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	Comments on: ADD or Hashimoto&#8217;s Brain Fog?	</title>
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	<description>Feel better with hypothyroidism, finally</description>
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		<title>
		By: Laura		</title>
		<link>https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-34950</link>

		<dc:creator><![CDATA[Laura]]></dc:creator>
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					<description><![CDATA[In reply to &lt;a href=&quot;https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-31753&quot;&gt;Victoria McLachlan&lt;/a&gt;.

Victoria, very interesting.  I, too, had been prescribed Ritalin.  I am 60 yrs old and have had Hashi&#039;s/hypothyroidism since 1996. Was poorly managed by an endocrinologist for most of those yrs.  Changed doctors 10 yrs ago, and they tried me on antidepressants. Paxil and Wellbutrin is what I settled on.  Ritalin added on top of that. Was always tired on that mixture. Thyroid labs looked good too.  Finally after a couple years and a 20 lb. weight gain (137 lbs - 157 lbs.), my tsh elevated to 4.  
My primary doctor said my labs look great!  And I thought, &quot;walks like a duck, talks like a duck, it is a duck&quot;.  So I decided to increase my Synthroid to see what would happen.  Joint pains are going away, I&#039;m not sleeping 9 hours a night with a 3 hour nap in afternoon.  I can take my dog for walks and not be exhausted for two days after. sleep is returning to normal. Went from Synthroid 100 mcg to 106 to 112 to 118 to 125mcg. over the course of 3 months. Will get labs in a couple weeks on the 125 dose.   I did stop the Ritalin and Wellbutrin, as I felt it was masking symptoms, but may add Wellbutrin back in at some point, as I&#039;m still experiencing brain fog.  One change at a time.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-31753">Victoria McLachlan</a>.</p>
<p>Victoria, very interesting.  I, too, had been prescribed Ritalin.  I am 60 yrs old and have had Hashi&#8217;s/hypothyroidism since 1996. Was poorly managed by an endocrinologist for most of those yrs.  Changed doctors 10 yrs ago, and they tried me on antidepressants. Paxil and Wellbutrin is what I settled on.  Ritalin added on top of that. Was always tired on that mixture. Thyroid labs looked good too.  Finally after a couple years and a 20 lb. weight gain (137 lbs &#8211; 157 lbs.), my tsh elevated to 4.<br />
My primary doctor said my labs look great!  And I thought, &#8220;walks like a duck, talks like a duck, it is a duck&#8221;.  So I decided to increase my Synthroid to see what would happen.  Joint pains are going away, I&#8217;m not sleeping 9 hours a night with a 3 hour nap in afternoon.  I can take my dog for walks and not be exhausted for two days after. sleep is returning to normal. Went from Synthroid 100 mcg to 106 to 112 to 118 to 125mcg. over the course of 3 months. Will get labs in a couple weeks on the 125 dose.   I did stop the Ritalin and Wellbutrin, as I felt it was masking symptoms, but may add Wellbutrin back in at some point, as I&#8217;m still experiencing brain fog.  One change at a time.</p>
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		<title>
		By: Erika Miller		</title>
		<link>https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-34493</link>

		<dc:creator><![CDATA[Erika Miller]]></dc:creator>
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					<description><![CDATA[In reply to &lt;a href=&quot;https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-31858&quot;&gt;KerryAnn Millin&lt;/a&gt;.

I am 27 and was diagnosed at 13 with Hashis. I know exactly how you feel. It’s hard enough as is, but being young with Hashimotos adds an additional layer of difficultly. I would like to say it gets easier, but yikes. Lol. The struggles are real on the daily. I hope you’re doing better over the years. Here if you ever need someone to relate to! It definitely makes me feel good to know someone understands me. ❤️]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-31858">KerryAnn Millin</a>.</p>
<p>I am 27 and was diagnosed at 13 with Hashis. I know exactly how you feel. It’s hard enough as is, but being young with Hashimotos adds an additional layer of difficultly. I would like to say it gets easier, but yikes. Lol. The struggles are real on the daily. I hope you’re doing better over the years. Here if you ever need someone to relate to! It definitely makes me feel good to know someone understands me. ❤️</p>
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		<title>
		By: Hannah Mulligan		</title>
		<link>https://hypothyroidmom.com/add-or-hashimotos-brain-fog/#comment-33955</link>

		<dc:creator><![CDATA[Hannah Mulligan]]></dc:creator>
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					<description><![CDATA[These are the exact issues I have on that medication. I am currently in the midst of struggling to get a diagnosis because my TSH was slightly elevated. Doctors will not consider a diagnosis unless your TSH is 9-10+ and you basically cannot walk or talk anymore. Nvm that I&#039;m having troubling putting together coherent sentences, my thyroid gland is swollen, I can&#039;t stay awake, my WBC is bordering the flagged range. I cannot stand the healthcare system we have, I&#039;m at the end of my rope. The doctors, all they can do is tell you, you are sensitive to the medication and or maybe you are abusing the medication. There must be no other reason for why you can&#039;t sleep till 4-6 in the morning, have constant aches and pains, energy fluctuations, feel like fainting, are losing your hair and through all of that still choose to take the medication. I can&#039;t stay awake if I don&#039;t take it, I wouldn&#039;t be in university if it weren&#039;t for Adderall. The only thing that can keep me going is amphetamines, coffee is not strong enough to keep me awake. I&#039;m tempted to go after every doctor who decided to put me on ADHD medication rather than test my blood for common deficiencies or a thyroid issue.]]></description>
			<content:encoded><![CDATA[<p>These are the exact issues I have on that medication. I am currently in the midst of struggling to get a diagnosis because my TSH was slightly elevated. Doctors will not consider a diagnosis unless your TSH is 9-10+ and you basically cannot walk or talk anymore. Nvm that I&#8217;m having troubling putting together coherent sentences, my thyroid gland is swollen, I can&#8217;t stay awake, my WBC is bordering the flagged range. I cannot stand the healthcare system we have, I&#8217;m at the end of my rope. The doctors, all they can do is tell you, you are sensitive to the medication and or maybe you are abusing the medication. There must be no other reason for why you can&#8217;t sleep till 4-6 in the morning, have constant aches and pains, energy fluctuations, feel like fainting, are losing your hair and through all of that still choose to take the medication. I can&#8217;t stay awake if I don&#8217;t take it, I wouldn&#8217;t be in university if it weren&#8217;t for Adderall. The only thing that can keep me going is amphetamines, coffee is not strong enough to keep me awake. I&#8217;m tempted to go after every doctor who decided to put me on ADHD medication rather than test my blood for common deficiencies or a thyroid issue.</p>
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