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My journey with POTS. | and a side of salt, please.

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My journey with POTS. | and a side of salt, please. | thesyncopejournal.wordpress.com Reviews

https://thesyncopejournal.wordpress.com

and a side of salt, please.

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Dear POTS, dear Big Beast. | My journey with POTS.

https://thesyncopejournal.wordpress.com/2015/03/09/dear-pots-dear-big-beast

My journey with POTS. And a side of salt, please. Dear POTS, dear Big Beast. March 9, 2015. It’s nice to finally see you but I am not your friend. You are a beast and you continue to take but you will not win. You do not get to be the victorious one in this battle, it’s my turn to win. Your not friend,. My story is the story of a carrier. In those 5 minutes, we become one. →. March 9, 2015 at 7:18 pm. I love you,. Leave a Reply Cancel reply. Enter your comment here. Email (Address never made public).

2

I was on the mountain last week, now I’m in the valley.  | My journey with POTS.

https://thesyncopejournal.wordpress.com/2015/05/01/1426

My journey with POTS. And a side of salt, please. I was on the mountain last week, now I’m in the valley. May 1, 2015. It goes like this:. Maybe someone can work on making that happen. If so, I’ll take Maya Angelou on my shoulder. In those 5 minutes, we become one. I built my own Wall of China, you probably have one too. →. May 1, 2015 at 11:27 am. May 1, 2015 at 2:39 pm. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. A Whole Lot of Everything.

3

In those 5 minutes, we become one.  | My journey with POTS.

https://thesyncopejournal.wordpress.com/2015/04/09/in-those-5-minutes-we-became-one

My journey with POTS. And a side of salt, please. In those 5 minutes, we become one. April 9, 2015. Dear POTS, dear Big Beast. I was on the mountain last week, now I’m in the valley. →. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Email (Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. Notify me of new comments via email. I am not a superhero.

4

meridethkathryn | Mentions | My journey with POTS.

https://thesyncopejournal.wordpress.com/mentions/meridethkathryn

My journey with POTS. And a side of salt, please. May 25, 2016. View all 2 comments. I’ve really never had flashbacks of that part of the accident, I assume it’s because I don’t remember most of it. The only really strong memory I have is trying to look around but all I could see was what was up above me because my head was strapped into a collar. I wonder if these next 4 years will be like the last 4, who knows what the earth will throw my way but I’m so ready for it. I want to thank each and everyone o...

5

Resources | My journey with POTS.

https://thesyncopejournal.wordpress.com/resources-2

My journey with POTS. And a side of salt, please. For more information on Dysautonomia these sites may be helpful:. Http:/ www.dynainc.org/living/new-patients. Http:/ www.dinet.org. Http:/ www.ninds.nih.gov/disorders/dysautonomia/dysautonomia.htm. For more information on POTS these sites may be helpful:. Http:/ www.patient.co.uk/health/postural-orthostatic-tachycardia-syndrome. Http:/ www.stars.org.uk/patient-info/conditions/pots. Http:/ pots-disease.webs.com. Leave a Reply Cancel reply. Just Hold. On.

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August 2015 – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/2015/08

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. August 31, 2015. August 27, 2015. In Ehlers Danlos Syndrome. As August draws to a close were you aware it was Gastroparesis awareness month? So with all this in mind what is Gastroparesis? It is a chronic condition in which the stomach cannot empty itself in the normally. It means food passes through the stomach more slowly than usual, leading to symptoms such as:. So what causes Gastroparesis?

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Also Featured On – Living With Ehlers-Danlos Syndrome Type 3

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Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. Guest Post for @mummybarrow :. Http:/ www.mummybarrow.com/gadget-show-live-review/. Review post for @thinkcountry. Http:/ www.thinkcountry.co.uk/? Reviewer and Social Media Queen for W21 Music🙂. Proud to be linking up with Love all Blogs. 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). My Hospital Short Stay.

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Visiting my GP – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/2015/08/17/visiting-my-gp

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. August 17, 2015. August 15, 2015. In Ehlers Danlos Syndrome. Ive said before that I hear people complain all the time about getting on the day appointments at our Drs surgery. Well thanks to Patient Access and their amazing app, I just log on and fingers crossed there are on the day, or urgent appointments available. We asked him briefly about the nomad packs for my monthly medications, with limi...

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Useful Links – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/useful-links

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. These are websites that I have been resourcing since my PoTs diagnosis and now I suspect I have Ehlers-Danlos Syndrome. I hope they help you. Http:/ www.potsuk.org/. Http:/ www.dinet.org/. Http:/ www.stars.org.uk. Http:/ en.wikipedia.org/wiki/Postural orthostatic tachycardia syndrome. Https:/ www.ehlers-danlos.org. Leave a Reply Cancel reply. Enter your comment here. Address never made public).

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March 2015 – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/2015/03

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. The Parapet Breast Clinic. March 31, 2015. March 23, 2015. In Ehlers Danlos Syndrome. Two friends in the last eighteen months have been diagnosed with breast cancer, both have dealt with it in very different ways and I’m not sure now I would feel if it were to happen to me. How often do you check your breasts? Do you know how often you should check them? Now it’s just a waiting game, I know...

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Paul Carella Gig at The Borderline – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/2015/08/15/paul-carella-gig-at-the-borderline

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. Paul Carella Gig at The Borderline. August 15, 2015. August 14, 2015. It’s the home grown talent that needs our support on the UK Country Music scene, they are all amazing, talented and worth traveling to see. Paul is due to be at the Bull’s Head in Barnes, London tonight, tickets are 8 in advance or 10 on the door, do make the effort he’s well worth a look😉. Silent Sunday – 16th August. And eve...

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Hard Decisions – Living With Ehlers-Danlos Syndrome Type 3

https://livingwithedsuk.wordpress.com/2015/08/14/hard-decisions

Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. August 14, 2015. August 14, 2015. In Ehlers Danlos Syndrome. My lunch arrived and it was a case of not wanting to eat in case I jeapordised any procedure they may want to do at any point that day. It had been two hours since the PALS lady had been to see me, midday was my cutoff so I gave her a call and asked what should I do? She asked had Zoe been to see me, no! I didn’t know! They felt there w...

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Disclosure Policy – Living With Ehlers-Danlos Syndrome Type 3

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Living With Ehlers-Danlos Syndrome Type 3. And everything that goes with it – Raising Awareness #zebrastrong. These are written by friends, often on a topic important to them, and have either been written because I asked them to guest post on my blog, or because they asked me if they could. Done because I love and support the blogger and am happy to promote whatever it is they are talking about. No money has changed hands, just love. Thanks to @mummybarrow for allowing me to borrow her disclosure policy.

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My journey with POTS. | and a side of salt, please.

My journey with POTS. And a side of salt, please. My Soul Is Healing. August 17, 2015. View all 2 comments. It has to be a good thing that I didn’t make the connection right? I mean it’s not like it’s a date you mark on your calendar and celebrate every year like a birthday, HOORAH you get a debilitating chronic illness congratulations! August 1, 2015. I have teamed up with Elizabeth Powe who runs a shop called PearlsByPowe and together we have come up with a beautiful freshwater pearl necklace, but here...

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