My autoimmune/ anti-inflammatory diet starts tomorrow!

Today my husband asked me if I had done any research on this diet that I’m about to begin. I haven’t and don’t want to, but I thought that maybe I will start writing separate posts about my diet experience and what I wind up eating/cooking in case it can help others. I mean, there are a million cooking/recipe/food blogs out there, so people must be interested and maybe it’ll help or inspire somebody.

The diet and supplement plan was designed to help autoimmune conditions and inflammation. Apparently, there has been some success treating autoimmune diseases with this restrictive, evil, soulless regimen. But, seriously, I would pretty much do anything to feel better, so I am determined to find the will power. Stay tuned for my diet installments and I hope they’re not too boring!

Diet details: https://ldndiary.wordpress.com/2012/08/22/this-new-diet-of-mine/

Supplement details: https://ldndiary.wordpress.com/2012/08/23/my-new-supplement-plan/

LDN Day 6…a better night.

Last night, I slept better than I have in the past 5 nights. That doesn’t mean I slept well, but I slept better. I think I might have actually hit 8 hours. Zeo says 6 hours and 50 minutes but it looks like the headband fell off or lost contact with my forehead for over an hour. I still had crazy dreams (about saving my dogs from danger. I always have this dream. What do parents of human children do? I think I would never stop dreaming about keeping them safe). I also woke up with no blood in my arms multiple times and pain in my neck, as usual, but what was different from the other nights? Well, yesterday, I got a bit of exercise at the park (walking slowly, but something), I used arnica and took a painkiller for the muscle pain, I took my antihistamine nasal spray twice, I used my neck stretcher thingy (like a mini-rack for your spine), I did mild leg and arm stretches, I didn’t eat last night after 5 or 6pm, and I did a little mental preparation before I went to sleep, telling myself that everything was great and the diet would be exciting and tomorrow I would have energy and, oh, I LOVE bed! (lie ~ this year, bed has become all things bad) Also, the temperature dipped last night and my room was much colder than usual (which is typically not a good thing for me because I get chilled and my head and ears get cold. Back in January, when this sickness started in earnest, I would wear a woolly cap to bed every night, as well as have the electric heater on, as well as cuddle a hot water bottle. I’m going to invest in an electric blanket this winter). I don’t know what, if anything, helped me get more sleep, but I want to track it. I know if I just popped a bigger, better painkiller and a muscle relaxer, I would sleep much better, but I still refuse. It freaks me out. If I stop the LDN, maybe I will try other options, but, for now, one drug at a time, sweet jesus.

Today, I am stiff and achy, of course. My eyes are VERY swollen. I am going to chalk that up to sleeping longer and maybe a bit deeper and pretend it is a good thing. My hands still hurt and are swollen and the left thumb is still one raw nerve. Oh, I keep forgetting to tell you about this one crazy side effect I’ve been having at night since starting the LDN. I wake up in the night from a light in my eyes, but, when I open them, the room is black. This keeps happening! From behind closed eyes, I think someone has opened the blind or something, but when I come fully awake and open my eyes: darkness. Bizarre. Also, LDN seems to be affecting my skin ~ I have a bit of a break out on my chest (never happens) and face.

Yesterday, I did make it to the dog park, but not the pharmacy or the grocery store. I was just so wasted and the weather was crappy. So, I haven’t started the diet or the supplements yet. I’m having my tea with milk and splenda and savouring every sip. The Good Doctor dropped another bombshell about my diet late last night via email: NO BEANS. That means NO PEANUT BUTTER, NO HUMMUS. That kills me. Hummus can replace so much ~ eat it with veg to feel more full, put in on sandwiches (or, in my case, lettuce wraps. Yum), baked hummus chicken is good… But peanut butter I will truly mourn. Peanuts are my go-to food. She also said it is essential to have no refined sugar. That made me want to punch her in the face. If you ever read this, Good Doctor, I don’t really mean that. I don’t want to hurt you, you are my only hope, but I am just so overwhelmed by what I have to do, what I can’t do, how NOT easy eating is going to be.

I’ll start the diet tomorrow. I promise. I’ll go shopping today. I’ll have to make homemade soups. Lots of homemade soups, salads, nuts for snacks and … what about breakfast? I still feel discouraged about breakfast. I’ll have to develop a liking for the fake yogurts made with soy or coconut milk. I could add fruit and crumbled Lara Bar and pretend it’s granola or muesli. Then, to stop my blood sugar dropping, eat a bunch of almonds. This is going to fun. You are going to feel great.

Have I mentioned my blood sugar? If I have, forgive me ~ no memory. I have reactive hypoglycemia. I can fast for 10 hours and my sugar is fine, but, as soon as I eat breakfast, I have to watch out. An hour or two later (depending on what I had to eat), my BS plummets. I usually catch it in the 60s and 70s, once I start to feel the shakes. Last week, it was 58. The week before it was 43. That’s low. Way too low. It had an effect on my whole day. So, now I am trying to be very mindful of what I eat in the mornings.

Day 5… Later. Feeling low.

