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Friday, December 27, 2013

Response to Ms. Cahan Director of Communications NIA/NIH

We continue to fight for our rare disease research! How can you help?

1. Sign the petition:

2. Write to your senator:
Ask your senator to write a letter to NIH asking why this study was halted and to request to have study reinstated.

Dear Ms. Cahan,

I appreciate you contacting me regarding the request for reinstatement NIA Protocol 2003-086. Unfortunately your response does not address the many concerns that I have. This study was closed prematurely, without a reasonable explanation.  You stated, "The goal from analyzing these data was to identify biological pathways that might serve as targets for new treatments Unfortunately you did not meet this goal as you would have the public believe. 

You have stated,  "We want to make it clear to participants and to the community interested in this research, however, that the data and samples are being archived and will be maintained. When the NIA has completed organizing and processing data and samples, they will be made available to qualified researchers for analyses. 
How is this being done specifically? Will you allow the lead investigator Dr. McDonnell access to this data so she can continue this imperative research? 

I will continue on this plight for reinstatement until this study is reinstated fully and the investigators, who have expertise  of these diseases have access to the data. The 10 years worth of data is best used by the investigators who are most knowledgable about my disease.  I will not stop the petition or contacting my congress until these issues are addressed to my satisfaction.

I hope we can continue the dialogue to get this very important research reinstated immediately. Many lives depend on this research. It is very disheartening to say the least that NIA states the major goals of this study have been met, when in fact we have no biomarkers or responsible gene for this disease, not even a treatment protocol. How can it be possible for major goals to be made when NIH/NIA never brought back the participants of the longitudinal study? You had over 500 people waiting to go to the study. NIA has a responsibility to me and other patients to finish what you have started. Do not waste any more tax money or time, this work is important on so many levels.

Warmest Regards,

Kari Ulrich
Rare Disease Patient

On Dec 27, 2013, at 10:45 AM, Cahan, Vicky (NIH/NIA) [E] <> wrote:

Dear Ms. Ulrich,
Thank you for contacting leadership at the National Institutes of Health (NIH) and the National Institute on Aging (NIA) about the NIA’s natural history study on inherited connective tissue disorders.  I am the Director of Communications at the NIA, and your note was forwarded to me for response.
We thank you for your interest and participation in the study. I am writing to help clarify some of the points about the study that you have raised in your note and petition, and the attached document should provide reassurance on issues of concern. While data collection has stopped, we want to assure you that the data collected over the course of the study are being organized and archived so that they can be made available as soon as possible to qualified researchers. No samples are being destroyed, unless a participant has formally asked that we do so.
Further, the attachment offers telephone numbers at NIA for patients who feel that their condition is not presently being addressed. Your communications with us suggest, however, that you are working with knowledgeable medical team.
Again, thank you and your family for your valuable time and effort participating in this study. We very much appreciate your interest in NIH-supported research.
Best regards,
Vicky Cahan
Director of Communications
National Institute on Aging
National Institutes of Health
From: Kari Ulrich []
Sent: Saturday, November 30, 2013 4:01 PM
To: Collins, Francis (NIH/OD) [E]; Hodes, Richard (NIH/NIA) [E]; Gottesman, Michael (NIH/OD) [E]
Subject: NIA Protocol 2003-086 “Clinical and Molecular Manifestations of Heritable Disorders of Connective Tissue"
Dear Drs.
It is with great respect that I contact you all today regarding my petition to reinstate NIA Protocol 2003-086. I am hoping you can offer me some insight as to why this study was closed abruptly without a reasonable explaination. More importantly we have received over 5,000 signatures asking for this study to be reinstated. 
I would like to start a conversation with you about making this happen. I value your time, and look forward to hearing your response.
I remain confident that a positive resolution can be made. 
Warmest Regards,
Kari Ulrich
Albert Lea, Minnesota

Wednesday, December 11, 2013

Vascular Ehlers-Danlos Lessons in Life

David's Lessons in Life
Today I want to share with you an experience that will hopefully touch your soul as it has mine. 
Why should we care about rare disease research? Hopefully you will find the answer in the words below.

Cathy and her son David
Not too many people know this but David left us with a profound message after his death. I share this to bring/give you HOPE. There are so many things that happened over the last 17 years, that I could never begin to fully explain them all.  There are just too many to include in this post. I learned that there are no coincidences. Some of these events would be called a"mystery"....the "unexplainable."

