Thursday, November 10, 2016

Another Diagnosis: Erythromelalgia

Like many of us, I already have an alphabet soup of diagnoses that seems to grow every year: ME/CFS kicked everything off almost 15 years ago. It causes Orthostatic Intolerance (OI), which for me includes both POTS and NMH. Plus I recently realized I still have Lyme disease which seems to flare up every few years.

Classic EM on toes & feet (mine is much milder)
Now, I can add one more to the list: Erythromelalgia or EM (yay, another acronym!) This started 3 years ago but was just diagnosed at the end of last winter. Because mine goes dormant in the warmer months, I have just begun to read and research EM, to learn more about it and how to treat it because it gets very painful at this time of year. EM is likely caused by/directly related to ME/CFS in my case, so it is possible that some of you may have it as well and quite likely if you do that it hasn't yet been diagnosed. It is considered a rare condition.

According to the Erythromelalgia Association:
"Erythromelalgia is a rare and frequently devastating disorder that typically affects the skin of the feet or hands, or both, and causes visible redness, intense heat and burning pain."
My EM began abruptly almost 3 years ago. It was the first week of December, the weather had turned cold, and my family made our annual trip to a local Christmas tree farm to cut down our tree. It was, as always, a pleasant time with my family, except that by the time I got home, my toes were burning with pain. I was desperate to tear off my warm socks and boots and was almost in tears. From that day on, the burning pain and redness in my toes continued until spring. The podiatrist guessed maybe it was a fungal infection, but the antifungal cream he prescribed did nothing. My primary care doctor had no idea what was wrong (is this sounding familiar?).

On my next visit to the dermatologist, I showed him my toes and described the pain. He said it sounded like chilblains. I told him someone else had suggested that, and I had looked it up, but my problem seemed to be the opposite. Apparently, with chilblains, cold temperatures make the condition flare and it feels better if you keep your feet warm. I had discovered, by trial and error, that heat made my feet worse. I explained to him that the only relief I got was from soaking my feet in cold water, which led him to conclude this was definitely not chilblains. He was also stumped, but - to his great credit - he didn't give up on me. He went off and did some research and called me back to his office.

He said he thought he'd figured out what I had: Erythromelalgia. He'd found information online on the Mayo Clinic's website, and he let me watch a video (at the link) about it on his tablet. He was right - it sounded exactly like what I had! Unfortunately, since it was a relatively rare condition, there didn't seem to be a lot of information on treatments. He prescribed a cream for me for the pain & burning feeling and advised me to use cold water soaks sparingly (and cool, not ice cold water) so as not to damage the skin. I limped (sometimes literally) through the rest of the cool season and breathed a sigh of relief when it disappeared again in the warmer months.

Two weeks ago, it began to flare up again - right on time as the outdoor temperature cooled. By the way, my seasonal fluctuations seem to be unusual; for most people, summer is worse, and the warm outdoor temperatures cause bad flare-ups of their EM. My theory, from what I've read and the photos I've seen, is that mine is milder, and it flares up when I start to wear shoes and socks in the cooler weather and switch from flip-flops to slippers indoors. This time when it started, I looked up erythromelalgia online and began to educate myself about the condition and its possible treatments.

For starters, my EM is almost certainly related to ME/CFS. ME/CFS causes autonomic nervous system dysfunction, which causes OI and can also lead to EM. Interestingly, I already take several medications for ME/CFS that are sometimes used for EM (beta blockers for OI/POTS and tricyclic antidepressants - low dose at bedtime - for correcting sleep dysfunction). Perhaps that is another reason why my EM seems milder than most and goes dormant for part of the year.

I was happy to find that there have been some studies on various treatments (though not many), and I eagerly read all that I could find on the subject and made a list of what might work for me. They divide EM into two categories: primary, which has a genetic marker, and secondary, which is caused by other conditions. I think with ME/CFS and its autonomic dysfunction, I fall squarely in the secondary camp (I also checked my genetic results and I don't have the marker). So, that somewhat limits my treatment options, but there are several things I'd like to try. My dermatologist doesn't feel qualified to treat EM - he'd never even heard of it before he dug it up for me! - but I have learned there are two potential doctors sort of nearby - one at Temple and one at Johns Hopkins - who might be able to treat it. So, that's my next step.

