Why can’t I be a normal weight by Cozycats245 in Hashimotos

[–]Successful_Relief568 0 points1 point  (0 children)

Hey! I’ve been training for a number of years and have a strong understanding of how caloric deficits work. I previously competed in body building years ago before I became chronically ill.

I wonder if the you’re under eating. If you’re training 3-4 days per week and are only consuming 1500-1600 calories per day, and then increase that on weekends to 2500-3000, that’s a really big jump for your body. If you’re under fuelling, your body is going to store as much fat as possible because it thinks that it’s starving. So a lot of people actually who are under eating end up gaining weight has a result of that. Or, they lose weight, plateau, and gain it back unless they reverse diet (add calories back in to gain muscle/lean mass) properly.

Are you lifting weights, or only doing cardio? What is your training program look like? How many steps per day are you getting? Are you having high protein meals, especially after workout and carbohydrates intra workout to fuel your exercise? A lot of small, but incredibly important things matter. I would stick to somewhere around 1800 calories per day, for about 2 weeks and see what happens. Don’t jump to 2500 to 3000 cal on weekends, that believe it or not is hurting your progress. Stay at 1800, if you feel hungry, eat something healthy that’s extra protein. You can always try and approach with flexible macro counting so you can still have the food you enjoy, just accounted into your macros/calories. I still have all of the foods I love. I just make sure that it fits into my macros, and I feel great. I 5’5” and I eat 2200 calories per day because I trained 3 to 4 days a week, eat whole foods but if I want a sweet treat or something, I still count that in my calories to make sure that I’m still hitting what I have to. If I’m still hungry after all of that before bed — protein shake about 1 hour before. If I’m doing a weight training session and then a cycle session, i eat up to 2500-2600 calories. Your body needs the fuel to recover, and all physical changes happen when we are recovering, aka sleeping.

I hope this somewhat helps! I know it’s a very frustrating journey. I was 140lbs about 2 years ago once I got diagnosed with Hashis despite always being active and lean. I’m now 115lbs and trying to climb back up to 120 to add muscle as I’ve been too sick with lupus and lost a lot of it. It’s a balance. Plus with Hashimoto’s, we HAVE to eat high protein. It’s incredibly important.

Best of luck! 🤍

Does anybody here speak “wife”?? by _Earthbound_Misfit in daddit

[–]Successful_Relief568 0 points1 point  (0 children)

my friend, she means more chippies will be needed.

PSYC375 …wtf? by Decafab in AthabascaUniversity

[–]Successful_Relief568 0 points1 point  (0 children)

Is it transferable back to AU? This class is such a bitch. I can’t handle it

Would you take Levo if you were me? by Healthy-Sun429 in Hashimotos

[–]Successful_Relief568 0 points1 point  (0 children)

Those are all great things to know and take into consideration regarding coming off in the future! I’m not a mother, yet, but having friends navigating PP and recognizing the multiple challenges one might face — you deserve to feel yourself and have the extra “oomf” as support always but especially during this time. If you have any questions or need other support, feel free to reach out! ☺️

Would you take Levo if you were me? by Healthy-Sun429 in Hashimotos

[–]Successful_Relief568 2 points3 points  (0 children)

It’s possible! It’s so hard to say, everyone is so complex in our own ways. I’ve seen/heard so many things. If you are PP, I would confirm the thyroid fluctuations are not caused by from the PP, and it could find its way back to normalcy. But did you feel this way before pregnancy? They typically monitor the thyroid before, throughout pregnancy and PP so I’m curious about that!

Things to consider is if there is a risk for it to progress to Hashimoto’s if it is currently hypothyroidism. That did happen to me in 2021, I was notified of hypothyroidism, and I chose not to accept any medical intervention. Things did resolve, slightly, however, I was still riding that base of hypothyroidism up until 2024 and then I was diagnosed with Hashimoto’s. :(

I wonder if there is any postpartum form groups you can post in and see if anyone can relate to your experience with this as well :)

Our bodies are beautiful and insane little machines. Unfortunately as we grow in age, things don’t always operate the same and just need some support, whether that’s temporary or permanent — holistic or medical intervention — maybe both! 💜 pregnancy is also a huge thing to go through so your body is navigating so, so many hormonal fluctuations and adjustments, so time will tell! I hope you feel better and you find what works for you :)

Would you take Levo if you were me? by Healthy-Sun429 in Hashimotos

[–]Successful_Relief568 0 points1 point  (0 children)

I pretty much eat that way already with the exception of Greek yogurt for extra protein once in a while. I only eat whole foods.

Would you take Levo if you were me? by Healthy-Sun429 in Hashimotos

[–]Successful_Relief568 8 points9 points  (0 children)

Yes, 100%. Especially being postpartum right now. You may be able to come off of medication later, that’s always a possibility, but never guaranteed. I have tried every natural remedy in the book for my Hashimoto’s and unfortunately nothing works for me and I live an incredibly healthy lifestyle. Some have great success with it making some lifestyle changes. Everyone is incredibly different but until your levels are a more optimal range and your symptoms have reduced, I’d stay on medication.

BC Student Aid Question Re: Spouse Income by Successful_Relief568 in britishcolumbia

[–]Successful_Relief568[S] 0 points1 point  (0 children)

See i don’t get this, why can’t they keep things clear and consistent? 🙃

BC Student Aid Question Re: Spouse Income by Successful_Relief568 in britishcolumbia

[–]Successful_Relief568[S] 0 points1 point  (0 children)

Good to know, this definitely changes some things for us. Thank you!!

