Allodynia

Allodynia is a type of pain that many of us with Fibromyalgia have. It is basically a extreme sensitively to touch. People with this can have extraordinary pain from simple every day contact like combing one’s hair.

My Allodynia

I don’t know if my situation is unique, but mine seems come and go, and it can vary depending on the amount of pressure.

Some days I’m golden. I have zero issues. Other days, I will shed a hair from my head and when it falls on to my unsuspecting arm I am in excruciating pain. Other times I with just come in light contact with something and the pain is agonizing, but I can have firm contact like a hug and there’s nothing. I don’t get it.

There appears to be no rhyme or reason as to which circumstances will crop up on any given day. Fortunately, it does not change from one to another on the fly. I’m more likely to switch from one to another on different days. So on one day I’m good, but the next day it hurts to brush my hair or even my teeth (yes, it can impact my gums).

I have found that the most noticable instigator of this type of pain is from a hair touching my skin, either stopping, caught on hard or leg hair, or feeling it as the single hair strand bounces on my skin as it falls. Because of this, I tend to brush or comb my hair fairly frequently. My sister was surprised when I mentioned that I will brush my hair several times a day, vs the once or twice she brushes her hair. I also tend to pull my hair back or up to prevent loose hairs from falling.

The other way it frequently hurts is a casual touch. A light hand on the shoulder. Someone brushing by me. My mom no longer touches me because of the number of times I have flinched unless I have asked her to, like rubbing A535 into my back. My sister is the same. My neices & nephew tend to forget. My intimate relationships don’t seem to be impacted as much cuz those touches tend to be more firm.

The hardest part is incidental touches by others who don’t know me as well. I am a leader in scouting. I’ve had youth come and touch my shoulder from behind so I’m in prepared, or a hug from a child who forgets they aren’t allowed to touch without consent.

There are also times when I know to expect contact. A perfect example is another scouting situation. As the ‘head’ leader (usually called Akela, but the Scouts named me Koolaid before I went to Cubs) I do opening & closing. This includes the challenge. I yell “Pack! .. Pack Pack Pack!” and the youth come running to challenge me, as I am the head wolf (hence wolf cubs). They come to a tight circle around me, but every meeting someone will run too far or have a hand out or jostle with another youth & contact is made Because I know it’s likely coming from somewhere, I can prepare for it and it’s less of an issue.

Lately, it doesn’t seem to be as much of an issue as it has been in the past. I don’t know why. Is it the improvement in my overall health? Is it my weight-loss? Is it than my activity level has changed? Is it that my pain levels had dropped? Is it a change in medications? I have no clue.

if you experience this condition, how does it impact you?

30 Facts!!

Originally written for the 25th Anniversary with 25 facts,, this is a list of things you should know, from someone with Fibromyalgia. From someone who experiences it, not just studies it. I have taken the original, modified it and added to it from *my* perspective as my experiences with fibro are not the same as hers. OP info available at the bottom.

