Apparently its stronger than other fish oils. Hope it helps.
FyMyArt
in
Pain Concern
6 months ago
Prep For Thyroid Blood Test?
Hi folks. I’m sending off a blood test next Monday for FT3, FT4, TSH, anti-Tg, anti-TPO and want to prepare properly for taking the bloods. I’ve taken in doing it before 9am, drink only water. But unsure about vits, I’m taking Fish Oil, magnesium, B Complex, D3+K. I also SI B12. I think I heard one
Hi folks. I’m sending off a blood test next Monday for FT3, FT4, TSH, anti-Tg, anti-TPO and want to prepare properly for taking the bloods. I’ve taken in doing it before 9am, drink only water. But unsure about vits, I’m taking Fish Oil, magnesium, B Complex, D3+K. I also SI B12. I think I heard one
B12again
in
Thyroid UK
6 months ago
When shall I start 10K ??
OK, so I've decided to do a 10K race, and have my eye on a local one on 20 October 2024 (which is 1 day short of my first ever 5K Parkrun). I'm running 3 times a week (including a weekly Parkrun) and swimming twice weekly too. While the weather is not so "run friendly" - ie windy, dark and cold (I
OK, so I've decided to do a 10K race, and have my eye on a local one on 20 October 2024 (which is 1 day short of my first ever 5K Parkrun). I'm running 3 times a week (including a weekly Parkrun) and swimming twice weekly too. While the weather is not so "run friendly" - ie windy, dark and cold (I
adnewg73
in
Bridge to 10K
6 months ago
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#1 Symptom Reducer
I am a PwP and 56 years old. I'm a bit overwhelmed with all of the information, sometimes conflicting, out there regarding treatments and supplements. I am trying to determine what to try first. I am a predominantly tremor parkie. I exercise regularly & eat well. I take levadopa 25/100 4x a day.
I am a PwP and 56 years old. I'm a bit overwhelmed with all of the information, sometimes conflicting, out there regarding treatments and supplements. I am trying to determine what to try first. I am a predominantly tremor parkie. I exercise regularly & eat well. I take levadopa 25/100 4x a day.
staceysack
in
Cure Parkinson's
6 months ago
Rasagiline/Azilect?
Hi ! My hwp (77) diagnosed 2017. But of course with hindsight symptoms manifested earlier. Started C/L last year : 25/100 @ 3 times a day. Azilect 1 mg once a day . Walking became a really serious problem a month ago. Partly because of ongoing "sciatica" but also freezing a few times a day. Two weeks
Hi ! My hwp (77) diagnosed 2017. But of course with hindsight symptoms manifested earlier. Started C/L last year : 25/100 @ 3 times a day. Azilect 1 mg once a day . Walking became a really serious problem a month ago. Partly because of ongoing "sciatica" but also freezing a few times a day. Two weeks
ghoegap
in
Cure Parkinson's
6 months ago
Edoxoban Update
I recently posted that my Cardiologist had put me on Edoxoban 30mg daily, instead of Aspirin which I had been taking for years. He said the Edoxoban was both safer, and unlike Aspirin would prevent the risk of stroke. A day after starting Edoxoban, I either came down with a cold, or allergy symptoms
I recently posted that my Cardiologist had put me on Edoxoban 30mg daily, instead of Aspirin which I had been taking for years. He said the Edoxoban was both safer, and unlike Aspirin would prevent the risk of stroke. A day after starting Edoxoban, I either came down with a cold, or allergy symptoms
Budken
in
AF Association
6 months ago
Interferon reaction
Hi all,I've recently joined the group and already have found it a great source of information & reassuring messages. I started interferon back in August and it's going okay. I am having a reaction at the injection site. My skin is rash looking, bright red and dry. Is there anything that works? The nurses
Hi all,I've recently joined the group and already have found it a great source of information & reassuring messages. I started interferon back in August and it's going okay. I am having a reaction at the injection site. My skin is rash looking, bright red and dry. Is there anything that works? The nurses
RuaSaoirse
in
MPN Voice
6 months ago
Dry eye syndrome - and castor oil!