Besides digging up all the information I could find, I also joined two Facebook groups on erythromelalgia. I know from experience that nothing beats talking to other patients in the same situation about what has worked for them (that's where I found out about the two doctors in the area).

So, briefly, erythromelalgia symptoms often include:
  • Burning pain and redness on extremities - often toes and feet, sometimes fingers and hands, and occasionally up the legs or arms, too. For some people, it also affects the face and ears.
  • Some swelling and inflammation of affected extremities.
  • Cold makes symptoms better; heat makes them worse - this is key and differentiates EM from many other possible diagnoses.
I miss my whimsical sock collection!
First-line of defense is simply keeping the affected extremities cool. For me, this means going barefoot or in flip-flops all the time in the house, keeping the house temperature cool (at least until my husband gets home in the evening!), sleeping with my bare feet outside of the covers, and occasionally - not too long or too often - using a brief cool water soak when the pain gets unbearable. It's not easy having cold feet all winter long, but it helps a lot! I am already missing my slippers and all my cute, colorful socks that I used to love wearing. Going out is tricky for me at the moment. Wearing loose slip-on canvas sneakers without socks seems to work best, if I really can't bear being out in flip-flops. Right now, my pinky toe is swollen, so even those hurt a lot.

If you think you, too, might have erythromelalgia (I'm getting better at saying & typing that!), here are some resources - information and groups - to help:

So, I'm curious, does anyone else with ME/CFS or Lyme have EM or think they may have it? So far, in the two groups I joined, there seem to be quite a few EM patients who also have ME/CFS, POTS, or Lyme disease.

9 comments:

  1. Anonymous1:38 AM

    A friend of mine has this! She wrote this post about it a few years ago: http://lymetwistontherocks.blogspot.com/2011/01/pain-that-lyme-can-cause.html

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    1. Thanks for the link! It's a great post & very informative. She and I seem to have a lot in common.

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  2. It may be that I have this also. In the picture, the veins are popped up. This happens to me, along with slight swelling and, sometimes, burning. I will look into the links you have provided (Thank you!) when up to it, but are the popped veins part of erythromelalgia also?

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    1. I haven't seen that mentioned, but it makes sense based on the underlying mechanism. EM often occurs when there is poor control of autonomic nervous function, including dilation & constriction of blood vessels. Dilation of blood vessels can cause that sudden flare-up of EM (just as heat does), and it makes sense that the blood vessels would appear more swollen & prominent in that condition.

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  3. I have Lyme and was diagnosed with ME/CFS last year but not sure if it was that or reactivation of EBV (still have high titers of that) along with CMV, HHV-6. If you are well read on CFS which you sound to be. I recently visited Mayo Clinic and was diagnosed with 'probable' EM. Going back soon for a final diagnosis. So - sounds like we have some similar health issues. I wonder if a researcher would want to study a group of us.

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    1. Lyme, like ME/CFS, is known to cause re-activation of dormant viruses, like EBV, CMV, and HHV-6. For that reason, I stayed on antivirals (Valtrex or Famvir) during the 3 years that I was being treated for Lyme. You should look into that - treating those reactivated viruses could help you feel a lot better and even possibly help the EM! Glad to hear the EM clinic at Mayo was helpful.

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  4. I think I may have this condition as I suffer extreme burning of hands and feet when the blood rushes through, veins swell up and becomes very painful. I also have POTS secondary to EDS.
    Thank you

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    1. So sorry to hear that - your symptoms do sound like EM - the key indicator is if heat makes it worse & cold makes it better. Since you have EDS & POTS, secondary EM does make sense.

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  5. Oh gosh, this sound incredibly painful :( I am so sorry that you are having to deal with this on top of your other health challenges

    Donna- http://www.februarystars.co.uk

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