Patient's Story - Treatment of Chronic inflammatory demyelinating polyneuropathy (CIDP)

"It's like when you see a light at the end of the tunnel", expressed Nabeeh's mother, after the 16-year-old boy underwent treatment at Vejthani Hospital and is finally ready to return home. Nabeeh has been suffering from a loss of strength and balance in the body. Upon consultations with two doctors at Vejthani Hospital, Nabeeh was diagnosed with CIDP and at last, given proper treatment.
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[@blacksun496]

I was diagnosed with CIDP back in 2007. Ive learned a lot since then and am living an almost normal life again. A few tips to help anyone dealing with this disease: A keto style diet works best for me. Lots of organic healthy meats, veggies and fruits. I tried a vegan diet but it made it worse. A diet of good fatty meats, eggs and avocados is good because it helps to regrow the myelin sheets that was stripped off the nerve endings by the immune system. Cut out all processed food especially sweet foods. Sugar is your number one enemy. It’s best to avoid all forms of sugar even stevia etc. you may can get away with a “little” manuka honey. Avoid smoking and drinking any alcohol, including wine. Exercise as much as possible and lift heavy weights (at least what is heavy to you). This will keep you stronger than the disease itself. Workout your entire body especially legs and arms. This is how I regained my balance. Get plenty of rest. When showering. Switch from hot to cold to stimulate your nerves, ending your shower with cold. Get a vibrating foot massager to stimulate your nerve endings in your feet. By doing all of these things I am 90% back to normal without taking any steroids or ivig, haven’t been back to my neurologist in ten years after he told me I will be wheelchair bound if I stopped the treatment. I’m not advising you stop treatment I’m just saying that’s what I did. I didn’t abruptly stop, I slowly reduced the amount of steroids I was taking and weaned myself off of them as I was doing everything I wrote in the comment. The stronger I got the more I weaned myself off. Hope this helps someone

[@adv.satadrusovonghosh.bhar8090]

Happy to know your testimony. Hope you are well now by the grace of God. What are your symptoms?

[@fatinaz1191]

Thank you for your kind advice. May God keep you blessed always ❤️

[@thecreative4688]

You have guided very well. May you live healthy happy life.

[@morechange7454]

Wich hospital in India You mentioned

[@jaigarg1364]

Hi I’m suffering from cidp disease I need your help please

[@SaifaldeenMahmoud]

من اين انت؟ where you de life?

[@jaigarg1364]

@@SaifaldeenMahmoud means?

[@ARIF-md7hn]

​@@jaigarg1364have u got any relief?

[@smartonlinelearning23]

I am suffering from same problems plz give nabee contact

[@blacksun496]

I was diagnosed with CIDP back in 2007. Ive learned a lot since then and am living an almost normal life again. A few tips to help anyone dealing with this disease: A keto style diet works best for me. Lots of organic healthy meats, veggies and fruits. I tried a vegan diet but it made it worse. A diet of good fatty meats, eggs and avocados is good because it helps to regrow the myelin sheets that was stripped off the nerve endings by the immune system. Cut out all processed food especially sweet foods. Sugar is your number one enemy. It’s best to avoid all forms of sugar even stevia etc. you may can get away with a “little” manuka honey. Avoid smoking and drinking any alcohol, including wine. Exercise as much as possible and lift heavy weights (at least what is heavy to you). This will keep you stronger than the disease itself. Workout your entire body especially legs and arms. This is how I regained my balance. Get plenty of rest. When showering. Switch from hot to cold to stimulate your nerves, ending your shower with cold. Get a vibrating foot massager to stimulate your nerve endings in your feet. By doing all of these things I am 90% back to normal without taking any steroids or ivig, haven’t been back to my neurologist in ten years after he told me I will be wheelchair bound if I stopped the treatment. I’m not advising you stop treatment I’m just saying that’s what I did. I didn’t abruptly stop, I slowly reduced the amount of steroids I was taking and weaned myself off of them as I was doing everything I wrote in the comment. The stronger I got the more I weaned myself off. Hope this helps someone