1. Every morning is a tough morning.
2. I can sleep all day and still feel like I just ran a marathon.
3. If I went out last night, I need a day or two or three to recover — its okay, it was worth it.
4. When i’m tired, let me sleep.
5. Certain foods make me flare up, For me that’s items like Ice cream breaded food products (like fish sticks or chicken fingers), mayo & salad dressing, KD, etc.. Some I know why, others no clue.
6. When I’m in a flare, leave me alone in a dark room but please check in, even if I don’t answer. It makes me feel cared for & loved .If I am flaring and I am responding, I’m likely asking for a ride to the ER.
7. Yes, diet matters, but in flare mode, all bets are off.
8. Yes, my face is swollen. No, I didn’t gain 5 pounds overnight… Well I could have gained, but not on my face.. So, Yes, that is a tell that I am in a flare.
9. I have many different sizes of clothes in my closet to accommodate flare vs. non-flare days. I currently have clothing from a medium ( very generous medium) to 3x.. I’ve lost weight, so likely only a few items & eventually they will go too.
10. Fibro Fog sucks. Ya know when you get absent-minded every once in a while? Misplaced your keys? Misread something? Forgot to water the plants? That’s Brain or Fibro Fog. While it happens to everyone at some point, it not the norm. For people with Fibromyalgia this is the norm. Every day. I have even lost my train of thought, mid-sentance. It happens enough that those close to me don’t bat an eyelash when it happens. Some even see it happening & will remind me of what I was saying. The worst, is fogging out when I drive & I love to drive, but have to be super careful to make sure I am clear minded.
11. Ask before you touch. Some days, I can barely tolerate the feel of clothing or even my hair on my skin. When I’m ok, give gentle hugs please — my skin & muscles may still be tender. But if I give you a bear hug, you can give me one back!
12. Bright lights, loud noise and too many smells can overload the senses and can cause nauseous (or worse) or kick in a migraine.
13. Allergies play havoc on my body. Scented products like perfumes & body products are typical culprits Sometimes I don’t even know I’m allergic until I experience it, So it’s a bit of Russian Roulette when I go into public because I can’t control what scents other people wear. Food allergies/sensitivities do not make life any easier either, especially when eating out.
14. I am a human barometer ( there’s a post around about that.. I can typically tell it’s gonna be too cold, too wet, too hot.
15. Yes, i am on medications, sometimes even alot of them. I have a decent relationship with the pharmacy staff, and I know exactly what all my medications are, the dosage, and why I’m on it & how it helps.
16. To me, car rides are joy rides cuz I really love to drive. I need to stop every hour or two to keep my legs from going numb or seizing up. It, for me, is so worth it! But so many with fibro feel differently than I do & equate it to a highly painful roller coaster ride.
17. Some days it’s OK to let my Fibro win. It’s a marathon, not a sprint.
18. I can get moody. You would be too if you were in pain all the time, be patient with me.
19. Don’t be surprised if I can tell your mood as soon you walk in the room. My Fibro/spidey-senses are tingling.
20. My day, week and month are carefully planned to accommodate my Fibro. Only important events & people like you are scheduled.
21. If I cancel my plans with you, don’t be mad.. Remember, I made plans with you, because you are important to me. I am trying and obviously want to hang out with you, so please keep any nasty commentator yourself as I already feel guilty.
22. Your friend with Fibro that says they have no pain doesn’t make me feel any better. Plus if they have no pain, they may not have fibro cuz *all* Fibromites have *some* level of pain at *all* times Alternatively they could simply lying either about having fibro or about being totally pain-free. Also, just cuz someone says they are “Good” that’s does not mean pain-free
23. “You should exercise.” ROTFLMAO. Have you considered going to the gym while you are in the middle of the flu with body-wide aches & pain, fatigue? Didn’t think so, so how can you expect me to when I have body-wide aches & pain and fatigue? Yes, I do exercise, but I’m not a hypocrite. Do you know how long it took from me to go from bobbing in the water during aquafit to get to my current level of exercise? Years!! It helps, that I have lost weight. Before you use me as an example of of someone with fibro who is ‘fit’, remember that I started my journey to become healthier & to increase my fitness level in the winter of 2012, almost 9 years ago. And I would not consider myself ‘fit’
24. Going to the doctor makes me sad & sometimes overwhelmed— it’s a reminder of my condition. And it doesn’t help that I have at minimum a half dozen medical appointments each month – GP, Pain Doc, RMT, Physio/Osteo therapy, Gyn, Neuro, Dental, Psych, mental health support groups, and one offs for tests like bloodwork, ultrasound, x-ray, MRI or CT.
25. There are zero no-pain days, but my low-pain days are my happy days. So if I’m looking good and acting good and I’m social, I’m better, right? No, just a good *low* pain day. Fibromyalgia is chronic & will not go away
26. Because of Fibro, the mandated downtime gives me the opportunity to write this blog, and I’m grateful. Unfortunately, some of that downtime does not even permit blog writing because the pain or fatigue is*too* intense, so I have missed posts.
27. Because of Fibro, some Fibromites get to spend more time with their families than if they were healthy.
28. if i am being a dick about my health, you will not change my mind. I have to figure it out myself. For those in my life who put up with that for years, I am sorry.
29. Because of Fibro, I’ve become part of a strong, supportive community that reminds me I’m never alone.
30. Yes, I have depression. No, it’s not because of my fibro. My depression started at age 16, but fibro, we believe, started from Mono when I was 19-20. So, obvs they started at different times plus I do know the triggering event that started my depression.

