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Alendronic acid / Colecalciferol
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Steroid injection for OA in shoulder
I experienced severe pain in shoulder at 8mg of Pred, and increasing dose had no affect. An X-ray showed bone on bone OA. I continued with taper now on 7mg. and shoulder pain has virtually gone. I think it flared up with too much use on recent holiday, and existing conditions do tend to assert themselves
I experienced severe pain in shoulder at 8mg of Pred, and increasing dose had no affect. An X-ray showed bone on bone OA. I continued with taper now on 7mg. and shoulder pain has virtually gone. I think it flared up with too much use on recent holiday, and existing conditions do tend to assert themselves
Marymon
in
PMRGCAuk
5 years ago
Steroid injection for OA in shoulder
I experienced severe pain in shoulder at 8mg of Pred, and increasing dose had no affect. An X-ray showed bone on bone OA. I continued with taper now on 7mg. and shoulder has virtually gone. I think it flared up with too much use on recent holiday, and existing conditions do tend to assert themselves
I experienced severe pain in shoulder at 8mg of Pred, and increasing dose had no affect. An X-ray showed bone on bone OA. I continued with taper now on 7mg. and shoulder has virtually gone. I think it flared up with too much use on recent holiday, and existing conditions do tend to assert themselves
Marymon
in
PMRGCAuk
5 years ago
Alendronic acid
Hi all, Is there anyone who has had good Dexa scan results when taking Alendronic acid. If so, how long did you take it for, and how long have you been off it.
Hi all, Is there anyone who has had good Dexa scan results when taking Alendronic acid. If so, how long did you take it for, and how long have you been off it.
Walkingdogs
in
Bone Health and Osteoporosis UK
5 years ago
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Itchy Scalp for months - slightly hair thinning but no visible scalp issues.
For the last 5 months, I have been suffering from an itchy scalp, primarily on the crown of my head. This happened essentially overnight and after scratching for a day, I coincidentally saw that my hair had thinned slightly in those itchiest areas by the next day. I went to see a General Practioner a
For the last 5 months, I have been suffering from an itchy scalp, primarily on the crown of my head. This happened essentially overnight and after scratching for a day, I coincidentally saw that my hair had thinned slightly in those itchiest areas by the next day. I went to see a General Practioner a
tombomslom
in
MY SKIN
5 years ago
PD amino acids miscellany
Open access PDF of each can be found online. https://www.ncbi.nlm.nih.gov/pubmed/23981689 https://www.ncbi.nlm.nih.gov/pubmed/25059457 https://www.ncbi.nlm.nih.gov/pubmed/25073474
Open access PDF of each can be found online. https://www.ncbi.nlm.nih.gov/pubmed/23981689 https://www.ncbi.nlm.nih.gov/pubmed/25059457 https://www.ncbi.nlm.nih.gov/pubmed/25073474
aspergerian
in
Cure Parkinson's
5 years ago
PK protocol
Patricia Kane protocol Share The Patricia Kane protocol (PK protocol) is an experimental treatment for neurological disease involving intravenous infusion of phospholipids and methylation factors, along with dietary changes and supplements. It is based on the theory that in diseases Kane classes as
Patricia Kane protocol Share The Patricia Kane protocol (PK protocol) is an experimental treatment for neurological disease involving intravenous infusion of phospholipids and methylation factors, along with dietary changes and supplements. It is based on the theory that in diseases Kane classes as
akgirlsrock
in
Cure Parkinson's
5 years ago
Agitated sleep
Hi everyone, I need ideas/advice to cope with my husband’s agitated sleep. He clasps and unclasps his hand and rubs constantly and rocks the boat which wakes me up. Or he rubs his face so hard he has red marks in the morning. I’m not sure about giving him a sleep aid or cbd oil: what have you experienced
Hi everyone, I need ideas/advice to cope with my husband’s agitated sleep. He clasps and unclasps his hand and rubs constantly and rocks the boat which wakes me up. Or he rubs his face so hard he has red marks in the morning. I’m not sure about giving him a sleep aid or cbd oil: what have you experienced
Caro2132
in
PSP Association
5 years ago
Newbie to this forum
Hi everyone just a little intro on myself I am 57 years old female was 5’3”now 5’1” Was diagnosed osteoporosis in 2013 after my eldest brother diagnosed real bad was advised his siblings get tested I drew the next short straw so as to speak. My T score as of Dec 2018 is 3.8 I been on calcium 2 x daily
Hi everyone just a little intro on myself I am 57 years old female was 5’3”now 5’1” Was diagnosed osteoporosis in 2013 after my eldest brother diagnosed real bad was advised his siblings get tested I drew the next short straw so as to speak. My T score as of Dec 2018 is 3.8 I been on calcium 2 x daily
Babyr1996
in
Bone Health and Osteoporosis UK
5 years ago
Dad 60 years young, Advance stage, Multiple Mets, Had first round of chemotherapy. Need help and guidance on what to expect.
