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The medicine I'm taking.

I was hospitalized for testing in August 2023

Hypopituitary dysfunction (designated intractable disease 78)

Since becoming

I take this medicine every day.

Cortril (a corticosteroid agent) is not right

predonine, the corticosteroid hormone

decadrone, a corticosteroid.

I always drink it every day

As a side effect, I have a fever every day

To lower the heat.

Are you drinking Loxonin 💊

i can't regulate my temperature.

I have a fever every day and it s really hot 😣

Because it's a disease that can't be cured

i have to drink for the rest of my life.

I can't help it, but...

Pituitary hypofunction

# adrenocortical _ hormone

21 hours agoEdited to

... Read more私も下垂体機能低下症の診断を受けてから、毎日副腎皮質ホルモン剤を服用しています。記事の中で紹介されているデカドロンも私の処方薬の一つです。私の場合、最初はコートリルやプレドニンを試しましたが、副作用や効果の薄れを感じて医師と相談しながらデカドロンに変更しました。 副腎皮質ホルモン剤は体内のホルモンバランスを調整し、下垂体機能低下症の症状を抑えるために不可欠な薬ですが、その副作用として体温調節が難しくなり、発熱が続くことがあります。私も熱が頻繁に出る経験があり、そのたびにロキソニンを使用して熱を下げていますが、それでも完全に熱が収まらず辛い時もあります。 体温調節の問題は本人の努力だけで完全にコントロールするのは難しく、生活の中で体温変化に注意を払いながら無理をしないことが重要です。例えば、適度な室温管理や水分補給、規則正しい生活リズムを保つことが役立ちました。 また、体調が悪くなる時があるため、家族や友人に自分の症状と対処法を理解してもらうことも心強い支えになります。そして、定期的な検診で医師とコミュニケーションを取り、副作用や効果の変化に応じて薬の調整を忘れずに行うことが大切です。 この病気は完治が難しいですが、適切な薬の服用と生活管理で症状を軽減し、できるだけ快適な生活を目指しています。同じ病気で悩んでいる方には、薬の副作用に対する正しい知識と、自身の体調変化に敏感になることをおすすめしたいです。皆さんと情報交換しながら前向きに過ごしていきましょう。

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