Aug. 1, 2017

It is becoming apparent that the management of pain in patients with sickle cell disease is not as straightforward as once thought. The frequency of painful episodes is grossly underestimated, largely because of prior beliefs that healthcare utilization adequately represents the incidence of crises. Recent studies, however, have shown that the majority of a patient’s pain is actually managed at home. Although the variety of analgesic medication to treat sickle cell pain is seemingly endless, we have seen that each medication has its own set of drawbacks. It is therefore imperative that the clinician tailor medication regimens to the individual patient while being vigilant in recognizing and managing possible complications of each treatment.

We have also observed that the nature of the patient’s pain, whether acute or chronic, can vary during the course of the illness. The subtleties distinguishing these two types of pain can often be overlooked, especially when clinicians fail to recognize key descriptors the patient may use to describe the pain. Better communication between patients and physicians may help to create a clearer understanding of what the pain patients are experiencing away from the healthcare setting. Not only does this aid in more effective management of the patient’s pain, but it also helps to foster a stronger doctor–patient relationship, which in turn works to dissolve many of the social stigmas that currently exist regarding sickle cell disease.

Mar. 26, 2017

Yes...I have so many journals and recordings to help me REMEMBER because Sickle Cell is just so ruthless and I was painfully accepting the judgement of people thinking that I didn't care for them or their time instead of just saying I FORGOT/I DIDN'T REMEMBER bc the truth sounds so flaky. SICKLE CELL IS SO CRUEL AND RUTHLESS...I AM DOING THIS TRIAL (http://curec.lk/2npFawV) because I am so tired of the feeling of fear of what my FUTURE holds. I am freaking 45 y'all! This has been going on for about 5yrs and I don't want to not know my kids. I am sorry for my emotions but I can't ask you to share if I won't. Sooo please share guys! 


Feb. 2, 2017

I seem to ALWAYS have the Sickle Cell Cravings when I am sick and hospitalized. ALLLL WAYS! Atm I the only one who can relate to this? WHAT do you crsve? Stay Tuned bc I am researching as we speak.

Dec. 21, 2016

Good morning Testimony, how was your health? Hope you're doing good? please, i need your help i noticed it yesterday that my palms and fingers are yellow be the first time in my health. am so scared what should i take or do? Am looking forward to your reply. thanks

Dec. 17, 2016

The folks who read my posts often can always tell when something is going sideways with me. They are the ones that reach out and ask "You Good"...Well I love you guys for that and yes you right! I am so dealing with trying to REMAIN professional while advocating for a fellow soldier. Even though the #Mistreatment was aimed at another...I STILL felt some type of way when witnessing the ignorance. Like I was telling @chazaqah As a person you don't want to sit here and admit that they have that effect on you and it is still bothering you to this day but it's the truth. I can get emotional thinking about it because the treatment was unwarranted and I didn't understand at that was going on. I thought I was doing something wrong because they were the professionals. I thought I was losing my mind because it was how the professional made me feel and they kept telling me that it couldn't be that bad and kept telling me that it's in my head and they kept telling me that it's not my sickle cell bc the blood work came back great.

THAT ignorance is like body punches to the soul. Can you not understand why a Sickle Cell patient may seem untrusting, hostile or a little rude? When you get burned like that...why would we go back into the fire?


So yes it's FRUSTRATING for us and we may exude all of that when I see a nurse or doctor I don't know.

I know that the trauma is hard to forget bc it cuts within but I do try.

I call it the #SickleCell #PTSD.