• Home
  • About Us
  • Blog

Pulmonary Hypertension RN

  • What is Pulmonary Hypertension?
    • What is Pulmonary Hypertension?
    • Pulmonary Hypertension Symptoms
    • Types of Pulmonary Hypertension
    • Causes of Pulmonary Hypertension
    • PH vs. PAH
    • Diastolic Heart Failure vs. PAH
    • WHO Group 3 Pulmonary Hypertension, IPF & COPD
    • Pulmonary Veno-Occlusive Disease
    • Hereditary Hemorrhagic Telangiectasia (HHT)
      • Hereditary Hemorrhagic Telangiectasia (HHT) Treatment
    • Functional Classification of Pulmonary Hypertension
    • Congenital Heart Disease
      • Eisenmenger’s Syndrome
      • Update on Management of PAH-CHD
      • Congenital Heart Disease & Sleep Apnea
      • Complex Congenital Heart Disease
      • Atrial Septal Defect and Pulmonary Arterial Hypertension
    • Pediatric Pulmonary Arterial Hypertension
    • Sickle Cell and Pulmonary Hypertension
    • Stimulant Associated Pulmonary Arterial Hypertension
    • Porto-Pulmonary Syndrome
    • Research, Life Expectancy & Prognosis for PH
  • Diagnosing & Monitoring PAH
    • Pulmonary Arterial Hypertension Diagnosis
    • How Am I Doing? Assessing Your PAH.
    • Blood Tests
    • Cardiopulmonary Exercise Test (CPET)
    • CT (Computed Tomography) Scan
    • Echocardiogram: An Overview
    • Echocardiogram: A Detailed Look
    • Pulmonary Function Tests (PFTs)
    • Right Heart Catheterization
    • Six Minute Walk
    • Ventilation Perfusion Scan (VQ Scan)
    • CTEPH
      • CTEPH: WHO Group 4 Pulmonary Hypertension
      • PTE (Pulmonary Thromboendarterectomy) Surgery
      • Adempas used to Treat PAH and CTEPH
  • PAH Treatment
    • Pulmonary Hypertension Centers
    • Pulmonary Hypertension Treatments
    • Continuously Infused Therapies Used to Treat PH
    • Prostanoids for Treatment of PH
    • Adcirca and Revatio Used to Treat Pulmonary Arterial Hypertension (PAH)
    • Adempas used to Treat PAH and CTEPH
    • Tracleer, Letairis, and Opsumit Treatments
    • Oxygen Therapy for Pulmonary Hypertension
    • Salt and Water Restrictions
    • Exercise & PAH
    • Diuretics
    • Blood Thinners
    • Getting the Most Out of PAH Therapy
      • Letairis
      • Opsumit
      • Sildenafil (Revatio)
  • Research
  • FAQ’s
    • Implanted Remodulin Pump, Right Heart Catheterization, PAH & Pregnancy
    • Oral Treatments, Care Centers & Hole in Heart
    • FAQ’s: Altitude, Cold & Allergy Medications
    • FAQ’s: Psoriasis, Idiopathic PAH, Contraceptives & PAH
    • FAQ’s: Causes of Pulmonary Hypertension, Symptom Frequency & Care Centers
    • FAQ: PAH Experts, Pregnancy, Mild PAH & Vacationing
    • FAQ’s: CTEPH, Blood Clots, Corrective Surgery & PAH Care Centers
    • FAQ’s: VQ Scans & PAH Curable?
    • FAQ’s: Mild Pulmonary Hypertension?
    • FAQ’s: Boating, Swimming & Eating with PAH
    • FAQ’s: Borderline Pulmonary Hypertension, Hand Swelling, Children with PAH, Costs

5 Steps For Making Moving with PAH Less Stressful

September 5, 2014 By Dr. Jeremy Feldman

Moving can be both exciting and stressful for everyone. Finding a new place to live, learning a new neighborhood, meeting new friends all takes time and energy. For PAH patients there is an added stress of finding a PAH expert to transfer medical care to.

