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Tylenol with Codeine #4
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Back pain and surprises
Hey y’all!!! Now that I’ve recouped from family matters, I have yet another surprise. Been having low back pain for about 3 yrs. Managed with PT and NSAIDs for almost 2 years. Beginning of this year, pain just wouldn’t let up so I asked for meloxicam. Meloxicam worked amazingly well but was nixed after
Hey y’all!!! Now that I’ve recouped from family matters, I have yet another surprise. Been having low back pain for about 3 yrs. Managed with PT and NSAIDs for almost 2 years. Beginning of this year, pain just wouldn’t let up so I asked for meloxicam. Meloxicam worked amazingly well but was nixed after
Jmiller623
in
LUPUS UK
3 years ago
Can PD get better?
A DAT scan shows I have PD. I take Rytary but Dr Google suggests other meds might help. So I also take cinnamon, phosphatidyl serine, Super B-complex, Vitamin D, Green tea capsules, fish oil, a statin, CoQ10, baby aspirin, miralax, dulcolax, tylenol and melatonin. Some of these are for PD
A DAT scan shows I have PD. I take Rytary but Dr Google suggests other meds might help. So I also take cinnamon, phosphatidyl serine, Super B-complex, Vitamin D, Green tea capsules, fish oil, a statin, CoQ10, baby aspirin, miralax, dulcolax, tylenol and melatonin. Some of these are for PD
kaypeeoh
in
Cure Parkinson's
3 years ago
TSI Results
High TSI usually means that the Graves Disease is surviving and thriving in us correct? Now with my thyroid that was ablated via RAI in Jan 2020 will these high antibodies attack something else in my system? Should I worry about TED? This disease has changed me mentally already never had constant nervousness
High TSI usually means that the Graves Disease is surviving and thriving in us correct? Now with my thyroid that was ablated via RAI in Jan 2020 will these high antibodies attack something else in my system? Should I worry about TED? This disease has changed me mentally already never had constant nervousness
Shaf3938
in
Graves Disease Support
3 years ago
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TSI information
Hello, I was diagnosed with Graves Disease end of 2019 and had RAI in Feb 2020! I just want more info on TSI results so with this value it means it’s surviving and thriving in my body! Now with high numbers like this I will be prone to get other diseases right? Is there anyway to get these numbers
Hello, I was diagnosed with Graves Disease end of 2019 and had RAI in Feb 2020! I just want more info on TSI results so with this value it means it’s surviving and thriving in my body! Now with high numbers like this I will be prone to get other diseases right? Is there anyway to get these numbers
Shaf3938
in
Thyroid UK
3 years ago
Where can I buy Tylenol or do I need a prescription?
Do I need a prescription for Tylenol for my arthritis
Do I need a prescription for Tylenol for my arthritis
Gooby1
in
Arthritis Action
3 years ago
Help needed to understand blood results please
Hi All, I wrote a post several weeks ago with regards to being diagnosed with Graves' Disease 23 years ago and undergoing radioactive iodine 6 years later. I have been on 175mcg levothyroxine daily indefinitely since then but a year ago I was diagnosed with anaemia (reduced mean cell volume of red cells
Hi All, I wrote a post several weeks ago with regards to being diagnosed with Graves' Disease 23 years ago and undergoing radioactive iodine 6 years later. I have been on 175mcg levothyroxine daily indefinitely since then but a year ago I was diagnosed with anaemia (reduced mean cell volume of red cells
RachFow85
in
Thyroid UK
3 years ago
Switch to Beovu?
I would like further information about the drug Beovu. I have had 20 plus injections of Eyelea over the past 2 years and after an initial improvement things have gone down hill. My sight has got worse despite the injections and I have various problems with my reaction to iodine and corneal abrasions
I would like further information about the drug Beovu. I have had 20 plus injections of Eyelea over the past 2 years and after an initial improvement things have gone down hill. My sight has got worse despite the injections and I have various problems with my reaction to iodine and corneal abrasions
3furryfiends
in
Macular Society
3 years ago
Should You Get the COVID-19 Vaccine If You Have a History of Allergic Reactions to Infused or Injectable Medications?
Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication. Learn more about our FREE COVID-19 Patient Support Program for chronic illness patients and their loved ones. Biologic Infusions
Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication. Learn more about our FREE COVID-19 Patient Support Program for chronic illness patients and their loved ones. Biologic Infusions
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
3 years ago
Age 41. Third IVF cycle with ARGC. When should I call it a day?
Hi everyone, This is my first time writing here and hoping to get some advice from you all. I've had two unsuccessful IVF rounds at ARGC so far, which was devastating. The first was a frozen cycle, due to the fact that I had to get surgery to remove fibroids. This one yielded 8 eggs, 6 fertilized and
Hi everyone, This is my first time writing here and hoping to get some advice from you all. I've had two unsuccessful IVF rounds at ARGC so far, which was devastating. The first was a frozen cycle, due to the fact that I had to get surgery to remove fibroids. This one yielded 8 eggs, 6 fertilized and
Janie79
in
Fertility Network UK
3 years ago
Not Sure What I Should Do
I've been diagnosed with Hashimoto's Thyroiditis and I currently take Levothyroxine. Previously I took Levothyroxine and Levothyronine. My current Endocrinologist only believes in testing the Free T4 and the TSH. She won't take any other tests. The nurse from my GPs office looked for another Endocrinologist
I've been diagnosed with Hashimoto's Thyroiditis and I currently take Levothyroxine. Previously I took Levothyroxine and Levothyronine. My current Endocrinologist only believes in testing the Free T4 and the TSH. She won't take any other tests. The nurse from my GPs office looked for another Endocrinologist
HealthyOldPerson
in
Thyroid UK
3 years ago
My 21 year old brother has HSE. Mom isn't coping, but I think he seems to be progressing well? Advice/support?
My little brother has had an unknown autoimmune disease since Sept 2017. Something with his pituitary gland, although with a very unhelpful GP we haven't been able to get very far. Overall he'd been doing well. On the weekend before the 15th of March he started to get a fever and low appetite, and on
My little brother has had an unknown autoimmune disease since Sept 2017. Something with his pituitary gland, although with a very unhelpful GP we haven't been able to get very far. Overall he'd been doing well. On the weekend before the 15th of March he started to get a fever and low appetite, and on
heidichanel
in
Encephalitis International
3 years ago
Update 3 years on
I joined this forum in 2018 whilst at a low ebb. Thank you to everyone who posted encouragement at the time. I weighed in at 134KG then, down from my top weight of 141KG. (At my recent weigh-in, I was a whisker over 110KG). After I read the replies to my post, I went to my Buddhist altar and
I joined this forum in 2018 whilst at a low ebb. Thank you to everyone who posted encouragement at the time. I weighed in at 134KG then, down from my top weight of 141KG. (At my recent weigh-in, I was a whisker over 110KG). After I read the replies to my post, I went to my Buddhist altar and
pondlotus
in
Weight Loss Support
3 years ago
PMR after Moderna 2 Doses
Stayed at 4.5mg/d Pred since 3/4 didn’t want to further increase a risk of a flare by dropping to 4mg. Dose 1 was 2/26. Had no side affects at all. Even my right arm where I got the shot didn’t hurt. Dose 2 was 3/26. Left arm did get sore at the injection site, it escalated to the point I took 2 Advil
Stayed at 4.5mg/d Pred since 3/4 didn’t want to further increase a risk of a flare by dropping to 4mg. Dose 1 was 2/26. Had no side affects at all. Even my right arm where I got the shot didn’t hurt. Dose 2 was 3/26. Left arm did get sore at the injection site, it escalated to the point I took 2 Advil
Boss302Fan
in
PMRGCAuk
3 years ago
Anyone else feels the same?
