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Potsitivity | A blog about Pots, my personal experience and reassurance for you

A blog about Pots, my personal experience and reassurance for you (by Potsitivityy)

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Potsitivity | A blog about Pots, my personal experience and reassurance for you | potsitivityy.wordpress.com Reviews

https://potsitivityy.wordpress.com

A blog about Pots, my personal experience and reassurance for you (by Potsitivityy)

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1

Heat and Hot Weather – Potsitivity

https://potsitivityy.wordpress.com/2015/07/01/heat-and-hot-weather

A blog about Pots, my personal experience and reassurance for you. Heat and Hot Weather. July 1, 2015. July 2, 2015. Summer is what I spend the year working towards : No School, Sleeping, Sun, Sea and Sand. Recently with PoTs I’ve gotten quite sensitive to the heat . Lots of pots patients do, so I thought I’d provide a quick guide to surviving the sun so that it doesn’t effect your enjoyment . Sometimes the hot air can make it hard for me to breathe, and at other times I just get very easily over heated.

2

You can do this – Potsitivity

https://potsitivityy.wordpress.com/2015/07/17/you-can-do-this

A blog about Pots, my personal experience and reassurance for you. You can do this. July 17, 2015. July 17, 2015. The ultimate positive post. I suggest you read this, re-read it, read it again and read it whenever you doubt yourself, lose confidence or need a pick me up. Read this to yourself and believe every word of it –. I can do this . View all posts by Potsitivityy. 8216;What If.’. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:.

3

‘Get well soon’ – Potsitivity

https://potsitivityy.wordpress.com/2015/06/26/get-well-soon

A blog about Pots, my personal experience and reassurance for you. 8216;Get well soon’. June 26, 2015. June 26, 2015. No matter how many times you explain to people about your illness, they often respond with ‘oh I hope you feel better soon’, or ‘ but you’re looking well! View all posts by Potsitivityy. Heat and Hot Weather. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). Notify me of new comments via email. Create a...

4

Potsitivityy – Potsitivity

https://potsitivityy.wordpress.com/author/potsitivityy

A blog about Pots, my personal experience and reassurance for you. The Past Few Years. For me, this last year has been the busiest. I knew this time last year what I had ahead of me and got nervous every time I thought of it. But now I look back at everything I’ve done and it shows me how far I’ve come with my health. And I’ve come a long way. Here’s to the next year of new starts, holidays, memories and milestones. August 16, 2016. 1) Making comparisons can spoil your happiness. Striving for happiness w...

5

‘What If..’ – Potsitivity

https://potsitivityy.wordpress.com/2015/07/04/what-if

A blog about Pots, my personal experience and reassurance for you. 8216;What If.’. July 4, 2015. When you realise you’ve got 99 problems but you don’t need to worry about 1. I say ‘What If-‘ at least 5 times a day . Since I was diagnosed I’ve been very cautious about what could happen to me when I’m out and about. My most popular phrases being ‘What if I don’t feel well? 8217; and ‘What if I need to sit down and there’s no where to sit? View all posts by Potsitivityy. Heat and Hot Weather. You can do this.

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findinglifessilversun.wordpress.com findinglifessilversun.wordpress.com

The Sunshine Blogger Award | Finding Life's Silver Sun

https://findinglifessilversun.wordpress.com/2015/08/12/the-sunshine-blogger-award

Finding Life's Silver Sun. Making the Most of Life with Chronic Illnesses. The Life of the Lizz. Zazzle Shop – Link. The Crazy People I Call Family. Things That Make Me Smile. The Story of the Silver Sun. What’s in a Name? The Great Ear Saga of 2015. Send Cow Mail to the Silver Sun. I AM NOT A DOCTOR! Help Support The Silver Sun. Medical bills can get a little insane, so I've started designing products on Zazzle. Check out my store using this link: Finding the Silver Sun. Follow Blog via Email. My husban...

tissuetales.com tissuetales.com

Marfan Syndrome – Tissue Tales

https://tissuetales.com/category/health-issues/marfan-syndrome-health-issues

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. July 20, 2016. The hospital stay: part 2. The spinal fluid leak and post-dural puncture headache. In the way that they handle my case. This can be both frustrating and scary because your connective tissue is. And when it’s weak it has the potential to change nearly. Pain, vomiting and frustration. Think that it was a good time or decision to start me on a diuretic in order to. Lower my ICP (which can be dangerous!