Some weeks ago someone posted they were using castor oil for dry eyes. I was rather sceptical that that was a good idea - it sounded as if they were putting it IN their eyes. Anyway - today I got a notification of this study of castor oil as a potential natural remedy for dry eyes: https://www.medicalnewstoday.com
Some weeks ago someone posted they were using castor oil for dry eyes. I was rather sceptical that that was a good idea - it sounded as if they were putting it IN their eyes. Anyway - today I got a notification of this study of castor oil as a potential natural remedy for dry eyes: https://www.medicalnewstoday.com
PMRpro
Ambassador
in
PMRGCAuk
6 months ago
Ear dilema
Hi folks 💛 I recently followed some bad advice and put warmed, diluted tea tree oil in my slightly clogged, itchy ear not realising that Tea Tree can be Ototoxic to the Cochlear. I diluted 3 drops of Tea Tree oil in 30ml of Olive oil and put 0.5 ml in my ear. I let it sit there for around 10 minutes
Hi folks 💛 I recently followed some bad advice and put warmed, diluted tea tree oil in my slightly clogged, itchy ear not realising that Tea Tree can be Ototoxic to the Cochlear. I diluted 3 drops of Tea Tree oil in 30ml of Olive oil and put 0.5 ml in my ear. I let it sit there for around 10 minutes
bodytronic
in
Tinnitus UK
1 month ago
UPDATE: Cod Liver Oil Supplements with Prednisolone
Thank you everyone for your replies. I have lots of information to read and questions for my GP tomorrow. I'm feeling far more in control with the knowledge I now have from you on this group. Really appreciate all the time you've taken to respond to my question. Thank you all once again. I'll sign
Thank you everyone for your replies. I have lots of information to read and questions for my GP tomorrow. I'm feeling far more in control with the knowledge I now have from you on this group. Really appreciate all the time you've taken to respond to my question. Thank you all once again. I'll sign
Sew_And_Sew
in
PMRGCAuk
1 month ago
My Tumour is shrinking
I am at the end of chemo cycle. In August my tumour was 1cm after I had the MRI. So 80% removed from right side of my brain. I have gone to 1cm to 1.5cm. In the three MRI's. My latest one has shunk so much I think it is now a 1/4 in size, comparing August mri to this mri. I am so pleased. I have
I am at the end of chemo cycle. In August my tumour was 1cm after I had the MRI. So 80% removed from right side of my brain. I have gone to 1cm to 1.5cm. In the three MRI's. My latest one has shunk so much I think it is now a 1/4 in size, comparing August mri to this mri. I am so pleased. I have
Denni60
in
Glioblastoma Support
6 months ago
Cod Liver Oil Supplements with Prednisolone
Been on prednisolone (UK) since 01/11/2022. I'm currently taking 3mgs/4mgs on alternate days. 3mgs was too much for me. Anyway if on pred, can we take cod liver oil supplements please? The tablets are ginormous so my husband has bought the liquid. Don't want to start unless it's OK to do so. Any opinions
Been on prednisolone (UK) since 01/11/2022. I'm currently taking 3mgs/4mgs on alternate days. 3mgs was too much for me. Anyway if on pred, can we take cod liver oil supplements please? The tablets are ginormous so my husband has bought the liquid. Don't want to start unless it's OK to do so. Any opinions
Sew_And_Sew
in
PMRGCAuk
1 month ago
Low ferritin
I was diagnosed with PV in November 2020. Initially, I had a few phlebotomies to reduce my hematocrit but thankfully I've passed my last three blood tests and haven't had one since January 2023. I take aspirin, a spoonful of cod liver oil and half a tin of grapefruit every day to keep my haematocrit
I was diagnosed with PV in November 2020. Initially, I had a few phlebotomies to reduce my hematocrit but thankfully I've passed my last three blood tests and haven't had one since January 2023. I take aspirin, a spoonful of cod liver oil and half a tin of grapefruit every day to keep my haematocrit
M1ndMyB100d
in
MPN Voice
1 month ago
Blood test results - anxiety
Hi everyone, I posted this same message in my previous post but I don't think it has been seen by anyone so creating a new post here... I got my blood test results back this morning. Here they are – TSH mIU/L: <0.005 (range 0.27 - 4.2) FT3 pmol/L: 7.7 (range 3.1 – 6.8) FT4 pmol/L: 18.2 (range 12 –
Hi everyone, I posted this same message in my previous post but I don't think it has been seen by anyone so creating a new post here... I got my blood test results back this morning. Here they are – TSH mIU/L: <0.005 (range 0.27 - 4.2) FT3 pmol/L: 7.7 (range 3.1 – 6.8) FT4 pmol/L: 18.2 (range 12 –
ci00aaj
in
Thyroid UK
2 months ago
vitamin results and advice on tweaking or changing supplements
Advice on supplements please and please tell me if I’m over thinking or worrying about this. I currently take: Better You Vit D with K2 / Thorne Basic B / Vegavero folate / Omega 3 fish oil / Magnesium / Zinc I’ve had my results back from Medichecks and would like some advice on what I can do to further
Advice on supplements please and please tell me if I’m over thinking or worrying about this. I currently take: Better You Vit D with K2 / Thorne Basic B / Vegavero folate / Omega 3 fish oil / Magnesium / Zinc I’ve had my results back from Medichecks and would like some advice on what I can do to further
Slowrunner1208
in
Thyroid UK
7 months ago
RA overlap just diagnosed. Who else? Tips?