Sometimes I feel like I had a panic attack when I’m feeling sleepy or have a headache. Like today especially I hadn’t eaten all day and finally got to eat something around 6 pm Felt very tired and sleepy and had a headache due to my sinuses. Once I take a nap or some Tylenol I feel much better. It
Sometimes I feel like I had a panic attack when I’m feeling sleepy or have a headache. Like today especially I hadn’t eaten all day and finally got to eat something around 6 pm Felt very tired and sleepy and had a headache due to my sinuses. Once I take a nap or some Tylenol I feel much better. It
alfreddy7
in
Anxiety and Depression Support
3 years ago
Tips for handling chronic pain!!!
I suffer chronic pain from an autoimmune disease called polymigria (muscle pain) and take steroids for it, i also fell in Jan of this year and broke my femur and left arm and am suffering such severe pain from the limb its almost unbearable. My doctor gives me codeine 30mgs but is talking about reducing
I suffer chronic pain from an autoimmune disease called polymigria (muscle pain) and take steroids for it, i also fell in Jan of this year and broke my femur and left arm and am suffering such severe pain from the limb its almost unbearable. My doctor gives me codeine 30mgs but is talking about reducing
Molefosey
in
Pain Concern
3 years ago
Duloxetine
Hi Paige, I have taken Duloxetine for 10 years. I take the highest dose of 120mg slow release once a day in the morning. I am very susceptible to drugs but apart from piling weight on I have had none. It keeps me sane. I also take Amitryptyline 20mg at night and 30/500 Codeine phosphate Paracetamol.
Hi Paige, I have taken Duloxetine for 10 years. I take the highest dose of 120mg slow release once a day in the morning. I am very susceptible to drugs but apart from piling weight on I have had none. It keeps me sane. I also take Amitryptyline 20mg at night and 30/500 Codeine phosphate Paracetamol.
merlinmac
in
Fibromyalgia Action UK
3 years ago
Does tylenol help?
I have PMR and am on low dose 1mg prednisone. It works quite well, but not so well the fluey feeling and all over misery when high humidity. Is Tylenol any benefit? Thanks, Jane
I have PMR and am on low dose 1mg prednisone. It works quite well, but not so well the fluey feeling and all over misery when high humidity. Is Tylenol any benefit? Thanks, Jane
Jane424
in
PMRGCAuk
3 years ago
For info: Just had a big rant on government survey on women's health
UK Government are doing a consultation on women's health until 13 June (although in England only sadly) You don't have to be a woman to complete it i..e you can complete as an ally (friend/family member) Sure this has been shared before but i found it very therapeutic to have a rant by completing the
UK Government are doing a consultation on women's health until 13 June (although in England only sadly) You don't have to be a woman to complete it i..e you can complete as an ally (friend/family member) Sure this has been shared before but i found it very therapeutic to have a rant by completing the
jsy_girl
in
Thyroid UK
3 years ago
I am new to this and I was wondering...
Is it still possible to have a flare even on 400mg of Plaquenil?? My rash on my face has spread to a spot on my forehead. And my joints are very stiff in the morning, and sometimes during the day at work. I do a lot of writing, and work a lot with my hands, and I worry if it gets any worse, I won’t be
Is it still possible to have a flare even on 400mg of Plaquenil?? My rash on my face has spread to a spot on my forehead. And my joints are very stiff in the morning, and sometimes during the day at work. I do a lot of writing, and work a lot with my hands, and I worry if it gets any worse, I won’t be
Willow7733
in
LUPUS UK
3 years ago
I hate my nose
7 pm in Orange County And my head is throbbing since 1 Am. I really I really hate my sinuses. I hate having to take Tylenol or any other sinus relievers.
7 pm in Orange County And my head is throbbing since 1 Am. I really I really hate my sinuses. I hate having to take Tylenol or any other sinus relievers.
alfreddy7
in
Anxiety and Depression Support
3 years ago
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