After the initial perforation and his recovery, Dave was afraid that something would happen to him, that he might die. So, I would sit with him at bedtime every night until he fell asleep for the first couple of weeks after he got home from the hospital.  He eventually gained all his strength back and was doing great. He wasn’t afraid anymore. Then it was time to go back in the hospital to have the colostomy reversed.     

The weeks before his death David was fully aware of everything, he never hallucinated or talked crazy. The day before his death he started talking in his sleep. I thought he was asking me something so I went over to him and woke him to ask him if he was talking to me. He opened his eyes and looked right at me and said, “No mom, when I close my eyes I see a whole other scene and I’m talking to “THEM””. This took me aback and I regretted that I never asked him who “they” were.    

My sister-in-law and I both worked for our local school system. The next day after David’s died a teacher at his school went into the computer room to work on something, when he started the computer this poem popped up. He must of read it and then closed it out. When he was finished he went into the office that’s when he found out that Dave had passed away. He told them about what just happened and he went back into the computer and printed the poem out. A friend of my sister-in-law called her to tell her what just happened and then she went to get the poem. She called me to tell me and I told her that I couldn’t hear it right now. My brother told me it was very profound (it seemed to mean different things to different family members and it affected my brother as well) I asked him to read it at his funeral if he would.

Now understand that Dave wasn't a reader or a writer the only thing he ever read on his own was the stats on his favorite hockey team,the Philadelphia Flyers. So, I was really reluctant to believe that he had written this poem when he went back to school in May (it was dated June 7th, 1996 for a class project). He didn't tell me about it, he usually always told me everything...this is what was really strange.


At the end of Dave’s funeral at the cemetery my brother started to read his poem. As he read his voice started shaking and cracking from the emotion he felt. My brother was always tough as nails and never showed his feelings. I was so moved that he was so deeply touched by these words. What I heard the most was the last few lines that touched my core and it was as if I heard Dave's voice whispered in my head...saying, "See Mom, now I can do ANYTHING"

I immediately knew it was in response to when I was in that conference room (3 days before his death) with the doctor and the Geneticist.They told me that they thought Dave had vascular EDS and that at any time something could happen to him. That if he survived he would be very limited and would never be able to obtain his dream of playing ice hockey one day.  After that blow, I had to suck up all these emotions so that Dave wouldn't see the anguish on my face, because he knew me so well. He never knew what was said in that room that day. He never knew about vascular EDS.

I knew that's what he was telling me in that poem where the answers to all the questions that had been going around in my head. That he saw God's face and He's the blinding light that he speaks of. And that he reached the goal...HEAVEN, and that it was meant to be and sadly nothing could of changed this, and that he NOW can do everything that they told me he would NEVER be able to do.

Two years after his death, I was asked to call this mother who had just lost her daughter because of EDS. Within the first five minutes of our conversation she said to me, “Then she started talking to “THEM”. I almost feel off my chair as my breath was sucked right out of my body. I asked her, “WHAT”, who were they?” She said her daughter told her, “They were her three friends and they were angels.” She then preceded to tell me everything her daughter told her about “THEM.”  That they took her up to see God, it was a long staircase that she walked and when she got to the top…God was as bright as the sun. No one in her family had believed in God prior to this. She told her mother and sister that God was real. She said that there is an angel for every problem and they are sent to help. The only one she mentioned to her mother was the angel for a broken heart. She began to sit in the sun or in front of bright lights…she at peace there and would sit for hours. It reminded her of her visit with God. She kept asking her if she would be alright if something ever happened to her, she was worried about her mother. She was preparing and helping her mother for what was about to happen. She died on Christmas night…her name is Mehsonia and she was 16 years old. Dave and her were born the same year.

When Dave died, I died and so did my faith. It took me many, many years to absorb the full impact and meaning of his poem. I analyzed it till I was insane and finally I came to believe that he did in fact write it, but I believe the meaning was meant for after his death. It is just too profound, so very spiritual and for him not to tell me that he wrote something so AMAZING...he wouldn't have been able to wait to share that with all of us. This is why it was so very hard for me to believe. He just wouldn't do that, so the only explanation was that it had to be inspired…this was the gift that God allowed David to leave for his father, his sister, me…and now all of you!!!