Here are 5 easy steps for making moving with PAH less stressful.

1.  Plan ahead: speak with your PH Care Center as soon as you know a move may be happening.

  • You may want to coordinate planned tests or procedures such as echocardiograms or right heart catheterizations to be done with your current physician in a familiar environment prior to your move.
  • Your physician may know of PH experts in your new area but if not this will allow for you and your physician to look into what centers and resources may be available in your area.   It may be helpful to do some research online to find out which physicians will be closest to your new home and then discuss those options with your current physician. The PHA’s (Pulmonary Hypertension Association’s) website at www.phassociation.org is a great place to start. They list physicians by state and are currently in the process of certifying Centers of Excellence.
  • It is helpful for your physician’s office to have a heads up that you will need a copy of your chart and one sent to a new provider. Electronic medical records can be difficult to sift through and don’t always paint a complete picture. Ask your physician to write a summary or speak to your knew provider personally before your first appointment.
  • New prescriptions may have to be written or transferred to new pharmacy locations which will require signatures from your physician. Speak to your current pharmacy providers, both retail and specialty, and let them know about the move.

2.  Find a physician and a back-up physician:PAH Expert talking with PH patient

  • Work with your current provider to find a PH Center in your new area. Research them and speak with their office to make sure you feel confident in the care they can provide for you. Have a back-up plan of which center you might choose next should the need arise.
  • If you’re moving within your region your current physician may be able to continue to provide care for you. You would need a local pulmonologist or cardiologist that you could see regularly that would be willing to work closely with your current provider and you would need to have the ability to see your PH Expert at preset intervals.

3.  Make an appointment:

  • Make an Appointment as soon as you know your move date.  Keep this Appointment.  It is important for the new physician to meet you and review your records before you have a PAH emergency.  This is a great opportunity for you to learn about the center, what number to call or which facility to go to in case of an emergency, and learn about local resources such as PAH support groups to get connected to.
  • Although medical records were probably sent to the new physician it is a good idea to come to your first appointment with a copy of your chart.

4.  Pace yourself and ask for help: Help with boxes

  • Remember that PAH patients have good days and bad days. Listen to your body and don’t’ push too hard to pack or unpack those moving boxes. Rest when you need to rest and ask for help from friends and family to make the job easier.
  • Avoid lifting heavy objects and place boxes on a table or counter rather than the floor when unpacking. This will help to avoid bending head down at the waist.

 5.  Stay connected to your support system while working on building a new support system:Connecting to support system

  • Moving doesn’t have to signal the end of interacting with your current support system. If you have friends or support group members that have helped you cope with your disease stay in contact with them. Facebook, skype, and facetime make it easier than ever to stay connected. Don’t avoid meeting new people but don’t forget about the valuable relationships you have already developed.

Filed Under: Blog, Home Page, Living with PAH

PAH Life Expectancy

PAH Research

Research, Life Expectancy & Prognosis for PH

Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

Where to Get Treatment?

CCCs for PAH

Pulmonary Hypertension Centers

Where to get treatment for pulmonary hypertension? Pulmonary arterial hypertension is a

Popular Posts

PAH Research

The Pulmonary Hypertension Team

By Dr. Jeremy Feldman

I would like to acknowledge the role of our PH nurse coordinators and support staff.  The care of pulmonary hypertension

good news re PAH

Entire Implantable System for Remodulin Approved by the FDA

By Dr. Jeremy Feldman

It is finally here! The Food and Drug Administration approved Remodulin in its implantable delivery system for treatment

good news in pah

 

Disclaimer

Recent Blog Posts

  • In Memoriam:  Greg Ahearn, MD June 16, 2024
  • Sotatercept (Winrevair) Approved! June 1, 2024
  • Disappointing News for Rodatristat Ethyl October 11, 2023

Categories

Archives