Dear All, Thank you for your support and guidance. My Dad is 60 years young with 59.6 kg body weight. He is based in India and currently getting his treatment in Medanta The Medcity hospital in Gurugram (Near New Delhi). I forgot to mention that he is diabetic as well. Diabetes was also diagnosed at
Dear All, Thank you for your support and guidance. My Dad is 60 years young with 59.6 kg body weight. He is based in India and currently getting his treatment in Medanta The Medcity hospital in Gurugram (Near New Delhi). I forgot to mention that he is diabetic as well. Diabetes was also diagnosed at
Shahbazahmedazmi
in
Advanced Prostate Cancer
5 years ago
HIFU and Metabolic Control
Good day fellow brothers and sufferers. This is my first post and my story. I am in the UK, so all of my treatment, whatever it entails is totally free of charge, so cost has no part to play in my treatment choice. I am 68 years old. In February 2018 I had a routine PSA – came back at 4.8ng/ml UK units
Good day fellow brothers and sufferers. This is my first post and my story. I am in the UK, so all of my treatment, whatever it entails is totally free of charge, so cost has no part to play in my treatment choice. I am 68 years old. In February 2018 I had a routine PSA – came back at 4.8ng/ml UK units
TFBUNDY
in
Advanced Prostate Cancer
5 years ago
What medicines to be cautious of....
I am seeing my rheumatologist in 5 days, for the first time since my diagnosis for PMR and possibly GCA. I know prednisone will most likely become a part of my life again, but I had terrible side effects 20 years ago. So, if the doctor were to try anything else like Alendronic Acid (scarey!), are there
I am seeing my rheumatologist in 5 days, for the first time since my diagnosis for PMR and possibly GCA. I know prednisone will most likely become a part of my life again, but I had terrible side effects 20 years ago. So, if the doctor were to try anything else like Alendronic Acid (scarey!), are there
pollymarierose
in
PMRGCAuk
5 years ago
Alendronic Acid 70mg tablets my experience.
I am new here, I just want to warn other people about taking Alendronic Acid 70mg tablets. I had my 2nd dexa scan about 2 weeks ago the one i had two and a half years previously showed i had osteopenia i was perscribed calcium and vit D at the time. The 2nd dexa report was sent to my gp it showed
I am new here, I just want to warn other people about taking Alendronic Acid 70mg tablets. I had my 2nd dexa scan about 2 weeks ago the one i had two and a half years previously showed i had osteopenia i was perscribed calcium and vit D at the time. The 2nd dexa report was sent to my gp it showed
buddygirl234
in
PMRGCAuk
5 years ago
Bone & Liver Metastatis
Hello Doctor, My mom had been detected breast cancer in 2015 and had been successfully operated in January 2016 and was on tamoxifen 20 mg, But in May 2018 we got to know that the cancer had come back in the bones, it had spread to her bones in the left ala of the Sacrum, now a year after receiving
Hello Doctor, My mom had been detected breast cancer in 2015 and had been successfully operated in January 2016 and was on tamoxifen 20 mg, But in May 2018 we got to know that the cancer had come back in the bones, it had spread to her bones in the left ala of the Sacrum, now a year after receiving
shiviangels
in
Breast Cancer India
5 years ago
What options do I have left?
