Can’t sleep, pain, part 2 (Ankylosing Spondylitis)

Can't sleep, pain, part 2 (Ankylosing Spondylitis)

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11 Comments on "Can’t sleep, pain, part 2 (Ankylosing Spondylitis)"

  1. PipenFalzy
    21/04/2013 at 10:44 am Permalink

    I have AS and it sucks although biologics has helped. Iam on enbrel and dont have those big flair ups as i use too. Iam 36 and still take med for pain but stopped taking those nsaids that ruin your stomach since on enbrel.

  2. shagtreez209
    21/04/2013 at 10:54 am Permalink

    im 17 years old with AS and it fuckin sucks. cant sleep or sit for very long or stand or basically anything. any advice on how to improve my quality of life? or am i just fucked? and also,food has a huge effect on my inflamation response,is that the same for you?

  3. Emmachka2000
    21/04/2013 at 10:59 am Permalink

    Lovely people, THERE IS HOPE!!! check out the doctor who cured himself from AS, and he can help you. GoldbergClinic in atlanta. Google Paul Goldberg. He is Awesome!!!!! go to his site. Read. Be informed! He IS an answer to my prayers! if you come to see him, contact me and I’ll help you with your visit to atlanta as I only live about 2 miles from his clinic. Lovely people, there IS HOPE. NEver give up. NEVER!!!!!! There ARE answers! God bless you!

  4. Emmachka2000
    21/04/2013 at 11:20 am Permalink

    Lovely people, THERE IS HOPE!!! check out the doctor who cured himself from AS, and he can help you. GoldbergClinic in atlanta. Google Paul Goldberg. He is Awesome!!!!! an answer to my prayers! if you come to see him, contact me and I’ll help you with your visit to atlanta as I only live about 2 miles from his clinic. Lovely people, there IS HOPE. NEver give up. NEVER!!!!!! There ARE answers! God bless you!

  5. tweeters54
    21/04/2013 at 12:16 pm Permalink

    Hey guy, liked your vid..can sure identify..have had it since 1975, dx at 21, female..took them forever to figure it out..had extreme blood shot eyes..which was tale tell sign for the doctors..am 56 now..not doing well..vision is affected now..can’t walk without cane alot and sitting upright difficult sometimes..very tired and hard to think sometimes..but other than that, things couldn’t be better!! LOL…stay in touch for more good news!! smiles

  6. steffiejoable
    21/04/2013 at 12:27 pm Permalink

    please post some updates…..i found you youtube yesterday and it helped me make it thru a bad day of pain. we need to spread the word and you haven’t made a video in a long time. you must be doing better. keep the faith my new found friend.

  7. eiwaz
    21/04/2013 at 12:33 pm Permalink

    LOL, you sound like me when I move.

  8. NewRiverAngel
    21/04/2013 at 12:43 pm Permalink

    dude it definitely says you suffer from musculoskeletal PAM! and the drug you mentioned in the last vid. right before vicoden is my favorite! my sister was just diagnosed with AS and FINALLY her lifelong suffering makes sense. we went through everything from “you have MS” to “nothing’s wrong with you” to “you have lupus” and then they found she had Chiari Malformation. But now after all these years she’s going for her first Remicade infusion tomorrow! Thank you for helping me see AS as it is.

  9. oaxqro
    21/04/2013 at 1:22 pm Permalink

    Hello. My name uis gerard and i am from Mexico. I have AS.
    I understand your pain, because it is same to mine.
    Do you hace e mail, i want to chat with persons with this kind of desease.
    Sorry by my bad engkish, i will try to explain me better.
    take care.

  10. Surf2130
    21/04/2013 at 1:41 pm Permalink

    yes.. more males than Females have this disease. Your right.

  11. Surf2130
    21/04/2013 at 2:38 pm Permalink

    Yes.. I was on Enbril injections for some time. They helped when I wasn’t as sick as I am now. It is a good drug tho. Much more easy than the Remicade infusions! Hope you, and are doing well!

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