His name tells how it is for him
He wonders, whether he should go on
But he feels so strong on reaching his goal
There are many things that happen to him
but he just pushes on
The goal is like a shining light,
that is blinding him
The only way of stopping the light
is to reach the goal
Something happens and he thinks about stopping,
but the way is now drawn for him
and he knows after getting through this
has helped him see the light
even brighter now
The way he feels now he can do


Thursday, December 5, 2013

NIH: Keep Hope Alive and Restore Lifesaving Study

Alone we can do so little; together we can do so much. —Helen Keller
The words of Helen Keller spoke greatly to me as I have reflected on accomplishments of the past few weeks. 
The National Institute of Health (NIH) has halted the only national study on rare genetic connective tissue disease. These diseases result in severe disability and even death for those afflicted. It represented the only hope thousands of families had in finding the cause and cure for these rare disease. We are asking the NIH to restore the 10 year study.
We have over 5,000 signatures supporting our petition. It is my goal to get 10,000 signatures to present to NIH/NIA. With this it is my expectation that the study will be reinstated and we will be assured that our data and specimens will not be lost. I remain confident that with each signature we are spreading awareness.
After a full nights sleep my body woke in pain, reminding me of a chronic illness that I have finally given into. It was that morning reminder that inspired me to work past the pain and start doing what so many of us with invisible illness have been speaking about. I wrote my first petition asking the NIH/NIA to reinstate research that is has been going on for over a decade. Although I  have not yet reached my goal of 10,000 signatures something has incredible has been happening. 
This is no longer my goal, but our goal. The patient organizations have come together united in our voice. We are empowering each other to do more. By collaborating we have shown the medical community that we will remain steadfast in our words. 
So today I would like to thank each organization for collaborating with each other for the betterment of the patient. I also would like to thank all the patient communities that have come together from EDS and Sticklers, to FMD and Brain Aneurysms, Marfans there are too many to list. Although we are far from done with our mission we will continue to support and care for each other in years to come. 
Croatian Alliance for Rare Diseases

Orphan Druganaut Blog

I encourage other organizations to get involved and help make a difference for the good of the patient. Today I am reaching out to all rare and genetic disease patient organizations and I am asking you for your support. 
Restoring the study will return hope, continuing the extensive work done over the last 10 years. It will ensure all the progress we have made will not have been in vain and keep us on a path to a cure. 
If the NIH continues with their current plan to end the study it will leave victims and their families without a place to turn for answers and send a message our lives are not worth the investment of finding a cure. Even worse, the samples and results already gathered could be lost, leaving scientists to start over.
Warm Regards,
Kari Ulrich

Monday, November 4, 2013

Fibromuscular Dysplasia (FMD) - Common Symptoms for an Uncommon Disease

Sunday, November 3, 2013

Tuesday, October 29, 2013

Stroke Awareness - Mayo Clinic

Saturday, September 14, 2013

Friday, September 13, 2013

FMD Chat Together 2013 — Sharing is Caring

Posted: 12 Sep 2013 11:21 PM PDT
In an effort to reach out to the fibromuscular dysplasia community, FMD Chat will be making much of its annual retreat available via the web.

While no livestream can replace the experience of meeting other FMD patients and caregivers face-to-face, FMD Chat realizes that many patients are unable to travel due to physical or financial constraints. Patients and others are encouraged to tune in to FMD Chat's YouTube channel from 9:30 a.m. to 3:30 p.m. ET on Saturday, Sept. 14 as presentations are streamed live. On Twitter, follow @FMDChat or the #FMDaware hashtag. Updates also will be posted to FMD Chat's Facebook page.

Need some help getting connected? Check out the following resources!

What is YouTube?

Twitter Tutorials
How To Sign Up
How To Tweet, Reply, Follow, Etc
How to Engage

What is Facebook?

When is it Where I am? 
Time Zone Converter 

Monday, August 5, 2013

Social SecurityDisability Benefits for Fibromuscular Dysplasia

Guest Blogger: Ram Meyyappan
 Senior Editor and writer for Social Security Disability Help

