Thursday, January 7, 2010

Avoiding Caregiver Burnout


A recent article in the American Pain Foundation’s newsletter was entitled “Avoiding Caregiver Burnout”. This title reminded me of my caregivers. They were first my mother, now my husband and soon to be my children.

I thought about these people, who did not ask for the job, and what they must be feeling while I’m in the hospital getting blood and morphine pumped into my veins. They sit in hospital rooms, doctor’s offices and watch while I suffer. Their lives are affected by Sickle Cell Disease as much as mine is.

Before reading the Pain Foundation’s article, I personally imagined that caregiver burnout must surely be a reality for some people dealing with sick family and friends. Working full-time just adds more stress to this situation.

Here’s what the Pain Foundation suggests to reduce caregiver burnout:

  1. Stay positive. Your metal health is just as important as the person who is being cared for.
  2. Balance your life by taking breaks to do hobbies or things you love.
  3. Protect your health. (Put your mask on first, then help others) Get rest, eat well, and take vitamins.
  4. Seek out help. There are support groups and resources for information. Know what you can do and acknowledge what you can’t. (ask for help)
  5. Keep communication open and be patient. Pain affects people differently; they need your patience and kindness.
  6. If people offer help, have a list ready of what needs to be done. (Grocery shopping, help cooking, cleaning the house, or raking the yard.)
There is no shame in asking for help from family members, church members or neighbors. People who see you care for a sick loved one will jump in to help….don’t be afraid to ask

Resources:


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Tuesday, December 22, 2009

Part 2 - Stem Cell Transplant


Part 2 - Anyone Want a Bone Marrow Transplant or
maybe a Stem Cell Transplant?


I couldn’t sleep thinking about this “cure”. I was wondering is there is a rush to yell cure?

Researchers gave 10 patients ages 16 to 45 bone marrow Stem Cells. They gave them low levels of radiation, chemotherapy and high levels of immune suppressant drugs.

People with SCD normally have spleen problems; this makes them more prone to infection. Think about the infection possibilities when you give a person, who’s already catching everything that blows by, an immune suppressant drug. You may have received a cure for sickle cell, but now you may get cancer to replace it.

Researchers said, “Though most patients in the study are still taking immune-suppressant drugs, researchers hope to eventually wean them off the medications.” Check out the side effects of Alemtuzumab, a drug used to suppress immune system T-cells, and Sirolimus, an immune suppressant to fight rejection.

Let’s not run to the hills crying CURE until you can give a person a better quality of life, not replace their problem with another one.

Tuesday, December 15, 2009

Stem-Cell Transplantation for Sickle Cell Disease


Anyone Want a Bone Marrow Transplant or
maybe a Stem Cell Transplant?

The airways are popping. The media blitz is in full affect. Massive editorial posts have been sent all over the internet. The word is out. There MAY be a cure for Sickle Cell Disease.

According to a New England Journal of Medicine report dated December 10, 2009, researchers at the U.S. National Institutes of Health say that a new method of bone marrow transplantation cured nine out of 10 adult patients with sickle cell disease.

NEW…hmmmm. I’ll take a big mac, fries and a bone marrow transplant…. please.

Here’s what I’ve gathered from reading the media stuff.

Old Bone Marrow Transplant Method - In conventional bone marrow transplants, high doses of chemotherapy drugs and radiation were given. Chemotherapy and radiation is used to wipe out the person's own bone marrow, which makes the faulty red blood cells. There are many complications including destroying fertility

Adults were usually not good candidates for bone marrow transplants because they were thought to be too sick to handle the high doses of chemotherapy and radiation needed to prep the body for the procedure.

New Bone (Stem Cell) Marrow Method - Senior study author, Dr. John Tisdale, a senior investigator at the U.S. National Institutes of Health explained the new method allows for less grueling pre-transplant routines, which adults with severe sickle cell can tolerate.