Good evening everyone, So after many emails and phone calls to PALS, they have finally given me an appointment for this Friday compared to waiting till July for my follow up regarding Zoladex treatment. I have been struggling the last 3 months on this injection so today I decided to stop anyways I am
Good evening everyone, So after many emails and phone calls to PALS, they have finally given me an appointment for this Friday compared to waiting till July for my follow up regarding Zoladex treatment. I have been struggling the last 3 months on this injection so today I decided to stop anyways I am
princessk09
in
Endometriosis UK
5 years ago
Dizziness
The past couple weeks have been great. I dare say most of my anxiety symptoms are gone but the dizziness persists. I’m left wondering if it’s my Zoloft or the anxiety. I didn’t have dizziness until I upped my dose to 150 since then I’ve gone back down to 125 but it hasn’t subsided much. Anyone have
The past couple weeks have been great. I dare say most of my anxiety symptoms are gone but the dizziness persists. I’m left wondering if it’s my Zoloft or the anxiety. I didn’t have dizziness until I upped my dose to 150 since then I’ve gone back down to 125 but it hasn’t subsided much. Anyone have
Mongea
in
Anxiety Support
5 years ago
Update - 8 weeks of injections and some new symptoms
Hi, I am having injections from last 8 weeks and have seen improvements in some areas. Blurred vision has improved and so does night vision. But shimmering effect is still there. Eyes try to move around the focused object and it feels like words have slight to and fro motion. This is probably the strangest
Hi, I am having injections from last 8 weeks and have seen improvements in some areas. Blurred vision has improved and so does night vision. But shimmering effect is still there. Eyes try to move around the focused object and it feels like words have slight to and fro motion. This is probably the strangest
TACCT
in
Pernicious Anaemia Society
5 years ago
Pain relief query
Hi everyone - I’m currently taking the mini pill which is keeping the pain at a pretty nonexistent level which is amazing! However without the mini pill, the endo is debilitating, mefanamic acid does nothing, I can’t leave th house and it really impacts my bowels too! My question is there will be a
Hi everyone - I’m currently taking the mini pill which is keeping the pain at a pretty nonexistent level which is amazing! However without the mini pill, the endo is debilitating, mefanamic acid does nothing, I can’t leave th house and it really impacts my bowels too! My question is there will be a
Pinkblossom1
in
Endometriosis UK
5 years ago
Walsh protocol
Have you ever read about Walsh protocol? It’s interesting and if you are against any medication, maybe this is something you can try. This is about our chemicals in the body, vitamins, minerals, amino acids, nutrients, etc. My son is suffering for so many years of depression, anxiety, OCD, and many more
Have you ever read about Walsh protocol? It’s interesting and if you are against any medication, maybe this is something you can try. This is about our chemicals in the body, vitamins, minerals, amino acids, nutrients, etc. My son is suffering for so many years of depression, anxiety, OCD, and many more
SGV66
in
Anxiety and Depression Support
5 years ago
New member
Hi. I was diagnosed with PMR at the end of January and been taking 20mg of Prednisone. Yesterday started reducing to 15 mg by alternating between 3 and then 4 tablets alternately. Dr recommended taking alendronic acid? Not keen on this idea. Any thoughts?
Hi. I was diagnosed with PMR at the end of January and been taking 20mg of Prednisone. Yesterday started reducing to 15 mg by alternating between 3 and then 4 tablets alternately. Dr recommended taking alendronic acid? Not keen on this idea. Any thoughts?
Bowls70
in
PMRGCAuk
5 years ago
Infusion Reaction Now What...?
Hi In January this year 2019 I had my 1st (and last!!) Infusion of Zoledronic Acid, I was told that I could have flu type symptoms for a week and my joints may ache more, (I have Hypomobility Ehlers Danlos Syndrome hEDS, & Gut Dismortility GD) but I wasn't prepared for the awful reaction that I had,
Hi In January this year 2019 I had my 1st (and last!!) Infusion of Zoledronic Acid, I was told that I could have flu type symptoms for a week and my joints may ache more, (I have Hypomobility Ehlers Danlos Syndrome hEDS, & Gut Dismortility GD) but I wasn't prepared for the awful reaction that I had,
Charlie50
in
Bone Health and Osteoporosis UK
5 years ago
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