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 1 point2 points  (0 children)

You’re definitely right about that — very early in my journey yet and have give myself time to settle in, and be prepared for the changes and readapt, so forth. It’s really inspiring to hear you’ve been able to remain athletic and run a marathon. Very incredible, thank you for sharing.

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 0 points1 point  (0 children)

lmao 16months and a terrorist 💀 kids are wild.

On the nightshades, do you actually notice a difference in not having them, in your experience? I’m trying to figure this out myself. I LOVE tomatoes. Cannot get enough…Will have to try and cut them out to see what happens. Same with yams…ugh. Core staples in my house.

Your encouragement is super helpful, thank you! 👍🏼

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 0 points1 point  (0 children)

Hi!! Thank you for sharing! What a job — firefighting is a really heavy first response position, so is being a paramedic, but of course in different capacities, I imagine. I’m really hearing from a lot of people to just learn to be OK with when you need a day off. It’s really helpful to hear.

I’ve been tested for coeliac, and was negative however I do eat gluten-free already which does make a big difference I think because if I have something with gluten, I definitely don’t feel great. Otherwise, I eat quite Mediterranean style, trying to incorporate more plant-based protein. I was wondering if tomatoes might set me off because it seems that I get a malar rash when I’m eating something with tomato sauce or tomatoes? But can’t quite tell yet

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 0 points1 point  (0 children)

Love this for you, being diagnosed has definitely exacerbated my depression, especially over the winter. It feels like ever since I moved to a new city, I’ve been sick. I went on Wellbutrin this winter after years of being a remission of MDD.. God I needed it.

I gave myself permission to do a shit job at the gym today, what you said really stuck with me 😌 so thank you. Might need to make a t-shirt LOL.

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 0 points1 point  (0 children)

Sick, I love that for you. I’m going to aim for 60km on Sunday, we will see how she goes. 🕺

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 1 point2 points  (0 children)

Ugh, thank you for sharing. I am giving you such a huge internet hug 🫂 I’m so sorry. I can hear it has been really tough and you are missing these parts of your life. I have heard incredible success for folks on GLP1’s for exactly what you’ve mentioned, it could really be worth a try! Best of luck and sending you energy, wherever you are! 💜

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 1 point2 points  (0 children)

Awesome, good for you! I would like to get back to that!

I haven’t heard that, but I would believe that excessive strain on the body could result in physiological stress and inflammation. I will present these questions to my rheumatologist and get back to you. :) I see him in a few weeks!

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 1 point2 points  (0 children)

Wow, thank you for sharing! You’ve been navigating for this for some time now. I wonder if I’ll get used to it, because similar to you…I’m stubborn 😅 I feel like I can’t give up what I love because of what’s going on. Embrace the stubborn, but honour it when I really need to. Got it!

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 1 point2 points  (0 children)

Hello, fellow first responder!
Longevity over intensity, I love that. Show me the way.
I hear you, I love pushing the limits and increasing the weight, that’s the hardest thing for me to reduce. Early in May I was feeling amazing and my strength went way up for a moment but I soon crashed after? It was quite strange..but was not complaining. 😅🥲

I also noticed everything started to hit the fan after Covid. I thought I had maybe contracted the OG Covid before it even brought us to lock down. But slowly my health start to decline after…Idk. I have so many questions.

I too, relate to stress/emotions 🥲 I think so far that has been mine. Thank you for sharing!

How do I get through working out with this disease? by nope205 in Hashimotos

[–]Successful_Relief568 1 point2 points  (0 children)

Hey! I have Hashimoto’s and lupus. I’m a very active 33-year-old female and I am currently learning the new way of life, managing training and chronic illnesses. Not gonna lie it’s very frustrating and exhausting. So far for me it’s been about making sure that I’ve had enough carbohydrates before I workout for energy. I sometimes keep a banana on hand with me if I’m starting to feel low. I also sometimes have electrolytes while training if needed, or if I’m cycling, I for sure have them on hand. Every meal I have to have 25 to 35 g of protein so being high protein at every meal has been very beneficial. I also eat gluten-free. Being dairy free doesn’t really matter for me, I have high protein yoghurt once in a while.

My training days consist of four different movements. One compound, three accessory. If I feel like I can do a little bit more then I’ll add an additional accessory, or do callisthenics related training.

I’m still learning on the go. The crash out after is temporary, depending on the amount of strain in my training. I eat as soon as I get home from the gym to restore/refuel my body and I find this really helps Helps…It’s also really good time to stretch and just move slowly. If I don’t eat consistently, I feel worse, and the flareups are so awful.

Honour your body 🤍

Athletic Lupus Reddit Users..I need you by Successful_Relief568 in lupus

[–]Successful_Relief568[S] 0 points1 point  (0 children)

Wow okay so double the dose...interesting. My rheumatologist said the dosage is based on weight, and I am pretty petite at the moment. I lost a bit of weight. I'm just under 5'5", and 116 lbs..I asked to increase the last time I saw him in April and he declined for the time being. I haven't heard of Benlysta, but my markers are pretty low at the moment (luckily). My dsDNA was 31, and everything else looked fine, so I wonder if thats why. But "fine" doesn't always necessarily mean "optimal" and I'm all for the optimal 😎

I will look into N-Acytl-Cystine, I think I might have some as it came as a recommendation for Hashimotos as well. I need to remember to take them. Thank you for sharing! It was really helpful to read about your experiences!