Radiation Induced Lumbar Plexopathy


A few weeks ago someone left me a comment on Twitter after I tweeted about my balance problems. She mentioned Radiation Induced Lumbar Plexopathy, something I never heard of it, so I did some research. From what I read, I could very well have this.

My balance problems became evident after I was weaned off pain meds. Before that my doctors thought I was wobbly because of the heavy-duty pain meds I was taking. But when I was drug-free, they checked me over and all they could tell me was “I don’t know.”

I looked around the Internet to see if I could find out for myself and the only thing I came up with was… maybe the chemotherapy attacked my nervous system. I only had two doses but the first one they gave me was accidently over-dosed, so I figured that’s when the damage was done. Since I found nothing concrete and my doctors didn’t seem interested to pursue the cause any further, I gave up.

At first my legs were so bad, I had to get around in a wheelchair if I went out for long periods. My legs were too weak to walk farther than half a block… but after some rehab and getting into gentle yoga, I got better; not back to normal but at least I didn’t need a wheelchair anymore. Now I use a walker when I go out alone.

Radiation Induced Lumbar Plexopathy is a fancy term for; your nerves are screwed up around your lumbar pelvic area from all the radiation treatment you got to kill the tumors. When my 30 treatments were finished, my radiation doctor told me, ” I’m surprised you finished the treatment, I gave you more radiation than any of my other  patients.” At the time I didn’t fully appreciate his comment, but now I see how it probably affected my nerves. Before I started radiation the same doctor assured me that only the tumors would be affected; none of the surrounding tissue would be damaged.

Silly me, I believed him.

Within a couple weeks the entire area around my upper thighs and groin area turned gray. My pubic hair fell out. The radiation beam was aimed at my lower left butt-cheek and yet the front of my body clearly was affected. I shutter to think what my ovaries, vagina and other lady-parts must have looked like. Did my doctor really not know the radiation would spread out to connecting tissue or was he feeding me a line of crap, thinking I wouldn’t do the treatment if he was honest with me? My experience is another example why patients should do their own research before doing ANY treatment. You have to be your own advocate! I don’t care what your doctor tells you, you aren’t getting the full story.

I can’t go back and change what happened and I probably would have done the radiation anyway. I was in bad shape and I knew time was not on my side, but it would have been nice (and ethically responsible) to give me all the information. Now I have a “new normal” life. Everyday I practice gentle yoga (I have some listed in the yoga section of this blog if you want to check them out for yourself) and I go for walks. If I miss a few days, I feel my muscles tightening. My lower back was so tight after radiation I couldn’t bend over to pick something off the floor. It felt like my muscle was tearing; that’s why I started a daily yoga practice. It took a year for me to be able to touch my toes or come close to sitting cross-legged. But each day it got easier and easier.


If you are experiencing balance problems or nerve pain and/or numbness, after getting radiation, you might have Radiation Induced Lumbar Plexopathy. There’s a Facebook support group you can join and find out what other’s do to relieve their symptoms.

Be well and stay informed!



Mesothelioma Survival – Resources for Patients and Families

Almost daily I read stories about people who got cancer from their environment and/or the foods they were eating. Often times these patients have no idea that the environment where they live or work contains cancer causing chemicals.


Sure, the law requires Prop 65 signs be posted in public places, warning us that “something” in that area can cause cancer, but they never say exactly what. So what good does that silly sign do? I’ll tell you what…nothing! It’s a big game of smoke and mirrors. For example: Asbestos was been making people sick for decades before something was done about it. Since it takes just as long for the symptoms to manifest, people are still getting sick. According to the Mesothelioma website:

“… Individuals who worked in industries that used asbestos as insulation are most vulnerable. Anyone who worked with asbestos while removing it, installing it or as it was used for insulation may be at risk. This mainly includes shipbuilders, steel workers, military veterans, automotive industry workers and construction workers but can involve others as well…”

You can bet none of those people knew they would get sick from just going to work and trying to make a living. Getting a cancer diagnosis (no matter what kind) is a life altering event. There is so much to do and think about…and trying to find help while going through treatment is nearly impossible. This is one of the main reasons I write this blog…to help you find help. When I was sick, my family got the run around by government agencies that were supposed to be there to help us. It’s disgusting if you ask me, since our government should be looking out for us before we get sick…like having these cancer causing chemicals “independently” tested before they are used in public.

Luckily, there is an organization that provides help for those who have been diagnosed with mesothelioma or some other asbestos-related disease. Someone from Mesothelioma Survival contacted me and asked if their organization could be added to my Helpful Resource section. I am more than happy to do that. I also found out that May is Mesothelioma Awareness Month. So if you have been recently diagnosed or know someone who has, please go to their website and share their information. We have to depend on each other because the ones who we elect to “protect” us certainly won’t do it.

Be well and stay informed!


September 8 2021

I was recently contacted a member of the Public Outreach Department for the Mesothelioma Center (Asbestos.com). They are an advocacy group that works to spread awareness of asbestos-related diseases and help those currently suffering from them.

Here are some things they offer patients that set them apart from other advocacy sites:

• A monthly online support group where we discuss a variety of topics pertaining to cancer patients.
• An on-staff doctor and nurse available to answer any medical-related questions.
• 24-hour live chat support.
• Patient Advocates that work 1-on-1 with individuals to help them find local doctors, treatment centers and support groups.

You can learn more about them by visiting their website: https://www.asbestos.com/mesothelioma/

Be well!