Sai Chand. Gurujala
  • Male
  • Hyderabad, Telangana
  • India
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Sai Chand. Gurujala's Friends

  • K s sai punith
  • Gloria Chen
  • Zachary Strobeck
  • Sampreet
  • TW
  • Sanja Kogelnik
  • Galia Ben Ishay

Sai Chand. Gurujala's Discussions

Exon Duplications

Started Sep 11, 2017 0 Replies

Hi All,Clinical research is going on Deletions. Anybody has any idea on Duplication's research.Serepta Pharma working on 40-53 Deletions.Does Gene Therapy is applicable for Duplication's as well.…Continue

Exon Duplications of 2 to 4

Started Feb 10, 2017 0 Replies

I request you to please help us. My nephew is diagnosed with DMD in 2016.His age is 7.5 years.Hemizygous Duplication of Exons 2 - 4.MLPA probe ratio : 1.83 - 1.98CPK level - 12100I request you to…Continue

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Sai Chand. Gurujala's Page

Profile Information

About me:
I am from India.
State - Telangana, Hyderabad
Phone# 9866723131
About my family:
My Nephew is diagnosed with DMD (Hemizygous Duplication)
3 (Exons 2 - 4).
MLPA Ratio : 1.83 - 1.98
CPK Level - 12100
Name(s) of child(ren)/individual(s) with Duchenne:
Abhinav Goud
Age(s) of child(ren)/individual(s) with Duchenne:

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Comment Wall (7 comments)

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At 12:53pm on March 11, 2017, Zachary Strobeck said…
I'm take lisinopril and coreg to maintain my heart. I also use a sleep apnea machine when I sleep in order to maintain my respitory muscles. I also have an internal cardiac defibrillator (icd).
At 11:56am on March 9, 2017, Zachary Strobeck said…
I'm doing okay, I am in a wheelchair though, haha. I went into one around the time I was in 4th grade. I'm here to let everyone know that life still can be good in this situation even though it can be quite difficult.
At 11:29am on March 9, 2017, Zachary Strobeck said…
Hey there!
Sorry for the lat response, I don't know much about steroid treatment as I have not had any during the course of my disease so I don't know a lot about the side affects. It might be a good idea to do some research and weigh out the pros and cons for steroid therapy. I do know from experience that consistent physical therapy is important because it will maintain range of motion and help slow the process of phibrosis.
Also again, I'm sorry that I'm not familiar with that drug on trial and I don't know that it will completely cure dmd, it doesn't seem that medicine has arrived at a full cure but I can tell you that there have been huge breakthroughs and that diseases like this will be cured some day and it's quite possible that this could happen in your nephews lifetime.
Also something else that is of great importance is that your nephew should be seeing a cardiologist and a pulmonologist who have a background in treating patients with dmd as the heart and respiratory muscles are the very most important muscles and the treatment to maintain them will greatly extend your nephews life span. Men with dmd are now able to live well into their 40's because of all of the treatments that are available today. I hope this helps!
At 12:33am on March 1, 2017, TW said…

I looked up creatine in discussions.  I'm going to change the supplements that my son is taking.  If you read down the page-Maria shared what her son was taking.  L-glutamine, l caritine, grape seed, etc.  Im a believer  natural supplenents.

At 11:34pm on February 28, 2017, TW said…

He is taking omega-3, calcium, Co q10, d3,-THESE 2X DAYmultivitamin.   I just started him on the nicotin amide riboside supplement.-500.-AFTER reading the posts on it.  He is taking deflazacort too.  He is still active.  The time period is shorter and gets more fatigued than before. 

At 12:13am on February 28, 2017, TW said…

What is your nephew taking for supplenents?

At 12:10am on February 28, 2017, TW said…

He is doing well.  We noticed he is falling more.  Tamoxifen sounds so promising.  I wish we could try what they are doing in Isreal.  How is your nephew?


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