Social Security Disability Benefits for Fibromuscular Dysplasia
If you are suffering from fibromuscular dysplasia, the condition may have left you unable to work. Without the ability to work, you are left without an income and insurance. The lack of income and mounting medical bills can quickly spiral out of control. Fortunately, in many cases, Social Security Disability benefits can help. 
Qualifying for Social Security Disability Benefits with Fibromuscular Dysplasia
When you apply for Social Security Disability benefits, the Social Security Administration (SSA) will compare your condition to a listing of conditions known as the Social Security Blue Book ( The Blue Book contains a listing of all of the conditions that could possibly qualify an individual for Social Security Disability benefits, along with the criteria that must be met in order to be approved for benefits under each listing.
Unfortunately fibromuscular dysplasia is not listed in the SSA's Blue Book. If you have an associated condition that is listed in the Blue Book, however, such as aneurysms or dissections, you may be able to qualify under those Blue Book listings. 
For those who are suffering from aneurysms, you could apply for benefits under Section 4.10 of the Blue Book. According to this listing, in order to qualify for benefits you must be able to prove that:
  • You suffer from an aneurysm of aorta or major branches due to any cause
  • The aneurysm has been demonstrated by medically acceptable imaging
  • The aneurysm is with dissection and not controlled by prescribed treatment
If you do not have any conditions that are listed in the Blue Book, you may still qualify for Social Security Disability benefits under a vocational allowance. In order to do this, you must prove to the SSA that you are unable to perform any type of work activity that you are qualified for due to your disabling condition. For example, if you have only worked in a warehouse and your doctor has told you that you must avoid lifting and strenuous activity, which can strain the arteries, a written statement from your treating physician stating that you cannot continue to work due to your limitations may help support your Social Security Disability claim. This will affect the SSA's residual functional capacity assessment of your condition.
Technical Requirements for Social Security Disability Benefits
In addition to proving that you are disabled according to the SSA's guidelines, you must also meet technical requirements to be eligible for Social Security Disability benefits. There are two different disability programs available from the SSA and both have their own technical requirements.
Qualifying for SSDI
In order to qualify for Social Security Disability Insurance (SSDI), you must have earned enough work credits through your previous work history. If you are age 31 or older, you must have 20 work credits in order to qualify for SSDI benefits. If you are under the age of 31, you must have worked half of the years since turning age 21. For example, if you are 27, you must have worked for three of the past six years to qualify for SSDI benefits.
Qualifying for SSI
If you do not have enough work credits to qualify for SSDI benefits, you may be able to qualify for SSI (Supplemental Security Income) benefits. SSI is a needs-based program. It is intended for low-income individuals and families. In order to qualify for SSI benefits, your monthly income cannot exceed $710 as an individual or $1,060 as a couple. Your household assets must also not exceed $2,000 as an individual or $3,000 as a couple. 
Applying for Social Security Disability Benefits
You can apply for Social Security Disability benefits online ( or in person at your local Social Security office. If you are applying in person, make sure that you bring copies of medical records that prove that your condition meets a Blue Book listing, as mentioned above, or that you are unable to perform any type of work activity whatsoever. You will also be asked to fill out a number of forms. Make sure you fill out each form in its entirety and answer the questions with as much detail as possible so the SSA understands how your condition prevents you from performing any type of work activity. If you are applying online, you will be provided with a cover sheet that will allow you to fax your medical documentation in. You will receive a decision regarding your disability claim within three to six months of the date of your application. 

Article by Ram Meyyappan
Social Security Disability Help

Monday, June 10, 2013

the afternoon nap society: Dr. Mike Sevilla Has Left The Virtual Building

Bravo Afternoon Napper! Dr. Sevilla is a leader and an ethical mentor to many. He leaves behind a legacy of of empathy, compassion and defines what participatory medicine is. Many have learned from his wisdom and knowledge. 

the afternoon nap society: Dr. Mike Sevilla Has Left The Virtual Building: Hearing of Dr. Mike Sevilla's decision to leave the realm of healthcare and social media was like stumbling across the obituary notice o...

Thursday, February 28, 2013

Rare Disease Day 2013

I have not blogged in awhile, but today has been an incredible day! I have little energy to write so here is my video blog:
Thank you President Obama for addressing rare disease with our nation!

To my elected officials:
President Obama
Representative Walz
Senator Franken
Senator Klobuchar

We need funding for Fibromuscular Dysplasia (FMD)/ Ehlers Danlos Syndrome
(EDS) National Institute on Aging/NIH's Connective Tissue Disorders;
Clinical and Molecular Manifestations of Heritable, Disorders of
Connective Tissue Study, Principal Investigator: Nazli McDonnell, M.D.,

Please support rare disease research.

Warmest Wishes on Rare Disease Day 2013!

Kari Ulrich

Fibromuscular Dysplasia and Ehlers Danlos Syndrome