As the home of the stem cells that produce blood and immune system cells, bone marrow is a complicated tissue for people with lupus.
Bones are vital, hardworking parts of the body – they protect organs, provide structure, and enable all forms of movement, large or small. People with lupus often have issues with these important structures.
Systemic lupus erythematosus (SLE,) has the capacity to affect any organ in the body, but it is most well-known for its affects on the joints, the lubricated, soft areas of cartilage in between different bones that allow limbs to bend and move. SLE attacks the joints, causing them to become inflamed, swollen, and damaged, locking up the limbs and making it difficult and painful to move. When the joints are attacked, the bones are often not spared, and the ends of the bones can often be directly damaged by lupus.
Lupus medications, such as glucocorticoids, are notorious for causing bone loss. Osteoporosis is the general catch-all term for bone that has either been thinned and weakened or has been encouraged by disease to grow in ways that make it weaker – thicker bone in the wrong places can be just as structurally unsound as less bone! However, people with lupus usually experience bone loss and more fragile bones.
Lupus itself causes pain and fatigue, which leads to inactivity, a contributor to osteoporosis. You can read more about fatigue here. Because the weakened bone from osteoporosis might make it risky to do certain activities, this creates a vicious cycle of inactivity, which can make all lupus symptoms worse – including the weakened bones!
So, lupus does have an effect on the bones, but what about the bone marrow inside many of the larger bones of the body? And how is this bone marrow important for people with lupus?
I don’t know if I will get an answer or not but I have lupus and because I have not had a positive Ana, everything keeps getting overlooked as though it’s skin only but yet I get sick really easy if somebody has a cold I get it and it’s worse for me if I eat something that says will affect a person with lupus, like garlic, I flare … I’m starting to have things happen to me that no doctor can answer nobody and I’ve been able to get myself to three different hospitals and they have no answers! Is it possible for me to experience the same organ failure the same attacks on organs as it is for someone who has had a positive Ana? I am starting to have problems with my kidneys out of nowhere I am starting to not be able to go to the restroom I am starting to have all these issues that somebody that has had a positive ANA will experience. I’m so tired of no doctor me and able to tell me what is going on with me and then they threw up that my ana has not been positive and so I cannot have these types of things happen to me, and that, I just do not believe. Any advice?
You should seek the advise of a Rheumatologist as there are a host of blood tests they can do to see if your immune system is off. This would at least give you a starting point to find out what is going on. My doctor does these test every 3-4 months to give her an accurate look at how my immune system is doing.
Hope this helps!
You should seek the advise of a Rheumatologist as there are a host of blood tests they can do to see if your immune system is off. This would at least give you a starting point to find out what is going on. My doctor does these test every 3-4 months to give her an accurate look at how my immune system is doing.
Hope this helps!
You should seek the advise of a Rheumatologist as there are a host of blood tests they can do to see if your immune system is off. This would at least give you a starting point to find out what is going on. My doctor does these test every 3-4 months to give her an accurate look at how my immune system is doing.
Hope this helps!
You should seek the advise of a Rheumatologist as there are a host of blood tests they can do to see if your immune system is off. This would at least give you a starting point to find out what is going on. My doctor does these test every 3-4 months to give her an accurate look at how my immune system is doing.
Hope this helps!
Ask for a referral and go to a teaching hospital. These teaching hospitals are usually at universities or Mayo Clinic. I had to go to several doctors and had a positive ANA and still couldn’t get treatment until my ‘numbers were higher’. Basically I had to wait until I couldn’t walk and by then my numbers were too high. Some people do t get treatment until they have organ failure. Keep pushing and don’t be passive. It took me 9 years to get a diagnosis and treatment with a family history of SLE. It’s hard for women to get diagnosed because of our gender and we aren’t taken seriously. You can be nice or be firm , be firm.