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Patient Stories

Testimonials

Read stories and experiences from patients, caregivers, and medical professionals who have worked with the National Leiomyosarcoma Foundation.

These testimonials reflect the impact of NLMSF's dedication to providing support, education, and resources to the LMS community, as well as our commitment to advancing research initiatives.

Research Clinicians

Learn how clinician leaders and researchers describe the impact of NLMSF and the LMS community.

Dr. M. Druta

Dr. M. Druta

Research Clinician

"You are doing so much for so many" You should be proud of all you have accomplished within the Foundation.

Dr. Sant Chawla

Dr. Sant Chawla

Research Clinician

"NLMSF is recommended for patients and care givers looking for information on Leiomyosarcoma."

Dr. Raphael Pollock

Dr. Raphael Pollock

Research Clinician

The NLMSF provides a vital link between the community, including LMS patients, and the oncology researchers who work tirelessly to help develop a better understanding of this rare disease, with the direct intent to provide sorely needed new...

Dr. Roberta Sanfilippo

Dr. Roberta Sanfilippo

Research Clinician

The LMS Roundtable offers the possibility to work with all researchers in the world dedicated to a rare tumor such as LMS - gathering the community of experts dedicated to LMS and hearing the patients' perspectives as well. It is an honor t...

Dr. S. Okuno

Dr. S. Okuno

Research Clinician

"You and Mitch are doing great things in the Foundation, and the Research Roundtable approach to taking things to the next level - this is a good thing!"

Dr. Rebecca Gladdy

Dr. Rebecca Gladdy

Research Clinician

"I am very much engaged in understanding LMS and hoping to improve care. Annie and Mitch are such great patient advocates which I admire."

Dr. Evan Rosenbaum

Dr. Evan Rosenbaum

Research Clinician

No better way to advance LMS research - the Roundtable is an achievement to focus on LMS-specific study, and harness scrambled data with different histology's of various sarcomas - a clear signal for this disease type.

Dr. W. J. Van Houdt

Dr. W. J. Van Houdt

Research Clinician

I strongly support the NLMSF in their efforts to fight LMS by bringing together world-wide experts - this is a major achievement. Together we are stronger and smarter to fight this disease.

Dr. B. Van Tine

Dr. B. Van Tine

Research Clinician

This is exciting - and the way the Research Roundtable has unfolded is the right approach.

Wantong Yao, PHD

Wantong Yao, PHD

Research Clinician

Thank you so much for all you have done for us and for LMS research community! We really appreciate!

Dr. Matthew Hemming

Dr. Matthew Hemming

Research Clinician

The essential benefit arising from Foundation's LMS Roundtable working groups is the opportunity to bring an assembly of researchers and clinicians into a conversation that spans basic research to clinical application. By working together w...

Dr Seth Pollack

Dr Seth Pollack

Research Clinician

I love the NLMSF - I love the patient programs held - your signature support advocacy to collaborate with sarcoma centers. LMS is common enough to have had a specific focus initiative- and the NLMSF was many steps ahead of the curve, to lau...

Dr. Sebastian Bauer

Dr. Sebastian Bauer

Research Clinician

Dear Annie and Mitch - Thank YOU for supporting the cause You could have just done other stuff. But you choose to fight for this disease. It makes and will further make a difference!!

Bruce and Beverly Shriver

Bruce and Beverly Shriver

Research Clinician

You have made a huge difference in the infrastructure of the NLMSF. You should be proud of what you have done. Beverly and I congratulate you both! It is a great Foundation.

Dr. Arun Singh

Dr. Arun Singh

Research Clinician

I think that the LMS Research Roundtable is a valuable model of bringing clinicians and scientists together to discuss the state of LMS and to develop ideas for pushing the field forward.

Dr Sandra D'Angelo

Dr Sandra D'Angelo

Research Clinician

Annie and Mitch! Thanks for all you for our patients.

Patient Stories

Voices from patients and caregivers sharing the impact of NLMSF support and guidance.

Catharine

Catharine

Patient

You and Mitch are heroes to our family.

Rebecca

Rebecca

Patient

"Thank you, you both are a light where there is fog."

David Matanic

David Matanic

Patient

I was diagnosed with LMS just one week ago. Annie Achee and her husband called me and spent about 45 minutes telling me what to expect, what questions to ask and the kind of specialists I would need. It was the most valuable 45 minutes of m...

Mary

Mary

Patient

Thank you 100x's over, thank you. I have been praying and asking God to send me someone good and kind to help me. Thank you both for all your doing. Only wish you could be with me and hold my hand. You're wonderful! Thank you. Sincerely, Ma...

Sharon

Sharon

Patient

Annie and Mitch are both so special, and make me want to live in this world. I love you guys and NLMSF.

Carolyn

Carolyn

Patient

NLMSF: Thank you so much for your kind words and your recommendations regarding speakers and your great passion and commitment got us to the finish line in pulling this Rare Cancer / Sarcoma Webinar program together. All is possible with ou...

ED

ED

Patient

We are all interconnected through one big LIFE, Annie, so it is each of our duty to be mutually supportive. Looking forward to your new and useful insights.

Cathie

Cathie

Patient

NLMSF is a wonderful place to help you feel that you are not alone in your LMS journey. You will have access to knowledge, practical tips, resources, and, best of all, contact with others who may be newly diagnosed or long term thrivers. It...

Hanna

Hanna

Patient

Thank you so much with all of your help, if my situation is getting worst, I will contact you to ask for help again. Here is Canada, it is so different to US, and in Vancouver, we dont have many options. In my heart, I am always thinking of...

Edith

Edith

Patient

Annie thanks for your warm words for me and for my country. Yaacov is getting all the best treatment that our country can offer, but now its only a miracle or a new medicine that can help. I feel lucky to have you in my life.

Darlene

Darlene

Patient

Dear Annie and Mitch, thank you so very much for your Godly service, direction, precious time, and great knowledge. You have given me a new perspective. You are an awesome duo and I am grateful for your wonderful work.

Pamela

Pamela

Patient

In 2012, I was diagnosed with leiomyosarcoma, but had never heard of it. God allowed me to be part of something that changed how I wanted to fight this. I learned that I must fight and teach as many people as I can that are fighting cancer....

Sharon

Sharon

Patient

NLMSF is a wonderful place to help you feel that you are not alone in your LMS journey. You will have access to knowledge, practical tips, resources, and, best of all, contact with others who may be newly diagnosed or long term thrivers. It...

Evan

Evan

Patient

From the bottom of our hearts, thanks for all the great work that you do for LMS. It is clear that your organization goes above and beyond the call of duty. I admire the work and the diligent efforts to research and aid in moving forward in...

Michelle

Michelle

Patient

I found NLMSF 3 years after my diagnosis of LMS; wish I'd found them sooner. The resources and information they provide is so helpful and the foundation's commitment to furthering research on this disease is vital.

Christina

Christina

Patient

Thank you NLMSF and Annie for your support and giving me information to get under the best hospital and doctor care.

Emily

Emily

Patient

Thank you so much for your note. You two make our whole family feel enfolded in your care and love. We are so grateful for you.