I cured my PMR simply by cutting out all vegetable oils, ultra-processed food, sugar and cut down on carbohydrates. In addition I ate more olive oil and tried to eliminate food containing lectins from my diet. This includes wheat, beans (unless thoroughly soaked) and nightshades. This diet not only cured my PMR but my general health improved. I would never eat the diet that I once had, it's toxic to many.
Thank you for this wonderful youtube. I have had PMR for several years and due to side effects have ditched all pharmaceutical medications. Pain is almost untenable but I'm determined I won't go back on prednisone or other meds. I did these exercises along with the video. A couple (shoulder-focused) were challenging but when I'd finished I could not believe how much better my body felt when I needed to move, walk, reach for something or stoop. I am thrilled. I will do them every morning now (and try and stick with the anti-inflammatory diet I've been reading about) - now there's a challenge - fish?? green tea?? Eeeeek! Thank yhou again for sharing your expertise. I'm very grateful to you. Greetings and Happhy New Year from down under.
I am not worse in the morning thankfully and my shoulders and knees are the affected places . Over the counter analgesia helps a lot as well as some THC and microdosing particularly good for my spirits . Being creative with singing in a choir is paramount to staying positive and with a strict diet, meditation, and prayer maybe this will improve as I’ve read from others in this very thread. Thank you for your concern with these exercises.
78 yr old w/ PMR. MAKE SUPREME EFFORT TO QUIT CAFFEINE! The best thing you can do for yourself. Suggestion: avoid lactic acid from yogurt, sauerkraut and kim chi pickles. Also oxalic acid in spinach, beets etc. Yes to Brassica greens. Suggestion: avoid chairs for long periods. Sit crosslegged for computer use. Suggestion: avoid all sugars and high GI starches. Avoid fried anything. Yes to olive oil drizzled not fried. Try out "food combining". Lots of veg fiber rich foods.
First time I've seen this channel today. Crazy disease is crippling! I'm no longer taking Prednisone but slight pain persists. Thank you for doing this! Will do it every day!
The following is what helped me, big time, with my polymyalgia rheumatica. Oh Zone treatment, moringa, celery juice, broccoli and cauliflower juice. All within appropriate instructions. Go to sleep early around 9 PM, light exercise such as the one exposed in this video. Avoid animal product, avoid caffeine, avoid sugars, avoid highly processed foods, avoid refined products such as white flour and white bread, cookies etc. Avoid junk food, avoid canned food, Try to eat everything organic as much as possible, it all the raw food you can. A lot of praying to our God. Avoid hard times, enjoy life, 15 minutes of sunlight every day and breath. Air. Avoid third toxic and smelly chemicals to clean the house. It will be blessed just like me. My pain, nowadays, it’s not really a pain. My symptoms it’s more like a discomfort. I came long ways from not being able to walk or move hardly any bit to being able to go back to my normal life activities within some limitations. God bless you all. 7:15
Thank you. Will try these exercises to see how I go. Diagnosed polymalgia 12 months ago. Started 25 mg prednisolone. Now reduced to 5 mg. Muscles still hurt.
Thanks so much for these helpful movements. Do you think it's necessary to warm up a bit before doing them? Thinking maybe some marching, low kicks, gentle kickbacks, ham curls, definitely with the arms (right now, my shoulders, rot cuffs and upper arms are the most painful). Glad you included that swimming movement with upper elbow lifting. That hurt a bit, but little by little I'll get there. Not sure how to warm the arms for this swim movement. Thanks so much again. Great that you used the whole body.
Nothing works for me and I'm sick and tired of failure. I ride my bike, even foregoing my E bike for my old lightweight. I walk up the local hills, go to a spa pool and gym and try to eat sensibly. I have a persistent trapped nerve in my right shoulder, a right knee that prevents me from standing on my pedals and my balance is shot. I've just kicked Prednisolone after four years of the stuff and I have to pop Paracetamol night and morning. I'm sick of reading about diets that cure, being robbed by joint supplement hawkers and NHS Doctors that don't care. Isn't it about time the wretched health authority got to grips with this plethora of conflicting treatments???
I hear you ! And I agree I don’t think I’ll last 4 yrs on the stuff it’s made me so ill in so many other areas I feel like it’s destroying me , I dread the pred
I like the new stopwatch outline of your logo on your shirt. Any news on the clothing line? I had a shirt made for myself that’s similar:) Top fan haha.
Ha ha! Great. No not yet as I'm still working full time as well as running my martial arts business on top. This is still a "hobby" but hopefully as it grows, I will be able to focus more time to it and give up my day job! That's the plan anyway. Thank you No.1 fan
Congratulations for 1.11 lakh Subscriber❤❤❤❤....... I have Weak muscles and Weak bone... Weak Spine \ Backbone.. 🙏🙏 spinal cord \. The waist bends Downward After Some time ....there is difficulty in keeping the spine \Backbone straight...🙏🙏 Any Excercise 🙏Suggestions 🙏
Thank you! It sounds like you need to strengthen your core muscles to help with your back issues. Take a look at this playlist as there may be something in here that will help you: ru-vid.com/group/PLf9i8qFtMBBI6ua6m3OgL5_wBVw7JkNk-
My rheumatoloist says I have pmr. I cant use my left hand..cant Bend fingers..it is stiff and swells up...i can use my right but cant make a fist. Am on 20 mg of prednisone. Some of my toes feel numb. The bone and joint doctor I see isnt buying the rhumatologists notion. My knee reflexes are hyper but arm reflexes are not. I wish someone had an answer. Been this way since September.
If rheumatologist says you have pmr you have it, depending on your tests results. I get numbness in my toes and top foot pad too. I didn't numbness was a symptom , thought it could be my chronic fatigue syndrome
I’ve been diagnosed with PMR. My morning stiffness lasts for at least 3 hours and on a bad day can be six hours. Does anybody only have it for an hour?
Yes, before I started on Prednisone I had great pain and stiffness for an hour. I have no pain now. As I go down from 9 mg. to 8 mg., (Drop one mg. every two weeks) I may start to experience pain and stiffness again or even a relapse with very low dosages. Exercise is a great idea if you can get enough sleep. I am 79 now.
I'm same as you. I'm now 4/5 weeks in - Strangely I seem to have about once a week or so that I wake up with no pain, think i've cracked it and then next day the return is so deflating - but yeah the general advice being its approx first hour it's not been for me i'm far more in line with 3 hours or more often up to 6. I am on treatment with GP and now hospital consultant.
I don’t know anyone who only has stiffness and pain for one hour but that is the description that the nhs gives ! 15mg of pred gave me some movement I’m not down to 8 and in agony most of the time I’d say 4 hours in morning and returning about 6 hours after meds . I do have other health issues As far as this video is concerned if I could move like that I doubt I would ever have been referred to rhuematology !