I’ve been debating whether I should be honest on this blog about just how hopeless things can feel and how low I can get with this sickness. Part of me thinks I should keep it factual, try to report the facts, not make things sound so dire and depress those that might be reading. But, things often feel dire and, if I’m going to use these posts for the therapeutic purposes they’ve taken on, maybe I should be honest with my feelings.

So, honestly, I’m scared and feeling pretty hopeless – today. I know, from the last nine months, when my physical symptoms are better, my mood lightens immediately, so I’m trying to keep things in perspective. You will have a better day than today. Take one day at a time. You’ll live to a ripe old age. You will have a quality of life. It’s just difficult to stay positive. It’s virtually impossible. In the simplest description, I have had the flu for nine months. That’s not the half of it, obviously, but, it’s the best way to get across how it feels. Tonight I feel like shit. It’s the same thing I keep describing: I can’t breathe, every muscle is stiff and painful, I have a headache and feel weak, my throat is sore, I have chills, low grade fever and no appetite. I just want to get better. I just want ...to…feel…better. To feel strong. To feel stable. To feel pain free. To feel carefree. To not notice how I feel!

The truth is, I can’t do this for years and it feels selfish. Things could be so much worse. I could be much sicker or I could be much poorer or I could have no husband, friends or family. I could live in a different country, I could be in a war zone, I could have no access to healthcare, I could have no bed, no blankets. I could be much sicker. I have to find the strength to be grateful every day. We all do. So, in that spirit: I am grateful to be alive. As long as you are breathing, there is more right with you than wrong with you.

My new supplement plan from the Good Doctor.

For those of you who are curious about the supplement plan my new Good Doctor has put me on, here it is:

For nutritional immunomodulation:

Vitamin A: 10,000 iu/day, “preformed” or “mixed carotenoids”, not beta carotene

Vitamin D: 4,000iu/day

Alpha lipoic acid: 400mg 3xday = 1,200mg total/day

Borage oil for GLA 1,000mg/day

Fish oil for EPA+DHA = apx 1,000mg/day

For Mitochondrial dysfunction:

CoQ-10: 100mg/day

Acetyl-L-carnitine: 1,000mg 2xday = 2,000mg total/day

I also take:

Thyroid hormones (T3 and T4)

Fiber

Colace

Ortho-Biotic probiotics

Vitamin B-complex

Biomins mixed minerals

Vitamin E

And Emergen-C once in a while.

 

LDN Day 5… still no sleep

Ugh. I am so tired. I had another terrible night. I took the LDN and was in bed at 10pm and didn’t get up until 9am. In 11 hours, I managed to get 6.5 hours sleep. I woke up constantly again. (Check out the Zeo graph. “W” at the top = “wake”) I had to go to the bathroom constantly. I was uncomfortable and in pain. I had crazy dreams. I was sweaty, but cold. Extreme hunger finally forced me out of bed. Ugh.

There’s this thing I do in my sleep that always wakes me up. I wake up with all of my muscles tensed from head to toe, my back in an arch, my hands in fists, my arms and legs rigid, my jaw clamped down so hard it feels like my teeth might break (and they have). I have no idea why it happens or how to stop it, but I am always afraid that I am going to throw my neck out while doing it. I have degenerative disc disease issues in my neck (cervical spine). When my neck goes out, it is the most acute pain I have ever experienced in my life. I am paralysed when this happens. I have been seeing a physical therapist for years with minimal progress. She said I had the worst case of hypermobility she had ever treated. I have an at-home TENS unit (transcutaneous electrical nerve stimulation) which I use every day. It helps me not have to use pain killers and I basically stopped going to the PT, because now I have the equipment they use at home. Today, as I type this, I have it zapping my back and neck ~ I tweaked something in the night with all the tensing and thrashing about.

I haven’t had a “good” day since the day I started LDN. I have felt fluish and chilled every day this week. The pain in my back, shoulders and neck makes it difficult to do much ~ even walking up and down the stairs. My chest is tight the past 5 days and my nose is either running or stuffed up. My hands ache. My left thumb has been virtually useless for days because there is a painful electric jolt that runs down it every time I press it into a certain position. After lunch yesterday with my friend, I had planned on going shopping for groceries and supplements for the new regimen, but, after two hours of visiting, I was weak, felt faint, my muscles were buzzing, my concentration was totally shot. I was having such a hard time focusing on our conversation and the responses I should give… That doesn’t happen a lot to me. I have had some cognitive disturbances with memory, but having to put so much effort into focusing on what you are hearing and what you should say… that’s a new one.

I would love to tell you about the stool sample kit that I have to do, but I won’t. It might be the most disgusting thing I’ve ever dealt with. Well, that’s not true. I’ve dealt with more disgusting things (work in an elderly care facility and restaurants long enough and you see things you don’t want to). In fact, I’ve experienced more disgusting things just surfing the internet.

Today, I am determined to go to the dog park, the pharmacy and the grocery store. I’m determined to finish the laundry and laugh and PLEASE GOD get a better night’s sleep. Maybe I should take a melatonin…. but I hate mixing drugs. Stay tuned.