I have had PBC since 2009. I have just been diagnosed with overlap rheumatoid arthritis. UGH! I know some of you have too. Would appreciate any tips. Unfortunately for me because of both PBC and the fact I am allergic to sulpha the list of medications is small. Starting with hydroxicholriquine.
I have had PBC since 2009. I have just been diagnosed with overlap rheumatoid arthritis. UGH! I know some of you have too. Would appreciate any tips. Unfortunately for me because of both PBC and the fact I am allergic to sulpha the list of medications is small. Starting with hydroxicholriquine.
CeeCee101
in
PBC Foundation
7 months ago
supplements and lifestyle
Hello guys, I’ve found the advice from you folks to be really helpful since I’ve been on here moaning and groaning so I just wondered if any of you have experienced any measurable improvement in arthritis symptoms using supplements and lifestyle changes? I have just been recommended for TKR surgery
Hello guys, I’ve found the advice from you folks to be really helpful since I’ve been on here moaning and groaning so I just wondered if any of you have experienced any measurable improvement in arthritis symptoms using supplements and lifestyle changes? I have just been recommended for TKR surgery
Wolf68
in
Arthritis Action
2 months ago
First IVF Cyle - Endo sufferer - What should I be doing to prepare?
Hi All! Just looking for some advice about what to do prior to a IVF cycle. Bit of background… I have stage 4 endometriosis, kissing ovaries, 5cm cyst on one ovary and a small fibroid. My partner and I have been TTC for 6 years. The years of lack of success led to a lot of weight gain as I took
Hi All! Just looking for some advice about what to do prior to a IVF cycle. Bit of background… I have stage 4 endometriosis, kissing ovaries, 5cm cyst on one ovary and a small fibroid. My partner and I have been TTC for 6 years. The years of lack of success led to a lot of weight gain as I took
Behind_Hazel_Eyes
in
Fertility Network UK
7 months ago
second time lucky ?
Can I hope for a totally different result? Has anyone gone from NOTHING first round and then had a decent result on the second round? As I approach my second nhs icsi cycle I’m anxious, nervous and hopeful that I will get a better result this time. We collected three eggs which were quite small
Can I hope for a totally different result? Has anyone gone from NOTHING first round and then had a decent result on the second round? As I approach my second nhs icsi cycle I’m anxious, nervous and hopeful that I will get a better result this time. We collected three eggs which were quite small
Cuppppatea
in
Fertility Network UK
7 months ago
Just Started Levothyroxine 25mcg, and scared/need advice please,as not feeling good at all after starting the Meds (And Worsened Tinnitus)
Hi All, This is my first post,hope you can help. I had full blood works tested at the start of the year,as i have always suffered anxiety as well as mild depression and OCD,as well as tired often,thinning hair,and mild tinnitus in the right ear etc,and reading many forums i was led to believe i could
Hi All, This is my first post,hope you can help. I had full blood works tested at the start of the year,as i have always suffered anxiety as well as mild depression and OCD,as well as tired often,thinning hair,and mild tinnitus in the right ear etc,and reading many forums i was led to believe i could
Foxy147
in
Thyroid UK
3 months ago
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