Thank you so much for sharing ❤ i have had psa for 12 years and i am on 25mg of methotrexate injectopen. I've just started more pain jumping everywhere so they are looking in to it now as so struggling with the pain and fatigue xx
Becky thank you so much for sharing your journey with us! I'm so sorry that you are having such a hard time finding medication that helps and doesn't cause an allergic reaction *hugs* I've had psoriasis for many years and was just diagnosed with psoriatic arthritis. I have stiffness and pain throughout my body with the bottoms of my feet tender sore and painful and 2 swollen toes. Plus the fatigue. My rheumatologist said to avoid alcohol and sugar and in the past I have had increased pain after eating whole wheat, so I am mostly gluten free. I am finding that since I have cut out any added sugars (I still eat sugar naturally occurring in fresh fruits and vegetables) and am avoiding refined carbohydrates which quickly turn into sugar in the body, my fatigue has gone away, which is wonderful! Have you tried any dietary changes to see if they might help you feel a little better? It's hard when cooking is so painful for you though. I am starting methotrexate this week and am hoping it will work well for me. Did the Talz (spelling?) end up helping you? I hope that you and your doctor have been able to find a treatment that is helping you feel better. Sending you lots of love and hugs Becky!
Thank you for sharing your story. You are right, there are not many videos by sufferers telling there story, I think I have seen just about all there is apart for the new ones I have open ready to watch including yours. I've lived with it for 30 years now.... I keep falling off the medical wagon, I find it difficult to trust doctors as I'm always put on Methotrexate and never been put on anything else and it never works, only for a short time. Plus there was the 10 years I wasn't listened to prior to my diagnosis. I just feel there is no hope, that the medicines ware off and doctors don't have many options to give us. I have lost my quality of like a long time ago. 47 now.
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Thank you so much. I'm just on the start of my journey. But I sound exactly like yours. Really appreciate your help ❤
Thank you so much for sharing ❤ i have had psa for 12 years and i am on 25mg of methotrexate injectopen. I've just started more pain jumping everywhere so they are looking in to it now as so struggling with the pain and fatigue xx
Thank you for sharing
Becky thank you so much for sharing your journey with us! I'm so sorry that you are having such a hard time finding medication that helps and doesn't cause an allergic reaction *hugs* I've had psoriasis for many years and was just diagnosed with psoriatic arthritis. I have stiffness and pain throughout my body with the bottoms of my feet tender sore and painful and 2 swollen toes. Plus the fatigue. My rheumatologist said to avoid alcohol and sugar and in the past I have had increased pain after eating whole wheat, so I am mostly gluten free. I am finding that since I have cut out any added sugars (I still eat sugar naturally occurring in fresh fruits and vegetables) and am avoiding refined carbohydrates which quickly turn into sugar in the body, my fatigue has gone away, which is wonderful! Have you tried any dietary changes to see if they might help you feel a little better? It's hard when cooking is so painful for you though. I am starting methotrexate this week and am hoping it will work well for me. Did the Talz (spelling?) end up helping you? I hope that you and your doctor have been able to find a treatment that is helping you feel better. Sending you lots of love and hugs Becky!
Thank you for sharing your story. You are right, there are not many videos by sufferers telling there story, I think I have seen just about all there is apart for the new ones I have open ready to watch including yours. I've lived with it for 30 years now.... I keep falling off the medical wagon, I find it difficult to trust doctors as I'm always put on Methotrexate and never been put on anything else and it never works, only for a short time. Plus there was the 10 years I wasn't listened to prior to my diagnosis. I just feel there is no hope, that the medicines ware off and doctors don't have many options to give us. I have lost my quality of like a long time ago. 47 now.
Thank you gratefully received 🏴❤🙏