REBLOZYL® (luspatercept-aamt) logo
Now approved for earlier treatment of MDS-related anemia badge


REBLOZYL® (luspatercept-aamt) is a prescription medicine used to treat anemia (low red blood cells) without previous erythropoiesis stimulating agent use (ESA-naïve) in adult patients with very low- to intermediate-risk myelodysplastic syndromes (MDS) who may require regular red blood cell (RBC) transfusions.

It is not known if REBLOZYL is safe or effective in children under 18 years of age.

Now approved for earlier treatment of MDS-related anemia badge

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Hypothetical patient with anemia in myelodysplastic syndromes with ring sideroblasts (MDS-RS)
Hypothetical patient

Caregiver Information

Caregiver Information

After being diagnosed with myelodysplastic syndromes (MDS) and MDS-related anemia, a person may feel overwhelmed and nervous about the future. That’s where caregivers like you can help. Whether a spouse, family member, or friend, a caregiver plays a major role in supporting someone living with MDS.

But no matter how you’re helping, remember—at every step of the way, the support of a caregiver can make all the difference in your loved one’s treatment journey. Your help is noticed and appreciated.

How can I help my loved one with their MDS-related anemia?

You can learn more about MDS and anemia

One of the most helpful things you can do as a caregiver is to learn about these conditions. The MDS Education Brochure provides useful information that will help you better understand MDS, anemia, and what can be expected over time. If learning about MDS-related anemia feels overwhelming on your own, ask a friend or family member to learn with you.

You can share how you’ve seen MDS-related anemia impact them

It can be hard sometimes for people to understand how their symptoms are affecting them, or to put these changes into words. But as a caregiver, you have a unique perspective. Speaking up with your loved one's healthcare team and discussing the answers to these questions will help you know what symptoms might need attention.

During the treatment journey, think about questions like:

  • What parts of my loved one’s routine have changed over time?
  • What tasks do they need help with? What parts of their day have become difficult for them, and when did things start getting harder?
  • What changes in their health or behavior have they (or I) attributed to aging? When did these changes start?
  • Have they brought up any feelings of discomfort or tiredness to me recently? If so, what situation prompted them to share this?

Talk about your answers to these questions with your loved one and with their healthcare team. This information may give greater insight into your loved one’s health.

You can help them set their goals

When treating anemia, the healthcare team will set treatment goals that are important for everyone to understand and remember. Communicating with your loved one's healthcare team is one of your most important roles as caregiver, so ask questions if you need to.

You can also help with setting activity-based goals, which are goals that can be measured in terms of a person’s day-to-day life. Speaking up with your loved one's healthcare team and discussing the answers to these questions will help you know what symptoms might need attention.

You can help them stay organized

There will be a lot of information for your loved one to keep track of. Helping with note-taking, organization, and tracking is a great way for you to make a difference.

At appointments, help them track:

  • Test results, including hemoglobin (Ηgb) levels
  • Transfusion information, including dates and units
  • Treatment information, including dates and dosages
  • Progress toward treatment goals, including any updates from their healthcare team
  • Any follow-up appointment details

At home and between appointments, help them track:

  • How they feel right after a transfusion (usually pretty good)
  • How they feel in the time leading up to their next transfusion (usually not as good)
  • Their progress toward their goals
  • Changes in their symptoms

Get more information about tracking

You can speak up with their healthcare team

People living with MDS-RS can sometimes find it hard to speak up with their healthcare team, but their caregivers can help. When you’re interacting with their healthcare team, you can advocate for them by:

  • Asking questions and taking notes during appointments
  • Arranging for a translator, or acting as a translator if necessary
  • Sharing any health and symptom information you and your loved one have tracked
  • Making sure healthcare providers from different facilities are sharing information
  • Reminding the healthcare team of your loved one’s treatment goals and progress so far
Hypothetical patient with anemia in myelodysplastic syndromes with ring sideroblasts (MDS-RS) with doctor and loved one

Not sure what to ask in appointments?
The MDS Education Brochure has example questions

You can connect with MDS advocacy groups

MDS advocacy groups were created to support you and the person you’re caring for. These groups have valuable resources made specifically for people living with MDS and anemia and their caregivers, including:

  • Disease education materials
  • Opportunities to connect with other MDS caregivers and patients
  • Expert opinions and up-to-date research

It’s worth taking the time to explore everything MDS advocacy groups can offer you and your loved one. Visit the REBLOZYL resources section for a list of some of our advocacy group partners.

Hypothetical patient with healthcare provider and loved one

You can take care of yourself, too

Caregivers can sometimes become so focused on the people they care for that they forget about their own well-being. But you can be an even better caregiver for your loved one when you’re also taking good care of yourself. Here are some self-care strategies:

Care for your mind:
Set aside time for your hobbies, your friends, and any activities that help you relax—even just watching TV.

Care for your body:
Try your best to eat well, get good sleep, exercise when you can, and visit your doctor regularly.

Care for your connections:
Look for community with other caregivers, and talk to your friends, family, or even a therapist about how you’re doing.

It’s normal to sometimes feel scared, lonely, sad, or like you’re handling everything yourself. Remember: you’re not alone, so don’t feel guilty if you need support from friends or family. Communicating and asking for help are both important for your own well-being.

Visit REBLOZYL Resources