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Connective Tissue Disorder – Tissue Tales

https://tissuetales.com/tag/connective-tissue-disorder

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. August 29, 2016. As an example, here is an incomplete overview from Wikipedia. Of the most common symptoms:. Weakness or “heaviness” in the lower legs. Fluctuations in weight, memory. Pallor, or sweating. High as it often did without and prolonged tachycardia (of any kind) can be hard on the heart, particularly with my disorder. This was my pulse and blood pressure while sitting down. Posted in Ehlers-Danlos Syndrome.

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Katie Michele – Tissue Tales

https://tissuetales.com/author/katiemichele

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. August 29, 2016. As an example, here is an incomplete overview from Wikipedia. Of the most common symptoms:. Weakness or “heaviness” in the lower legs. Fluctuations in weight, memory. Pallor, or sweating. High as it often did without and prolonged tachycardia (of any kind) can be hard on the heart, particularly with my disorder. This was my pulse and blood pressure while sitting down. Posted in Ehlers-Danlos Syndrome.

tissuetales.com tissuetales.com

Resources – Tissue Tales

https://tissuetales.com/helpful-links

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. For blogs related to the topics below be sure to check out the beneficial blogs. To register and become a part of the Marfan Net community. Provides information on the different types of lens implants that may be used by those with lens subluxation (ectopia lentis). Chronic Pain Association of Canada. Teaches “effective chronic pain self management” through various means such as retreats, education, pain...Their mis...

tissuetales.com tissuetales.com

Health – Tissue Tales

https://tissuetales.com/tag/health

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. August 29, 2016. As an example, here is an incomplete overview from Wikipedia. Of the most common symptoms:. Weakness or “heaviness” in the lower legs. Fluctuations in weight, memory. Pallor, or sweating. High as it often did without and prolonged tachycardia (of any kind) can be hard on the heart, particularly with my disorder. This was my pulse and blood pressure while sitting down. Posted in Ehlers-Danlos Syndrome.

tissuetales.com tissuetales.com

Eye Problems – Tissue Tales

https://tissuetales.com/category/health-issues/eye-problems

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. Posts and information regarding my eye problems and surgeries. July 20, 2016. The hospital stay: part 2. The spinal fluid leak and post-dural puncture headache. In the way that they handle my case. This can be both frustrating and scary because your connective tissue is. And when it’s weak it has the potential to change nearly. Pain, vomiting and frustration. Lower my ICP (which can be dangerous! The importance of t...

tissuetales.com tissuetales.com

We always carry on, and sometimes it gets easier. – Tissue Tales

https://tissuetales.com/2014/12/11/we-always-carry-on-and-sometimes-it-gets-easier

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. December 11, 2014. We always carry on, and sometimes it gets easier. First of all, I want to thank each and every one of you for all of your support. It seems so strange to think about how many people took the time to read it or share it on Facebook – I’ve never had that happen with such a personal post before and I really appreciate the response. Photograph by Jeremy Taylor. Big hugs to you all. xx. And thank you f...

tissuetales.com tissuetales.com

Disclaimer – Tissue Tales

https://tissuetales.com/disclaimer

My journey, navigating through life with a Connective Tissue Disorder. Me, Myself, and I. Any medical terms and/or definitions featured on this blog have been thoroughly researched by me in order to prevent any false or unsubstantiated information from being presented to the followers of Tissue Tales. Though, that aside;. I am not a doctor. I will happily comply with any regulations or wishes you have about the presentation of your photos and will remove them immediately if you wish. Click to share on Tu...

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Potsitivity | A blog about Pots, my personal experience and reassurance for you

A blog about Pots, my personal experience and reassurance for you. I was invited to the cinema by friends on a Saturday evening to go the following day. My initial response was ‘No, I can’t do that’ : But I can and I did. Why should my excuse automatically be ‘ I can’t as I’m not feeling great’ even if it’s just because I’m worried about how I’ll feel when I’m there? My Company and Support. Tell yourself that you can do this, you’ll be surprised at what you can do, and if it doesn’t go to pla...I suggest...

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