Original published by Puja Rios on May 11, 2007 at https://www.huffpost.com/entry/25-facts-for-fibromyalgia-awareness-day_b_59148663e4b01ad573dac1c2

Remission! What is it?

What does this look like? Honestly, it’s not that different. Most people who have chronic illnesses only go out when they are having good day.. In remission, you are having primarily good days.. So, the big change is that people will see more of that person. Instead of once every 2-3 weeks, depending on your relationship, you might see them 2-3 times in a week!

What does it look like for me? It looks like better connections with family & friends as I can see and interact with them more.. It looks like consistent cubs meetings with a higher participation. It looks like I can do something from before but without the bad consequences like I was able to go for a hike down by the lake today and tomorrow I may be a little sore, instead of a nice big crash that used to happen.

Remission means a temporary relief from pain, fatigue & other dymptoms. I can do so much more than I could!

Do I still crash? Absolutely.. Does it happen as much right now? No. Is it as bad, as painful, right now? No, actually the pain is better right now. Does it last as long? Not usually.

So, I’m sure you are wondering, can I return to ‘normal’ life? No.. I’m still having off days. I still can & do overdo it. I crashed out one day last week for no particular reason. Today I am toast cuz of the weather shift earlier in the week. I having been slowly adding more ‘normal’ things to my life including friendships, romantic relationships, scouting commitments, family interactions, increased activity including exercise.

Am I still in pain? Am I symptomatic? Sbsolutely. That one reason I know I’m not ‘cured’ I still have pain evety single day. But lately it’s only a 2 or 3 on the pain scale these days.. I still am exhausted, but I don’t necessarily need the 12+ hours of sleep to recover from a regular day. IBS? Oh yeah., Fibro Fog? Definately.. Sensitivities? Sure, some less intense.. Morning stiffness? Oh yeah, but it’s usually less..

Why am I in remission? What did I do? I can’t say for sure, but the timing of the end of a toxic even abusive long-term relationship may have something to do with it. I returned home, slowly rebuilt relationships, re-establishing connections, increased fitness, weight loss, changed my meds & got off several, decreased dosages of others.. Lots of good changes, all of which may have contributed to my current status.

Will this last? I wish, but I doubt it.

Who Do You Sleep With?

Who do you sleep with? A partner? A pet? Alone? Myself, I tend to sleep with a partner.. There are many advantages & disadvantages to sleep with a partner..

 

Disadvantages:
*(S)He may snore or talk while sleeping
*(S)He may be a restless sleeper and putting two together could be a nightmare
*(S)He may be used to having the whole bed and becomes a bed hog
*(S)He may not be used to sharing and becomes a blanket hog
*(S)He may like to cuddle and tho may consciously know not to cuddle, do so unconsciously while asleep
*(S)He may like to connect while asleep and reach out and touch you, but we know there are times when any unexpected touch hurts
*(S)He may have different sleep hours which could disrupt your sleep *(S)He may have a small bladder and needs to use the bathroom several times a night *(S)He may be more sexual and try to initiate some hanky-panky while still asleep
*(S)He may prefer a different room temperature or room darkness
*(S)He be a total morning person who wakes bright, cheerful and alert. To be honest, I don’t think *any* Fibromite wakes bright, cheerful or alert let alone all three! Advantages:
*You are not alone, and you *know* this. You know there is some there for you. You know that there is someone who cares and will be there for you. You know that (s)he loves you and will support you. You know that there is someone who ‘gets it’, or is at least understanding & compassionate, or if your are lucky, both. It’s this knowledge that, as a single advantage, easily outweighs the potential disadvantages. Do you agree with my conclusion? Can you think of any other advantages or disadvantages?