10 patients ages 16 to 45 with severe sickle cell disease received bone marrow from donors that were siblings with matched HLA (human leukocyte antigen) in their blood.

Lower levels of radiation were used in the new method which does not seem to destroy fertility. The bone marrow is replaced with stem cells from a donor's marrow, which then takes over and begins to produce new, healthy red blood cells.

NOTE: When doing the new bone marrow transplants, the researchers noted that not all of the patient's own marrow was wiped out. Some remained and seemed to co-exist with the donor marrow without causing problems. Dr. Tisdale said, "That meant we didn't necessarily have to kill the entire bone marrow of the patient to make this work." Tisdale said, this opens the possibility of using an even less toxic means of preparing the body for transplant.

Patients in the new method study were also given:

Alemtuzumab, a drug used to suppress immune system T-cells
Side Effects of Alemtuzumab - events include hypotension, rigors, fever, shortness of breath, bronchospasm, chills, rash, syncope, pulmonary infiltrates, ARDS, respiratory arrest, cardiac arrhythmias, myocardial infarction, and cardiac arrest. Some cases of cardiac adverse events have resulted in death. http://www.drugs.com/sfx/alemtuzumab-side-effects.html

Sirolimus, an immune suppressant to fight rejection
Side Effects of Sirolimus – acne, back pain, constipation, diarrhea, headache, joint pain, nausea, trouble sleeping, vomiting and weakness. http://www.drugs.com/cdi/sirolimus.html#side-effects

After 30 months, all 10 patients are alive, and nine of the patients had successful grafts where none of the patients experienced graft-versus-host disease (where the body rejects the new bone marrow). They are also considered cured of sickle cell disease, according to the study. Though most patients in the study are still taking immune-suppressant drugs, researchers hope to eventually wean them off the medications.

The new procedure doctor’s say is promising, especially since it could eventually include those who don't have an HLA-matched sibling. Dr. Tisdale said, "These were the sickest of the sick patients. Some were in the hospital every other week for pain or other crises. Today, some have gone back to school and to work. One patient had a baby."

In the past, these older/sicker patients were excluded from transplant studies as they are very poor candidates for high dose chemotherapy regimens. This study makes it possible to offer patients with severe sickle cell disease stem cell transplants."

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My conclusion: This is a “study”….also know as a “trial”. We won’t see this stem cell treatment given to “us” for a while. But, I’m hopeful.
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Links related to this report:

Bone Marrow Transplants May Cure Sickle Cell in Adults http://www.dreddyclinic.com/forum/viewtopic.php?f=25&t=22080&p=34580#p34580

Bone Marrow Transplants May Cure Sickle Cell in Adults - http://www.nlm.nih.gov/medlineplus/news/fullstory_92818.html

Stem Cell Researcher Dr. MM Hsieh – Co-author of report http://www.stemcellscience.org/showauthor.php?surname=Hsieh&initials=MM

New England Journal of Medicine report dated December 10, 2009
“Allogeneic Hematopoietic Stem-Cell Transplantation for Sickle Cell Disease”
http://content.nejm.org/current.dtl

National Institute of Health

Sunday, December 13, 2009

Finally, Someone Heard Me

I've been screaming from rooftops that SCD affects all people, not just those of African ancestry. Thank God the Sickle Cell Disease Association of America finally heard.




The SCDAA 2009 poster child
http://www.sicklecelldisease.org/
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Monday, November 30, 2009

Live On!!!

I'm baaaaack.

Not 100%, using one good eye, but living my motto "Live On". No pity party here, just information, education and support.

Now on to business.

Get Educated: The Department of Education is accepting applications for new SSS Program awards for FY 2010. The purpose of this program is to increase the number of disadvantaged low-income college students, first generation college students, and college students with disabilities who successfully complete a program of study at the postsecondary level.

Eligible applicants include institutions of higher education. Application deadline is December 7, 2009. Check out these sites for more information:

http://www.disability.gov/education/news_%26_events
http://www.ed.gov/news/fedregister/index.html
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