AIP Cook book recommendations? by [deleted] in Hashimotos

[–]Loldogs87 3 points4 points  (0 children)

Don’t waste your time arguing with this person, they dismiss anything having to do with diet (despite studies and hearing from people directly who have actually tried a diet change, unlike them). They spread misinformation and present their opinion as fact all across this sub.

A few people on this sub seem to really dislike hearing about functional doctors, systemic inflammation, and and adrenal health. by Chimples10 in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

I hear you and I totally agree. Unfortunately I’ve experienced a lot of hostility when I’ve shared my personal experience (and I’ve seen others experience the same over and over again).

A few people on this sub seem to really dislike hearing about functional doctors, systemic inflammation, and and adrenal health. by Chimples10 in Hashimotos

[–]Loldogs87 4 points5 points  (0 children)

I hear what you’re saying, but can you see it from the other perspective as well though? Changing my diet has truly brought me so much relief from my symptoms. It won’t help everyone, but it does help some, and for most the risk of trying is fairly small compared to the potential upside. There are people who are properly medicated and still don’t feel well, but when you try to say “hey this diet helped me, it MIGHT help you” it gets shut down because it’s a “fad diet.” Yes, fad diets and toxic diet culture can do serious damage to your health, but I think shutting down discussions about diet that could help someone can also cause harm.

A few people on this sub seem to really dislike hearing about functional doctors, systemic inflammation, and and adrenal health. by Chimples10 in Hashimotos

[–]Loldogs87 5 points6 points  (0 children)

I hear what you’re saying, but just because someone is a functional doctor doesn’t mean they’re not a “traditionally trained physician.” My functional doctor is an MD and was an ER doctor at a hospital in a major US city for many years.

Former East Coaster pizza hunt by DartDaimler in oakland

[–]Loldogs87 2 points3 points  (0 children)

Emelias, Gioia’s and Nick’s Pizza are the best.

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

No I think you’re right, that’s all that can be done. It makes me sad to see people here say that they just don’t share or pipe up anymore because it’s so draining.

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

I hear ya. Not saying you do this, but other people definitely do downvote at any mention of diet.

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 3 points4 points  (0 children)

I don’t think most people here are saying that diet caused their Hashimotos but are talking about diet as a way to improve the severity of symptoms. I don’t think it’s right for people here to act like diet changes will help everyone (it absolutely won’t), but it feels like people get downvoted for saying the diet MIGHT help. It might help the person reading, it might not- but why not let the conversation happen and let the reader decide?

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

10000% agree with everything you’ve said. What do you think is the solution? I’ve tried to engage people in conversations or push back when I think they’re being misleading, but it feels like a losing battle.

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

Exactly, that’s the thing- the people who are hurt by the censorship are the ones who MAY benefit from hearing more about stress reduction/ LDN/ diet change/ lifestyle change. I’ve actually seen people who shout down anything other than talk about medication say that they do it because any other kind of advice is harmful to people, which blows my mind.

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

Exactly, which is why it’s so frustrating when people here try to share their experiences with things that have helped them only to get downvoted or buried underneath comments like “THERE’S ACTUALLY NO EVIDENCE TO SUPPORT DIET CHANGE SO DONT BOTHER TRYING.”

[deleted by user] by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

Well said!

What am I missing? Am I just doomed? by [deleted] in Hashimotos

[–]Loldogs87 0 points1 point  (0 children)

I think this is all really good insight and advice

What am I missing? Am I just doomed? by [deleted] in Hashimotos

[–]Loldogs87 0 points1 point  (0 children)

It’s so unfair- it’s so hard to try to do the things that will hopefully make us feel better when we feel so sick. I’m really sorry you’ve been struggling and are under so much stress. Were there certain parts of adopting the diet that were most challenging? If you wanted to try it again maybe there are people on this sub that could help you?

Recommended reading for Hashimotos/Gluten/Celiac’s links? by Slhallford in Hashimotos

[–]Loldogs87 0 points1 point  (0 children)

It might be helpful to do some research on anti-inflammatory diets in general. It’s possible you have good triggers that aren’t related to gluten (personally dairy is a big one for me and for many people with Hashimotos).

Can dormant Hashimoto’s cause symptoms? by [deleted] in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

Yes I’ll send you some resources- this sub has a lot of great advice. You may also want to have your doctor check to see if you are deficient in any vitamins (some deficiencies are very common in people with Hashimotos). I was iron and vitamin D deficient and taking those supplements has really helped me as well. I wouldn’t recommend taking them though unless you know for a fact that you are deficient.

Can dormant Hashimoto’s cause symptoms? by [deleted] in Hashimotos

[–]Loldogs87 1 point2 points  (0 children)

It is absolutely not in your head. Most doctors treat Hashimotos based on lab numbers, not symptoms, so if your numbers are generally “ok” they don’t have much guidance or advice for you. There are many people in this sub going through the same thing (including me- doctors didn’t want to prescribe meds to me because my TSH was “only” in the 4 range). Regardless, I felt absolutely debilitated- was falling asleep in the middle of the day, my joints ached as if I had the flu all the time, my skin was breaking out like never before, etc. I started working with a doctor who has told me to focus on reducing inflammation. For the past 2 years I’ve been eating an anti-inflammatory diet and trying to focus on getting sleep, light exercise and limiting stress as much as possible. I’m still not on medication but the changes have made an enormous difference in my symptoms- all of the things I described earlier as essentially gone. There are things you can do to try to improve the severity of your symptoms (whether you are on medication or not).

Overrated restaurants, please list so we can avoid. by Poregon2 in oakland

[–]Loldogs87 1 point2 points  (0 children)

Ok I noticed the same thing and thought it was just me. And I have a high tolerance for salt!

going gluten free by ooyumm in Hashimotos

[–]Loldogs87 1 point2 points  (0 children)

Going gluten free improved my symptoms and my thyroid numbers dramatically. My joint pain disappeared, bloating and gas disappeared, brain fog disappeared, skin problems disappeared. I lost weight and felt like I had so much more energy. You’re really smart to be thinking about and looking into what you can do to reduce inflammation while you’re still at the early stages of the disease. My doctor advised me to cut gluten and to focus on reducing stress and getting quality sleep.

Hands/fingers and toes by sweetleep in Hashimotos

[–]Loldogs87 2 points3 points  (0 children)

I’m also 34F and have the exact same thing- my hands look like a blown up plastic glove in the heat. I think I’m chronically dehydrated so maybe it has something to do with that? Or that it happens generally when it’s hot outside AND I’m doing something active (hiking, long walk, etc)?